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Written Exposure Therapy for Suicide Prevention
N/A
Waitlist Available
Led By Brian P Marx, PhD
Research Sponsored by Boston University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline,10 weeks, 20 weeks, 30 weeks
Awards & highlights
Study Summary
This trial will evaluate an evidence-based intervention, WET-SP, to reduce risk of self-injury & rehospitalization for military service members after psychiatric hospitalization.
Who is the study for?
Active duty military service members hospitalized for suicidal thoughts, plans, or attempts and showing significant suicidal ideation. Participants must be able to read, write, and speak English.Check my eligibility
What is being tested?
The trial is testing WET-SP—a brief psychotherapy aimed at reducing distress from suicidal crises—against the usual care (TAU). It involves writing about stressful experiences during hospitalization with follow-ups after discharge.See study design
What are the potential side effects?
As WET-SP is a form of psychotherapy involving writing about personal stressors, side effects may include emotional discomfort or temporary increases in distress.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline,10 weeks, 20 weeks, 30 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline,10 weeks, 20 weeks, 30 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Suicidal ideation (SI)
SI at 20 weeks
SI at 30 weeks
Secondary outcome measures
Most severe SI
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Written Exposure Therapy-for Suicide Prevention (WET-SP) +TAUExperimental Treatment2 Interventions
Participants randomized into this arm will be offered WET-SP which will consist of 5 treatment sessions, conducted daily while the participant is hospitalized, allowing for the largest dose of treatment possible while inpatient. If a patient is discharged prior to the completion of WET-SP, the remaining sessions will be conducted in outpatient sessions. Participants in this arm will also be offered TAU.
Group II: Treatment as usual (TAU)Active Control1 Intervention
Participants randomized into this arm will be offered TAU which consists of daily contact and patient centered care by the acute psychiatric inpatient unit provider team (e.g., psychiatrists, therapists, case managers, behavioral health techs). Participants will engage with the provider team daily throughout the duration of hospitalization.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
TAU
2016
Completed Phase 3
~8350
Find a Location
Who is running the clinical trial?
Boston UniversityLead Sponsor
454 Previous Clinical Trials
9,941,410 Total Patients Enrolled
United States Department of DefenseFED
861 Previous Clinical Trials
227,034 Total Patients Enrolled
School of Medicine, Anschutz Medical Campus, Colorado UniversityUNKNOWN
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My main reason for hospital care is not due to active psychosis.I have trouble understanding basic questionnaires.I was admitted to CRDAMC for suicidal thoughts or actions.I am unable to understand and agree to the study's details on my own.
Research Study Groups:
This trial has the following groups:- Group 1: Treatment as usual (TAU)
- Group 2: Written Exposure Therapy-for Suicide Prevention (WET-SP) +TAU
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there any remaining slots available for enrolment in this investigation?
"According to clinicaltrials.gov, the enrolment period for this medical trial has passed as it was first posted on July 1st 2023 and last updated on May 18th of that year. Nonetheless, 181 alternative studies are actively recruiting patients at present."
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