Primary Care iSBIRT to Reduce Serious Teen Health Risks
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
Tobacco, Alcohol and Drug Use Seat-belt and Bicycle/Sports Helmet Use Weapon Carrying and Associating With Peers Who Carry Weapons Depression and Suicidality High Risk Sexual Behaviors |
Behavioral: iSBIRT Behavioral: iSBIRT/TE |
Phase 1 Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Screening |
| Official Title: | Primary Care Internet/Intranet-based Screening, Brief Intervention, and Referral to Treatment (iSBIRT) System to Reduce Serious Teen Health Risks |
- frequency of substance use and other risk behaviors [ Time Frame: 3 months ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 699 |
| Study Start Date: | September 2009 |
| Estimated Study Completion Date: | September 2011 |
| Estimated Primary Completion Date: | September 2011 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: iSBIRT
Participants will complete the iSBIRT system.
|
Behavioral: iSBIRT
Participants will receive the internet/intranet based screening, brief intervention, and referral to treatment program.
Other Name: SBIRT
|
|
Experimental: iSBIRT/TE
Participants will receive the internet/intranet screening, brief intervention, and referral to treatment system and technological extenders
|
Behavioral: iSBIRT/TE
Participants will receive the internet/intranet screening, brief intervention, and referral to treatment system along with technological extenders
Other Name: SBIRT
|
|
No Intervention: TAU
Participants will receive Treatment as Usual from their primary care provider.
|
Detailed 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.
Eligibility| Ages Eligible for Study: | 12 Years to 21 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
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
Contacts and Locations| United States, Massachusetts | |
| Children's Hospital Boston | |
| Boston, Massachusetts, United States, 02115 | |
| Principal Investigator: | John R Knight, MD | Children's Hospital Boston |
More Information
Additional Information:
No publications provided
| Responsible Party: | John R. Knight, MD, Children's Hospital Boston |
| ClinicalTrials.gov Identifier: | NCT00891631 History of Changes |
| Other Study ID Numbers: | iSBIRT RFA-od-09-003 |
| Study First Received: | April 30, 2009 |
| Last Updated: | March 7, 2011 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Children's Hospital Boston:
|
tobacco alcohol marijuana drug use seat-belt |
weapons depression suicidality sexual risk behaviors |
Additional relevant MeSH terms:
|
Depression Depressive Disorder Behavioral Symptoms Mood Disorders Mental Disorders |
ClinicalTrials.gov processed this record on June 17, 2013