Changes in trauma symptoms of discrimination after MDMA-assisted psychotherapy for posttraumatic stress disorder
This preliminary study (n=5) examined MDMA-assisted psychotherapy for post-traumatic stress disorder and found that discrimination-related trauma symptoms fell after treatment in a small, diverse group of participants. All participants reported marked improvement, but the sample was very small.
1 linked clinical trial·6 references indexed in Blossom
Authors
- Williams, M. T.
- Faber, S. C.
- Sloshower, J.
Published
Abstract
This preliminary study explored the effects of MDMA-assisted therapy on trauma symptoms related to discrimination, as measured by the Trauma Symptoms of Discrimination Scale (TSDS). A total of five diverse participants, who experienced multiple types of discrimination (e.g., gender, racial/ethnic, social class, age, sexual orientation), were assessed before and after treatment. A paired-samples t‐test indicated a significant reduction in TSDS scores following therapy, with mean scores decreasing by 38% (t(4) = 2.85, p = .046). The effect size was large (Cohen’s d = 1.28), though this estimate should be interpreted cautiously given the small sample size. All participants reported marked improvements in discrimination related trauma symptoms following MDMA-assisted therapy in this sample, and across different racial/ethnic identities and discrimination histories. These findings provide preliminary evidence that MDMA-assisted therapy may effectively alleviate discrimination-related trauma in marginalized populations. We discuss the importance of culturally-informed treatment approaches for psychedelic-assisted psychotherapy. These early results warrant further investigation in larger, more diverse cohorts.
Research Summary of 'Changes in trauma symptoms of discrimination after MDMA-assisted psychotherapy for posttraumatic stress disorder'
βBlossom's Take
MDMA-assisted psychotherapy was linked to lower discrimination-related trauma symptoms in a five-person substudy
SourcedDid trauma symptoms tied to discrimination change after treatment?
- 38%
- mean TSDS reduction after therapy
- 63.20
- baseline mean TSDS score
- 39.40
- post-treatment mean TSDS score
- 1.28
- Cohen's d effect size
Participants in the final analysable sample
Open-label, uncontrolled substudy within an expanded access programme, so the results are preliminary and cannot separate MDMA effects from psychotherapy, expectancy, or regression to the mean. The numbers here come from the paper's own TSDS pre and post analysis in five participants, not from a controlled trial.
Introduction
Williams and colleagues frame the study around a gap in psychedelic and trauma research: although MDMA-assisted psychotherapy has been investigated for post-traumatic stress disorder, little is known about whether it also reduces trauma symptoms linked to discrimination, oppression, and marginalisation. The authors note that earlier psychedelic studies have included relatively few Black, Indigenous, and other people of colour, and that most trauma research has focused on discrete events rather than chronic social stressors such as racism, class-based oppression, and bias related to gender or sexual orientation. They also point out that the Trauma Symptoms of Discrimination Scale (TSDS) is a validated way to assess anxiety-related trauma symptoms caused by oppression-based trauma, but that no clinical trials had yet examined changes in such symptoms before and after psychedelic therapy. The purpose of this substudy was to add the TSDS to an expanded access programme of MDMA-assisted psychotherapy for treatment-resistant PTSD and examine whether symptoms of discriminatory trauma changed after treatment. The authors describe this as an exploratory, real-world assessment of feasibility and possible efficacy in a small subgroup of participants who experienced discrimination-related trauma. They present the work as an early step towards understanding whether culturally informed psychedelic-assisted psychotherapy may help people with marginalised identities.
Methods
This study was nested within MAPS’ expanded access programme for MDMA-assisted psychotherapy for patients with treatment-resistant PTSD who could not join a clinical trial. The parent programme provided up to 50 patients with access to treatment and was intended to generate real-world evidence on both therapeutic outcomes and the logistics of delivery. Participants were told about study risks and benefits and gave written informed consent. The treatment model consisted of three non-drug preparatory psychotherapy sessions, followed by three MDMA-assisted therapy sessions, with three non-drug integrative sessions after each MDMA session. The extracted text does not clearly report the MDMA dose or detailed session procedures in this substudy. The TSDS was added as an additional measure to assess discrimination-related trauma symptoms alongside standard safety and efficacy outcomes. Although 28 participants completed treatment and 24 completed the TSDS at post-treatment, only nine had TSDS data at both screening and post-treatment. Four of those nine reported no symptoms at either time point and were excluded, leaving a final analysable sample of five participants. The low paired completion rate was attributed to the late addition of the TSDS and inconsistent administration across participants. The main analysis was a paired-samples t-test comparing TSDS scores before and after treatment, with a reported correlation between pre- and post-treatment scores and an effect size estimate (Cohen’s d).
Results
Five participants formed the final sample for the discrimination-trauma analysis. They completed the TSDS at screening and again after treatment. Baseline mean TSDS score was 63.20 (SD 16.44), falling to 39.40 (SD 10.74) after treatment. This represented a mean reduction of 24 points, or about 38%. The paired-samples t-test showed a statistically significant decrease in TSDS scores after MDMA-assisted psychotherapy, t(4) = 2.85, p = .046 (two-sided). The reported effect size was large, with Cohen’s d = 1.28 (95% CI 0.02 to 2.46). The correlation between baseline and post-treatment TSDS scores was weak, r = .10 (p = .87), suggesting little association between initial and final scores in this very small sample. The authors report that all five participants showed a decline in discrimination-related trauma symptoms. They also state that participants spanned multiple discrimination domains, including race/ethnicity, gender, class, age, and sexual orientation, and that some experienced more than one form of discrimination. The extracted text does not provide more detailed subgroup results, and it does not report adverse events in this substudy section.
Discussion
Williams and colleagues interpret the findings as preliminary evidence that MDMA-assisted psychotherapy may reduce trauma symptoms associated with discrimination and oppression. They emphasise that the average TSDS reduction was substantial and that the improvement reached statistical significance despite the very small sample. In their view, the large effect size suggests that the treatment may meaningfully alleviate discrimination-related trauma symptoms across people with different marginalised identities. The authors position these results alongside earlier research suggesting that psychedelic interventions can reduce racial or discrimination-related stress symptoms. They argue that the study adds value because trauma research has often overlooked chronic social harms, and because psychedelic trials have historically under-represented BIPOC participants and other marginalised groups. They also highlight the apparent improvement seen in both racialised participants and White participants, which they present as suggestive of culturally inclusive efficacy when care is provided in a culturally sensitive setting. The main limitations they acknowledge are the extremely small sample size, limited statistical power, and exploratory nature of the analysis. They note that the TSDS was introduced late, creating a low rate of paired completion and possible selection bias. They also state that the open-label design without a control group means placebo effects and the effects of psychotherapy alone cannot be separated from MDMA effects. In addition, overlap between discrimination types made it difficult to isolate the influence of any single form of discrimination, and the sample may not generalise to all people with discrimination-related trauma, particularly those less willing to engage in MDMA-assisted therapy. The authors’ broader implication is that psychedelic-assisted psychotherapy should be culturally attuned and intersectional, with therapists actively recognising racism, marginalisation, historical mistrust, and identity-specific stressors. They suggest that future studies should use larger samples and more consistent measurement to examine moderators such as type and chronicity of discrimination, intersectional identity burden, therapist-participant cultural match, prior therapy, and expectancy effects. They also argue that culturally competent and affirming care is central to optimising outcomes, not merely an added feature.
Conclusion
The authors conclude that this small substudy provides encouraging preliminary evidence that MDMA-assisted psychotherapy may reduce symptoms of discriminatory trauma in marginalised populations. They state that the TSDS scores fell significantly after treatment and that both Asian and White participants showed large improvements, with no sign that any subgroup failed to benefit. However, they stress that these findings are only exploratory because of the very limited sample size, and that any apparent group differences or associations should be treated as speculative.
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BACKGROUND
Investigational drugs that have not yet been approved by the FDA for prescription use can be made available to qualified patients through clinical trials. In cases where a patient is not able to enroll in a clinical trial or there are no ongoing clinical trials available, doctors may seek an alternate pathway called "expanded access" (also known as "compassionate use") for their patients. The Expanded Access Program (EAP) can allow patients with a serious or life-threatening disease or condition for which there are no comparable or satisfactory therapies to gain access to promising investigational drugs (US FDA, 2020). Through the EAP, Lykos (formerly MAPS PBC) received FDA authorization to establish an expanded access program for MDMA-assisted therapy for up to 50 patients with PTSD who met specific eligibility criteria. In addition, this program collects data on safety and tolerability of MDMA-assisted therapy in treatment-resistant patients with PTSD. Clinical trials of psychedelic therapies, including MDMA-assisted psychotherapy, have not adequately included Black, Indigenous or other people of color (BIPOC), or those with other marginalized identities. A review byfound that approximately 16% of participants self-identified as BIPOC in the 18 included psychedelic studies from 1993-2017. The failure to include BIPOC in psychedelic research trials neglects the ethnic, racial, and cultural factors that may impact individual responses to psychedelic therapies and thereby prevents generalizability of findings. Likewise, very few research studies address the experience of being a sexual or gender minority. "Oppression describes an asymmetrical power dynamic characterized by domination and subordination of a group by restricting access to social, economic, and political resources". Members of these disenfranchised groups may subsequently experience fear, stress, and even negative perceptions of themselves. As a chronic stressor, oppression can exacerbate poor mental health, leading to a concentration of health disparities within marginalized communities,. Increased exposure to stress from racial discrimination is a strong predictor of depression and anxiety for BIPOC, and similar findings exist for intersectional oppressions based on class, sexual orientation and race. Studies also consistently link poverty and lower socioeconomic status (SES) with increased vulnerability to negative physical and mental health conditions. Most trauma research is focused on discrete events, such as assault, combat, or natural disasters, with less attention paid to social conditions which can be traumatizing. The Trauma Symptoms of Discrimination Scale (TSDS;) is a clinical measure that demonstrates strong reliability and validity in the measurement of anxiety-related trauma symptoms due to oppression-based trauma. This measure was used in a series of studies examining the impact of psychedelics on racial trauma. One retrospective study included 313 diverse BIPOC in the US and Canada who reported a memorable experience connected with psychedelics that helped them cope with racial trauma. Participants reported their symptoms both before and after the experience, and there was a significant decrease in symptoms of racial trauma as measured by the TSDS after the psychedelic experience. However, to date, no clinical trials have measured changes in symptoms of oppression-based trauma before and after psychedelic-therapy.
PURPOSE
In addition to standard safety and efficacy outcome measures collected in MAPS' EAP for MDMAassisted psychotherapy of PTSD, we incorporated a validated measure of discriminatory trauma in order to assess the impact of treatment on oppression-based trauma symptoms in this subset. By measuring changes in TSDS scores, this study seeks to explore the feasibility and potential efficacy of MDMAassisted psychotherapy in alleviating discrimination-related trauma symptoms, paving the way for more effective trauma-focused treatments for people of color and others with marginalized identities.
PROCEDURE
The title of the parent study was "An Intermediate-size Multi-site Expanded Access Program for MDMAassisted Psychotherapy for Patients With Treatment-resistant PTSD,". The goal of this EAP was to provide access to MDMA-assisted therapy for eligible patients with treatment-resistant PTSD who were not able to enroll in another MDMA-assisted therapy clinical trial. Participants underwent three nondrug preparatory therapy sessions followed by three MDMA-assisted therapy sessions. Each MDMAassisted therapy session is followed by three non-drug integrative therapy sessions.
A R T I C L E I N P R E S S
other constraints. This study aimed to generate real-world evidence on both therapeutic outcomes and logistical feasibility of delivering MDMA-assisted therapy post-approval (MAPS Public Benefit Corporation [MAPS PBC], 2020). All participants were informed of study risks and benefits. All participants provided written informed consent to participate. Of the 28 participants who completed treatment, 24 completed the TSDS at post-treatment, and 9 completed the measure at both screening and post-treatment timepoints. Four of these participants reported no symptoms at either time point and were excluded, resulting in a final analyzable sample of 5 participants (see Table). The low rate of paired completion reflects the late addition of the TSDS within the Expanded Access Program and variability in providing it to participants.
RESULTS
Participants (N = 5) completed the TSDS before treatment during screening (Time 1) and again after treatment (Time 2). As shown in Table, the mean TSDS score at Time 1 was 63.20 (SD = 16.44), whereas at Time 2 it was 39.40 (SD = 10.74). A paired-samples t-test revealed that, despite the small sample size, this reduction in TSDS scores was statistically significant, t(4) = 2.85, p = .046 (two-sided). The effect size for this change was large, with Cohen's d = 1.28 (95% CI [0.02, 2.46]). The correlation between pre-and post-treatment TSDS scores was r = .10 (p = .87), indicating that baseline TSDS scores were only weakly related to post-treatment scores in this small sample. Overall, these findings suggest a notable decrease in discrimination-related trauma symptoms following MDMA-assisted therapy.
DISCUSSION
Participants included in this substudy had experienced discrimination in a range of identity domains (including race/ethnicity, gender, class, etc.), with some reporting multiple types of discrimination. All five participants showed a decline in discriminatory trauma symptoms following MDMA-assisted therapy for PTSD. The mean TSDS score realized a 24-point reduction, which represents approximately 38% improvement in these symptoms. This represents a large decrease in trauma symptoms and was statistically significant despite the small sample. This corresponds to a large effect size, suggesting that MDMA-assisted therapy may be able to substantially reduce discrimination-related trauma symptoms. These results are notable in the context of trauma among people with marginalized identities -they imply that a novel therapy like MDMA-assisted psychotherapy can potentially alleviate discriminationbased trauma symptoms across diverse individuals. This aligns with emerging research suggesting psychedelic interventions can reduce racial/discrimination-related stress symptoms. Despite the limitations, this substudy provides valuable insight for trauma research in marginalized populations. The substantial reduction in TSDS scores post-therapy suggests that MDMA-assisted psychotherapy may be a promising approach for treating trauma related to systemic discrimination and oppression. It is especially encouraging that members of racialized groups (in this case, Asian) showed healing alongside White participants, as historically there have been concerns that people of color might
A R T I C L E I N P R E S S
respond differently or face unique barriers in trauma treatment. Here, both groups benefited, hinting at the potential for culturally inclusive efficacy by way of culturally sensitive support, though larger trials are needed to confirm this. The results also reinforce the importance of an intersectional lens; clinicians and researchers should consider that individuals with multiple marginalized identities are susceptible to a greater burden of cumulative, systemic trauma (i.e., higher baseline severity)), yet the substantial reduction in TSDS scores suggests they showed comparable efficacy and improvement when given effective therapy tailored to their needs.
IMPLICATIONS FOR CULTURALLY ATTUNED PSYCHEDELIC-ASSISTED THERAPY
Given these valuable insights, this substudy emphasizes the importance of culturally attuned psychedelic-assisted therapy that reinforces an intersectional lens so that the burdens of cumulative, systemic trauma can be properly addressed. Culturally attuned PAT incorporates not only standard therapeutic competencies, but a keen and explicit recognition of sociocultural contexts, such as racism, marginalization, and historical mistrust with research and medicalized institutions. Such approaches require that therapists engage in ongoing cultural humility, actively validate experiences of racism, and create therapeutic environments which actively showcase diversity in its clinical care team so that participants can feel psychologically and culturally safe throughout treatment. Importantly, culturally responsive PAT extends beyond surface-level matching by racial and cultural identifiers, to involve deeper structural and relational considerations, such as integrating culturally relevant meaning making, attending to identify specific-stressors, and adapting an intersection and culturally attuned preparation and integration process that aligns with the participant's living experience. Inclusivity of culturally responsive PAT and, in conventional contexts, therapeutic care, is critical, as unaddressed cultural dynamics have been shown to shape both the therapeutic process and its outcomes. At the same time, culturally inclusive practices, whether inclusive of MDMA or otherwise, improve outcomes for BIPOC. Emerging evidence suggests that when BIPOC receives highquality, affirming, and culturally competent care, substantial therapeutic gains can occur regardless of therapeutic modality. In this sense, MDMA-assisted therapy may function as an enhancing catalyst by which BIPOC openly processes previously subverted psychological wounding as a result of negative experiences of marginalization in an environment that garners trauma-informed practices and cultural responsibility.
A R T I C L E I N P R E S S
Taken together, MDMA-assisted therapy may not exclusively account for the reductions in TSDS scores, but rather serve as an enhancement to already present trauma-informed therapeutic practices, provided within a culturally attuned context. The findings of this study highlight that the effectiveness of PAT is likely not only a function of the interventions themselves, but also of the context in which it is delivered. Ensuring that PAT is culturally attuned and provided by culturally competent clinicians is not ancillary, but rather a critical integration for ethical and optimized treatment. Future research should prioritize larger sample sizes to investigate the development and empirical testing of culturally competent PAT models to determine how best to optimize treatment efficacy for these individuals and their intersecting identities.
LIMITATIONS
The primary limitation of this substudy is its small sample size. With only 5 participants statistical power is very limited and observations are exploratory.. Additionally, the low rate of paired TSDS completion may introduce selection bias, as the measure was introduced late into the data collection process. Future studies should prioritize consistent administration of discrimination specific measures across all timepoints to improve data completeness. While the withinperson improvement was strong enough to reach statistical significance, comparisons between racial groups or gender would be unreliable. Several plausible moderators may influence treatment response which would be valuable to examine in a larger sample, such as type and chronicity of discrimination, intersectional identity burden, baseline PTSD severity, cultural identity match between participant and therapists, prior therapy experience, and expectancy effects. Future research with larger samples should examine these variables to better understand heterogeneity in treatment response and to inform more tailored, culturally responsive interventions. Additionally, the study was open-label and there were no control groups, thereby making it impossible to discern the role of placebo effects or the effect of psychotherapy alone. Moreover, the types of discrimination reported overlapped between participants (for example, most experienced racial/ethnic bias, often alongside other types), making it hard to isolate the effect of any single discrimination type on outcomes. We also note that all participants in this sample were willing to undergo MDMA-assisted therapy. As such, their experiences might not generalize to all individuals who have trauma from discrimination. Similarly, it is possible the ethnoracial demographics of the sample were skewed against the inclusion of racialized people from groups that have been historically subjected to unethical research practices due to fears of being harmed (e.g., Black Americans;.
CONCLUSION
Despite the limitations, this small substudy provides encouraging preliminary data for the role of MDMA-assisted psychotherapy in alleviating symptoms of discriminatory trauma among marginalized populations. Using the TSDS, we found that MDMA-assisted therapy was associated with significant reductions in trauma symptoms related to discrimination. Both Asian and White participants experienced large improvements in TSDS scores, with no evidence of any group failing to benefit, and those with multiple discrimination experiences responded equally well as those with fewer. These preliminary findings support the feasibility and potential effectiveness of addressing trauma from marginalized identity-based stressors with novel therapeutic approaches. However, due to the very limited sample size, any group differences or associations observed must be interpreted as speculative.
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Study Details
- Study Typeindividual
- Populationhumans
- Characteristicsobservational
- Journal
- Compound
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References (6)
References cited by this study and indexed in Blossom.
Ching, T. H., Williams, M. T., Wang, J. B. et al. · Journal of Psychopharmacology (2022)
Davis, A. K., Xin, Y., Sepeda, N. D. et al. · Chronic Stress (2021)
Goldy, S. P., Sepeda, N. D., Hilbert, S. N. et al. · Psychiatry Research (2026)
Halstead, M., Reed, S., Krause, R. et al. · Clinical Case Studies (2021)
Strauss, D., de la Salle, S., Sloshower, J. A. et al. · Journal of Medical Ethics (2021)
Williams, T. M., Davis, A. K., Xin, Y. et al. · Drugs Education Prevention and Policy (2020)
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