Mobile Continuing Care Approach for Youth
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Purpose
The primary purpose of this study is to test the effectiveness of a pilot mobile based continuing care program (monitoring/feedback texting) relative to standard continuing care as usual in reducing relapse and improving psychosocial functioning outcomes in a youth population (under 24) with substance abuse problems.
| Condition | Intervention |
|---|---|
|
Addiction |
Behavioral: Mobile Continuing Care Other: Standard Continuing Care as Usual |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Supportive Care |
| Official Title: | Mobile Continuing Care Approach for Youth |
- Substance use (methamphetamine, marijuana, other) [ Time Frame: over the 9 month study period ] [ Designated as safety issue: No ]The primary efficacy measure is substance use measured by urine specimen and self-reports over the 12-week intervention period anf over time measured by repeated measures from baseline to discharge and follow-up: months 3, 6 and 9
- Psychosocial functioning [ Time Frame: over the 9-month study ] [ Designated as safety issue: No ]The effects of the intervention (mobile continuing care) will be compared to standard continuing care as usual in improving psychosocial outcomes (criminal behaviors, HIV risk, health status and mental health outcomes - mood and stress) using repeated measures at baseline and follow-up: months 3, 6 and 9
- Recovery motivation, self management and confidence (self-efficacy) [ Time Frame: over the 9-month study ] [ Designated as safety issue: No ]The effects of the intervention (mobile continuing care) compared to standard continuing care as usual will be assessed in terms of change/improvements in recovery motivation, recovery self-management (drug avoidance behaviors), and recovery confidence over time (measured by repeated measures from baseline to discharge and 3 follow-up: 3-, 6- and 9-months post-discharge)
- Social Support Utilization [ Time Frame: Over the 9-month study ] [ Designated as safety issue: No ]The effects of the intervention (mobile continuing care) compared to standard continuing care will be assessed in terms of change/improvements in recovery service utilziation over time (measured by repeated measures from baseline to discharge and follow-up: 3-, 6- and 9-months post-discharge)
| Estimated Enrollment: | 80 |
| Study Start Date: | February 2012 |
| Estimated Study Completion Date: | June 2015 |
| Estimated Primary Completion Date: | December 2014 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Mobile Continuing Care
Behavioral: 12-week Structured Texting intervention focused on recovery monitoring, feedback for self-management, social support and education
|
Behavioral: Mobile Continuing Care
Behavioral: Mobile Texting 12-week intervention. Delivers daily Recovering monitoring, self-management feedback, and education/social support
|
|
No Intervention: Standard Continuing Care as Usual
Other: Continuing care as usual to 12-step facilitation (Anonymous group)
|
Other: Standard Continuing Care as Usual
Facilitation to 12-step recovery/anonymous groups
|
Detailed Description:
This study will include approximately 80 participants randomized to either 12 weeks of mobile continuing care (intervention) or standard continuing care as usual (control). Participants will be recruited from the treatment programs in Los Angeles County, including Matrix Institute on Addictions, Tarzana Treatment, Twin Town, Phoenix House, and Cri-Help. During the 12-week active program, participants will be monitored monthly via telephone data collection. Both groups will be followed for 10-months using repeated assessments (self-report and urine specimens) at baseline (month 0) and at follow-up points (months 3, 6, and 9).
Eligibility| Ages Eligible for Study: | 12 Years to 24 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Youth between 12 and 24 years old
- Youth in treatment for substance abuse
- Youth who complete treatment (minimum 12 weeks)
- Youth who have the cognitive capacity to understand study procedures and agree to participate
Exclusion Criteria:
- Presence of an adverse (life threatening) medical condition that could interfere with study participation.
- Presence of psychiatric co-occurring illness or symptoms warranting safety concerns or continued treatment, including acute suicide risk; and
- Current homelessness (unless residing in recovery home for which contact information can be provided).
Contacts and Locations| Contact: Christina Zavalza, BS | 626-815-6000 ext 2417 | czavalza@apu.edu |
| United States, California | |
| Azusa Pacific University Psychology Department | Recruiting |
| Azusa, California, United States, 91702 | |
| Contact: Christina Zavalza 626-815-6000 ext 2417 czavalza@apu.edu | |
| Contact: Sarah Cousins, MPH 310-267-5519 SCousins@mednet.ucla.edu | |
| Principal Investigator: Rachel Gonzales (Castaneda), MPH, PhD | |
| Principal Investigator: | Rachel Gonzales-Castaneda, MPH, PhD | Azusa Pacific University |
More Information
No publications provided
| Responsible Party: | Azusa Pacific University |
| ClinicalTrials.gov Identifier: | NCT01632735 History of Changes |
| Other Study ID Numbers: | 5K01DA027754-03, 1K01DA027754-01A1 |
| Study First Received: | June 29, 2012 |
| Last Updated: | July 2, 2012 |
| Health Authority: | United States: Institutional Review Board United States: Federal Government |
Keywords provided by Azusa Pacific University:
|
Continuing Care Youth Substance Abuse Recovery Support Mobile Texting |
Additional relevant MeSH terms:
|
Behavior, Addictive Compulsive Behavior Impulsive Behavior |
ClinicalTrials.gov processed this record on May 21, 2013