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:
2025-12-25 @ 12:36 AM
Ignite Modification Date:
2025-12-25 @ 12:36 AM
NCT ID:
NCT02707367
Eligibility Criteria:
Inclusion Criteria:
Clients:
* Age of majority
* Receipt of mental health services within the participating program;
* Directly work with a provider participating in the study
* The ability to participate in the activities as determined by the client's clinical team
* Willing and able to engage in a six month PCRP intervention and participate in follow-up research activities (24 months total including follow up assessments).
Providers: Providers must meet the following inclusion criteria:
* Age of majority
* Directly work with clients willing to participate in the study;
* Have access to and basic navigation skills for using the Internet (for online coaching
* Work for a participating program
* Have a willingness to engage in a six-month PCRP intervention and participate in follow-up research activities (24 months total).
Administrators: Inclusion criteria for administrators participating in key informant semi-structured interviews include:
* Age of majority
* Being administrator of a program participating in the study or umbrella organization
* Have access to a computer to view tool components
* Knowledge about the market for this type of product for use in adult mental health. The team will develop a screening tool for administrators to ensure they meet basic criteria for the study.
Exclusion Criteria:
Clients:
* Non-English speakers
* Clients who are unable to participate in study activities (per clinical team determination) and individuals who are unable to understand the informed consent process (per the Quiz of Understanding for Informed Consent) will be excluded from the study.
Providers:
* Non-English speakers
* Providers who have prior experience with RR tools will be excluded from the study.
Administrators:
• Non-English speakers
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02707367
Study Brief:
Protocol Section:
NCT02707367