Web-based support for caregivers of heart failure patients
Web-based Support to Caregivers Supporting a Person With Heart Failure - a Randomised Controlled Trial With a Process Evaluation
This study is testing an online support program for caregivers of heart failure patients to see if it helps them feel more prepared and connected while caring for their loved ones.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 300 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Linkoeping University Government |
| Locations | 1 site (Linköping, Östergötland) |
| Trial ID | NCT04885465 on ClinicalTrials.gov |
What this trial studies
This study aims to provide an internet-based support program for caregivers of individuals with heart failure, developed in collaboration with these caregivers. The program focuses on enhancing caregivers' preparedness and knowledge about heart failure, while also allowing them to share experiences with others in similar situations. The effectiveness of the program will be evaluated through various scales measuring caregiver competence, rewards of caregiving, and the impact on healthcare consumption. The ultimate goal is to improve the caregiving experience and health outcomes for both caregivers and patients.
Who should consider this trial
Good fit: Ideal candidates for this study are close relatives of patients diagnosed with heart failure who are actively involved in caregiving.
Not a fit: Patients whose caregivers are unable to participate due to language barriers, cognitive issues, or other serious health conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could significantly enhance the support and preparedness of caregivers, leading to better health outcomes for heart failure patients.
How similar studies have performed: Other studies have shown positive outcomes with similar web-based support interventions for caregivers, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * A close relative identified by the patient who cares for, supports or helps this patient with a verified heart failure diagnosis ICD codes within I42 or I50 (i.e. all types of heart failure). Exclusion Criteria: * Relatives who are unable to carry out the data collection or participate in intervention (e.g. non-Swedish speaking, cognitive problems, severe mental illness, addiction) * The patient or the close relative have a serious disease with expected short survival of \< 6 months.
Where this trial is running
Linköping, Östergötland
- Linköping University Hospital — Linköping, Östergötland, Sweden (Recruiting)
Study contacts
- Principal investigator: Anna Strömberg, PhD — Linkoeping University
- Study coordinator: Anna Stromberg, PhD
- Email: anna.stromberg@liu.se
- Phone: +46-73-6569265
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.