Impact on Opioid Use of Bundling Medication-assisted Treatment With mHealth

NCT02712034 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 417

Last updated 2020-04-14

No results posted yet for this study

Summary

The primary aim of this study is to measure and explain the impact on long-term opioid use when medication-assisted treatment (MAT) is bundled with an evidence-based mobile-health system (A-CHESS).

Conditions

Interventions

BEHAVIORAL

MAT + A-CHESS

Subjects randomized to MAT + A-CHESS will receive MAT plus the A-CHESS recovery support system which provides: 1. Self-directed, interactive modules that teach basic recovery support, harm-reduction, and psychosocial functioning skills. 2. The latest information about addiction and recovery support, monitoring prompts, and peer and family support. 3. Advice on where to go for help and on how to make the best use of health and human services; and 4. A way to talk with experts in the area of addiction and other study participants by sending anonymous messages in the A-CHESS discussion groups. 5. A way to keep your health care team up to date through reports based on information entered into A-CHESS (i.e. alcohol and drug use, depression, MAT side effects).

OTHER

MAT

Patients will receive treatment consisting of a recovery plan, appropriate pharmacology, routine urine screens, and regularly scheduled behavioral interventions, such as monthly group counseling sessions or sessions with a recovery coach. "Appropriate pharmacology" may include methadone; naltrexone; buprenorphine; and in the case of overdose, naloxone; and other medications and combinations of medications as part of the patient's standard clinical care.

Sponsors & Collaborators

  • Stanley Street Treatment and Resources (SSTAR)

    collaborator UNKNOWN
  • Gosnold on Cape Cod

    collaborator UNKNOWN
  • ARC Community Services, Inc.

    collaborator UNKNOWN
  • National Institute on Drug Abuse (NIDA)

    collaborator NIH
  • University of Wisconsin, Madison

    lead OTHER

Principal Investigators

  • David H Gustafson, PhD · UW Madison

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-04-21
Primary Completion
2020-04-08
Completion
2020-04-08

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02712034 on ClinicalTrials.gov