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Behavioral Intervention

Social Media Interventions for Reducing Suicide Risk

N/A
Recruiting
Research Sponsored by Harvard University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Active RallyPoint users who had at least one post flagged by a machine learning risk algorithm for containing concerning language (e.g., descriptions of suicidal thoughts or behaviors).
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 hrs post intervention
Awards & highlights

Study Summary

This trial tests a way to help veterans and servicemembers get mental health support when they need it.

Who is the study for?
This trial is for active users of RallyPoint, a social media platform for U.S. servicemembers and veterans, who have posted content flagged by an algorithm as containing concerning language related to suicide or emotional distress.Check my eligibility
What is being tested?
The study tests a psychoeducational intervention designed to encourage distressed individuals to seek mental health resources like suicide hotlines. It's part of a randomized controlled trial (RCT) series on RallyPoint.See study design
What are the potential side effects?
Since this is a psychoeducational intervention rather than a medical treatment, traditional side effects are not applicable. However, participants may experience varying psychological impacts from the information provided.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 hrs post intervention
This trial's timeline: 3 weeks for screening, Varies for treatment, and 24 hrs post intervention for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Number of participants reporting use of resources

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: InterventionExperimental Treatment2 Interventions
Participants will be identified using a machine learning risk algorithm developed by the investigators that will automatically identify concerning posts (e.g., those mentioning suicidal thoughts or behaviors). RallyPoint members whose posts are flagged will randomly be assigned to the intervention group or the control group.
Group II: ControlActive Control1 Intervention
Participants will be identified using a machine learning risk algorithm developed by the investigators that will automatically identify concerning posts (e.g., those mentioning suicidal thoughts or behaviors). RallyPoint members whose posts are flagged will randomly be assigned to the intervention group or the control group.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Treatment as usual
2010
N/A
~6760

Find a Location

Who is running the clinical trial?

Harvard UniversityLead Sponsor
229 Previous Clinical Trials
473,505 Total Patients Enrolled
7 Trials studying Suicide
80,950 Patients Enrolled for Suicide

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are researchers currently recruiting volunteers for this research endeavor?

"According to clinicaltrials.gov, this trial is actively recruiting participants since its original posting on November 20th of 2023 and most recent editing on the 30th of that same month."

Answered by AI

How many individuals have voluntarily enrolled in this experiment?

"Affirmative. Clinicaltrials.gov's data displays that the trial, originally posted on November 20th 2023, is actively seeking participants. 1000 individuals are required for recruitment from 1 site."

Answered by AI
~0 spots leftby May 2024