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N/A N=40 Single-blind Prevention

Technology Assisted Programs That Promote Mental Health for Teenagers

Depression

Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Nov 2018
Primary outcome: Primary: Program Logins Per Participant by Week. — 9.15; 8.17; 3.6; 6.06 number of program logins

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Networked Peer Support with Peer Guide (Behavioral); Networked Peer Support with Clinician Coach (Behavioral)
Age
Pediatric, Adult · 14+ yrs
Sex
All
Sponsor
Northwestern University
Primary completion
Jun 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Program Logins Per Participant by Week.
9.15; 8.17; 3.6; 6.06; 2.8; 3.39
PRIMARY
USE (Usefulness, Satisfaction and Ease of Use) Questionnaire
4.04; 4.4; 4.36; 4.53; 5.21; 5.55
PRIMARY
SUS (System Usability Scale) Questionnaire
61.53; 71.91; 66.72; 69.53

Summary

The mission of this project is to develop novel systems of care that can provide efficacious, scalable, cost-effective, participant friendly behavioral intervention technologies (BITs) for the prevention of depression in adolescents. The investigators define BITs as interventions that use information and telecommunications technologies such as the internet, mobile or traditional phones, computers and/or other technologies to support and deliver psychological and behavioral interventions. Through usability testing, focus interviews, and field trials, investigators may modify the technologies and intervention based on immediate usage data.

Eligibility Criteria

Inclusion Criteria

  • Has a score of 12-39 (males) / 15-39 (females) on the Center for Epidemiologic Studies Depression Scale (CES-D) OR reported past month use of marijuana, cigarettes, alcohol or other substances on the Center for Disease Control Youth Risk Behavior Survey (YRBS).
  • Is familiar with the use of computers and the Internet, as well as mobile phones
  • Is able to speak and read English
  • Is between 14-19 years of age

Exclusion Criteria

  • Is currently taking an antidepressant medication or has taken one in the previous 3 months
  • Has visual, hearing, voice, or motor impairment that would prevent completion of study procedures or use of the Internet or mobile phone
  • Is diagnosed with a psychotic disorder, bipolar disorder, dissociative disorder, current substance dependence, or other diagnosis for which participation in this trial is either inappropriate or dangerous. Inclusion of participants with symptoms of anxiety disorders, eating disorders and substance abuse disorders will be made on a case-by-case basis.
  • Is severely suicidal (has ideation, plan, and intent in the past 12 months) .
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01912729). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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