RECRUITING

MBC2OTP Project (Measurement-Based Care Implementation in Community Opioid Treatment Programs)

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The goal of this clinical trial is to evaluate the effectiveness and implementation of measurement-based care, which involves the systematic use of client self-report data to inform and enhance treatment, in opioid treatment programs using a pilot hybrid effectiveness-implementation study design. The main questions this study aims to answer are: 1) is measurement based care effective for improving patient treatment attendance and opioid abstinence, and 2) can measurement based care be implemented with fidelity in opioid treatment programs? Participants in this study will be opioid treatment program leaders and treatment providers. Leaders and treatment providers will participate in measurement-based care implementation strategies such as training and consultation to help them use measurement-based care with their patients. There is no comparison group for this study, however researchers will compare effectiveness outcomes prior to and post measurement-based care implementation and will evaluate changes in measurement-based care use with fidelity post implementation.

Official Title

Pilot Implementation of Measurement-Based Care in Community Opioid Treatment Programs

Quick Facts

Study Start:2024-04-24
Study Completion:2026-02
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06345274

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Kelli Scott, PhD
CONTACT
312-503-0347
kelli.scott@northwestern.edu

Study Locations (Sites)

Family Guidance Centers, Inc.
Aurora, Illinois, 60505
United States
Northwestern University Feinberg School of Medicine
Chicago, Illinois, 60611
United States
Family Guidance Centers, Inc.
Chicago, Illinois, 60654
United States
Family Guidance Centers, Inc.
Des Plaines, Illinois, 60016
United States
Family Guidance Centers, Inc.
Joliet, Illinois, 60435
United States

Collaborators and Investigators

Sponsor: Northwestern University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-04-24
Study Completion Date2026-02

Study Record Updates

Study Start Date2024-04-24
Study Completion Date2026-02

Terms related to this study

Keywords Provided by Researchers

  • Opioid Use Disorder
  • Opioid Treatment Programs
  • Measurement-Based Care
  • Implementation Science

Additional Relevant MeSH Terms

  • Opioid Use Disorder