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Culturally Adapted Stress Management for Preventing Suicide in Adolescents
N/A
Recruiting
Led By LaVome Robinson, PhD
Research Sponsored by DePaul University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up assessments will be administered through study completion, an average of every six months.
Awards & highlights
Study Summary
This trial is examining whether a stress-management intervention can reduce suicide and violence rates among African American youth when delivered by social workers who are familiar with the school system.
Who is the study for?
This trial is for African American 9th graders enrolled in participating high schools. Their parents or guardians must consent to their participation, and teachers are involved if they have students in the study. It's not open to those who aren't in 9th grade at enrollment or lack parental permission.Check my eligibility
What is being tested?
The trial tests a culturally adapted stress coping course (A-CWS) taught by social workers from the school system against standard care. The goal is to see if it can boost resilience, improve coping strategies, and reduce violence and suicide among these youths.See study design
What are the potential side effects?
Since this intervention involves educational sessions rather than medication, traditional side effects are not expected. However, participants may experience emotional discomfort discussing sensitive topics like stress and suicide.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ assessments will be administered through study completion, an average of every six months.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~assessments will be administered through study completion, an average of every six months.
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Suicide Ideation
Secondary outcome measures
Change in Adaptive Coping
Change in Hope
Change in Hopelessness
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Robinson's Culturally Adapted Coping with Stress CourseExperimental Treatment1 Intervention
Group II: Standard Care Control ConditionActive Control1 Intervention
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Who is running the clinical trial?
DePaul UniversityLead Sponsor
8 Previous Clinical Trials
7,983 Total Patients Enrolled
1 Trials studying Suicide
939 Patients Enrolled for Suicide
National Institute of Mental Health (NIMH)NIH
2,802 Previous Clinical Trials
2,660,804 Total Patients Enrolled
113 Trials studying Suicide
1,151,605 Patients Enrolled for Suicide
LaVome Robinson, PhDPrincipal InvestigatorDePaul University
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I am a 9th grader enrolled at a participating high school.
Research Study Groups:
This trial has the following groups:- Group 1: Robinson's Culturally Adapted Coping with Stress Course
- Group 2: Standard Care Control Condition
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.
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