Study Stopped
Grant application was not funded
Primary Care iSBIRT to Reduce Serious Teen Health Risks
Primary Care Internet/Intranet-based Screening, Brief Intervention, and Referral to Treatment (iSBIRT) System to Reduce Serious Teen Health Risks
1 other identifier
interventional
N/A
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
Started Sep 2009
Typical duration for phase_1
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 30, 2009
CompletedFirst Posted
Study publicly available on registry
May 1, 2009
CompletedStudy Start
First participant enrolled
September 1, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2011
CompletedOctober 7, 2016
October 1, 2016
2 years
April 30, 2009
October 6, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
frequency of substance use and other risk behaviors
3 months
Study Arms (3)
iSBIRT
EXPERIMENTALParticipants will complete the iSBIRT system.
iSBIRT/TE
EXPERIMENTALParticipants will receive the internet/intranet screening, brief intervention, and referral to treatment system and technological extenders
TAU
NO INTERVENTIONParticipants will receive Treatment as Usual from their primary care provider.
Interventions
Participants will receive the internet/intranet based screening, brief intervention, and referral to treatment program.
Participants will receive the internet/intranet screening, brief intervention, and referral to treatment system along with technological extenders
Eligibility Criteria
You may qualify if:
- years old
- arriving for non-urgent care
- provide informed assent/consent
You may not qualify if:
- less than 6th grade reading level
- unavailable for follow-up questionnaires
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Children's Hospital Boston
Boston, Massachusetts, 02115, United States
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
John R Knight, MD
Boston Children's Hospital
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SCREENING
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor of Pediatrics, Harvard Medical School; Senior Associate in Medicine; Associate in Psychiatry, Director, Center for Adolescent Substance Abuse Research, Boston Children's Hospital
Study Record Dates
First Submitted
April 30, 2009
First Posted
May 1, 2009
Study Start
September 1, 2009
Primary Completion
September 1, 2011
Study Completion
September 1, 2011
Last Updated
October 7, 2016
Record last verified: 2016-10
Data Sharing
- IPD Sharing
- Will not share