MDMA-Assisted Psychotherapy for Anxiety Associated With a Life-Threatening Illness
Brief Summary
Condition or Disease
- Anxiety
Phase
Study Design
Study type: | Interventional |
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Status: | Completed |
Study results: | Has Results |
Age: | 18 Years and older (Adult, Older Adult) |
Enrollment: | 18 () |
Funded by: | Other |
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Clinical Trial Dates
Start date: | Apr 01, 2015 | |
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Primary Completion: | May 01, 2018 | |
Completion Date: | Jul 01, 2018 | |
Study First Posted: | Apr 28, 2015 | |
Results First Posted: | Aug 02, 2021 | |
Last Updated: | Jan 13, 2022 |
Sponsors / Collaborators
Location
Individuals facing, or who have faced, a life-threatening illness contend with more than just the physical symptoms of their condition and may experience anxiety, depression, anger, and despair that can exacerbate their distress. Research suggests that diagnosis of, and living with a life-threatening illness can result in symptoms similar to those seen in posttraumatic stress disorder (PTSD).
3,-4-methylenedioxymethamphetamine (MDMA) is a monoamine releaser with a unique pharmacological profile that include decreased feelings of fear, increased positive mood and increased interpersonal trust. Findings from clinical trials in people with PTSD and anecdotal reports suggest that MDMA-assisted psychotherapy may assist people who have anxiety related to having a life-threatening illness.
This Phase 2 pilot study is a randomized, double-blind, placebo-controlled study in 18 participants comparing the effects of MDMA-assisted therapy vs. placebo with therapy. Thirteen participants were randomized to the active dose condition of 125 mg of MDMA (plus an optional supplemental dose of 62.5 mg MDMA) with therapy and five participants were randomized to the placebo with therapy condition. The study will consist of two blinded experimental sessions of MDMA-assisted therapy or placebo with therapy, each session lasting six to eight hours and scheduled two to four weeks apart. Each participant will be unblinded one month after their second experimental session in Stage 1. After unblinding, participants receiving MDMA will complete a third open-label experimental session of MDMA-assisted therapy and participants who originally received placebo will have the opportunity to cross over to open-label Stage 2 and receive active MDMA-assisted therapy in 3 sessions.
The primary objective of the study is to assess changes in trait anxiety in subjects receiving active dose MDMA compared to those receiving placebo as measured by State-Trait Anxiety Index (STAI) Trait scores from Baseline to the Primary Endpoint (one month after the second experimental session).
Eligibility Criteria
Sex: | All |
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Minimum Age: | 18 |
More Details
NCT Number: | NCT02427568 |
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Other IDs: | MDA-1 |
Study URL: | https://ClinicalTrials.gov/show/NCT02427568 |