Integration of (iSBIRT) for Teen Drug Use Into a Pediatric Network
This study has been withdrawn prior to enrollment.
(The project was not funded)
Sponsor:
Children's Hospital Boston
Information provided by (Responsible Party):
Children's Hospital Boston
ClinicalTrials.gov Identifier:
NCT01454206
First received: October 5, 2011
Last updated: January 2, 2013
Last verified: January 2013
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Purpose
The Goal of this project is to integrate a previously-tested internet-facilitated Screening, Brief Intervention, and Referral to Treatment (iSBIRT) system for adolescent substance use into a large network of primary care offices, the Pediatric Practices of Children's Hospital Boston (PPOC).
| Condition | Intervention | Phase |
|---|---|---|
|
Substance Use |
Behavioral: iSBIRT |
Phase 2 Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Crossover Assignment Masking: Open Label Primary Purpose: Prevention |
| Official Title: | Integration of Internet-facilitated Screening, Brief Intervention, Referral to Treatment (iSBIRT) for Teen Drug Use Into a Pediatric Network |
Further study details as provided by Children's Hospital Boston:
Primary Outcome Measures:
- Provider attitude toward iSBIRT [ Time Frame: 12 months post baseline ] [ Designated as safety issue: No ]We will evaluate providers' acceptance of and attitude toward integrating iSBIRT into their practices.
Secondary Outcome Measures:
- Youth connectedness to provider [ Time Frame: Baseline ] [ Designated as safety issue: No ]We will measure adolescents' attitudes toward their providers' advice regarding the health effects of substance use given during the visit
- iSBIRT sustainability [ Time Frame: 12 months post ] [ Designated as safety issue: No ]We will measure rates of continued use of iSBIRT by practices 12 months after iSBIRT recruitment and implementation ends
- Change in rates of adolescent substance use [ Time Frame: 3 months post baseline ] [ Designated as safety issue: No ]We will measure the change in rates of adolescent substance use from baseline to 3 months post study visit.
- Change in rates of adolescent substance use [ Time Frame: 6 months post baseline ] [ Designated as safety issue: No ]We will measure the change in rates of adolescent substance use from baseline to 6 months post study visit.
- Change in rates of adolescent substance use [ Time Frame: 12 months post baseline ] [ Designated as safety issue: No ]We will measure the change in rates of adolescent substance use from baseline to 12 months post study visit.
| Enrollment: | 0 |
| Study Start Date: | July 2012 |
| Estimated Study Completion Date: | December 2016 |
| Estimated Primary Completion Date: | October 2016 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| No Intervention: Treatment as Usual | |
|
Experimental: iSBIRT
Participants will receive the internet-facilitated screening, brief intervention and referral to treatment (iSBIRT intervention)
|
Behavioral: iSBIRT
Participants will be screened for substance use, view information about the health effects of substance use on the computer, and receive advice from the primary care provider regarding the health effects of substance use. Those found to be at "high risk" will complete an internet-based program encouraging them to change their substance use.
|
Eligibility| Ages Eligible for Study: | 12 Years to 18 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- 12-18 year olds
- Coming for non-emergent care
- Access to a private computer
- Have email address
Exclusion Criteria:
- Not available for follow-up questionnaires
- Unable to read or understand English at a 6th grade reading level
- Medically or emotionally unstable on the day of the visit
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01454206
Locations
| United States, Massachusetts | |
| Children's Hospital Boston | |
| Boston, Massachusetts, United States, 02115 | |
Sponsors and Collaborators
Children's Hospital Boston
Investigators
| Principal Investigator: | John R Knight, MD | Children's Hospital Boston |
More Information
Additional Information:
No publications provided
| Responsible Party: | Children's Hospital Boston |
| ClinicalTrials.gov Identifier: | NCT01454206 History of Changes |
| Other Study ID Numbers: | CeASAR app RFADA12008 |
| Study First Received: | October 5, 2011 |
| Last Updated: | January 2, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Children's Hospital Boston:
|
cannabis abuse alcohol abuse substance abuse |
ClinicalTrials.gov processed this record on May 16, 2013