- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04885465
Web-based Support to Caregivers in Heart Failure
Web-based Support to Caregivers Supporting a Person With Heart Failure - a Randomised Controlled Trial With a Process Evaluation
Caregivers of people with heart failure experience a lack of support from health care in their caring role. They often want to become more involved in care, receive education and have the opportunity to share experiences with other caregivers.
Objectives and hypothesis: Our hypothesis is that an internet-based support program that is developed in collaboration with caregivers of people with heart failure will increase preparedness to care (Preparedness for Caregiving Scale). We will also evaluate the effects of the support program on the experiences of caring including positive experiences and the impact of care on health and lifestyle (Caregiver Competence Scale, Rewards of Caregiving Scale, Heart Failure-Caregiver Questionnaire) and their management of heart failure (knowledge of heart failure, support for heart failure self-care and perceived control over heart disease). We will also explore if the patients' healthcare consumption is altered when caregivers receive more support.
Method: The project is a randomized controlled study where 300 caregivers from four health care regions will be randomised to either receive a support program via 1177 care guide or to a control group waiting list who receive standard support from health care and municipalities. After the termination of the study participants in the control group will also be offered access to the support program. Data will be collected with questionnaires at baseline and after 3 and 6 months. A process evaluation with semi-structured interviews to describe the relatives' experiences of using the program with be conducted.
Relevance: Caregivers have been involved in all stages of the development of the Internet-based support program. The evaluation focuses on both the effects of the intervention and factors that affect implementation and equality. Caregiver support that is delivered through 1177 care guide enables a more equal, efficient and accessible support for caregivers.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Östergötland County
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Linköping, Östergötland County, Sweden, 581 85
- Linköping University Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention group
Study participants will receive a web-based support program
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Caregivers in the experimental group will have access to psycho-educational support through a web-based plattform during 3 months.
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No Intervention: Control group waiting list
Study participants in the control group waiting list will receive standard support from health care and municipalities.
After study termination they will receive access to the same web-based program as the experimental group
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline to 3 months in preparedness to care for a person with heart failure
Time Frame: Measured at baseline, after 3 months
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Total score of the Preparedness for Caregiving Scale including 8 items, min score 0, max score 32, higher score indicate better preparedness
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Measured at baseline, after 3 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline to 3 and 6 months in Rewards of Caregiving
Time Frame: Measured at baseline, after 3 and 6 months
|
Total score of the Rewards of Caregiving Scale including 10 items, min score 0, max score 40, higher score indicate better Rewards of caregiving
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Measured at baseline, after 3 and 6 months
|
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Change from baseline to 3 and 6 months in Caregiver Competence
Time Frame: Measured at baseline, after 3 and 6 months
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Total score of the Caregiver Competence Scale, including 4 item, min score 0, max score 12, higher score indicate better Caregiver Competence
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Measured at baseline, after 3 and 6 months
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Heart Failure-Caregiver burden and stress
Time Frame: Measured at baseline, after 3 and 6 months
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Total score and subscales of the Heart Failure-Caregiver Questionnaire including 21 item in three domains, namely physical (five items), emotional/psychological (11 items) and lifestyle (four items and one stem item).
Items are scored on a severity response scale ranging from 'Not at all = 0' to 'A lot = 4'.
The total score was the average of the sum of the three domain scores calculated from sum of scores for items answered/total possible score of items answered x 100.
The minimum and maximum scores ranged between 0 and 100.Higher score indicate higher caregiver burden.
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Measured at baseline, after 3 and 6 months
|
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Perceived control over the heart disease
Time Frame: Measured at baseline, after 3 and 6 months
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Total score of the Control Attitude scale- caregiver version 4 item, min score 4, max score 28, higher score indicate better perceived control
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Measured at baseline, after 3 and 6 months
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Change from baseline to 6 months in preparedness to care for a person with heart failure
Time Frame: Measured at baseline, after 6 months
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Total score of the the Preparedness for Caregiving Scale including 8 items, min score 0, max score 32, higher score indicate better preparedness
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Measured at baseline, after 6 months
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Change in knowledge about heart failure in the three subscales
Time Frame: Measured after 3 months
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Revised Dutch heart failure knowledge scale with 3 subscales: 1. Knowledge subscale 15 items, min score 0 max score 15, higher score indicate better heart failure knowledge.
2. Trust in own HF knowledge subscale 3 items, min score 3 max score 15, higher score indicare better trust.
3. Health literacy subscale 3 items, min score 3 max score 15, higher score indicare better health literacy.
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Measured after 3 months
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Change in caregiver support for heart failure self-care
Time Frame: Measured at baseline, after 3 and 6 months
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European Self-care Behaviour Scale - caregiverversion 7 items, Score from 0-100, higher score better support for self-care
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Measured at baseline, after 3 and 6 months
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Social support
Time Frame: Measured at baseline, after 3 and 6 months
|
Multidimensional Scale of Perceived Social Support, 12 items.
Each item is rated on a seven-point Likert-type response format (1 = very strongly disagree; 7 = very strongly agree).
A total score is calculated by summing the results for all items.
The possible score range is between 12 and 84, the higher the score the higher the perceived social support.
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Measured at baseline, after 3 and 6 months
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Symptoms of anxiety and depression
Time Frame: Measured at baseline, after 3 and 6 months
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Hospital anxiety and depression scale, 7 items for anxiety and 7 items for depression.
Min score 0 and max score 21 for each scale, Higher score indicate more symptoms of anxiety and depression
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Measured at baseline, after 3 and 6 months
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Health related quality of life
Time Frame: Measured at baseline, after 3 and 6 months
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EuroQol EQ-5D 5 level, index and VAS 0-100, higher score indicate better health
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Measured at baseline, after 3 and 6 months
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Anna Strömberg, PhD, Linkoeping University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Dnr 2019-05310
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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