Actively Recruiting

Phase 1
Age: 18Years +
All Genders
Healthy Volunteers
NCT07102576

MDMA-Assisted Therapy for Mental Healthcare Providers

Led by Rachel Yehuda · Updated on 2026-03-27

30

Participants Needed

1

Research Sites

201 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

MDMA-Assisted Therapy for Mental Healthcare Providers

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • At least 18 years old at the time of signing informed consent
  • Fluent in English
  • Able to swallow pills
  • Agree to have study visits audiovisually recorded
  • Able to provide a contact person reachable if participant becomes unwell or unreachable
  • Licensed, license-eligible, or trainee in a relevant healthcare or mental health profession
  • Learning or certified to conduct MDMA-assisted therapy through the Lykos MDMA-Assisted Therapy Training program or authorized affiliate
  • Body weight of at least 45 kilograms (100 pounds)
Not Eligible

You will not qualify if you...

  • Started a new form of psychiatric or mental health care within 12 weeks before enrollment
  • Current alcohol or cannabis use disorder within the past 12 months
  • Substance use disorder within the past 12 months
  • Suicidal thoughts within the last 6 months
  • Repetitive or recent use of Ecstasy/MDMA
  • Currently enrolled in another clinical study involving investigational treatment without approval
  • Current or recent (within 3 months) major depressive episode or current anxiety disorder
  • Current eating disorder with compensatory behaviors
  • History or current primary psychotic disorder or bipolar disorder
  • Previous participation in a clinical trial involving MDMA administration
  • Personal relationship with the site investigator
  • Pregnant, nursing, or able to become pregnant without effective contraception

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Parsons Research Center for Psychedelic Healing

New York, New York, United States, 10025

Actively Recruiting

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Research Team

L

Lily Fischer

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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