Stopped: COVID-19
Participants in the intervention study will be 120 caregivers with guilt feelings linked with care and high levels of emotional distress (anxiety and/or depression), randomly allocated to the intervention conditions: intervention group and cognitive-behavioral comparison group. The intervention will be provided in a group setting and will consist in 8 sessions plus 3 booster sessions. The effect of the intervention on guilt feelings, depressive and anxious symptomatology, and biomarkers of cardiovascular risk will be assessed after the intervention and at follow-ups at 6 months.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Guilt symptoms
Timeframe: Pre-intervention, post-intervention (two months after the intervention) and follow-up (6 months after the intervention)
Depressive symptoms
Timeframe: Pre-intervention, post-intervention (two months after the intervention) and follow-up (6 months after the intervention)
Anxiety symptoms
Timeframe: Pre-intervention, post-intervention (two months after the intervention) and follow-up (6 months after the intervention)