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Mobile Continuing Care Approach for Youth

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ClinicalTrials.gov Identifier: NCT01632735
Recruitment Status : Completed
First Posted : July 3, 2012
Results First Posted : August 21, 2015
Last Update Posted : August 21, 2015
National Institute on Drug Abuse (NIDA)
University of California, Los Angeles
Information provided by (Responsible Party):
Azusa Pacific University

Brief Summary:
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 or disease Intervention/treatment
Addiction Behavioral: Mobile Continuing Care

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).

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 80 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Supportive Care
Official Title: Mobile Continuing Care Approach for Youth
Study Start Date : February 2012
Primary Completion Date : December 2014
Study Completion Date : June 2015

Arm Intervention/treatment
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
Continuing care as usual to 12-step facilitation (Anonymous group)

Primary Outcome Measures :
  1. Primary Substance Use (Defined as Substance Received Treatment for) [ Time Frame: Baseline, discahrge, 3 month follow-up, 6 month follow-up, 9 month follow-up ]
    Primary substance use relapse was measured by urine tests (0 = negative, 1 = positive).

Secondary Outcome Measures :
  1. Participation in Recovery Behaviors Over Time [ Time Frame: baseline, discharge, 3-, 6- and 9-month follow-ups ]
    Recovery behaviors defined as mean number of days doing extracurricular/recovery-goal directed activities using repeated measures over time.

  2. Recovery Confidence (Self-efficacy) Over Time [ Time Frame: baseline, discharge, 3-, 6-, and 9-month follow-ups ]
    Change/improvements in mean recovery confidence score over time (measured by question "How confident are you in your ability to be completely abstinent (clean) from alcohol and drugs in the next 30 days?" (units on scale included 0=not at all, 1=slightly, 2=moderately, 3=considerably, 4-extremely).

  3. Social Support Utilization [ Time Frame: Baseline, discahrge, 3 month follow-up, 6 month follow-up, 9 month follow-up ]
    Self-help utilization was measured by the question: "In the past 30 days, how many days did you attend self-help meetings like AA or NA to support your recovery?"

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Ages Eligible for Study:   12 Years to 24 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  1. Youth between 12 and 24 years old
  2. Youth in treatment for substance abuse
  3. Youth who complete treatment (minimum 12 weeks)
  4. Youth who have the cognitive capacity to understand study procedures and agree to participate

Exclusion Criteria:

  1. Presence of an adverse (life threatening) medical condition that could interfere with study participation.
  2. Presence of psychiatric co-occurring illness or symptoms warranting safety concerns or continued treatment, including acute suicide risk; and
  3. Current homelessness (unless residing in recovery home for which contact information can be provided).

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01632735

United States, California
Azusa Pacific University Psychology Department
Azusa, California, United States, 91702
Sponsors and Collaborators
Azusa Pacific University
National Institute on Drug Abuse (NIDA)
University of California, Los Angeles
Principal Investigator: Rachel Gonzales-Castaneda, MPH, PhD Azusa Pacific University

Responsible Party: Azusa Pacific University
ClinicalTrials.gov Identifier: NCT01632735     History of Changes
Other Study ID Numbers: 5K01DA027754-03 ( U.S. NIH Grant/Contract )
1K01DA027754-01A1 ( U.S. NIH Grant/Contract )
First Posted: July 3, 2012    Key Record Dates
Results First Posted: August 21, 2015
Last Update Posted: August 21, 2015
Last Verified: July 2015

Keywords provided by Azusa Pacific University:
Continuing Care
Youth Substance Abuse
Recovery Support
Mobile Texting