PEM: Prosocial Effects of MDMA

Sponsor
University of Chicago (Other)
Overall Status
Recruiting
CT.gov ID
NCT05948683
Collaborator
National Institutes of Health (NIH) (NIH), National Institute on Drug Abuse (NIDA) (NIH)
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Study Details

Study Description

Brief Summary

In this study, the aim is to test the hypothesis that MDMA produces greater prosocial effects when administered in the presence of a familiar, compared to an unfamiliar, person

Condition or Disease Intervention/Treatment Phase
Early Phase 1

Detailed Description

MDMA has shown promise as an adjunct to psychotherapy in the treatment of PTSD and other disorders. When used clinically with psychotherapy, the drug is believed to interact with the interpersonal components of the psychotherapy, especially the patient-therapist interaction. Indeed, patients and therapists usually form a strong alliance during several preparatory sessions, even before a drug is administered. Experts believe that the patient's familiarity and trust of the therapist is critical to the success of the intervention. Whereas therapeutic alliance is critical to the success of any psychotherapy, it may be especially important when psychoactive drugs are part of the treatment. The importance of this trust-building component preceding drug-assisted therapy has not been investigated.

There are mechanistic reasons to expect that MDMA will be more effective when a patient interacts with a familiar and trusted other person, compared to a stranger. MDMA is thought to exert its "prosocial" effects by increasing the social bonding hormone, oxytocin, and this hormone may contribute to its therapeutic effects. However, there is evidence that oxytocin increases feelings of connectedness specifically with familiar "in-group" members, and that it may not produce affiliative effects with individuals who are unfamiliar, or perceived to be outside their groups. Thus, the pro-social effects of oxytocin may depend on the degree of familiarity and closeness of the interacting partner. As noted above, during preparatory sessions in drug-assisted psychotherapy the patient forms a bond with a therapists before the drug is administered, which may serve to increase the 'in-group' effect of the drug, and thus maximize the therapeutic potential of the MDMA.

Controlled laboratory studies (without psychotherapy) show that MDMA produces prosocial effects on measures of mood and socio-emotional function. However, most of these studies are conducted in isolated individuals, or with study partners who have no prior relationship with the participant. In this proposed study the study team will investigate whether the prosocial effects of MDMA are greater when interacting with a partner to whom the participant feels close and more connected, compared to a partner who is unfamiliar.

To establish familiarity in one of the study groups the study team will use a procedure designed to establish feelings of closeness and connectedness between two strangers. In this procedure, two same-sex partners, who are initially strangers, engage in a 45 min conversation with one of two sets of topics provided by the experimenter. In one condition the topics remain superficial ("small talk" condition) and in the other, they become progressively deeper ("deep talk" condition) over the 45 mins. The study team and others have shown that the deep talk condition produces feelings of connection between the partners, and participants report feeling understood and liking their partners.

In the present study, the investigator will use this procedure to establish familiarity between conversation partners. The investigator aims to test the hypothesis that MDMA produces greater prosocial effects when administered in the presence of a familiar, compared to an unfamiliar, person. Participants will participate in four sessions, in which they receive MDMA (100 mg) or a placebo and then engage in a 15-min conversation with a familiar or unfamiliar person.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
34 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Other
Official Title:
Effects of Familiarity on Prosocial Effects of MDMA
Anticipated Study Start Date :
Jul 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2024
Anticipated Study Completion Date :
Jun 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Familiar partner with placebo

Participant engages in social interaction with 'familiar' partner under placebo

Drug: Placebo
Dextrose

Experimental: Familiar partner with MDMA

Participant engages in social interaction with 'familiar' partner under MDMA

Drug: MDMA
The stimulant MDMA

Experimental: Unfamiliar partner with placebo

Participant engages in social interaction with 'unfamiliar' partner under placebo

Drug: Placebo
Dextrose

Experimental: Unfamiliar partner with MDMA

Participant engages in social interaction with 'unfamiliar' partner under MDMA

Drug: MDMA
The stimulant MDMA

Outcome Measures

Primary Outcome Measures

  1. Natural Language Processing using large language model [during 15 minute test conversation, occurring 1.5 hours after drug administration]

    Differences in speech content across all conditions

  2. Facial expression analysis using HUMEAI software [during 15 minute test conversation, occurring 1.5 hours after drug administration]

    Changes in emotional expressions during conversations

Secondary Outcome Measures

  1. Oxytocin [120 minutes post drug administration]

    Changes in oxytocin levels across all conditions

  2. Self-reported feelings of connection using Likert scale conversation questionnaires [Collected at the end of the session, 240 minutes post-drug administration]

    ratings of connectedness

  3. Affective touch [Post-drug, 2 hours post-drug administration]

    Ratings of pleasantness, intensity and want more touch (1-7) after differing velocities of touch

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 35 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • used MDMA or psychedelic between 1-40

  • high school diploma or equivalent

  • BMI between 19 and 30

  • verbal fluency in English

Exclusion Criteria:
  • History of adverse effects with MDMA

  • High blood pressure

  • Any medical condition requiring regular medication

  • Individuals with a current (within the last year) DSM-IV Axis 1 diagnosis

  • Women who are pregnant or trying to become pregnant.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Chicago Chicago Illinois United States 60637

Sponsors and Collaborators

  • University of Chicago
  • National Institutes of Health (NIH)
  • National Institute on Drug Abuse (NIDA)

Investigators

  • Principal Investigator: Harriet de Wit, University of Chicago

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Chicago
ClinicalTrials.gov Identifier:
NCT05948683
Other Study ID Numbers:
  • IRB23-0219
  • 5R01DA002812-35
First Posted:
Jul 17, 2023
Last Update Posted:
Jul 17, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jul 17, 2023