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Mobile Continuing Care Approach for Youth

A

Azusa Pacific University

Status

Completed

Conditions

Addiction

Treatments

Behavioral: Mobile Continuing Care

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT01632735
5K01DA027754-03
1K01DA027754-01A1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

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.

Full 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).

Enrollment

80 patients

Sex

All

Ages

12 to 24 years old

Volunteers

No Healthy Volunteers

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).

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

80 participants in 2 patient groups

Mobile Continuing Care
Experimental group
Description:
Behavioral: 12-week Structured Texting intervention focused on recovery monitoring, feedback for self-management, social support and education
Treatment:
Behavioral: Mobile Continuing Care
Standard Continuing Care as Usual
No Intervention group
Description:
Continuing care as usual to 12-step facilitation (Anonymous group)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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