Primary Care Internet Based Depression Prevention for Adolescents (CATCH-IT) Also Known as Promoting AdolescenT Health

NCT01893749 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1142

Last updated 2019-08-22

No results posted yet for this study

Summary

The purpose of this randomized multiple-site clinical study is to determine whether a revised CATCH-IT (Internet-based depression prevention program) is more effective than a general health education Internet intervention (Health Education)on teens ages 13-18 (inclusive). It is hypothesized that teens in CATCH-IT will exhibit lower levels of depressed mood and/or maintain lower depressive scores over 2 years long-term follow up as compared to teens in Health Education group.

Conditions

Interventions

BEHAVIORAL

CATCH-IT

It contains 14 modules focused on behavioral activation, cognitive behavioral therapy, interpersonal therapy and a resiliency building model, including elements such as narratives, video diaries, skill building exercises and a booster program (not yet initiated) with 6 modules that involves interaction with a live therapist. It also includes three 15-minute meetings with the primary care provider at baseline, 2 months and 12 months post intervention. These meetings are focused on the motivational interview approach where the patient and the doctor talk about the mental/physical health goals of the patient and determine the best approach for the patient by allowing the patient to have full input into the plan.

Sponsors & Collaborators

  • Wellesley College

    collaborator OTHER
  • Northwestern University

    collaborator OTHER
  • Harvard Vanguard Medical Associates

    collaborator OTHER
  • Access Healthcare Systems

    collaborator OTHER
  • Endeavor Health

    collaborator OTHER
  • Infant Welfare Society

    collaborator UNKNOWN
  • Wake Forest University Health Sciences

    collaborator OTHER
  • Franciscan St. Margaret Health - Franciscan Alliance

    collaborator UNKNOWN
  • Benjamin Van Voorhees, MD, MPH

    lead OTHER

Principal Investigators

  • Benjamin Van Voorhees, MD, MPH · UIC

  • Tracy Gladstone, PHD · Wellesley Center for Women

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
13 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-02-29
Primary Completion
2016-07-31
Completion
2016-07-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01893749 on ClinicalTrials.gov