We will conduct a pilot RCT (n = 60) as a test of the FN+ Program feasibility and preliminary effectiveness to improve individual-level variables, relative to Attention Control (AC). The primary outcome will be increased foster parent activation (P-PAM-MH). Secondary outcomes include reduced barriers to treatment and perceived change in parent capacity to manage youth MH care. Randomization: We will use simple randomization to assign foster parents to condition. Foster parents (n=60) will be randomized to the either the FN+ or AC. We will pilot all randomization procedures including those designed to prevent allocation bias. Randomization will be conducted by a research analyst who is blind to hypotheses and is not involved in any other aspect of the study. The research analyst will only share the names and condition assignment with the FNs who do not know study aims or hypotheses and will keep research staff blinded to condition. The ACHW will conduct all outcome data and remain blind to condition. The ACHW will remain masked to treatment assignment until the trial is complete. Success in masking will be monitored using the Evaluator Masking Assessment upon the completion of each data collection time point for each parent. Inclusion and Exclusion criteria are the same as Aim 2 with the addition that any foster parent that participated in Aim 1 or 2 will be excluded from the RCT.
Age
18–99
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Foster parent, kinship caregiver, or guardian, of a youth between the ages of 6 to 17 with mental health needs
Parent adopted child from foster care
Living in Illinois, United States
English speaking
Has access to internet and videoconferencing
You may not be if
Participated in the FN+ Focus Groups, Open Trial or PROACTIVE Parent Pilot Study
Clareo Health | Building Capacity for Youth Mental Wellness: Family Navigator Model for Foster Parents