Supporting Mental Health and Reducing Care Stress in Caregivers of Persons With Cardiovascular Disease
a study on Caregivers Mental Health Stress Depression Anxiety Cardiovascular Disease
Summary
- Eligibility
- for people ages 18 years and up (full criteria)
- Location
- at Sacramento, California
- Dates
- study startedstudy ends around
Description
Summary
The purpose of this study is to evaluate the preliminary efficacy, feasibility, acceptability, and barriers and facilitators to implementation of the Confident Caregiver intervention among family caregivers of persons with cardiovascular disease participating in cardiac rehabilitation. Caregivers receive four individualized intervention sessions focused on assessment of caregiving challenges, tailored coaching, stress reduction, education, and referrals to supportive resources. Outcomes include reductions in caregiving-related challenges, improvements in mental health, and reductions in stress.
Official Title
Supporting Mental Health and Reducing Care Stress in Caregivers of Persons With Cardiovascular Disease: A Hybrid Effectiveness-Implementation Study of Caregiving Support in Cardiac Rehabilitation
Details
This Type 1 hybrid effectiveness-implementation study evaluates the Confident Caregiver intervention among family caregivers of persons with cardiovascular disease enrolled in cardiac rehabilitation. The intervention consists of four individualized sessions delivered virtually by a trained interventionist over approximately 8 to 12 weeks. Sessions include assessment of caregiving challenges, tailored coaching and action planning to address caregiving challenges, stress reduction strategies, caregiver education, and referrals to services and supports.
Primary intervention efficacy endpoints are: improvement in caregiving challenges and improvement in caregiving-related difficulties
Secondary intervention efficacy endpoints are: improvement in caregiver mental health (depression, anxiety), improvement in caregiver stress (both general and caregiving-specific), and improvement in caregiver overall well-being
Exploratory intervention efficacy endpoints are: improvement in clinic-level cardiac rehab outcomes for cardiac rehab patients (average # of sessions attended, average program completion, program satisfaction, improvement in patient biomarkers, and improvement in person-centered patient outcomes)
Investigators will also evaluate the feasibility and acceptability of intervention for caregiver participants and clinicians in cardiac rehab
Keywords
Caregiver Burden, Stress, Depression, Anxiety, Cardiovascular Diseases, Cardiac Rehabilitation, Caregiver Support, Confident Caregiver, Anxiety Disorders, Confident Caregiver Intervention
Eligibility
You can join if…
Open to people ages 18 years and up
- 18 years of age or older
- Is a caregiver for a patient receiving care in our UC Davis Cardiac Rehabilitation Clinic. A caregiver is defined as someone who provides support to the patient with one or more basic or instrumental activities of daily living.
- Has one or more caregiving-related challenges or issues that they would like support with
- Is able to read and speak in English
You CAN'T join if...
- Is a paid professional caregiver with no family or fictive kin relationship with the care recipient
- Has a diagnosis of major cognitive impairment or Alzheimer's or related dementias
- Is unable to complete the protocol or participate in the intervention (e.g., unavailable during the intervention period, unable to access or use virtual meeting technology)
Location
- University of California Davis Health System
accepting new patients
Sacramento California 95817 United States
Details
- Status
- accepting new patients
- Start Date
- Completion Date
- (estimated)
- Sponsor
- University of California, Davis
- ID
- NCT07717723
- Study Type
- Interventional
- Participants
- Expecting 40 study participants
- Last Updated
Please contact me about this study
We will not share your information with anyone other than the team in charge of this study, which might include an external sponsor. Providing your contact details does not obligate you to participate in the research.
Thank you!
The study team should get back to you in a few business days.