Using Technology to Reduce Youth Substance Use

  • STATUS
    Recruiting
  • participants needed
    120
  • sponsor
    University of California, San Francisco
Updated on 19 February 2024

Summary

The research project will focus on conducting a trial of whether a tailored SMS text-messaging intervention is efficacious in improving justice-involved youths' substance use or dual diagnosis treatment attendance and engagement.

Description

The study will demonstrate how delivery of text messages for appointment reminders and motivational/coaching message to justice-involved youth and their caregivers will lead to greater youth substance use treatment attendance and engagement. The study will start with identifying the feasibility and acceptability of the SMS text-messaging intervention with community-supervised justice-involved youth. Then, the study will determine whether the tailored dyadic (youth and caregiver) SMS text-messaging intervention improves justice-involved youth substance use or dual diagnosis treatment attendance and engagement relative to standard of care (not receiving text messaging appointment reminders and motivational/coaching messages). Finally, the study will characterize patterns of key justice and behavioral health system-level factors that promote or hinder eventual adoption and sustainability of mHealth technology as a tool to improve treatment attendance for justice-involved youth.

Details
Condition Drug abuse, substance abuse, substance abuse
Age 13-18 years
Treatment SMS Text Messaging, Standard of Care Engagement Practices
Clinical Study IdentifierNCT04446910
SponsorUniversity of California, San Francisco
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

English-speaking youth
Ages 13-18
Justice-involved while living in the community
Own a mobile phone or tablet
Are willing to send and receive text messages
Are referred to community-based substance use and/or mental health treatment
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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