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Recruiting NCT07868588

Leveraging Interventions for Caregiver Growth, Health, Training, Empowerment and Navigation: Comparing Group Behavioral Interventions to Improve Dementia Caregiver Strain

Conditions: Elevated Caregiver Strain, Dementia Caregiver, Caregiver Stress

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 450
Sponsor: Massachusetts General Hospital

Location: Mass General Hospital Boston Massachusetts

Summary

The goal of this clinical trial is to compare two group-based interventions for caregivers of persons with memory loss (N=450) delivered via telehealth. The aim is to evaluate which program is most effective for different types of caregivers in reducing stress, improving coping, and increasing confidence related to caregiving. Participants will be randomly assigned to one of the two programs, as well as be asked to complete study assessments at baseline (week 0), post-intervention (week 7), and 6-month follow-up.

Eligibility Criteria

While the below criteria reference both the caregiver and care recipient, only caregivers will be enrolled in this study. Inclusion Criteria: * Caregiver of a person with memory loss currently * Care recipient currently living in community * Caregiver at least 18 years of age * Caregiver Zarit Burden Interview-6 (ZBI-6) greater than or equal to 9 or ZBI-22 greater than or equal to 34 * English or Spanish fluency/literacy * Able and willing to participate Exclusion Criteria: * Care recipient enrolled or planning to enroll in hospice * Severe, untreated mental illness or substance use (self or clinician report) * Active suicide risk * Residence outside the U.S. during study procedures

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07868588). StuddyBuddy aggregates publicly available trial information.