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FRRM Intervention for Behavioral Mechanisms (FRRM Trial)
N/A
Waitlist Available
Research Sponsored by New York University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up delayed follow up (9 months)
Awards & highlights
FRRM Trial Summary
This trial looks to develop a teen pregnancy prevention program specifically for adolescent males to help address the issue of teen pregnancy.
FRRM Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ delayed follow up (9 months)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~delayed follow up (9 months)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Secondary outcome measures
Adolescent Attendance at Educational Support Services
Adolescent Attendance at Job Training Services
Adolescent Attendance at Sexual and Reproductive Health Service
+10 moreFRRM Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: FRRM InterventionExperimental Treatment1 Intervention
The experimental arm will receive the FRRM intervention.
Group II: ControlActive Control1 Intervention
The control arm will not receive the FRRM intervention.
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Who is running the clinical trial?
New York UniversityLead Sponsor
226 Previous Clinical Trials
313,873 Total Patients Enrolled
Duke UniversityLead Sponsor
2,356 Previous Clinical Trials
3,418,614 Total Patients Enrolled
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