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NCT06114862

Brief Interventions on Social Media to Reduce Suicide Risk (Intervention 2)

Withdrawn NA Last updated 13 August 2025
What this trial tests

NA trial testing Stigma-reduction intervention in Stigma, Social. Withdrawn.

Timeline
1 October 2024
Primary endpoint
14 March 2025
14 March 2025

Quick facts

Lead sponsorHarvard University
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeprevention
Start date1 October 2024
Primary completion14 March 2025
Estimated completion14 March 2025
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Harvard University

Who can join

18 and older, any sex, with Stigma, Social or Mental Health Issue. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This clinical trial is part of a series of brief interventions to reduce suicide risk in collaboration with the social media platform RallyPoint, a site specifically designed for U.S. servicemembers and veterans to connect with one another. This RCT (Intervention 2: Stigma Reduction) is focused on decreasing the stigma associated with sharing one's personal experiences related to mental health on the RallyPoint site. Specifically, the investigators will test the effect of a psychoeducational intervention that will provide participants information on the potential benefits of self-disclosure.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Stigma-reduction intervention

Trials testing the same drug.

Other recruiting trials for Stigma, Social

Currently open trials in the same condition.

Other Harvard University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06114862.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing