This study aims to evaluate the implementation outcomes of a pilot randomized controlled trial and to assess the preliminary efficacy of Problem Management Plus (PM+) in reducing symptoms of depression and anxiety among users at a Primary Health Care center in Chile. Two intervention groups will be compared: PM+ versus care as usual (CAU). The process will include an evaluation of the feasibility of the study procedures, as well as the acceptability and fidelity of the PM+ intervention.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Implementation outcome: Feasibility
Timeframe: Feasibility outcome component A will be collected once recruitment is completed. Component B will be collected at week 6, starting from the first intervention week.
Implementation outcome: Acceptability
Timeframe: Acceptability outcomes will be collected during the post-intervention assessment at week 6, starting from the first intervention week.
Implementation Outcome: Fidelity
Timeframe: Fidelity outcomes will be collected throughout the intervention period, from the first to the final intervention week (week 5).