Phase II: Scalable Digital Delivery of CRAFT Training for Professionals to Maximize Treatment Rates of OUD in Families
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Digital Tutorial overview, Digital Tutorial plus training Materials, Digital Tutorial plus training Materials plus feedback and Coaching.
- Who it may be relevant to
- Registry conditions: Community Reinforcement And Family Training, Family Health, Substance-Related Disorders. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Phase II: Scalable Digital Delivery of Evidence-based Training for Addiction Professionals to Maximize Treatment Admission and Retention Rates of Opioid Use Disorder in Affected Families
Overview
The goal of this project is to demonstrate digital training efficacy at scale and commercial readiness. This pilot project will advance piloted digital training programs for CRAFT and maximize scalability. In this project, investigators will: Aim 1: Optimize the digital CRAFT training product based on data and feedback from the pilot and commercialization advisors. Aim 2: Conduct a fully powered randomized control trial of 3 levels of digital training (Level 1 - Digital tutorial only \[T\]; Level 2 - Tutorial \& digital training materials for self-study \[TM\]; Level 3 - Tutorial, digital materials, feedback and coaching \[TMC\]) to examine the effects of training on CRAFT knowledge, fidelity, and plus IP treatment entry/retention and counselor skill pre- and post-tutorial, at 12 weeks and at 6 months.
Interventions
- Behavioral Digital Tutorial overview
Self study of a digital tutorial covering an overview of CRAFT designed to be reviewed within 7 weeks and revisited over 6 months. - Behavioral Digital Tutorial plus training Materials
Self study of a digital tutorial covering an overview of CRAFT and deeper materials designed to be reviewed within 7 weeks and revisited over 6 months. - Behavioral Digital Tutorial plus training Materials plus feedback and Coaching
Self study of a digital tutorial covering an overview of CRAFT and deeper materials designed to be reviewed within 7 weeks and revisited over 6 months. Plus group coaching and feedback on audio recordings of CRAFT procedures used in sessions
Primary outcome measures
- CRAFT Procedure Fidelity [Time frame: 3 months, 6 months]
Secondary outcome measures (2)
- 3 months [Time frame: 3 months, 6 months]
- Program Implementation Potential Scale [Time frame: 3 months, 6 months]
Eligibility criteria
Inclusion criteria
- Be over 19
- Live in the US
- Work in a counselor-related profession
- Have counseling work that involves clients
- Work with CSOs impacted by OUD, or could work with this type of client
- Have not been certified in CRAFT
- Have not participated in the 2023 WTV counselor training pilot study
- Be able to provide at least 45-minute individual counselor sessions to at least one CSO (CSO)
- Be able and willing to complete intervention activities over the course of the 12-week study as determined by the random assignment including: participating in the tutorial and training and submitting the required session audiotapes
- Report having access to a computer and smartphone with internet access, email, and word processing capability
- Demonstrate complete understanding of the requirements for participation in the study by reading and signing the consent form and completing the online consent quiz or confirmation call
- Provide valid locator information to allow research and CRAFT training staff to contact them to schedule study-related appointments
- Complete the first assessment mock session with our standardized patient (SP) and pre-tutorial surveys
Exclusion criteria
- Does not agree to participate
- Does not complete the baseline assessment requirements
- Is not English-speaking
- Participated in the Qualitative Review aspect of the study
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Prevention
Study locations
United States · 1 center
- We The Village, Inc. — New York
Identifiers
NCT: NCT06685003 · 2403 · 4R44DA053845-02