Primary Care iSBIRT to Reduce Serious Teen Health Risks

Depression Clinical Trial

Official title:

Primary Care Internet/Intranet-based Screening, Brief Intervention, and Referral to Treatment (iSBIRT) System to Reduce Serious Teen Health Risks

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT00891631
• Other study ID #: iSBIRT RFA-od-09-003
• Status: Withdrawn
• Phase: Phase 1/Phase 2
• First received: April 30, 2009
• Last updated: October 6, 2016
• Start date: September 2009
• Est. completion date: September 2011

Study information

• Verified date: October 2016
• Source: Boston Children’s Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

The goal of the project is to develop and test an internet/intranet-based Screening, Brief Intervention, and Referral to Treatment (iSBIRT) system for adolescents that targets a broad range of serious health-risks and problem behaviors.

Description:

We have previously developed and tested a computerized substance use screening and feedback program for adolescents. We will expand this program to include other serious health risks, enhance the feedback and health risk information adolescents will receive on the computer, develop Technological Extenders to extend the effect of the intervention, develop a training video and protocol for providers, and pilot test the system among adolescents coming for non-urgent care at a variety of primary care sites.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: September 2011
• Est. primary completion date: September 2011
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 12 Years to 21 Years

Eligibility

Inclusion Criteria:

• 12-21 years old

• arriving for non-urgent care

• provide informed assent/consent

Exclusion Criteria:

• less than 6th grade reading level

• unavailable for follow-up questionnaires

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Screening

Related Conditions & MeSH terms

• Depression
• High-risk Sex
• Substance-related Disorders

Intervention

Behavioral:
• iSBIRT
Participants will receive the internet/intranet based screening, brief intervention, and referral to treatment program.
• iSBIRT/TE
Participants will receive the internet/intranet screening, brief intervention, and referral to treatment system along with technological extenders

Locations

Country	Name	City	State
United States	Children's Hospital Boston	Boston	Massachusetts

Sponsors (1)

Lead Sponsor	Collaborator
Boston Children’s Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	frequency of substance use and other risk behaviors		3 months	No

External Links

•   Web site of the Center for Adolescent Substance Abuse Research at Children's Hospital Boston