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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 weeks
Treatment ~ Varies
Follow Up ~delayed follow up (9 months)
This trial's timeline: 3 weeks for screening, Varies for treatment, and delayed follow up (9 months) for reporting.

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 more

FRRM 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.

Find a Location

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

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~53 spots leftby Apr 2025