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Behavioral Intervention

Digital Support Program for Suicide Prevention

N/A

Recruiting

Led By Alejandra Arango

Research Sponsored by University of Michigan

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be younger than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up up to week 14

Awards & highlights

Study Summary

This trial studies how effectively an online support system (eYST) helps youth, and looks for feedback from users.

Who is the study for?

This trial is for English-speaking youths who have attempted suicide or are having serious thoughts of harming themselves. They must own a smartphone, be able to understand the study with their guardian's consent, and provide an emergency contact. It excludes those in other treatment studies, unable to follow health safety guidelines like mask-wearing, with conditions that affect informed consent or participation, active psychosis, substance withdrawal issues, or high risk judged by the investigator.Check my eligibility

What is being tested?

The trial is testing the eYST website—an experimental digital platform designed to support young people dealing with suicidal thoughts. The goal is to gather user feedback on eYST and evaluate its effectiveness in aiding these individuals.See study design

What are the potential side effects?

Since this intervention involves using a digital platform rather than medication or medical procedures, traditional side effects are not applicable. However, there may be emotional or psychological impacts from participating in the program which will be monitored.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ up to week 14

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~up to week 14

This trial's timeline: 3 weeks for screening, Varies for treatment, and up to week 14 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Duration of use of app

Frequency of use of app

System Usability Scale (SUS) score System Usability Scale (SUS)

Secondary outcome measures

Acceptability of Intervention Measure (AIM)

Client Satisfaction Questionnaire (CSQ-I)

Feasibility of Intervention Measure (FIM)

+1 more

Trial Design

1Treatment groups

Experimental Treatment

Group I: eYST websiteExperimental Treatment1 Intervention

Do I qualify?Apply below to find out

Find a Location

Who is running the clinical trial?

National Institute of Mental Health (NIMH)NIH

2,786 Previous Clinical Trials

2,689,589 Total Patients Enrolled

112 Trials studying Suicide

1,156,699 Patients Enrolled for Suicide

University of MichiganLead Sponsor

1,798 Previous Clinical Trials

6,378,018 Total Patients Enrolled

18 Trials studying Suicide

11,525 Patients Enrolled for Suicide

Patricia SimonStudy DirectorOui Therapeutics, Inc.

Media Library

eYST website (Behavioral Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT05900700 — N/A

Suicide Research Study Groups: eYST website

Suicide Clinical Trial 2023: eYST website Highlights & Side Effects. Trial Name: NCT05900700 — N/A

eYST website (Behavioral Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05900700 — N/A

Frequently Asked Questions

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

Does the protocol of this trial only pertain to senior citizens?

"As per the standards of this research, only participants aged 13 to 17 may be enrolled."

Answered by AI

Are there any opportunities for prospective patients to participate in this research?

"As per information on clinicaltrials.gov, this trial is no longer enrolling volunteers; its initial posting was July 1st 2023 and the last revision was made June 2nd of that same year. That being said, there are still 180 other trials open to participants at present."

Answered by AI

What qualifications must be met for someone to participate in this research?

"Aspiring enrollees in this medical study must be adolescents aged 13 through 17 who have experienced suicidal ideation. Approximately 120 participants are necessary to complete the trial."

Answered by AI

What is the primary objective of this medical experiment?

"The main outcome of this trial, evaluated over a period of up to 14 weeks, is the frequency with which participants utilise the app. Secondary outcomes include acceptance (measured through Acceptability of Intervention Measure [AIM], scored on a 5-point scale ranging from 1 - 5), appropriateness (Intervention Appropriateness Measure [IAM] also measured on a 5-point scale) and satisfaction (Client Satisfaction Questionnaire [CSQ-I], an 8 item Likert Scale ranging from 8-32)."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

Digital Youth-Nominated Support Team (YST) Program

Alejandra Arango 2023. "Digital Youth-Nominated Support Team (YST) Program". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT05900700.