← Back to Search

Education Program to Reduce Risky Behavior in Adolescents Ph I (iTRAC Trial)

N/A
Waitlist Available
Led By Christopher D Houck, PhD
Research Sponsored by Klein Buendel, Inc.
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 baseline, after wireframe production (approximately 2 months after baseline)
Awards & highlights
No Placebo-Only Group

Summary

This phase will complete the TRAC adaptation to a web app. The pilot study (R21 HD089979) effectively translated the ER content of TRAC and the same procedures will be used to translate the remaining content.

Eligible Conditions
  • Risky Sexual Behavior
  • Emotional Regulation
  • Adolescent Behaviors

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, after study completion (approximately 2 months after baseline), 6-months after baseline
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, after study completion (approximately 2 months after baseline), 6-months after baseline for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Formative Research
Secondary study objectives
Abstinence Attitudes
Adolescent Risk Behavior Assessment (ARBA)
Non-sexual Risk Behaviors
+1 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

3Treatment groups
Experimental Treatment
Group I: Health Education Professionals Panel (HEPP)Experimental Treatment1 Intervention
This panel consisted of 6 health teachers and other school health professionals such as nurses and counselors. They were recruited at each participating school.
Group II: Adolescent Advisory Board MaleExperimental Treatment1 Intervention
This board consisted of 9 male adolescents recruited from the schools.
Group III: Adolescent Advisory Board FemaleExperimental Treatment1 Intervention
This board consisted of 9 female adolescents recruited from the schools.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Formative Research- Content Translation
2022
N/A
~30
Formative Research- Content Feedback and Acceptability
2022
N/A
~30

Find a Location

Who is running the clinical trial?

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)NIH
2,064 Previous Clinical Trials
2,746,331 Total Patients Enrolled
Klein Buendel, Inc.Lead Sponsor
39 Previous Clinical Trials
19,854 Total Patients Enrolled
University of OregonOTHER
85 Previous Clinical Trials
44,170 Total Patients Enrolled
1 Trials studying Emotional Regulation
12 Patients Enrolled for Emotional Regulation
Rhode Island HospitalOTHER
264 Previous Clinical Trials
68,749 Total Patients Enrolled
Christopher D Houck, PhDPrincipal InvestigatorRhode Island Hospital
1 Previous Clinical Trials
420 Total Patients Enrolled
~8 spots leftby Dec 2025