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Web-based Support to Caregivers in Heart Failure

Primary Purpose

Heart Failure, Family Caregivers

Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
web-based psychoeducational support
Sponsored by
Linkoeping University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Heart Failure focused on measuring heart failure, caregiver, carer, preparedness, Perceived control

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: A close relative identified by the patient, who cares for, supports or helps a 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) or have a serious disease with expected short survival.

Sites / Locations

  • Linköping University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention group

Control group waiting list

Arm Description

Study participants will receive a web-based support program

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

Outcomes

Primary Outcome Measures

Change from baseline to 3 months in preparedness to care for a person with heart failure
Total score of the Preparedness for Caregiving Scale including 8 items, min score 0, max score 32, higher score indicate better preparedness

Secondary Outcome Measures

Change from baseline to 3 and 6 months in Rewards of Caregiving
Total score of the Rewards of Caregiving Scale including 10 items, min score 0, max score 40, higher score indicate better Rewards of caregiving
Change from baseline to 3 and 6 months in Caregiver Competence
Total score of the Caregiver Competence Scale, including 4 item, min score 0, max score 12, higher score indicate better Caregiver Competence
Heart Failure-Caregiver burden and stress
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.
Perceived control over the heart disease
Total score of the Control Attitude scale- caregiver version 4 item, min score 4, max score 28, higher score indicate better perceived control
Change from baseline to 6 months in preparedness to care for a person with heart failure
Total score of the the Preparedness for Caregiving Scale including 8 items, min score 0, max score 32, higher score indicate better preparedness
Change in knowledge about heart failure in the three subscales
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.
Change in caregiver support for heart failure self-care
European Self-care Behaviour Scale - caregiverversion 7 items, Score from 0-100, higher score better support for self-care

Full Information

First Posted
May 9, 2021
Last Updated
January 23, 2023
Sponsor
Linkoeping University
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1. Study Identification

Unique Protocol Identification Number
NCT04885465
Brief Title
Web-based Support to Caregivers in Heart Failure
Official Title
Web-based Support to Caregivers Supporting a Person With Heart Failure - a Randomised Controlled Trial With a Process Evaluation
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 15, 2021 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Linkoeping University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Family Caregivers
Keywords
heart failure, caregiver, carer, preparedness, Perceived control

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention group
Arm Type
Experimental
Arm Description
Study participants will receive a web-based support program
Arm Title
Control group waiting list
Arm Type
No Intervention
Arm Description
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
Intervention Type
Behavioral
Intervention Name(s)
web-based psychoeducational support
Intervention Description
Caregivers in the experimental group will have access to psycho-educational support through a web-based plattform during 3 months.
Primary Outcome Measure Information:
Title
Change from baseline to 3 months in preparedness to care for a person with heart failure
Description
Total score of the Preparedness for Caregiving Scale including 8 items, min score 0, max score 32, higher score indicate better preparedness
Time Frame
Measured at baseline, after 3 months
Secondary Outcome Measure Information:
Title
Change from baseline to 3 and 6 months in Rewards of Caregiving
Description
Total score of the Rewards of Caregiving Scale including 10 items, min score 0, max score 40, higher score indicate better Rewards of caregiving
Time Frame
Measured at baseline, after 3 and 6 months
Title
Change from baseline to 3 and 6 months in Caregiver Competence
Description
Total score of the Caregiver Competence Scale, including 4 item, min score 0, max score 12, higher score indicate better Caregiver Competence
Time Frame
Measured at baseline, after 3 and 6 months
Title
Heart Failure-Caregiver burden and stress
Description
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.
Time Frame
Measured at baseline, after 3 and 6 months
Title
Perceived control over the heart disease
Description
Total score of the Control Attitude scale- caregiver version 4 item, min score 4, max score 28, higher score indicate better perceived control
Time Frame
Measured at baseline, after 3 and 6 months
Title
Change from baseline to 6 months in preparedness to care for a person with heart failure
Description
Total score of the the Preparedness for Caregiving Scale including 8 items, min score 0, max score 32, higher score indicate better preparedness
Time Frame
Measured at baseline, after 6 months
Title
Change in knowledge about heart failure in the three subscales
Description
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.
Time Frame
Measured after 3 months
Title
Change in caregiver support for heart failure self-care
Description
European Self-care Behaviour Scale - caregiverversion 7 items, Score from 0-100, higher score better support for self-care
Time Frame
Measured at baseline, after 3 and 6 months
Other Pre-specified Outcome Measures:
Title
Social support
Description
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.
Time Frame
Measured at baseline, after 3 and 6 months
Title
Symptoms of anxiety and depression
Description
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
Time Frame
Measured at baseline, after 3 and 6 months
Title
Health related quality of life
Description
EuroQol EQ-5D 5 level, index and VAS 0-100, higher score indicate better health
Time Frame
Measured at baseline, after 3 and 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility 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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Anna Stromberg, PhD
Phone
+46-73-6569265
Email
anna.stromberg@liu.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anna Strömberg, PhD
Organizational Affiliation
Linkoeping University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Linköping University Hospital
City
Linköping
State/Province
Östergötland
ZIP/Postal Code
581 85
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anna Strömberg, PhD
Phone
+46736569265
Email
anna.stromberg@liu.se

12. IPD Sharing Statement

Plan to Share IPD
No

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Web-based Support to Caregivers in Heart Failure

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