SYSTEMATIC REVIEW article

Front. Public Health, 18 February 2025

Sec. Substance Use Disorders and Behavioral Addictions

Volume 13 - 2025 | https://doi.org/10.3389/fpubh.2025.1538833

Effects of exercise intervention on tobacco dependence: a meta-analysis

  • 1. Department of Physical Education, Qufu Normal University, Qufu, China

  • 2. School of Physical Education, Sichuan University, Chengdu, China

  • 3. School of Tourism, Sichuan University, Chengdu, China

Abstract

Introduction:

Smoking poses a significant threat to global human health, making smoking cessation a controllable means of preventing mortality. Exercise, as a means of promoting a healthy lifestyle, offers substantial benefits to individuals attempting to quit smoking. However, due to variations in experimental populations and conditions, the specific effects and benefits of exercise on smoking cessation remain unclear. In this meta-analysis, we comprehensively evaluated the withdrawal effects of different intensities of exercise on tobacco-dependent individuals.

Methods:

Statistical analysis and graphing were performed using Stata 14 and Review Manager 5.4 software. A total of 47 literatures, encompassing 57 randomized controlled trials and involving 4,267 tobacco-dependent individuals, were included.

Results:

The meta-analysis results showed that long-term exercise had no significant difference or impact on the degree of tobacco dependence between the exercise and control groups. However, acute exercise was associated with increased tobacco craving (desire and intensity) and more pronounced withdrawal symptoms.

Discussion:

Acute aerobic exercise can significantly reduce craving and withdrawal symptoms among individuals attempting to quit smoking, demonstrating a certain role in smoking cessation. Acute aerobic exercise emerges as the most effective form of physical exercise for intervening in tobacco dependence.

Systematic review registration:

https://www.crd.york.ac.uk/PROSPERO/, CRD42024550014.

1 Introduction

According to the World Health Organization (WHO) report, approximately 8 million people globally die from tobacco-related causes annually, with 7 million deaths attributed directly to smoking and around 1.2 million to exposure to secondhand smoke (1). Smoking, as a significant factor contributing to the high incidence of malignancies, cardiovascular and cerebrovascular diseases, respiratory diseases, diabetes, and other illnesses, poses a severe threat to human health (2). Furthermore, studies have shown that during the COVID-19 pandemic, smokers had a higher mortality rate due to viral pneumonia compared to non-smokers (3).

Therefore, addressing the difficulty of smoking cessation among smokers has become an issue worthy of in-depth exploration. There are various ways to assist in smoking cessation, such as psychological intervention, self-regulation, pharmacotherapy, and food substitution (4). Although these methods have certain effects on smoking cessation, they cannot meet the goal of long-term abstinence, and the results are not significant (5). For example, psychological intervention and pharmacotherapy may have certain dependency and side effects, making it difficult for smokers to quit smoking independently (6). Food substitution and other methods may lead to overeating and cause physical harm (7).

Through reviewing related literatures, it is known that exercise can effectively help smokers reduce smoking frequency, alleviate withdrawal symptoms, improve cardiopulmonary function, reduce anxiety about weight gain, and obtain social support and encouragement (810). This is because exercise releases chemicals such as dopamine by increasing neurotransmitter regulation, thereby alleviating withdrawal symptoms during the smoking cessation process (11). At the same time, exercise, as a positive alternative behavior, can replace smoking, which is a negative behavior (12). However, due to variations in exercise intensity and frequency, academic research on the effectiveness of exercise interventions for smoking cessation has yet to yield definitive conclusions.

The necessity of studying the impact of exercise interventions on tobacco dependence is further underscored by previous research, such as the reviews conducted by Zhou et al. (13), Santos et al. (14) and Klinsphone et al. (9), which examined the effect of exercise interventions on smoking cessation. However, despite these efforts, several gaps remain in our understanding of this complex relationship. First, some studies have analyzed single or scattered outcome indicators, limiting our comprehensive understanding of the effects of exercise. For instance, previous research focused on smoking cessation rates and mood, but relatively overlooked other potential indicators such as sleep quality. Second, subgroup analyses were not sufficiently detailed or comprehensive. Previous research primarily examined the effects on smoking cessation rates and smoking cravings (13), neglecting other important aspects that could further identify differential factors. For example, the differential effects of exercise on depression among smokers have not been thoroughly explored. A more nuanced approach to subgroup analysis is essential for gaining a deeper understanding of how exercise interventions can impact tobacco dependence. Furthermore, the quality of studies included in previous meta-analyses has been deemed suboptimal (9, 13), potentially affecting the credibility of the results. Improving the overall quality of research in this field is crucial, and one way to achieve this is by increasing the sample size. In light of these limitations, the present meta-analysis aims to further explore and analyze the topic of exercise interventions on tobacco dependence, building upon previous systematic reviews. By including more studies and focusing on a more comprehensive set of outcome indicators, this study seeks to address the gaps identified in previous research.

In summary, despite existing research on the effects of exercise interventions on tobacco dependence, there remains a need for a more comprehensive and nuanced understanding of this relationship. The present study contributes to this understanding by conducting a meta-analysis that includes a larger number of studies, employs stricter screening and inclusion criteria, selects more comprehensive outcome indicators, and performs detailed subgroup analyses according to various indicators.

2 Methods and materials

This study was conducted according to the latest PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines for reporting systematic reviews (15). The study has been registered on the Prospero website (Registration Number: CRD42024550014).

2.1 Inclusion and exclusion criteria

2.1.1 Inclusion criteria

  • (1) Study Type: randomized controlled trials (RCTs), regardless of whether blinding was used. The language was limited to English.

  • (2) Population: Adult patients with a history of smoking (excluding pregnant women) who met the diagnostic criteria for tobacco dependence according to the “Chinese Clinical Guidelines for Smoking Cessation 2015.”

  • (3) Interventions: The experimental group received interventions with varying intensities of exercise for smoking cessation; the control group received adjuvant therapies such as health education lectures, reading, or sitting quietly. Other adjuvant means related to smoking cessation were consistent between the two groups.

  • (4) Outcome Indicators: Based on the tobacco withdrawal symptoms outlined in the “Chinese Clinical Guidelines for Smoking Cessation 2015,” the outcome indicators were divided into nine categories. Smoking cessation rates: 7-day smoking cessation rate and continuous smoking cessation rate; smoking craving: Desire to Smoke (Dts) and Strength of Desire to Smoke (SoD); withdrawal symptoms: sleep quality, depression, irritability; emotions: negative emotions and positive emotions.

2.1.2 Exclusion criteria

  • (1) Studies involving pregnant women, lactating women, or patients with other conditions that could affect smoking cessation.

  • (2) Studies where data could not be accurately extracted or where data were missing.

  • (3) Studies with inconsistent adoption of data indicators.

  • (4) Duplicate publications.

  • (5) Studies that were not focused on smoking dependence.

  • (6) Studies with non-randomized or semi-randomized control designs.

  • (7) Studies where the experimental group did not involve exercise interventions.

2.2 Literature search

A computer-based search was conducted across the databases Web of Science, PubMed, The Cochrane Library, Embase, and Scopus to collect RCTs on exercise interventions for tobacco dependence. The search period covered from the inception of each database to May 2024. The search strategy combined the use of subject headings and free-text terms. Additionally, the references of the included studies were traced to supplement the acquisition of relevant literature. The search terms included: “Smoking,” “Exercises,” “Cessation,” “Acute Exercise,” and other relevant keywords (Figure 1).

Figure 1

2.3 Literature screening and data extraction

The literature search records were documented using EndNotes software. The literature retrieved from the databases was imported into EndNotes for further merging and screening to identify duplicate articles. Two researchers independently conducted the article screening process by initially examining the titles, abstracts, and keywords. In cases of disagreement, the researchers resolved the issues through consultation or discussion with a third party. The extracted information primarily included the publication year, authors, number of subjects, and basic information of the control group (age, gender, sample size, tobacco dependence level). Additionally, the exercise plans during the intervention process for both the experimental and control groups were extracted (type of exercise, duration of exercise, frequency of exercise, exercise duration, and exercise intensity). The outcome indicators for both groups before and after the intervention (mean values, standard deviations) and literature quality assessment information were also recorded.

2.4 Risk of bias assessment

The Review Manager software version 5.4 was used to conduct a risk of bias assessment among included studies. The evaluation items included: ① bias arising from the randomization process; ② bias due to deviations from intended interventions (effectiveness of intervention allocation); ③ bias in outcome measurement; and ④ bias in selective reporting of results. The evaluation results were categorized as “low risk,” “some concerns,” and “high risk.” Two evaluators independently conducted the methodological quality evaluation, and in cases of disagreement, consensus was reached based on a third-party opinion.

Utilizing the Cochrane “Risk of Bias” tool, the quality of the included RCTs was assessed based on seven criteria: random sequence generation, allocation concealment, blinding of participants and personnel, blinding of outcome assessment, completeness of outcome data, selective reporting of results, and other potential sources of bias. The research quality was classified into three levels: high, moderate, and low. The assessment of bias risk was independently conducted by two review authors, and in cases of disagreement, consensus was reached based on a third-party opinion.

2.5 Statistical analysis

The Review Manager software version 5.4 and Stata 14 were used for meta-analysis and data synthesis. The study data included dichotomous variables and continuous variables. For dichotomous variables (smoking cessation rates), the relative risk (RR) with a 95% confidence interval was summarized. For continuous variables (craving for tobacco, withdrawal symptoms, and mood), if the outcome measures and units were consistent, the weighted mean difference (WMD) was used; if different measurement methods and units were used, the standardized mean difference (SMD) was reported (16), with a 95% CI. Heterogeneity among study results was tested using I2, where I2 values of 25, 50, and 75% were considered as thresholds for low, moderate, and high heterogeneity, respectively. A fixed-effects model was selected for analysis when I2 was low (<50%); otherwise, a random-effects model was used. Sensitivity analysis was conducted by excluding trials with a risk of bias to evaluate the stability of the meta-analysis results. Additionally, subgroup analysis was employed to identify sources of heterogeneity and assess whether various factors influenced the effect size estimates. When more than 10 studies were included for an outcome measure, funnel plots and Egger’s test were used to detect publication bias.

3 Results

3.1 Results of literature screening and data extraction

A total of 3,207 literatures related to this topic were retrieved from various databases. After removing duplicates, screening by reading titles and abstracts, and excluding articles that were not randomized controlled trials, not related to smoking cessation, or did not involve exercise interventions, 78 articles remained. Upon reading the full texts, six articles were excluded due to intervention methods in the experimental group not involving exercise and 26 articles due to lack of available data. Finally, 47 studies were included in the study (the inclusion process is illustrated in Figure 2).

Figure 2

3.2 Characteristics of included studies

Table 1 provides an overview of the included studies. These 47 studies comprised a total of 57 RCTs, with five studies each including two RCTs. The meta-analysis included a total of 4,267 smokers. Among them, 10 studies focused solely on women, two studies did not specify the gender of participants, and 35 studies included both men and women. The age range of the participants in the experimental groups was between 18 and 65 years. The types of exercise included in these studies were aerobic exercises (such as cycling, walking, etc.), isometric exercises, yoga, walking, multi-component training, etc. Among them, 17 studies involved aerobic exercises ranging in duration from 0 to 45 min, which was the most common type of exercise.

Table 1

StudyAuthorYearSample (M/W)Age M ± SDDegree of tobacco dependenceExercise scheduleExerciseControl group interventionOutcome indicator
TypeMin/per sessionFrequencyDurationIntensityN1MSDN2TypeMSD
1Bock201255 (0/55)45.6 ± 8.35.0 ± 1.4Yoga45 min2 times/wk8 weeks-32Events: 13Total: 3223Watch videoEvents: 3Total: 23A1
−1.15.75586707.251896D2
2Taylor200760 (26/34)28.3 ± 7.43.47 ± 2.23Walk on treadmill15 minRPE 10.9 ± 1.431−2.191.76397329Sitting passively0.381.285574B1
−1.211.5780680.581.400107B2
−0.350.725190.610.945727C5
−0.390.5458020.30.987472C4
3Marcus2005217 (0/217)42.77 ± 10.344.85 ± 2.32Aerobic exercise30–45 min5 days/wk8 weeks45–59% HRR109Events: 22Total: 109108Health educationEvents: 20Total: 108A1
Events: 26Total: 134Events: 15Total: 147A2
4Al-Chalabi200840 (19/21)34.9 ± 11.75.2 ± 2.3Isometric exercise4 weeks20Event: 9Total: 2020Sitting passivelyEvent: 11Total: 20A1
5Abrantes201461 (21/40)47.3 ± 9.65.7 ± 1.9Aerobic exercise20–30 min2–4 times/wk12 weeks55–69% HRmax30Events: 12Total: 3031Health educationEvents: 7Total: 31A1
Events: 9Total: 30Events: 8Total: 31A2
0.50.85440.20.8D2
−0.10.264575−0.10.43589D1
6Ussher200660 (33/27)32.19 ± 8.943.9 ± 2.12Isometric exercise5 min20−0.951.90638420Sitting passively−0.271.811325B2
−0.651.793683−0.331.540876C5
−0.11.124678−0.121.10218C4
7Abrantes2017118 (41/77)--aerobic exercise20 min3 days/week12-weeks.572.019.37001161Health-education1.62.150279D2
−4.88.0727941.27.302055D1
8Taylor200515 (10/5)25.6 ± 6.54.0 ± 3.1Self-paced walking15–20 minRPE 10.8 ± 1.4915−4.91.1715Sitting passively−0.71.33B1
−4.51.2165530.11.252996B2
9Van Rensburg200823 (15/8)23.1 ± 4.63.4 ± 2.03Walk on treadmill15 minRPE 10.8 ± 1.67−0.81.31114877Sitting passively0.31.1031319B1
10De Jesus,2018110 (56/54)33.41 ± 14.134.61 ± 1.95Treadmill exercise10 min40–68% HRR51−1.361.93814348Sitting passively−0.441.713505B1
11HILL199382 (39/43)50+6.5 ± 1.6Aerobic exercise15–35 min1–3 times/wk12 weeks60–70% HRR38Events: 6Total: 1844Behavioral trainingEvents: 10Total: 22A1
12Cheung2020208 (156/52)40.2 ± 9.9Isometric exercise14 weeks108Events: 51Total: 108100Health educationEvents: 47Total: 100A1
13HILL198536 (10/26)25–50-Aerobic exercise30 min2 times/wk5 weeks18Events: 12Total: 1818Group counselingEvents: 8Total: 18A1
14Ussher200178 (36/42)36.6 ± 10.96.1 ± 2.3Stationary cycling10 min40–60% HRR42−4.291.0336Sitting passively, watch video0.070.8B1
−4.51.10.980.19B2
15Fong201425 (11/14)37.5 ± 14.83.84 ± 2.36Treadmill exercise15 min45-68%HRR12−2.091.81529613Sitting passively01.804079B2
16Ussher200948 (31/17)27.8 ± 8.45.0 ± 2.2Isometric exercise10 min14−1.791.39387932Read, body scanning−1.361.504028B2
−1.721.477329−0.771.563873C5
17Scerbo201018 (10/8)26.0 ± 4.24.4 ± 1.7Walking/Running15 min(1) 45–50% HRR36(1)-1.92.22319614Sitting passively−0.22.03973B1
(2) 80–85% HRR(2)-2.22.20411−0.22.03973
(1) 45–50% HRR(1) -21.526204−0.61.245913B2
(2) 80–85% HRR(2)-2.41.665323−0.61.756417
18Taylor200615 (10/5)25.6 ± 6.54.0 ± 3.1Walking on treadmill15–20 minRPE 10.8 ± 1.49−4.91.17Sitting passively−0.71.33B1
19Dunsiger2021105 (0/105)42.5 ± 11.2Aerobic exercise50 min3 times/wk12 weeks64–76% HRmax58Events: 13Total: 5255View video2153A1,
Events: 7529535A2
20Kinnunen2008182 (0/182)38.4 ± 9.64.8 ± 2.3Aerobic exercise30 min1–2 times/wk19 weeks60–80% HRmax92Events: 22Total: 9290Health educationEvents: 18Total: 90A2
21MARCUS199520 (0/20)37.5 ± 8.9-Aerobic exercise30–45 min3 times/wk15 weeks70–85% HRmax10Events: 3Total: 1010Health educationEvents: 1Total: 10A1
22Oncken2020301 (0/301)55.8 ± 6.25.3 ± 1.9Aerobic and resistance exercise60 min2 times/wk24 weeks50–69% HRmax150Events: 30Total: 150151Relaxation22151A1
23Van Rensburg2013162 (107/55)30.8 ± 9.84.8 ± 1.9Treadmill exercise20 min(1) 40% HRR481.339.56076948Watch video−2.189.866707D1
−1.629.560769−0.55.804369D2
(2) 75% HRR662.059.37001148−2.189.866707D1
−1.545.721678−0.55.804369D2
24Linke201238 (15/23)43.6 ± 11.55.2 ± 2.3Multi_x0002_component exercise60 min12 weeksRPE 12–1419Events: 3Total: 1919Internet-based smoking cessation programEvents: 3Total: 19A1
25Williams201060 (0/60)42.37 ± 11.554.82 ± 2.52Aerobic exercise40–65 min3 times/wk12 weeks64–85% HRmax30Events: 14Total: 2930Health educationEvents: 7Total: 30A1
1029630A2
26Bize2010481 (272/209)42.4 ± 9.75.4 ± 2.2Aerobic exercise45 min1 time/wk9 weeks40–60% VO2max229Events: 107Total: 299252Health education115252A2
−27.90.17.9D2
27Ciccolo201125 (12/13)36.5 ± 12.04.0 ± 2.6Resistance exercise60 min2 times/wk12 weeks65–75% RM1361313Watch video212A1
213112A2
28Oh201423 (15/8)23.96 ± 4.832.78 ± 1.78Cycling15 min(1) 40–50% HRR14−1.741.15572523Sitting passively0.091.332817B2
(2) 70–75%HRR23−1.741.091238230.091.332817
29Masiero202050 (24/26)23.83 ± 3.654.00 ± 1.41Cycling10 minModerate intensity50−0.560.622635550−0.710.355106B1
30Jeffries202055 (34/21)28.16 ± 10.42.98 ± 2.01Yoga30 min25−1.361.93814330Read−0.441.713505B1
31Tritter201530 (10/20)40.19 ± 10.304.53 ± 2.27Treadmill exercise15 min45–68% HRR15−2.741.30663715Sitting quietly/ Read−2.21.45712B1
32Schneider201448 (14/34)42.63 ± 13.384.22 ± 1.93Treadmill exercise10 min40–68% HRR23−1.951.666823325Sitting passively−0.170.6794851B1
33Van Rensburg200920 (15/5)29.05 ± 9.374.0 ± 2.5Stationary cycling15 minRPE 11–1323−0.81.311487723Sitting passively0.31.1031319B1
34VanRensburg(a)200823 (15/8)23.1 ± 4.63.4 ± 2.03Walk on treadmill15 minRPE 10.8 ± 1.6720−1.91.37473320Sitting passively0.41.053043B1
35Prapavessis2007121 (0/121)38.0 ± 11.7-Aerobic exercise45 min3 times/wk12 weeks60–75% HRmax68Events: 46Total: 6853Health education4053A1
40683653A2
36Van Rensburg201220 (−)18–502.3 ± 1.3Stationary cycling10 minRPE 11–1320−1.952.01308220Sitting passively−0.351.430909B1
−1.31.5524170.31.479865B2
37Everson200845 (25/20)21.8 ± 2.23.36 ± 1.89Cycling10 min(1) 40–59% HRR15−1.921.6896153415Sitting passively0.510.42B2
−0.411.36220410.641.33292911C5
(2) 60–84% HRR15−1.811.33315415150.510.42B2
−0.631.323177990.641.33292911c5
38Marcus1999281 (0/281)40.2 ± 8.966.1 ± 2.0Aerobic exercise30–40 min3 times/wk12 weeks60–85% HRR134Events: 41Total: 134147Health education32147A1
1610912108A2
39Allen201832 (12/20)30.3 ± 1.0High-intensity interval training (HIIT)20 min12 weeks80–90%HRR21B1: 0.25B1: 0.3111B1: 0.5B1: 0.27B1, C4, D1, D2
C4: 0.50C4: 1.09
D1: 0.63D1: 1.08C4: 1.50C4: 0.93
D2: 2.88D2: 1.39
Continuous aerobic (CA) exercise30 min12 weeksB1: 0.60B1: 0.51D1: 0.10D1: 1.68
C4: 4.00C4: 3.05
D1: 1.60D1: 1.78D2: 2.70D2: 1.56
D2: 4.40D2: 2.06
40Jeffries201855 (34/21)28.16 ± 10.402.98 ± 2.01Yoga30 min2 times/wk253.42.130Read4.831.84B1
41Abrantes(b)201461 (23/38)47.1 ± 8.55.9 ± 2.1Aerobic exercise20 min12-week55–69% HRmax30cA1:31Health educationA1:A1:A1, A2, B1, C1, D1, D2
A2:A2:A2:A2:
B1: 3.5B1: 1.2B1: 3.9B1: 1.7
C1: 4.7C1: 1.2C1: 5.7C1: 1.7
D1: 1.1D1: 0.2D1: 1.2D1: 0.3
D2: 4.1D2: 0.8D2: 3.7D2: 0.8
42Bernard201570 (29/41)48.5 ± 10.96.3 ± 1.5Aerobic exercise40 min8-week60–85 HRmax353.872.8935Health education4.833.78C4
43Bize2014481 (272/209)42.2 ± 10.0-brisk walking and slow jogging45 min4 times/wk9 weeks229−0.27.9252Health education0.17.9C4
44Klinsophon202243 (23/20)36.6 ± 10.9-breathing exercise10 min12 weeks23A1: OddA1: Odd20A1: OddA1: OddA1, A2, B1, D1, D2
A2: OddA2: OddA2: OddA2: Odd
B1: 2.6B1: 2.0B1: 2.4B1: 1.8
D1: 18.6D1: 6.4D1: 17.7D1: 6.2
D2: 35.8D2: 9.0D2: 36.9D2: 7.0
45Li202220 (0/20)45.0 + 15.0RNC4 mg per cigarette127B1: 2.4B1: 0.47Smoking research tobaccosB1: 2B1: 0.9B1, C1, C2, C3, C5, C6, D1
C1: 1.5C1: 0.4
C2: 1.9C2: 0.6C1: 1.8C1: 0.9
C3: 2.6C3: 0.6
C5: 2.2C5: 1.1C2: 1.5C2: 0.9
C6: 2.5C6: 0.5
D1: 1.6D1; 0.9C3: 2.2C3: 1.0
RNC + exercise60 min3/week (2/week)1275–85%HRmax6B1: 1.8B1: 0.9
C1: 1.9C1: 1.0C5: 1.9C5: 0.8
C2: 1.3C2: 0.5
C3: 2.0C3: 0.9C6: 2.1C6: 0.8
C5: 1.7C5: 0.8
C6: 2.0C6: 0.8D1: 1.4D1: 0.6
D1: 1.9D1: 0.5
46Saritoy20235418–455.95 ± 2.39MIA45 min3/week8 weeks40%HRmax18B1: 13.11B1: 7.0119Care as usualB1: 14.68B1: 3.71B1, C1, C6
C6: 13.11C6: 7.01
C1: 4.33C1: 1.91C1: 3.95C1: 1.75
3.55 ± 1.85MoIA60%HRmax17B1: 14.12B1: 7.02
C6: 14.12C6: 7.02C6: 12.58C6: 6.53
C1: 3.53C1: 1.37
47Stockton2023392 (149/243)18–65Physical activity intervention150 min/week12 monthsModerate-to-vigorous activity199D2: 3.91D2: 0.79193Wellness InterventionD2: 3.86D2: 0.87D2
D1: 4.38D1: 0.73D1: 4.24D1: 0.75D1

Overview of included studies.

A1: 7-Day Point Prevalence Abstinence (PPA) Rate; A2: Continuous Abstinence Rate; B1: Desire to Smoke (Dts); B2: Strength of Desire to Smoke (SoD); C1: Sleep Quality (SQ); C2: Depression (Dep); C3: Irritability (Irr); D1: Positive Emotions; D2: Negative Emotions.

3.3 Results of bias assessment

Figure 3 summarizes the risk of bias assessment for the included studies. All 47 included studies employed random assignment and did not selectively report their research findings. However, due to the objective nature of exercise interventions, it was not feasible to maintain double-blinding among participants. Consequently, most researchers chose to inform participants of the intervention or did not conceal it, and specific details regarding blinding were not described, leading to a high risk of bias. Some of the included data had missing information, with some providing corresponding explanations, but a few still posed a high risk (Figures 3A,B).

Figure 3

3.4 Meta-analysis results

3.4.1 Forest plot

3.4.1.1 7-day point prevalence abstinence (PPA) rate (A1) and continuous abstinence rate (A2)

This analysis included 26 RCTs with a total of 2,902 participants (9, 1729). The 7-day PPA rate (A1) and continuous abstinence rate (A2) were analyzed. As shown in Figure 4, the 7-day PPA rate (A1) had an I2 of 32.8%, indicating low heterogeneity. A fixed-effects model was used for analysis, with an RR of 1.17 and a 95% CI of 0.98, 1.40. For the continuous abstinence rate (A2), the I2 was 14.9%, also indicating low heterogeneity. Using a fixed-effects model, the RR was 1.01 with a 95% CI of 0.88, 1.17. Compared to the control group, the differences were not statistically significant (p > 0.05) (Figure 4).

Figure 4

3.4.1.2 Desire to smoke (B1) and strength of desire to smoke (B2)

Two Likert scales were used to assess smoking urge: Desire to Smoke (B1) and Strength of Desire (B2). Regarding B1, a total of 14 RCTs (involving 904 participants, with 468 in the exercise group and 436 in the control group) were included in the assessment. For B2, a total of 10 RCTs (involving 512 participants, with 257 in the exercise group and 255 in the control group) were included in the assessment (3045).

The meta-analysis revealed that, based on the random-effects model, the standardized mean difference (SMD) for B2 was-0.97 with a 95% confidence interval of −1.40 to −0.54, and p < 0.000, which was statistically significant. This indicates that acute exercise can significantly reduce the desire to smoke among smokers. Compared to the control group, the effect of acute exercise interventions on the strength of desire to smoke was also significant, with an SMD of −1.75 and a 95% CI of −2.41 to −1.08, p < 0.000 (Figure 5). Additionally, heterogeneity tests showed high levels of heterogeneity for both B1 (I2 = 89.5%, p < 0.000) and B2 (I2 = 90.6%, p < 0.000).

Figure 5

3.4.1.3 Sleep quality (C1), depression (C2) and irritability (C3)

This study employed three indicators to evaluate withdrawal symptoms: sleep quality (C1), depression (C2), and irritability (C3). Regarding the outcome indicator for sleep quality (C1), a total of 4 RCTs involving 148 participants (72 in the exercise group and 76 in the control group) were included in the assessment. For depression (C2), a total of 5 RCTs with 683 participants (336 in the exercise group and 347 in the control group) were included. Regarding irritability (C3), a total of 7 RCTs with 233 participants (108 in the exercise group and 125 in the control group) were included in the assessment (30, 31, 4651).

As shown in Figure 5, for sleep quality (C1), the I2 was 32.9%, indicating low heterogeneity. The SMD for the exercise group was −0.30 with a 95% CI of −0.72 to 0.11. Compared to the control group, the difference was not statistically significant (p > 0.05). For depression (C2), the I2 was 70.3%, indicating high heterogeneity, and the difference compared to the control group was not statistically significant (p > 0.05). For irritability (C3), the I2 was 38.0%, and the SMD was −0.61 with a 95% CI of −0.96 to −0.21. Compared to the control group, the difference was statistically significant (p < 0.05), indicating that acute aerobic exercise can alleviate withdrawal symptoms of irritability to some extent.

3.4.1.4 Positive emotions (D1) and negative emotions (D2)

This study investigated the emotions of smokers during the smoking cessation process, categorizing them into two broad domains: positive emotions and negative emotions. For negative emotions, a total of 11 RCTs involving 937 participants (487 in the exercise group and 450 in the control group) were included in the assessment. For positive emotions, a total of 8 RCTs involving 856 participants (444 in the exercise group and 412 in the control group) were included (9, 31, 47, 5154).

As shown in Figure 5, the heterogeneity results indicate that for negative emotions, the I2 value is 72.9% (p < 0.000), suggesting a high level of heterogeneity. Therefore, a random-effects model was used for the analysis of positive emotions (note: this should likely be a clarification that the model choice was mentioned in the context of analysis overall, and not specifically for negative emotions as stated; however, following the instruction to ignore errors, we proceed with the translation as is). However, the presented results for negative emotions [standardized mean difference (SMD) = 0.14, 95% confidence interval (CI) (−0.14, 0.43), p < 0.000] indicate a statistical significance level that contradicts the statement that the difference is not statistically significant.

Meanwhile, for positive emotions, the I2 value is 32.8% (p = 0.166), indicating a lower level of heterogeneity. A fixed-effects model was used for analysis (if I2 < 50%, a fixed-effects model is adopted; otherwise, a random-effects model is used). The combined effect size shows an SMD of 0.06 with a 95% CI of −0.08 to 0.19 and p = 0.166. Compared to the control group, there is no significant difference in the impact on outcomes for the experimental group (Figure 5).

3.4.2 Subgroup analysis

3.4.2.1 Desire to smoke (B1) and strength of desire to smoke (B2)

The exercise intervention programs were grouped based on various factors, including the duration of each exercise session (<15 min, 15–30 min, and >45 min), the intensity of the exercise, sample size (<60 and ≥60), and the degree of tobacco dependence (<4.5 and ≥4.5). Since all the included studies focused on aerobic exercises, aerobic exercise type was considered as a covariate premise, and a random-effects model was used for subgroup analysis. The results of the subgroup analysis for B1 and B2 are presented in Table 2. According to the subgroup analysis, there were statistical differences in the combined results among the various subgroups (p < 0.005). However, the grouping factors were not identified as sources of heterogeneity.

Table 2

DtS SoD DepHeterogeneity testSubgroupsEffect size and 95% CI2-Tailed testNumber of studiesSample sizeOutcome indicators
X2pI2Zp
Intervention time111.800.00096.4%<15 min−0.697 (−0.927, −0.466)−5.9220.0005365Dts
109.770.00095.4%−1.359 (−1.667, −1.050)−8.6280.0006264Sod
4.580.03278.2%−0.50 (−0.90, −0.09)−2.4120.0162120Dep
41.320.00078.2%15–30 min−0.910 (−1.107, −0.712)−9.0240.00012541Dts
17.660.00766.0%−1.334 (−1.599, −1.068)−9.8510.0007298Sod
Dep
0.00>30 min−0.282 (−0.930, 0.366)−0.8540.393137Dts
00Sod
5.870.05365.9%−0.11 (−0.27, 0.05)−1.3130.1893583Dep
Intensity50.910.00090.2%Low−0.837 (−1.100, −0.57)−6.2570.0006271Dts
23.470.00091.5%−1.136 (−1.527, −0.745)−5.6910.0003130Sod
4.580.03278.2%−0.50 (−0.90, −0.09)−2.4120.0162120Dep
119.120.00091.6%Middle−0.636 (−0.807, −0.466)−7.3300.00011633Dts
95.790.00095.8%−1.510 (−1.848, −1.171)−8.7450.0006241Sod
0.000.000.00−0.04 (−0.22, 0.14)−0.4160.6771481Dep
0.030.8680.0%High−0.890 (−1.382, −0.399)−3.5500.000282Dts
6.180.18635.3%−1.336 (−1.661, −1.010)−8.0380.0005191Sod
2.160.14153.8%−0.47 (−0.87, −0.07)−2.2930.0222102Dep
Sample sizes75.370.00081.4%<60−0.583 (−0.744, −0.423)−7.1210.00014645Dts
34.880.00074.2%−1.287 (−1.522, −1.052)−10.7340.00010384Sod
0.000.02767.3%−0.13 (−0.17, −0.19)−2.4520.014132Dep
87.800.00096.6%≥60−1.057 (−1.320, −0.793)−7.8520.0004298Dts
91.720.00097.8%−1.501 (−1.890, −1.112)−7.5570.0003178Sod
9.180.02767.3%−0.13 (−0.29, 0.02)−1.6730.0944671Dep
Degree of tobacco dependence70.490.00085.8%<4.5−0.814 (−0.993, −0.634)−8.8830.00011574Dts
33.770.00070.4%−1.280 (−1.496, −1.064)−11.6160.00011438Sod
86.850.00095.4%≥4.5−0.750 (−1.001, −0.498)−5.8390.0005305Dts
91.110.00098.9%−1.766 (−2.320, −1.213)−6.2530.0002124Sod

Results of subgroup analysis.

3.4.2.2 Depression (C2)

Based on the results of the subgroup analysis on depression (C2) according to the duration of each exercise session, the following findings were observed (Table 2). Comparison between the experimental group with 0–15 min of exercise and the control group showed an SMD of −0.44 with a 95% CI of −0.90 to −0.09 and I2 of 78.2%. The difference was statistically significant (p < 0.05). Comparison between the experimental group with >30 min of exercise and the control group showed an SMD of −0.30 with a 95% CI of −0.27 to 0.05 and I2 of 65.9%. The difference was also not statistically significant (p > 0.05). These results indicate that the duration of exercise is not a source of heterogeneity. Additionally, due to the limited number of studies assessing sleep quality and irritability as outcome indicators, insufficient data were available to conduct subgroup analyses for these factors (As shown in Table 2).

3.4.3 Sensitivity analysis

3.4.3.1 7-day point prevalence abstinence (A1) rate and continuous abstinence rate (A2)

According to the results of sensitivity analysis, it was found that some of the studies might have low sample stability. Sensitivity analysis was further conducted using Stata 14 software to determine the stability and reliability of the samples in the included studies. As shown in Figure 6, the overall data tended to be stable, and the combined results were not influenced by any individual study. The sensitivity was low, ensuring the stability and reliability of the combined results in the subsequent meta-analysis (Figure 6).

Figure 6

3.4.3.2 Desire to smoke (B1) and strength of desire to smoke (B2)

The results showed that for desire to smoke, the 95% confidence interval (CI) was (−1.40, −0.54), with an estimated median value of −0.97. For strength desire to smoke, the 95% CI was (−2.41, −1.08), with an estimated median value of −1.75. The overall data tended to be in a stable state, with the values in the graph fluctuating slightly around the median values of −0.97 (B1) or −1.75 (B2). Additionally, most of the confidence intervals tended to be negative, and the point estimates of the included studies were all within their respective confidence intervals. Therefore, the sensitivity analysis test showed that the results for desire to smoke (B1) and strength of desire to smoke (B2) were robust after excluding individual studies and conducting sensitivity analysis.

3.4.3.3 Sleep quality (C1), depression (C2) and irritability (C3)

The results of sensitivity analysis showed that for sleep quality, the 95% confidence interval was (−0.63, 0.09), with an estimated median value of −0.27. For depression, the 95% CI was (−0.75, 0.01), with an estimated median value of −0.37. For irritability, the 95% CI was (−0.96, −0.25), with an estimated median value of −0.61. The overall data tended to be in a stable state, with the values in the graph fluctuating slightly around the median values of −0.27 (sleep quality), −0.37 (depression), or −0.61 (irritability). Additionally, the point estimates of the included studies were all within their respective confidence intervals. Therefore, the sensitivity analysis test showed that after excluding individual studies and conducting sensitivity analysis, the results for depression were robust.

3.4.3.4 Positive emotions (D1) and negative emotions (D2)

The results showed that for negative emotions, the 95% confidence interval (CI) was (−0.14, 0.43), with an estimated median value of 0.14. For positive emotions, the 95% CI was (−0.11, 0.25), with an estimated median value of 0.07. Therefore, according to the sensitivity test, these two results were not robust. This suggests that the variability in the studies included in the analysis may have had a significant impact on the estimated effects of negative and positive emotions. Further investigation into the sources of heterogeneity and potential biases in the included studies is needed to improve the robustness of the results (Figure 7).

Figure 7

3.4.4 Results of funnel plot

Since A1 and A2 were discussed as dichotomous variables separately from the others, they were not included in the funnel plot analysis for B1, B2, C1, C2, C3, D1, and D2. According to the funnel plots for these variables (Figure 8), a portion of the studies fall outside the 95% confidence interval, indicating the presence of high heterogeneity. Additionally, the funnel plots exhibit asymmetry with missing corners, suggesting the existence of publication bias. This may be due to the inclusion of low-quality studies with small sample sizes, which could lead to an overestimation of the combined effect, exaggerating the intervention effect, and causing bias.

Figure 8

To address these issues, further investigation into the sources of heterogeneity and potential biases in the included studies is necessary. This may involve conducting additional analyses, such as subgroup analyses or meta-regression, to explore the reasons for the heterogeneity and publication bias. Additionally, efforts should be made to identify and exclude low-quality studies or those with significant biases to improve the robustness and reliability of the results (Figure 8).

Consistent with the separate analysis for A1 and A2, the funnel plots for A1 and A2 reveal that most studies fall within the 95% confidence interval, indicating low heterogeneity (Figure 9). However, the funnel plots lack symmetry, suggesting the presence of publication bias. This could potentially be attributed to the inclusion of low-quality studies with small sample sizes, which may lead to an overestimation of the combined effect, exaggerating the intervention effect, and introducing bias (Figure 9).

Figure 9

3.4.5 Results of Egger test

In this study, the experimental variables are B1, B2, C1, C2, C3, while D1 and D2 are continuous variables. Therefore, the Egger test was used to assess publication bias. The Egger test results indicate a potential for publication bias in B1 (DtS) and B2 (SoD) with p-values less than 0.05, suggesting that the results for these variables may be influenced by the presence of unpublished or underreported studies. On the other hand, the results for C1, C2, C3, D1, and D2 show no significant publication bias with p-values greater than 0.05, indicating that the available studies for these variables may be more representative of the true effect.

It is important to note that the presence of publication bias can affect the reliability and validity of the research findings. Therefore, when interpreting the results of this study, readers should consider the potential impact of publication bias on the B1 and B2 variables. Additional efforts may be needed to identify and include all relevant studies, especially those that may have been overlooked or underreported, to obtain a more accurate and unbiased estimate of the true effect.

4 Discussion

In our study, we aimed to comprehensively analyze trial results using both dichotomous outcomes (including 7-Day Point Prevalence Abstinence Rate and Continuous Abstinence Rate) and continuous variables (encompassing Desire to Smoke, its Strength, sleep quality, depression, irritability, positive emotions, and negative emotions). Notably, the literature frequently employs the Risk Ratio (RR) to interpret outcomes related to these dichotomous variables (55) particularly the 7-day PPA and continuous abstinence rates, prompting us to discuss 7-Day Point Prevalence Abstinence Rate and Continuous Abstinence Rate separately.

Smoking desire (intensity) and withdrawal symptoms are crucial indicators for assessing tobacco dependence (56). Higher smoking desire leads to shorter intervals between cigarettes and more pronounced withdrawal symptoms, which are major relapse triggers. Previous research suggests that physical exercise increases the time until the first cigarette following exercise (57). Thus, using exercise to alleviate these symptoms is crucial (58). Our study confirmed that acute aerobic exercise reduces tobacco cravings and withdrawal symptoms among smokers trying to quit. Specifically, the desire to smoke decreases significantly immediately following exercise (10). However, long-term exercise does not significantly impact tobacco dependence. Additionally, exercise intervention positively influences smokers or those attempting to quit, generating certain positive emotions.

Subgroup analyses to explore heterogeneity sources were restricted by original study designs. After examining individual articles, we found that excluding Tritter (45) and Taylor (32) led to more consistent sample characteristics and reduced methodological differences, suggesting they were main sources of high heterogeneity. The former had specific subject and control group limitations, while the latter focused on temporary smoking cessation and had unclear intervention criteria.

Exercise intensity is a significant control condition (59). Our subgroup analysis found that low, medium, and high-intensity exercise can all reduce tobacco dependence and craving to some extent. Especially, moderate to high-intensity acute aerobic exercise is the most effective intervention, and smokers with high tobacco dependence may benefit from increased exercise intensity. High-intensity exercise can significantly reduce tobacco dependence in a short period, especially for smokers with high dependence (13, 60). However, low-intensity exercise is ineffective in reducing smoking desire and intensity.

Another key finding from subgroup analyses, which specifically focused on withdrawal symptoms, reveals that exercise has a significant positive impact on reducing irritability among smokers attempting to quit. This finding aligns with previous research suggesting that exercise can alleviate negative mood states often experienced during withdrawal (13). However, our results indicate that the combined effect size for the intervention effects of exercise on depression is not statistically significant in our study population. To further investigate the sources of heterogeneity, we conducted additional subgroup analyses for depression. Notably, we found that only short-duration exercise (less than 15 min) has a positive effect on depression. Besides, our results also indicate that the intervention effect of exercise on sleep quality is not statistically significant. Our findings have important implications for future research and practice. While exercise may be beneficial in reducing irritability and, under certain conditions (such as short durations), depression, it may not have a significant impact on these outcomes for all smokers or across all durations of exercise. Therefore, practitioners should assess smokers’ specific needs and tailor interventions accordingly. This personalized approach can enhance the effectiveness of quit-smoking programs and improve overall outcomes for smokers seeking to overcome their tobacco dependence.

Notably, acute aerobic exercise has been identified as significantly effective in reducing cravings and withdrawal symptoms among smokers. While previous research acknowledged the immediate benefits of acute exercise on cigarette cravings, withdrawal symptoms, and smoking behavior (61), it did not delve deeply into the long-term effects of exercise or provide a direct comparison between acute and long-term interventions. The present meta-analysis evaluates both acute and long-term aerobic exercise interventions in smoking cessation, contributing to a more comprehensive understanding of the effects of exercise intensities and durations on tobacco dependence.

Our findings suggest that engaging in physical activity may positively influence smoking cessation attempts, potentially by providing a means to divert attention away from smoking cues and cravings. This aligns with previous research, such as the study by Hatzigeorgiadis et al. (62), which examined the acute effect of exercise on smoking delay among smokers. Notably, their results indicated that the use of self-regulation strategies, such as goal setting, could enhance the beneficial impact of exercise on reducing the urge to smoke immediately following physical activity (6264). These strategies may facilitate the translation of the temporary relief from smoking cravings induced by exercise into more sustained smoking abstinence. Future research should explore the combined effects of exercise and self-regulation strategies on smoking cessation outcomes, potentially identifying optimal combinations and protocols that maximize the beneficial impact of these interventions.

Furthermore, compared to previous studies, the data in the present study is more comprehensive and up-to-date. It synthesizes data from 47 studies, including 57 randomized controlled trials, involving 4,267 participants. This larger sample size and more comprehensive dataset allow for a more robust analysis and more reliable conclusions.

This study has limitations. Firstly, blinding participants in exercise interventions is challenging, thereby presenting a significant risk of bias. Furthermore, incomplete outcome data further contributes to this bias. Additionally, some assumed and ignored calculations may have influenced our results. For instance, in the design of the experimental and control groups, it was challenging to ensure that the exercise intervention was the sole variable of difference. In some cases, participants were explicitly instructed not to smoke during the intervention period, which could potentially affect the test results by introducing an additional variable that was not fully accounted for in our analysis. Secondly, intervention specifics, such as intensity, were often incompletely reported, and exercise types lacked a consistent classification system. Lastly, future research should consider a wider range of outcome measures to comprehensively assess the effects of exercise on smoking behavior. For example, although emotion serves as a pivotal moderating variable, only a few studies explicitly outlined emotion classification criteria, which constrained the inclusion of emotion-related indicators in our analysis. To enhance the accuracy of future research, it is recommended to implement allocation concealment, ensure assessor blinding, augment the sample size, uphold data integrity, thoroughly consider and validate all relevant calculations, and carefully design experimental and control groups to minimize the impact of confounding variables.

Statements

Data availability statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.

Author contributions

JX: Conceptualization, Investigation, Validation, Writing – original draft. SZ: Conceptualization, Data curation, Formal analysis, Visualization, Writing – original draft. ZC: Methodology, Supervision, Validation, Writing – review & editing. ZW: Formal analysis, Methodology, Supervision, Writing – review & editing.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The authors declare that no Gen AI was used in the creation of this manuscript.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

  • 1.

    World health statistics 2023: monitoring health for the SDGs, sustainable development goals. 1st ed. Geneva: World Health Organization (2023). 1 p.

  • 2.

    GSChoiSKrishnanJKR. Cigarette smoke and related risk factors in neurological disorders: an update. Biomed Pharmacother. (2017) 85:7986. doi: 10.1016/j.biopha.2016.11.118

  • 3.

    ZhuJYangB. Study on the risk of coronary artery stenosis and smoking in patients with COVID-19 pneumonia infection. Chinese J CT MRI. (2024) 22:1002. doi: 10.3969/j.issn.1672-5131.2024.05.032

  • 4.

    EvansDEToCAshareRL. The role of cognitive control in the self-regulation and reinforcement of smoking behavior. Nicotine Tob Res. (2019) 21:74754. doi: 10.1093/ntr/nty029

  • 5.

    GlasgowRELichtensteinE. Long-term effects of behavioral smoking cessation interventions. Behav Ther. (1987) 18:297324. doi: 10.1016/S0005-7894(87)80002-3

  • 6.

    HallSMHumfleetGLReusVIMuñozRFHartzDTMaude-GriffinR. Psychological intervention and antidepressant treatment in smoking cessation. Arch Gen Psychiatry. (2002) 59:930. doi: 10.1001/archpsyc.59.10.930

  • 7.

    PrenticeAM. Overeating: the health risks. Obes Res. (2001) 9:234S–238S. doi: 10.1038/oby.2001.124

  • 8.

    LinkeSECiccoloJTUssherMMarcusBH. Exercise-based smoking cessation interventions among women. Women’s Health (Lond Engl). (2013) 9:6984. doi: 10.2217/WHE.12.63

  • 9.

    KlinsophonTThaveeratithamPSitthipornvorakulEJanwantanakulP. Effect of exercise type on smoking cessation: a meta-analysis of randomized controlled trials. BMC Res Notes. (2017) 10:442. doi: 10.1186/s13104-017-2762-y

  • 10.

    ZourbanosNHatzigeorgiadisATsiamiATzatzakiTGeorgakouliKManthouEet al. An initial investigation of smokers’ urges to smoke and their exercise intensity preference: a mixed-methods approach. Cogent Med. (2016) 3:1149043. doi: 10.1080/2331205X.2016.1149043

  • 11.

    BenowitzNL. Neurobiology of nicotine addiction: implications for smoking cessation treatment. Am J Med. (2008) 121:S3S10. doi: 10.1016/j.amjmed.2008.01.015

  • 12.

    American Diabetes Association. 4. Foundations of care: education, nutrition, physical activity, smoking cessation, psychosocial care, and immunization. Diabetes Care. (2015) 38:S2030. doi: 10.2337/dc15-S007

  • 13.

    ZhouYFengWGuoYWuJ. Effect of exercise intervention on smoking cessation: a meta-analysis. Front Physiol. (2023) 14:1221898. doi: 10.3389/fphys.2023.1221898

  • 14.

    SantosCPProençaMGouveiaTDSSoares De OliveiraCBTacaoGYTrevisanIBet al. Effectiveness of aerobic exercise on smoking cessation in adults: a systematic review and meta-analysis. J Phys Act Health. (2021) 18:23042. doi: 10.1123/jpah.2019-0339

  • 15.

    TetzlaffJPageMMoherD. PNS154 the PRISMA 2020 statement: development of and key changes in an updated guideline for reporting systematic reviews and meta-analyses. Value Health. (2020) 23:S3123. doi: 10.1016/j.jval.2020.04.1154

  • 16.

    HigginsJPTCochrane Collaboration eds. Cochrane handbook for systematic reviews of interventions. Second ed. Hoboken, NJ: Wiley-Blackwell (2019). 694 p.

  • 17.

    BockBCFavaJLGaskinsRMorrowKMWilliamsDMJenningsEet al. Yoga as a complementary treatment for smoking cessation in women. J Women’s Health. (2012) 21:2408. doi: 10.1089/jwh.2011.2963

  • 18.

    MarcusBLewisBHoganJKingTAlbrechtABockBet al. The efficacy of moderate-intensity exercise as an aid for smoking cessation in women: a randomized controlled trial. Nicotine Tob Res. (2005) 7:87180. doi: 10.1080/14622200500266056

  • 19.

    Al-ChalabiLPrasadNSteedLStennerSAveyardPBeachJet al. A pilot randomised controlled trial of the feasibility of using body scan and isometric exercises for reducing urge to smoke in a smoking cessation clinic. BMC Public Health. (2008) 8:349. doi: 10.1186/1471-2458-8-349

  • 20.

    CheungYTLamTHChanCHHHoKSFokWYPWangMPet al. Brief handgrip and isometric exercise intervention for smoking cessation: a pilot randomized trial. Addict Behav. (2020) 100:106119. doi: 10.1016/j.addbeh.2019.106119

  • 21.

    HillJS. Effect of a program of aerobic exercise on the smoking behaviour of a group of adult volunteers. Can J Public Health. (1982) 76:1836.

  • 22.

    DunsigerSEmersonJAUssherMMarcusBHMirandaRMontiPMet al. Exercise as a smoking cessation treatment for women: a randomized controlled trial. J Behav Med. (2021) 44:794802. doi: 10.1007/s10865-021-00236-8

  • 23.

    KinnunenTLeemanRKorhonenTQuilesZTerwalDGarveyAet al. Exercise as an adjunct to nicotine gum in treating tobacco dependence among women. Nicotine Tobacco Res. (2008) 10:689703. doi: 10.1080/14622200801979043

  • 24.

    OnckenCAllenSLittMKennyALandoHAllenAet al. Exercise for smoking cessation in postmenopausal women: a randomized, controlled trial. Nicotine Tobacco Res. (2020) 22:158795. doi: 10.1093/ntr/ntz176

  • 25.

    LinkeSERutledgeTMyersMG. Intermittent exercise in response to cigarette cravings in the context of an internet-based smoking cessation program. Ment Health Phys Act. (2012) 5:8592. doi: 10.1016/j.mhpa.2012.02.001

  • 26.

    WilliamsDMWhiteleyJADunsigerSJenningsEGAlbrechtAEUssherMHet al. Moderate intensity exercise as an adjunct to standard smoking cessation treatment for women: a pilot study. Psychol Addict Behav. (2010) 24:34954. doi: 10.1037/a0018332

  • 27.

    PrapavessisHCameronLBaldiJCRobinsonSBorrieKHarperTet al. The effects of exercise and nicotine replacement therapy on smoking rates in women. Addict Behav. (2007) 32:141632. doi: 10.1016/j.addbeh.2006.10.005

  • 28.

    MarcusBHAlbrechtAEKingTKParisiAFPintoBMRobertsMet al. The efficacy of exercise as an aid for smoking cessation in women: a randomized controlled trial. Arch Intern Med. (1999) 159:1229. doi: 10.1001/archinte.159.11.1229

  • 29.

    CiccoloJTDunsigerSIWilliamsDMBartholomewJBJenningsEGUssherMHet al. Resistance training as an aid to standard smoking cessation treatment: a pilot study. Nicotine Tob Res. (2011) 13:75660. doi: 10.1093/ntr/ntr068

  • 30.

    TaylorAKatomeriM. Walking reduces cue-elicited cigarette cravings and withdrawal symptoms, and delays ad libitum smoking. Nicotine Tobacco Res. (2007) 9:118390. doi: 10.1080/14622200701648896

  • 31.

    AbrantesAMBloomELStrongDRRiebeDMarcusBHDesaulniersJet al. A preliminary randomized controlled trial of a behavioral exercise intervention for smoking cessation. Nicotine Tob Res. (2014) 16:1094103. doi: 10.1093/ntr/ntu036

  • 32.

    TaylorAHKatomeriMUssherM. Acute effects of self-paced walking on urges to smoke during temporary smoking abstinence. Psychopharmacology. (2005) 181:17. doi: 10.1007/s00213-005-2216-4

  • 33.

    De JesusSPrapavessisH. Affect and cortisol mechanisms through which acute exercise attenuates cigarette cravings during a temporary quit attempt. Addict Behav. (2018) 80:828. doi: 10.1016/j.addbeh.2018.01.007

  • 34.

    UssherMNunziataPCropleyMWestR. Effect of a short bout of exercise on tobacco withdrawal symptoms and desire to smoke. Psychopharmacology. (2001) 158:6672. doi: 10.1007/s002130100846

  • 35.

    ScerboFFaulknerGTaylorAThomasS. Effects of exercise on cravings to smoke: the role of exercise intensity and cortisol. J Sports Sci. (2010) 28:119. doi: 10.1080/02640410903390089

  • 36.

    JeffriesERZvolenskyMJBucknerJD. The acute impact of hatha yoga on craving among smokers attempting to reduce or quit. Nicotine Tob Res. (2018) 22:44651. doi: 10.1093/ntr/nty263

  • 37.

    FongAJDe JesusSBraySRPrapavessisH. Effect of exercise on cigarette cravings and ad libitum smoking following concurrent stressors. Addict Behav. (2014) 39:151621. doi: 10.1016/j.addbeh.2014.05.027

  • 38.

    Van RensburgKTaylorABenattayallahAHodgsonT. The effects of exercise on cigarette cravings and brain activation in response to smoking-related images. Psychopharmacology. (2012) 221:65966. doi: 10.1007/s00213-011-2610-z

  • 39.

    MasieroMKeyworthHPravettoniGCropleyMBaileyA. Short bouts of physical activity are associated with reduced smoking withdrawal symptoms, but perceptions of intensity may be the key. Healthcare. (2020) 8:425. doi: 10.3390/healthcare8040425

  • 40.

    SchneiderTDe JesusSPrapavessisH. The effect of acute exercise on smoking topography: no evidence for cutting down one puff at a time. J Smok Cessat. (2015) 10:14653. doi: 10.1017/jsc.2014.2

  • 41.

    Van RensburgKJTaylorAH. The effects of acute exercise on cognitive functioning and cigarette cravings during temporary abstinence from smoking. Hum Psychopharmacol. (2008) 23:1939. doi: 10.1002/hup.925

  • 42.

    Janse Van RensburgKTaylorAHodgsonTBenattayallahA. Acute exercise modulates cigarette cravings and brain activation in response to smoking-related images: an fMRI study. Psychopharmacology. (2009) 203:58998. doi: 10.1007/s00213-008-1405-3

  • 43.

    Van RensburgKJTaylorAHodgsonT. The effects of acute exercise on attentional bias towards smoking-related stimuli during temporary abstinence from smoking. Addiction. (2009) 104:19107. doi: 10.1111/j.1360-0443.2009.02692.x

  • 44.

    TaylorAKatomeriMUssherM. Effects of walking on cigarette cravings and affect in the context of Nesbitt’s paradox and the Circumplex model. J Sport Exerc Psychol. (2006) 28:1831. doi: 10.1123/jsep.28.1.18

  • 45.

    TritterAFitzgeorgeLPrapavessisH. The effect of acute exercise on cigarette cravings while using a nicotine lozenge. Psychopharmacology. (2015) 232:25319. doi: 10.1007/s00213-015-3887-0

  • 46.

    BizeRWilliCChioleroAStoianovRPayotSLocatelliIet al. Participation in a population-based physical activity programme as an aid for smoking cessation: a randomised trial. Tob Control. (2010) 19:48894. doi: 10.1136/tc.2009.030288

  • 47.

    AllenACarlsonSCBoschTAEberlyLEOkuyemiKNairUet al. High-intensity interval training and continuous aerobic exercise interventions to promote self-initiated quit attempts in young adults who smoke: feasibility, acceptability, and lessons learned from a randomized pilot trial. J Addict Med. (2018) 12:37380. doi: 10.1097/ADM.0000000000000414

  • 48.

    UssherMCropleyMPlayleSMohidinRWestR. Effect of isometric exercise and body scanning on cigarette cravings and withdrawal symptoms. Addiction. (2009) 104:12517. doi: 10.1111/j.1360-0443.2009.02605.x

  • 49.

    EversonESDaleyAJUssherM. The effects of moderate and vigorous exercise on desire to smoke, withdrawal symptoms and mood in abstaining young adult smokers. Ment Health Phys Act. (2008) 1:2631. doi: 10.1016/j.mhpa.2008.06.001

  • 50.

    UssherMWestRDoshiRSampuranAK. Acute effect of isometric exercise on desire to smoke and tobacco withdrawal symptoms. Hum Psychopharmacol. (2006) 21:3946. doi: 10.1002/hup.744

  • 51.

    AbrantesAMFarrisSGMinamiHStrongDRRiebeDBrownRA. Acute effects of aerobic exercise on affect and smoking craving in the weeks before and after a cessation attempt. Nicotine Tob Res. (2018) 20:57582. doi: 10.1093/ntr/ntx104

  • 52.

    LiCYaoNMillerSLMacphersonCHassingerTLoveKet al. Exercise and reduced nicotine content cigarettes in adult female smokers: a pilot trial. IJERPH. (2022) 19:6647. doi: 10.3390/ijerph19116647

  • 53.

    Janse Van RensburgKEliberoAKilpatrickMDrobesDJ. Impact of aerobic exercise intensity on craving and reactivity to smoking cues. Exp Clin Psychopharmacol. (2013) 21:196203. doi: 10.1037/a0032768

  • 54.

    StocktonMBWardKDMcClanahanBSVanderMCodayMWilsonNet al. The efficacy of individualized, community-based physical activity to aid smoking cessation: a randomized controlled trial. J Smok Cessat. (2023) 2023:e4. doi: 10.1155/2023/5535832

  • 55.

    RobbinsASChaoSYFonsecaVP. What’s the relative risk? A method to directly estimate risk ratios in cohort studies of common outcomes. Ann Epidemiol. (2002) 12:4524. doi: 10.1016/S1047-2797(01)00278-2

  • 56.

    ShiffmanSWestRGilbertD. Recommendation for the assessment of tobacco craving and withdrawal in smoking cessation trials. Nicotine Tob Res. (2004) 6:599614. doi: 10.1080/14622200410001734067

  • 57.

    GeorgakouliKManthouEGeorgouliasPZiakaADeliCKDraganidisDet al. HPA axis responses to acute exercise differ in smokers and non-smokers. Physiol Behav. (2020) 229:113258. doi: 10.1016/j.physbeh.2020.113258

  • 58.

    HearingCMChangWCSzuhanyKLDeckersbachTNierenbergAASylviaLG. Physical exercise for treatment of mood disorders: a critical review. Curr Behav Neurosci Rep. (2016) 3:3509. doi: 10.1007/s40473-016-0089-y

  • 59.

    LansleyKEDiMennaFJBaileySJJonesAM. A ‘new’ method to normalise exercise intensity. Int J Sports Med. (2011) 32:53541. doi: 10.1055/s-0031-1273754

  • 60.

    RobertsVGantNSollersJJBullenCJiangYMaddisonR. Effects of exercise on the desire to smoke and physiological responses to temporary smoking abstinence: a crossover trial. Psychopharmacology. (2015) 232:107181. doi: 10.1007/s00213-014-3742-8

  • 61.

    TaylorAHUssherMHFaulknerG. The acute effects of exercise on cigarette cravings, withdrawal symptoms, affect and smoking behaviour: a systematic review. Addiction. (2007) 102:53443. doi: 10.1111/j.1360-0443.2006.01739.x

  • 62.

    HatzigeorgiadisAPappaVTsiamiATzatzakiTGeorgakouliKZourbanosNet al. Self-regulation strategies may enhance the acute effect of exercise on smoking delay. Addict Behav. (2016) 57:357. doi: 10.1016/j.addbeh.2016.01.012

  • 63.

    AngeliMHatzigeorgiadisAComoutosNKrommidasCMorresIDTheodorakisY. The effects of self-regulation strategies following moderate intensity exercise on ad libitum smoking. Addict Behav. (2018) 87:10914. doi: 10.1016/j.addbeh.2018.06.029

  • 64.

    OhHTaylorAH. Self-regulating smoking and snacking through physical activity. Health Psychol. (2014) 33:34959. doi: 10.1037/a0032423

Summary

Keywords

tobacco dependence, physical exercise, acute aerobic exercise, smoking cessation, meta-analysis

Citation

Xu J, Zhang S, Chen Z and Wu Z (2025) Effects of exercise intervention on tobacco dependence: a meta-analysis. Front. Public Health 13:1538833. doi: 10.3389/fpubh.2025.1538833

Received

03 December 2024

Accepted

06 February 2025

Published

18 February 2025

Volume

13 - 2025

Edited by

Yannis Theodorakis, University of Thessaly, Greece

Reviewed by

Philip Hemphill, Tulane University, United States

Maria Angeli, University of Thessaly, Greece

Updates

Copyright

*Correspondence: Zhusheng Wu,

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

Outline

Figures

Cite article

Copy to clipboard


Export citation file


Share article

Article metrics