Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 7:24 PM
Ignite Modification Date: 2025-12-24 @ 7:24 PM
NCT ID: NCT06685003
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
Healthy Volunteers: True
Sex: ALL
Minimum Age: 18 Years
Study: NCT06685003
Study Brief:
Protocol Section: NCT06685003