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 — DRUG
    Initial 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-Label
    One 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

Locations (1)

FacilityCityStateZIPSite coordinators
The Parsons Research Center for Psychedelic HealingNew YorkNew York10025
Tamar Glatman Zaretsky, PsyD
(914) 340-3669
Lily Fischer, MSc
‪(862) 253-1938‬
Rachel Yehuda, PhD (PRINCIPAL_INVESTIGATOR)

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