Your new experience awaits. Try the new design now and help us make it even better

MINI REVIEW article

Front. Psychiatry, 11 December 2025

Sec. Psychological Therapy and Psychosomatics

Volume 16 - 2025 | https://doi.org/10.3389/fpsyt.2025.1659841

How factors of the therapeutic alliance interact with oxytocin neurotransmission in psychotherapy

Marcus Eckert*Marcus Eckert*Eva SchandroEva Schandro
  • Apollon University of Applied Sciences, Bremen, Germany

Oxytocin (OT) neurotransmission has emerged as a promising target for alleviating psychiatric symptoms associated with depression, stress, and fear. This mini-review focuses on the therapeutic alliance, highlighting five core components: (1) attachment, (2) empathy, (3) social synchrony, (4) trust and cooperation, and (5) social support. We explore how these factors both influence and are modulated by the oxytocinergic system. Based on current empirical evidence, we propose a conceptual framework in which OT-mediated mechanisms dynamically and reciprocally strengthen the therapeutic alliance. We postulate that activation of the OT system by one or more of these components may synergistically enhance all alliance factors, creating a self-reinforcing cycle with potential therapeutic benefits. Finally, we discuss the clinical implications of this model and identify key avenues for future research.

Introduction

Oxytocin (OT) is a neuropeptide closely associated with both physical and mental health. Numerous studies indicate that OT can reduce stress and anxiety while promoting resilience and psychological well-being (1, 2). Moreover, OT has been implicated in various psychiatric disorders, including social anxiety disorder, affective disorders, autism spectrum disorder, schizophrenia, post-traumatic stress disorder, and borderline personality disorder (3). It is important to note, however, that findings vary depending on the methods used to measure OT—such as peripheral blood levels, central nervous system activity, or effects of exogenous OT administration—making direct comparisons challenging.

Due to these multifaceted associations, OT has increasingly gained attention as a potential therapeutic target in psychiatric treatment (2). Nevertheless, evidence regarding the therapeutic efficacy of OT-related interventions remains heterogeneous and sometimes contradictory, likely reflecting the influence of moderating variables such as individual differences, sex, and social context (4). Furthermore, methodological challenges persist, especially regarding the indirect nature of peripheral OT measurements as proxies for central oxytocinergic activity. Young (5) underscores the need for alternative pharmacological strategies to enhance OT neurotransmission, highlighting its therapeutic potential. Complementing this perspective, the present article focuses on psychological approaches to augmenting OT activity. Specifically, we emphasize the therapeutic alliance—a relational factor empirically linked to oxytocinergic processes (6).

It is crucial to acknowledge the considerable individual variability in OT effects, and that the relationships presented here provide only a preliminary overview that cannot fully capture the complexity and occasional inconsistencies in the literature. Nonetheless, we aim to introduce a conceptual model identifying five core factors empirically associated with both therapeutic alliance quality and OT activity: (1) attachment, (2) empathy, (3) social synchrony, (4) trust and cooperation, and (5) social support. First, while adult attachment theory does not map directly onto the therapeutic alliance, emerging evidence suggests that an attachment-based framework—particularly when considering oxytocin as a process marker—may offer valuable insights into relational dynamics in psychotherapy (7). Second, empathy, a widely recognized non-specific factor in psychotherapy outcomes (8), has a documented but context-dependent relationship with oxytocin (9). Recent research points to links between OT, behavioral synchrony, and even inter-brain synchrony during empathic engagement (10). Third, mutual trust and collaboration—core elements of the therapeutic relationship—have been associated with improved metacognitive functioning (11) and show dynamic, though sometimes inconsistent, associations with oxytocin (12). Finally, although often considered extra-therapeutic, social support has demonstrated bidirectional interactions with the therapeutic alliance (13) and is increasingly recognized as both a correlate and modulator of oxytocin-related processes (14, 15).

In the debate about the most suitable psychotherapy, Wampold (16) suggested non-specific factors such as the therapeutic alliance. The significance of the therapeutic alliance for psychotherapy outcomes has been robustly demonstrated—for example, Tschuschke et al. (17) report that alliance quality predicts treatment success more strongly than specific therapeutic modalities. Against this backdrop, OT has been proposed as a neurobiological substrate contributing to therapeutic effectiveness. A recent mini-review by Durante et al. (7) synthesized studies examining natural fluctuations and synchronization of OT levels between therapists and patients, finding preliminary evidence that OT covariation may be associated with treatment outcomes in major depressive disorder. However, this evidence is based on a limited number of studies, with no experimental or replication studies to date, highlighting the need for further research.

Studies employing exogenous OT administration have yielded mixed results. For instance, Grossman-Giron et al. (18) observed that intranasal OT improved concordance between patient and therapist perceptions of the alliance, while Ellenbogen et al. (19) reported that OT administration enhanced the therapeutic alliance particularly during early treatment phases. These findings suggest a potential for OT to strengthen the therapeutic relationship but also emphasize the necessity for more rigorous and replicable investigations.

In summary, this mini-review seeks to elucidate potential mechanisms through which OT may influence the quality of the therapeutic alliance. The hormonal context can generally be understood as a mediating factor in many psychological and social processes. This also applies to OT, of course. Studies involving exogenous OT administration often show its influence on behavior and experience. In addition, endogenous OT varies systematically with certain experiences and behaviors, often depending on the social context. This review postulates interactions between the factors of therapeutic alliance and OT on the one hand. On the other hand, the effect of OT on therapy outcomes is examined. In this analysis, OT emerges as a mediator of the therapeutic alliance’s effects on therapy outcomes. Furthermore, this review assumes reciprocal self-reinforcing processes whereby activation of the OT system promotes psychological processes that in turn make activation of the OT system more likely. We will also postulate spillover effects between the factors, which, however, must be confirmed by future research and which may offer valuable approaches for therapeutic action. In this sense, this conceptual framework provides a basis for future empirical studies and theoretical refinements.

Attachment theory

Attachment theory, initially formulated by Bowlby and Ainsworth, distinguishes three primary attachment styles: secure, anxious, and avoidant (20, 21). Secure attachment is generally linked to better mental health outcomes, whereas insecure styles—anxious and avoidant—are risk factors for psychopathology. Oxytocin (OT) has been implicated as a multifaceted neurobiological correlate of attachment, influencing social behaviors and emotional regulation in ways moderated by individual attachment styles (22).

Empirical findings reveal complex, sometimes contradictory interactions between attachment and OT. For example, Nawa et al. (23) observed that playful mother–child interactions following traumatic stress increased maternal OT, which was inversely related to maternal distress and predicted reductions in children’s behavioral problems two years later. Bosmans et al. (24) proposed an attachment learning model emphasizing how supportive caregiving buffers stress responses via OT- and dopamine-mediated neurobiological reinforcement, promoting future attachment-seeking behavior.

Parental caregiving behavior itself appears to be reinforced through OT activation (25), although OT’s social-cognitive effects vary by attachment style. Bartz et al. (22) and Fang et al. (26) demonstrated that intranasal OT administration enhances perceptions of care and cooperation only in individuals with low attachment anxiety or avoidance, respectively, while those with high attachment insecurity exhibit attenuated or no effects. Rockliff et al. (27) further showed that secure attachment facilitates engagement in compassion-focused imagery after OT administration, an effect diminished in less securely attached individuals.

Conversely, OT may also promote more secure attachment representations. Zhang et al. (28) meta-analysis suggests that intranasal OT reduces behaviors associated with attachment insecurity in ambiguous social contexts. Similarly, Buchheim et al. (29) found that OT administration increased attachment security experiences among insecurely attached adults. In this regard, it is worth noting that contemporary attachment research focuses on the dimensional nature of attachment. For instance, Fraley et al. (30) suggest attachment to be best described as a continuous variable. A taxometric analysis showed that both parental and romantic relationships show signs of dimensionality.

Regarding psychotherapy, attachment styles can shift through the therapeutic process, with anxiously attached patients benefiting particularly from a strong therapeutic alliance (31, 32). Therapists can function as attachment figures, potentially activating patients’ OT systems. Manvelian et al. (33) reported that pairing insecurely attached students with warm, securely attached mentors trained in Emotionally Focused Therapy increased mentees’ attachment security, possibly mediated by OT activation. However, Karl et al. (34) found that while secure attachment priming reduced physiological arousal, OT administration did not, suggesting OT-independent pathways for increasing attachment security.

Finally, the therapeutic alliance, attachment security, and OT are theoretically intertwined. Several reviews highlight OT as a potential biomarker of the alliance (7, 35), and empirical evidence supports associations between attachment security and alliance quality (36). Nonetheless, these links remain preliminary and require rigorous longitudinal and mechanistic research to clarify their interplay.

In sum, OT’s role in attachment is complex and moderated by individual differences in attachment style. Behavioral interventions aiming to enhance OT should consider these nuances and ideally incorporate strategies to foster secure attachment representations, thereby optimizing both neurobiological and relational outcomes.

Empathy

Empathy is widely recognized as a crucial factor influencing therapeutic alliance (37). Early work by Barraza and Zak (38) showed that inducing empathy via emotional video clips led to measurable increases in plasma OT, with greater empathic responses associated with larger OT changes. Building on this, Zak et al. (39) used similar stimuli in a quasi-experimental design, lacking a control group, limiting causal inferences. They reported age as a moderator, with older participants showing greater OT increases, and positive correlations between OT changes and empathic concern. Procyshyn et al. (40) also induced empathy through a video depicting a gravely ill child, observing a significant 14% rise in salivary OT among 173 healthy adults. Notably, individuals with a cognitive style biased toward empathizing, as conceptualized by Baron-Cohen and Wheelwright (41) empathizing–systemizing theory, showed more pronounced OT increases compared to those with systemizing biases (42). This bias is rooted in Baron-Cohen’s Empathizing–Systemizing (E-S) theory (41), which postulates two distinct cognitive dimensions—Empathizing and Systemizing—that are distributed continuously along a spectrum and associated with autism spectrum conditions. This means that individuals can exhibit different levels of each ability, with some people showing a strong preference for empathy, others for systematization, and still others a balance of both abilities. According to this theory, individuals high in empathizing are particularly attuned to the thoughts and emotions of others and possess a strong capacity to understand and respond appropriately to them. In contrast, individuals high in systemizing show a marked interest in, and aptitude for, analyzing and constructing technical, mechanical, or abstract rule-based systems (42). These findings suggest that individual differences modulate OT responses to empathy induction, highlighting the need to consider trait variability in therapeutic applications.

With regard to the therapeutic alliance, Fisher et al. (43) showed that therapists’ OT levels increased in response to patients’ negative emotions, thereby contributing to a reduction in patients’ depressive symptoms. This finding supports the assumption of an interaction in OT dynamics within clinical interactions. While the therapist’s empathy obviously influences her or his OT level, this increase appears to be accompanied by a reduction in the patient’s symptoms. Although no causality can be inferred here, it seems reasonable to assume that OT has an influence. Mu et al. (44), for example, found that the administration of OT not only increases behavioral synchrony in coordination games, but also promotes the synchronization of brain oscillations in the alpha band. Zilcha-Mano et al. (35) found that lower therapist-patient synchrony predicts changes in oxytocin levels during treatment, which in turn is associated with a smaller reduction in depressive symptoms during therapy.

While these findings support a model wherein empathy and OT form a self-reinforcing cycle that facilitates therapeutic progress (see Figure 1), several caveats apply. Measures of empathy vary widely across studies, complicating direct comparisons. Many studies rely on peripheral OT measures (e.g., plasma, saliva) or intranasal administration, which do not necessarily reflect central OT activity and differ in their ecological validity. Additionally, some designs lack appropriate control conditions, limiting causal conclusions. Individual differences, such as baseline attachment style or empathizing-systemizing cognitive profiles, further moderate these effects and deserve greater attention.

Figure 1
Flowchart depicting a cycle with three stages: Empathy, Activation of the Oxytocin System, and Therapeutic Progress (efficacy), connected by arrows indicating a cycle.

Figure 1. Self-reinforcing process of therapeutic alliance, OT activation and progress of psychotherapy.

These limitations can additionally be applied to our next construct of social synchrony.

Social synchrony

Social synchrony may underlie these OT-empathy links. Zilcha-Mano et al. (35) found that patient-therapist synchrony correlates with treatment success, with OT implicated as a mediating mechanism (6). Influs et al. (45, 46) implemented an eight-session intervention targeting synchrony and perspective-taking, reporting increases in both OT and empathy. Mimicry, a related synchronous behavior, is proposed to facilitate cognitive and emotional empathy (47). Reviews indicate that parent-infant synchrony correlates with parental OT levels (48), and experimental evidence shows that synchronous social interactions stimulate endogenous OT release in dyads (49). Moreover, oxytocin has been shown to enhance automatic imitation and facial mimicry, potentially mediating improved emotion recognition (50, 51).

As described in the before within the perspective of empathy, empirical evidence tentatively supports interaction effects in which social synchrony activates the OT system, which in turn enhances these social processes and therapeutic outcomes. However, more rigorous, longitudinal, and mechanistically informed research is needed to clarify causal pathways, measurement validity, and boundary conditions of this model.

Fostering trust and cooperation

Trust and cooperation are fundamental components of psychotherapy that significantly influence the therapeutic alliance (52). Both constructs appear to be interactively linked with oxytocin (OT), though findings in this area are complex, sometimes contradictory, and moderated by multiple factors.

Several experimental studies have reported that intranasal OT administration can increase trust and cooperative behaviors. For example, Kosfeld et al. (53) found that OT enhanced trust in a financial investment game, and Declerck et al. (54) observed increased cooperation following OT administration. However, subsequent research has yielded mixed results. Declerck et al. (55) failed to replicate the trust-enhancing effect of OT in a similar paradigm, and Baumgartner et al. (56) showed that while OT prevented the typical decline in trust after betrayal, the overall effects on trust were nuanced. A critical review by Nave et al. (57) concluded that there is no consistent, robust evidence for a general effect of OT on human trust. Supporting this, Walum et al. (58) conducted a meta-analysis highlighting considerable variability in OT effects on social behavior, emphasizing the influence of context, individual differences, and methodological factors in explaining inconsistent findings.

These inconsistencies may partly stem from methodological variations, including differences in OT dosage, timing of administration, participant characteristics, and experimental tasks. Additionally, the nature of “trust” itself varies across studies—ranging from situational trust in economic games to dispositional or relational trust—limiting direct comparability.

Contextual and individual differences appear to moderate OT’s effects on trust and cooperation. For instance, Van IJzendoorn and Bakermans-Kranenburg (59) meta-analysis suggested that OT preferentially enhances trust toward ingroup members, emphasizing the social context. Conversely, Bartz et al. (60) found that OT reduced trust in individuals with borderline personality disorder, highlighting the importance of personal traits. Shou et al. (61) proposed that OT’s effects might reflect reduced caution or fear of betrayal rather than genuine increases in trust. Moreover, Mikolajczak et al. (62) emphasized the dependency of OT’s prosocial effects on situational factors. Regarding cooperation, social context and individual social value orientation—whether a person tends toward prosocial or self-oriented behavior—moderate OT’s impact, especially in economic game paradigms (54). Other moderators such as age and gender have also been reported (63, 64).

Endogenous OT levels have also been linked to trust-related behaviors. Zak et al. (65) found positive correlations between peripheral OT and both intentions to trust and trustworthy actions (reciprocation) in economic games. Similarly, Kiss et al. (66) reported increased OT during a trust-based secret-sharing task compared to control conditions. However, it is important to note that peripheral OT measures (blood or saliva) may not directly reflect central OT activity, and the exact relationship between peripheral and central OT remains unclear.

Taken together, these findings suggest a complex, multidirectional relationship between trust, cooperation, and OT activity, strongly moderated by individual and contextual factors. We therefore propose a tentative self-reinforcing mechanism whereby therapeutic interventions that foster trust may elevate OT activity, which in turn facilitates trust-related cognitions and behaviors, further activating the OT system (see Figure 2). These self-reinforcing processes remain a theoretical model, requiring empirical validation, especially in clinical psychotherapy contexts.

Figure 2
Diagram illustrating the therapeutic alliance, focusing on the activation of the oxytocin system. It includes five components: attachment perspective, empathy, social synchrony, trust and cooperation, and social support. Each component has processes like working model activation, care, empathy, trust, cooperation, and perception of social support, all linked with arrows indicating interaction and feedback loops. The overall theme is enhancing the oxytocin system for therapeutic benefits.

Figure 2. Integration of the single broaden-and-build-cycles of OT from a therapeutic alliance perspective.

Social support

Social support is a psychological construct stemming from research on stress and health behaviors (67). Hence, it is considered a separate component in this mini review.

As early as the late 1990s, Carter (68) demonstrated that the accumulation of social support is associated with increased basal oxytocin responses to stress in animal models. Regarding the regulation of the hypothalamic-pituitary-adrenal (HPA) axis, oxytocin is hypothesized to mediate social buffering by attenuating physiological stress responses. In humans, Grewen et al. (69) found that self-reported partner support correlated with elevated plasma oxytocin levels following a warm contact intervention. Moreover, these authors suggested that partner support combined with increased oxytocin levels may have cardioprotective effects by modulating sympathetic nervous system activity and reducing blood pressure in women. However, it is important to note that plasma oxytocin levels represent peripheral measures and their relationship to central oxytocin activity remains indirect and not fully understood.

To further explore the interplay between social support, stress buffering, and oxytocin, Heinrichs et al. (70) conducted a placebo-controlled, double-blind study in humans. Participants received either intranasal oxytocin (24 IU) or placebo 50 minutes before exposure to the Trier Social Stress Test, combined with either social support or no support during the stressor. Results indicated an anxiolytic effect of oxytocin and, notably, the combination of oxytocin administration and social support was associated with the lowest cortisol responses and greater subjective calmness. These findings suggest that oxytocin may enhance the stress-buffering effects of social support, though further replication is needed to confirm these effects.

Neumann (71) discusses the mediating role of oxytocin in the positive effects of close social interactions on emotional well-being and health for many species, primarily based on rodent, sheep and primates’ studies. In these models, even subtle social stimuli activate oxytocin neurons. While such findings provide valuable insight into potential mechanisms, direct experimental evidence for similar oxytocinergic activation in the human brain following subtle social interactions—such as touch, hugging, or conversation — is currently lacking. Human research typically relies on peripheral oxytocin measurements in blood or saliva as indirect indicators of overall oxytocin system activation (72). The authors highlight that “activation of the brain OXT system even by subtle social stimuli is of particular relevance in the context of OT as a mediator of the positive effects of social support on stress responsiveness, as the OT system is closely linked to stress regulation” (72, p. 8), but emphasize the need for further research to substantiate these claims.

Consistent with the Tend-and-Befriend theory—which posits that social affiliation serves as a stress-coping mechanism, particularly in females—oxytocin responsiveness has been shown to predict the desire for social contact and support following social stress (73). Taken together, it is plausible that social stress induces support-seeking behavior, and that social support—especially emotional support—may alleviate psychological and physiological stress via oxytocinergic pathways. Nevertheless, no study to date has conclusively demonstrated direct activation of the central oxytocin system by social support in humans.

Despite these gaps, there is broad consensus that interventions aimed at enhancing social support positively impact health and well-being (74). It is hypothesized that oxytocin may partially mediate these beneficial effects (72), although this remains to be definitively established. Animal research supports the notion that partner support triggers oxytocin release and attenuates HPA axis responses to stress (75), but translating these findings to humans warrants cautious interpretation.

Discussion

Based on previous research, this paper proposes five distinct oxytocin-related reciprocal self-reinforcing processes that may contribute to the development and strengthening of the therapeutic alliance. Each cycle outlines specific psychological factors that are hypothesized to activate the oxytocin system. In turn, activation of this system is assumed to reinforce these very factors, potentially creating a reciprocal dynamic that further promotes oxytocin release.

Taking a broader perspective, it appears plausible that activation of the oxytocin (OT) system does not influence only the specific psychological factor that initially triggered it but also exerts effects on other related factors. We therefore propose a more complex interplay between these five reciprocal self-reinforcing processes, as illustrated in Figure 2. For instance, empathy and synchrony may lead to increased trust and cooperation (76). Empirical findings also suggest a link between empathy and the therapeutic alliance (37). From an attachment theory perspective, both empathy and supportive behavior are considered fundamental to the development of attachment security. Additionally, research has shown that OT can simultaneously influence empathy, trust, and cooperation (77). These findings support our hypothesis that OT may function as a general facilitating factor, amplifying the effects of single psychological mechanisms and contributing to a broader, self-reinforcing dynamic beyond isolated reciprocal self-reinforcing processes.

Theoretical and methodological considerations

While our model is informed by a growing body of evidence linking oxytocin (OT) to social bonding, stress regulation, and affiliative behaviors, we acknowledge that the current human literature remains heterogeneous, and in many areas, inconclusive. Notably, the association between classic attachment theory—primarily developed in the context of child–caregiver relationships—and the therapeutic alliance in psychotherapy is conceptually and empirically complex. Although both constructs involve interpersonal trust and perceived emotional safety, they emerge in distinct relational contexts and are typically assessed with different instruments. Current alliance measures (e.g., WAI) emphasize agreement on tasks and goals, and the perceived emotional bond, but do not directly map onto adult attachment styles such as avoidance or anxiety, which are usually measured in romantic or general interpersonal domains.

Moreover, while animal research robustly links oxytocin to attachment behaviors, direct evidence in humans remains limited. Studies suggest that early environmental factors—such as attachment experiences or early adversity—may moderate OT effects, rather than OT being a direct biological marker of secure attachment (22, 27). We therefore interpret the relationship between OT and attachment-related constructs with appropriate caution.

Similarly, although there are promising studies linking OT to aspects of the therapeutic process (e.g., 19, 35), the available evidence remains sparse, and findings are mixed. For instance, Ellenbogen et al. (19) showed that intranasal OT accelerated early alliance development in individuals with major depressive disorder, but this effect dissipated by mid-therapy as placebo recipients “caught up.” In other words, while OT may play a modulatory role in alliance formation, its therapeutic effects are likely time-sensitive and context-dependent.

Furthermore, methodological differences between studies make comparisons difficult. Endogenous OT levels measured in blood or saliva do not necessarily reflect central OT activity and may be influenced by numerous peripheral factors. Likewise, intranasal administration of synthetic OT introduces pharmacological effects that are not directly comparable to naturally occurring release. For this reason, we distinguish between findings based on (a) peripheral OT measurement, (b) intranasal OT administration, and (c) behavioral or psychological proxies of OT system activation (e.g., trust, synchrony, empathy).

While our broaden-and-build model posits reciprocal relationships between psychological processes and OT system activation, we fully recognize the preliminary nature of this proposal. The model is intended as a heuristic framework to stimulate further empirical research, not as a definitive account of OT function in psychotherapy. As such, we call for more rigorous, longitudinal, and mechanistically-informed studies to better understand the complex and likely bidirectional relationships between oxytocin, therapeutic processes, and clinical outcomes.

Conclusion

Taking an even broader perspective, it becomes clear that many of the assumptions put forward in this paper are based on fragmented evidence. We also acknowledge that numerous pieces of the puzzle are still missing. Therefore, we have identified several research gaps that should be addressed in future studies. Closing these gaps is both important and worthwhile in order to gain a deeper understanding of how the therapeutic alliance may influence broaden-and-build cycles and, ultimately, the oxytocin system. Both the therapeutic alliance and oxytocin have been independently associated with symptom reduction and enhanced well-being. It is therefore conceivable that their effects are closely intertwined—perhaps even two sides of the same coin, or more precisely, reflecting a common underlying mechanism.

Author contributions

ME: Conceptualization, Methodology, Supervision, Visualization, Writing – original draft, Writing – review & editing. ES: Conceptualization, Methodology, Writing – original draft, Writing – review & editing.

Funding

The author(s) declared that financial support was not received for this work and/or its publication.

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 author(s) declare that no Generative AI was used in the creation of this manuscript.

Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.

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. Jones C, Barrera I, Brothers S, Ring R, and Wahlestedt C. Oxytocin and social functioning. Dialogues Clin Neurosci. (2017) 19:193–201. doi: 10.31887/DCNS.2017.19.2/cjones

PubMed Abstract | Crossref Full Text | Google Scholar

2. Takayanagi Y and Onaka T. Roles of oxytocin in stress responses, allostasis and resilience. Int J Mol Sci. (2021) 23:150. doi: 10.3390/ijms23010150

PubMed Abstract | Crossref Full Text | Google Scholar

3. Peled-Avron L, Abu-Akel A, and Shamay-Tsoory S. Exogenous effects of oxytocin in five psychiatric disorders: a systematic review, meta-analyses and a personalized approach through the lens of the social salience hypothesis. Neurosci Biobehav Rev. (2020) 114:70–95. doi: 10.1016/j.neubiorev.2020.04.023

PubMed Abstract | Crossref Full Text | Google Scholar

4. Cochran DM, Fallon D, Hill M, and Frazier JA. The role of oxytocin in psychiatric disorders: a review of biological and therapeutic research findings. Harvard Rev Psychiatry. (2013) 21:219–47. doi: 10.1097/HRP.0b013e3182a75b7d

PubMed Abstract | Crossref Full Text | Google Scholar

5. Young LJ. Oxytocin, social cognition and psychiatry. Neuropsychopharmacology. (2014) 40:243–4. doi: 10.1038/npp.2014.186

PubMed Abstract | Crossref Full Text | Google Scholar

6. Zilcha-Mano S, Shamay-Tsoory S, Dolev-Amit T, Zagoory-Sharon O, and Feldman R. Oxytocin as a biomarker of the formation of therapeutic alliance in psychotherapy and counseling psychology. J Couns Psychol. (2020) 67:523–35. doi: 10.1037/cou0000386

PubMed Abstract | Crossref Full Text | Google Scholar

7. Durante C, Di Vincenzo G, Minutoli A, Nicolais G, and Carola V. The role of oxytocin as an indicator of outcome and therapeutic alliance. Res Psychotherapy: Psychopathology Process Outcome. (2025) 28:842. doi: 10.4081/ripppo.2025.842

PubMed Abstract | Crossref Full Text | Google Scholar

8. Elliott R, Bohart AC, Watson JC, and Greenberg LS. Empathy. Psychotherapy. (2011) 48:43–9. doi: 10.1037/a0022187

PubMed Abstract | Crossref Full Text | Google Scholar

9. Barchi-Ferreira AM and Osório FL. Associations between oxytocin and empathy in humans: A systematic literature review. Psychoneuroendocrinology. (2021) 129:105268. doi: 10.1016/j.psyneuen.2021.105268

PubMed Abstract | Crossref Full Text | Google Scholar

10. Schwartz L, Levy J, Shapira Y, Salomonski C, Hayut O, Zagoory-Sharon O, et al. Empathy aligns brains in synchrony. iScience. (2025) 28(6):112642. doi: 10.1016/j.isci.2025.112642

PubMed Abstract | Crossref Full Text | Google Scholar

11. Farina B, Liotti M, Imperatori C, Tombolini L, Gasperini E, Mallozzi P, et al. Cooperation within the therapeutic relationship improves metacognitive functioning: preliminary findings. Res Psychother (Milano). (2023) 26:712. doi: 10.4081/ripppo.2023.712

PubMed Abstract | Crossref Full Text | Google Scholar

12. Modic KU and Žvelc G. Helpful aspects of the therapeutic relationship in integrative psychotherapy. Int J Integr Psychother. (2015) 6:1–25.

Google Scholar

13. Mallinckrodt B. Change in working alliance, social support, and psychological symptoms in brief therapy. J Couns Psychol. (1996) 43:448. doi: 10.1037/0022-0167.43.4.448

Crossref Full Text | Google Scholar

14. Tsai TY, Tseng HH, Chi MH, Chang HH, Wu CK, Yang YK, et al. The interaction of oxytocin and social support, loneliness, and cortisol level in major depression. Clin Psychopharmacol Neurosci. (2019) 17:487. doi: 10.9758/cpn.2019.17.4.487

PubMed Abstract | Crossref Full Text | Google Scholar

15. Lindfors O, Ojanen S, Jääskeläinen T, and Knekt P. Social support as a predictor of the outcome of depressive and anxiety disorder in short-term and long-term psychotherapy. Psychiatry Res. (2014) 216:44–51. doi: 10.1016/j.psychres.2013.12.050

PubMed Abstract | Crossref Full Text | Google Scholar

16. Wampold BE. The great psychotherapy debate: Models, methods, and findings. London: Routledge (2001).

Google Scholar

17. Tschuschke V, Koemeda-Lutz M, von Wyl A, Crameri A, and Schulthess P. The impact of patients' and therapists' views of the therapeutic alliance on treatment outcome in psychotherapy. J nervous Ment Dis. (2020) 208:56–64. doi: 10.1097/NMD.0000000000001111

PubMed Abstract | Crossref Full Text | Google Scholar

18. Grossman-Giron A, Fisher H, Atzil-Slonim D, Maoz H, Nitzan U, Tzur Bitan D, et al. The effect of oxytocin administration on patient-therapist alliance congruence: results from a randomized controlled trial. Psychother Res. (2024) 34(8):1092–102.

PubMed Abstract | Google Scholar

19. Ellenbogen MA, Cardoso C, Serravalle L, Vadaga K, and Joober R. The effects of intranasal oxytocin on the efficacy of psychotherapy for major depressive disorder: a pilot randomized controlled trial. psychol Med. (2024) 54(9):1–11. doi: 10.1017/S0033291724000217

PubMed Abstract | Crossref Full Text | Google Scholar

20. Mikulincer M and Shaver P. Mental representations and attachment security. Interpersonal Cogn. (2005), 233–66.

Google Scholar

21. Mikulincer M and Shaver PR. An attachment perspective on psychopathology. World Psychiatry. (2012) 11:11–5. doi: 10.1016/j.wpsyc.2012.01.003

PubMed Abstract | Crossref Full Text | Google Scholar

22. Bartz JA, Zaki J, Bolger N, Hollander E, Ludwig NN, Kolevzon A, et al. Oxytocin selectively improves empathic accuracy. Psychol Sci. (2010) 21(10):1426–8.

Google Scholar

23. Nawa N, Nakamura K, and Fujiwara T. Oxytocin response following playful mother–child interaction in survivors of the great East Japan earthquake. Front Psychiatry. (2020) 11:477. doi: 10.3389/fpsyt.2020.00477

PubMed Abstract | Crossref Full Text | Google Scholar

24. Bosmans G, Bakermans-Kranenburg MJ, Vervliet B, Verhees MW, and van IJzendoorn MH. A learning theory of attachment: Unraveling the black box of attachment development. Neurosci Biobehav Rev. (2020) 113:287–98. doi: 10.1016/j.neubiorev.2020.03.014

PubMed Abstract | Crossref Full Text | Google Scholar

25. Ditzen B, Schaer M, Gabriel B, Bodenmann G, Ehlert U, and Heinrichs M. Intranasal oxytocin increases positive communication and reduces cortisol levels during couple conflict. Biol Psychiatry. (2009) 65:728–31. doi: 10.1016/j.biopsych.2008.10.011

PubMed Abstract | Crossref Full Text | Google Scholar

26. Fang A, Hoge EA, Heinrichs M, and Hofmann SG. Attachment style moderates the effects of oxytocin on social behaviors and cognitions during social rejection: Applying a research domain criteria framework to social anxiety. Clin psychol Sci. (2014) 2:740–7. doi: 10.1177/2167702614527948

PubMed Abstract | Crossref Full Text | Google Scholar

27. Rockliff H, Karl A, McEwan K, Gilbert J, Matos M, and Gilbert P. Effects of intranasal oxytocin on'compassion focused imagery'. Emotion. (2011) 11(6):1388.

PubMed Abstract | Google Scholar

28. Zhang K, Fan Y, Yu R, Tian Y, Liu J, and Gong P. Intranasal oxytocin administration but not peripheral oxytocin regulates behaviors of attachment insecurity: A meta-analysis. Psychoneuroendocrinology. (2021) 132:105369. doi: 10.1016/j.psyneuen.2021.105369

PubMed Abstract | Crossref Full Text | Google Scholar

29. Buchheim A, Heinrichs M, George C, Pokorny D, Koops E, Henningsen P, et al. Oxytocin enhances the experience of attachment security. Psychoneuroendocrinology. (2009) 34:1417–22. doi: 10.1016/j.psyneuen.2009.04.002

PubMed Abstract | Crossref Full Text | Google Scholar

30. Fraley RC, Hudson NW, Heffernan ME, and Segal N. Are adult attachment styles categorical or dimensional? A taxometric analysis of general and relationship-specific attachment orientations. J Pers Soc Psychol. (2015) 109:354. doi: 10.1037/pspp0000027

PubMed Abstract | Crossref Full Text | Google Scholar

31. Travis LA, Bliwise NG, Binder JL, and Horne-Moyer HL. Changes in clients' attachment styles over the course of time-limited dynamic psychotherapy. Psychotherapy: Theory, Research, Practice, Training. (2001) 38(2):149.

Google Scholar

32. Lange J, Goerigk S, Nowak K, Rosner R, and Erhardt A. Attachment style change and working alliance in panic disorder patients treated with cognitive behavioraltherapy. Psychotherapy. (2021) 58(2):206.

PubMed Abstract | Google Scholar

33. Manvelian A, Boyd S, O’Hara KL, Watters C, Liu Y, and Sbarra DA. Promoting attachment security during the transition to college: A pilot study of emotionally focused mentoring. J Soc Pers Relat. (2023) 40:4075–101. doi: 10.1177/02654075231195530

PubMed Abstract | Crossref Full Text | Google Scholar

34. Karl A, Carnelley KB, Arikan G, Baldwin DS, Heinrichs M, and Stopa L. The effect of attachment security priming and oxytocin on physiological responses to trauma films and subsequent intrusions. Behav Res Ther. (2021) 141:103845. doi: 10.1016/j.brat.2021.103845

PubMed Abstract | Crossref Full Text | Google Scholar

35. Zilcha-Mano S, Goldstein P, Dolev-Amit T, and Shamay-Tsoory S. Oxytocin synchrony between patients and therapists as a mechanism underlying effective psychotherapy for depression. J Consulting Clin Psychol. (2021) 89:49–57. doi: 10.1037/ccp0000619

PubMed Abstract | Crossref Full Text | Google Scholar

36. Diener MJ and Monroe JM. The relationship between adult attachment style and therapeutic alliance in individual psychotherapy: a meta-analytic review. Psychother (Chicago Ill.). (2011) 48:237–48.

PubMed Abstract | Google Scholar

37. Nienhuis JB, Owen J, Valentine JC, Winkeljohn Black S, Halford TC, Parazak SE, et al. Therapeutic alliance, empathy, and genuineness in individual adult psychotherapy: A meta-analytic review. Psychother Res. (2018) 28:593–605. doi: 10.1080/10503307.2016.1204023

PubMed Abstract | Crossref Full Text | Google Scholar

38. Barraza JA and Zak PJ. Empathy toward strangers triggers oxytocin release and subsequent generosity. Ann New York Acad Sci. (2009) 1167:182–9. doi: 10.1111/j.1749-6632.2009.04504.x

PubMed Abstract | Crossref Full Text | Google Scholar

39. Zak PJ, Curry B, Owen T, and Barraza JA. Oxytocin release increases with age and is associated with life satisfaction and prosocial behaviors. Front Behav Neurosci. (2022) 16:846234. doi: 10.3389/fnbeh.2022.846234

PubMed Abstract | Crossref Full Text | Google Scholar

40. Procyshyn TL, Watson NV, and Crespi BJ. Experimental empathy induction promotes oxytocin increases and testosterone decreases. Hormones Behav. (2020) 117:104607. doi: 10.1016/j.yhbeh.2019.104607

PubMed Abstract | Crossref Full Text | Google Scholar

41. Baron-Cohen S and Wheelwright S. The empathy quotient: an investigation of adults with Asperger syndrome or high functioning autism, and normal sex differences. J Autism Dev Disord. (2004) 34:163–75. doi: 10.1023/B:JADD.0000022607.19833.00

PubMed Abstract | Crossref Full Text | Google Scholar

42. Svedholm-Häkkinen AM, Halme S, and Lindeman M. Empathizing and systemizing are differentially related to dimensions of autistic traits in the general population. Int J Clin Health Psychol. (2018) 18(1):35–42.

PubMed Abstract | Google Scholar

43. Fisher H, Solomonov N, Falkenström F, Shahar B, Shamay-Tsoory S, and Zilcha-Mano S. Therapists' oxytocin response mediates the association between patients' negative emotions and psychotherapy outcomes. J Affect Disord. (2023) 338:163–70. doi: 10.1016/j.jad.2023.06.013

PubMed Abstract | Crossref Full Text | Google Scholar

44. Mu Y, Guo C, and Han S. Oxytocin enhances inter-brain synchrony during social coordination in male adults. Soc Cogn Affect Neurosci. (2016) 11:1882–93. doi: 10.1093/scan/nsw106

PubMed Abstract | Crossref Full Text | Google Scholar

45. Influs M, Pratt M, Masalha S, Zagoory-Sharon O, and Feldman R. A social neuroscience approach to conflict resolution: dialogue intervention to Israeli and Palestinian youth impacts oxytocin and empathy. Soc Neurosci. (2019) 14:378–89. doi: 10.1080/17470919.2018.1479983

PubMed Abstract | Crossref Full Text | Google Scholar

46. Influs M, Masalha S, Zagoory-Sharon O, and Feldman R. Dialogue intervention to youth amidst intractable conflict attenuates stress response to outgroup. Hormones Behav. (2019) 110:68–76. doi: 10.1016/j.yhbeh.2019.02.013

PubMed Abstract | Crossref Full Text | Google Scholar

47. Drimalla H, Landwehr N, Hess U, and Dziobek I. From face to face: the contribution of facial mimicry to cognitive and emotional empathy. Cogn Emotion. (2019) 33:1672–86. doi: 10.1080/02699931.2019.1596068

PubMed Abstract | Crossref Full Text | Google Scholar

48. Scatliffe N, Casavant S, Vittner D, and Cong X. Oxytocin and early parent-infant interactions: A systematic review. Int J Nurs Sci. (2019) 6:445–53. doi: 10.1016/j.ijnss.2019.09.009

PubMed Abstract | Crossref Full Text | Google Scholar

49. Spengler FB, Scheele D, Marsh N, Kofferath C, Flach A, Schwarz S, et al. Oxytocin facilitates reciprocity in social communication. Soc Cogn Affect Neurosci. (2017) 12:1325–33. doi: 10.1093/scan/nsx061

PubMed Abstract | Crossref Full Text | Google Scholar

50. De Coster L, Mueller SC, T'Sjoen G, De Saedeleer L, and Brass M. The influence of Oxytocin on automatic motor simulation. Psychoneuroendocrinology. (2014) 50:220–6. doi: 10.1016/j.psyneuen.2014.08.021

PubMed Abstract | Crossref Full Text | Google Scholar

51. Korb S, Malsert J, Strathearn L, Vuilleumier P, and Niedenthal P. Sniff and mimic—intranasal oxytocin increases facial mimicry in a sample of men. Hormones Behav. (2016) 84:64–74. doi: 10.1016/j.yhbeh.2016.06.003

PubMed Abstract | Crossref Full Text | Google Scholar

52. Trasmundi SB and Philipsen JS. Embodiments and co-actions: The function of trust and re-enactment in the practice of psychotherapy. Cogn Semiotics. (2020) 13:20202032. doi: 10.1515/cogsem-2020-2032

Crossref Full Text | Google Scholar

53. Kosfeld M, Heinrichs M, Zak PJ, Fischbacher U, and Fehr E. Oxytocin increases trust in humans. Nature. (2005) 435:673–6. doi: 10.1038/nature03701

PubMed Abstract | Crossref Full Text | Google Scholar

54. Declerck CH, Boone C, and Kiyonari T. The effect of oxytocin on cooperation in a prisoner’s dilemma depends on the social context and a person’s social value orientation. Soc Cogn Affect Neurosci. (2014) 9:802–9. doi: 10.1093/scan/nst040

PubMed Abstract | Crossref Full Text | Google Scholar

55. Declerck CH, Boone C, Pauwels L, Vogt B, and Fehr E. A registered replication study on oxytocin and trust. Nat Hum Behav. (2020) 4:646–55. doi: 10.1038/s41562-020-0878-x

PubMed Abstract | Crossref Full Text | Google Scholar

56. Baumgartner T, Heinrichs M, Vonlanthen A, Fischbacher U, and Fehr E. Oxytocin shapes the neural circuitry of trust and trust adaptation in humans. Neuron. (2008) 58:639–50. doi: 10.1016/j.neuron.2008.04.009

PubMed Abstract | Crossref Full Text | Google Scholar

57. Nave G, Camerer C, and McCullough M. Does oxytocin increase trust in humans? A critical review of research. Perspect psychol Sci. (2015) 10:772–89. doi: 10.1177/1745691615600138

PubMed Abstract | Crossref Full Text | Google Scholar

58. Walum H, Waldman ID, and Young LJ. Statistical and methodological considerations for the interpretation of intranasal oxytocin studies. Biol Psychiatry. (2016) 79(3):251–7.

PubMed Abstract | Google Scholar

59. Van IJzendoorn MH and Bakermans-Kranenburg MJ. A sniff of trust: meta-analysis of the effects of intranasal oxytocin administration on face recognition, trust to in-group, and trust to out-group. Psychoneuroendocrinology. (2012) 37:438–43. doi: 10.1016/j.psyneuen.2011.07.008

PubMed Abstract | Crossref Full Text | Google Scholar

60. Bartz J, Simeon D, Hamilton H, Kim S, Crystal S, Braun A, et al. Oxytocin can hinder trust and cooperation in borderline personality disorder. Soc Cogn Affect Neurosci. (2011) 6:556–63. doi: 10.1093/scan/nsq085

PubMed Abstract | Crossref Full Text | Google Scholar

61. Shou Q, Yamada J, Nishina K, Matsunaga M, Kiyonari T, and Takagishi H. Is oxytocin a trust hormone? Salivary oxytocin is associated with caution but not with general trust. PloS One. (2022) 17:e0267988. doi: 10.1371/journal.pone.0267988

PubMed Abstract | Crossref Full Text | Google Scholar

62. Mikolajczak M, Gross JJ, Lane A, Corneille O, de Timary P, and Luminet O. Oxytocin makes people trusting, not gullible. psychol Sci. (2010) 21:1072–4. doi: 10.1177/0956797610377343

PubMed Abstract | Crossref Full Text | Google Scholar

63. Frazier I, Lin T, Liu P, Skarsten S, Feifel D, and Ebner NC. Age and intranasal oxytocin effects on trust-related decisions after breach of trust: Behavioral and brain evidence. Psychol Aging. (2021) 36:10. doi: 10.1037/pag0000545

PubMed Abstract | Crossref Full Text | Google Scholar

64. Yao S, Zhao W, Cheng R, Geng Y, Luo L, and Kendrick KM. Oxytocin makes females, but not males, less forgiving following betrayal of trust. Int J Neuropsychopharmacol. (2014) 17:1785–92. doi: 10.1017/S146114571400090X

PubMed Abstract | Crossref Full Text | Google Scholar

65. Zak PJ, Kurzban R, and Matzner WT. Oxytocin is associated with human trustworthiness. Horm Behav. (2005) 48(5):522–7.

Google Scholar

66. Kiss I, Levy-Gigi E, and Kéri S. CD 38 expression, attachment style and habituation of arousal in relation to trust-related oxytocin release. Biol Psychol. (2011) 88:223–6. doi: 10.1016/j.biopsycho.2011.08.005

PubMed Abstract | Crossref Full Text | Google Scholar

67. Cohen S. Stress, social support, and disorder. In: The Meaning And Measurement Of Support. London: Taylor & Francis (2014). p. 109–24.

Google Scholar

68. Carter CS. Neuroendocrine perspectives on social attachment and love. Psychoneuroendocrinology. (1998) 23:779–818. doi: 10.1016/S0306-4530(98)00055-9

PubMed Abstract | Crossref Full Text | Google Scholar

69. Grewen KM, Girdler SS, Amico J, and Light KC. Effects of partner support on resting oxytocin, cortisol, norepinephrine, and blood pressure before and after warm partner contact. Psychosomatic Med. (2005) 67:531–8. doi: 10.1097/01.psy.0000170341.88395.47

PubMed Abstract | Crossref Full Text | Google Scholar

70. Heinrichs M, Baumgartner T, Kirschbaum C, and Ehlert U. Social support and oxytocin interact to suppress cortisol and subjective responses to psychosocial stress. Biol Psychiatry. (2003) 54:1389–98. doi: 10.1016/S0006-3223(03)00465-7

PubMed Abstract | Crossref Full Text | Google Scholar

71. Neumann ID. The advantage of social living: brain neuropeptides mediate the beneficial consequences of sex and motherhood. Front Neuroendocrinol. (2009) 30:483–96. doi: 10.1016/j.yfrne.2009.04.012

PubMed Abstract | Crossref Full Text | Google Scholar

72. Gryksa K and Neumann ID. Consequences of pandemic-associated social restrictions: Role of social support and the oxytocin system. Psychoneuroendocrinology. (2022) 135:105601. doi: 10.1016/j.psyneuen.2021.105601

PubMed Abstract | Crossref Full Text | Google Scholar

73. Sunahara CS, Wilson SJ, Rosenfield D, Alvi T, Szeto A, Mendez AJ, et al. Oxytocin reactivity to a lab-based stressor predicts support seeking after stress in daily life: Implications for the Tend-and-Befriend theory. Psychoneuroendocrinology. (2022) 145:105897. doi: 10.1016/j.psyneuen.2022.105897

PubMed Abstract | Crossref Full Text | Google Scholar

74. Reblin M and Uchino BN. Social and emotional support and its implication for health. Curr Opin Psychiatry. (2008) 21(2):201–5.

Google Scholar

75. Crockford C, Deschner T, and Wittig RM. The role of oxytocin in social buffering: what do primate studies add? Curr Top Behav Neurosci. (2017) 155–73.

PubMed Abstract | Google Scholar

76. Rumble AC, Van Lange PA, and Parks CD. The benefits of empathy: When empathy may sustain cooperation in social dilemmas. Eur J Soc Psychol. (2010) 40:856–66. doi: 10.1002/ejsp.659

Crossref Full Text | Google Scholar

77. De Dreu CK and Kret ME. Oxytocin conditions intergroup relations through upregulated in-group empathy, cooperation, conformity, and defense. Biol Psychiatry. (2016) 79:165–73. doi: 10.1016/j.biopsych.2015.03.020

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: oxytocin, therapeutic alliance, attachment, empathy, social synchrony, cooperation, social support

Citation: Eckert M and Schandro E (2025) How factors of the therapeutic alliance interact with oxytocin neurotransmission in psychotherapy. Front. Psychiatry 16:1659841. doi: 10.3389/fpsyt.2025.1659841

Received: 04 July 2025; Accepted: 21 November 2025; Revised: 19 November 2025;
Published: 11 December 2025.

Edited by:

Esben Strodl, Queensland University of Technology, Australia

Reviewed by:

Valery Krupnik, Naval Hospital Camp Pendleton, United States

Copyright © 2025 Eckert and Schandro. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Marcus Eckert, bWFyY3VzLmVja2VydEBhcG9sbG9uLWhvY2hzY2h1bGUuZGU=

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.