MDMA-Assisted Therapy for Mental Healthcare Providers
Part of paid clinical trials in New York, New York.
- Sponsor
- Rachel Yehuda
- Study ID
- NCT07102576
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Mental Wellbeing
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- MDMA Hydrochloride — DRUGInitial dose of 120 mg MDMA HCl in a therapeutic setting, followed 1.5 to 2 hours later by a supplemental dose of 40 mg MDMA HCl. Supplemental doses may be withheld if tolerability issues emerge or it is declined by the participant.
Study Details
This is a phase 1, open-label study to assess changes in mental well-being following MDMA administration within a therapeutic setting, in mental health providers who are in training to become MDMA assisted therapists. Secondary outcome measures will examine the effects on provider burnout, provider self-efficacy, mood, self-compassion, quality of life, and other psychological factors. Participants will work with a co-therapy pair as they engage in a preparatory session, one experimental session with MDMA, and an integration session the following day.
Key Dates
- Start date
- Feb 11, 2026
- Status verified
- Feb 2026
- Primary completion
- Sep 21, 2029
- Completion
- Dec 21, 2029
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- SUPPORTIVE_CARE
Arms
- Experimental: Open-LabelOne session of MDMA-Assisted Therapy
Primary Outcome Measure
Mental Health Continuum-Short Form (MHC-SF) [ Time Frame: At baseline and 28 days post-treatment ]
Central Contacts
- Lily Fischer862-253-1938
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| The Parsons Research Center for Psychedelic Healing | New York | New York | 10025 | Rachel Yehuda, PhD (PRINCIPAL_INVESTIGATOR) |