Psilocybin for Loneliness and Grief

This study is looking at how a single dose of psilocybin (25mg) affects feelings of loneliness and social connection in adults aged 21 to 65. You might be able to join if you are medically healthy, feel very lonely (based on a specific scale), or have unresolved grief. Researchers want to see if psilocybin can reduce how your brain reacts to negative social situations, and if this leads to better social connectedness. You would either receive psilocybin or a placebo (an inactive capsule). The study is currently unclear on its recruitment status.

Study design
This is a randomized, double-blind, placebo-controlled study, meaning participants are randomly assigned to receive either psilocybin or a placebo, and neither you nor the researchers will know which you receive. It plans to enroll 51 participants.
What's involved
You would have assessments at baseline (Day -1), Day +7, and Day +30. You would also have fMRI brain scans at Day -2 and Day +7.
Compensation
Not stated in the trial record.
Follow-up
Your loneliness and social connectedness will be measured up to Day +30 after treatment.

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NCT07693153

The Effects of Psilocybin on Social Connectedness

Not Yet Recruiting
PHASE1Ages 21–65Interventional
Yale University
~51 participants
Updated 2026-07-09 on ClinicalTrials.gov
What's tested:PsilocybinPlacebo

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Loneliness and social connectedness
Measured over Baseline (Day -1) and Day +7, Day +30
+1 more outcome measured
Loneliness
Grief
1 sites across 1 states
Connecticut1
  • Anahita Bassir Nia, MD · PRINCIPAL_INVESTIGATOR · Yale University

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Do you actually qualify for this trial?

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Eligibility criteria

Inclusion

Medically healthy
Ability to provide consent
High loneliness defined by the UCLA-3 Loneliness Scale
Willingness to comply with all study procedures and availability for the duration of the study

Exclusion

Any unstable medical condition, psychiatric disorder, or circumstance that, in the opinion of the investigator, could compromise participant safety, interfere with study participation, or hinder the participant's ability to comply with study procedures and requirements
Positive pregnancy test or women who are breastfeeding
Any contraindication to MRI such as a pacemaker or metal implants
  • Loneliness and social connectednessBaseline (Day -1) and Day +7, Day +30

    UCLA Loneliness Scale (UCLA-20)

  • fMRI Baseline AssessmentsDay -2, Day +7

    Hypervigilance to Social Threat: Facial Emotion Recognition Task (FERT)