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Acceptance and Commitment Therapy for Patients With Chronic Heart Failure and Their Caregivers on Their Quality of Life

Primary Purpose

Chronic Heart Failure

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
ACT (Acceptance and Commitment Therapy) plus brief CHF education
HE (Health Education)
Sponsored by
The Hong Kong Polytechnic University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Chronic Heart Failure focused on measuring Chronic heart failure, Acceptance and Commitment Therapy, Patient-caregiver dyads, Health-related quality of life, Randomized controlled trial

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Patient-caregiver dyads will be recruited as units if both are eligible as listed below.

  1. Patient

    • Inclusion Criteria:

      • 18 years or older
      • a confirmed diagnosis of Chronic Heart Failure (CHF) according to international guidelines
      • with New York Heart Association (NYHA) functional classification I to III
      • has been hospitalized in the past one year
      • able to nominate a primary family caregiver (if two or more family members where the primary caregivers of the patient, the one who had the highest average contact hours with the patient)
      • can understand and communicate in Chinese
      • can access Tencent VooV Meeting via smartphone for attending the intervention
    • Exclusion Criteria:

      • has a documented medical history of psychiatric illness, dementia, and life-threatening, such as end-stage renal failure, severe pulmonary disease and respiratory disease
      • has cognitive impairment evaluated with a score of 0-2 on the Mini-Cog scale
      • living in a nursing home
  2. Caregiver

    • Inclusion Criteria:

      • 18 years or older
      • can understand and communicate in Chinese
      • can access Tencent VooV Meeting via smartphone for attending the intervention
    • Exclusion Criteria:

      • paid caregivers
      • has a documented medical history of psychiatric illness, dementia, and life-threatening, such as end-stage renal failure, severe pulmonary disease and respiratory disease
      • has cognitive impairment evaluated with a score of 0-2 on the Mini-Cog scale

Sites / Locations

  • Taihe HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

ACT Group

HE group

Arm Description

The ACT intervention was structured to take place over one month on a weekly basis via Tencent's VooV platform. Each roughly 2-hour session will consist of a group-based ACT (1.5 hours) and a brief health education talk on CHF self-management (0.5 hours). Each training session will serve about 4-8 dyads. In addition, each participant will receive one set of session handouts on CHF education, ACT skills, and a homework assignment.

The participants of the control group will receive four weekly 2-hour sessions of structured health education on CHF self-management over four consecutive weeks via Tencent's VooV platform, delivered by a registered nurse. Each session will includea a review of the previous session (except the first session), a CHF education talk and a Q&A section to evaluate the participant's understanding of the key concepts. Each session will be offered to 4-8 patient-caregiver dyads. In addition, each participant will receive session handouts on the main topic related to CHF self-management and homework assignments.

Outcomes

Primary Outcome Measures

Change from baseline in patients' CHF specific health-related quality of life at immediately post-intervention
The short-form Kansas City Cardiomyopathy Questionnaire (KCCQ-12) will be used for patients. KCCQ-12 is a 12-item instrument with a score of 0-100, a lower score indicates a poorer quality of life.
Change from baseline in patients' CHF specific health-related quality of life at 3-month post-intervention
The short-form Kansas City Cardiomyopathy Questionnaire (KCCQ-12) will be used for patients. KCCQ-12 is a 12-item instrument with a score of 0-100, a lower score indicates a poorer quality of life.
Change from baseline in patients' generic health-related quality of life at immediately post-intervention
The five-dimensional descriptive system of the EuroQol Group 5-Dimension questionnaire (EQ-5D-5L) will be used to evaluate generic health-related quality of life for patients. The scores range from less than 0 to 1.0, with higher scores representing higher health utility.
Change from baseline in patients' generic health-related quality of life at three-month post-intervention
The five-dimensional descriptive system of the EuroQol Group 5-Dimension questionnaire (EQ-5D-5L) will be used to evaluate generic health-related quality of life for patients. The scores range from less than 0 to 1.0, with higher scores representing higher health utility.
Change from baseline in caregivers' health-related quality of life at immediately post-intervention
The five-dimensional descriptive system of the EuroQol Group 5-Dimension questionnaire (EQ-5D-5L) will be used to evaluate generic health-related quality of life for caregivers. The scores range from less than 0 to 1.0, with higher scores representing higher health utility.
Change from baseline in caregivers' health-related quality of life at three-month post-intervention
The five-dimensional descriptive system of the EuroQol Group 5-Dimension questionnaire (EQ-5D-5L) will be used to evaluate generic health-related quality of life for caregivers. The scores range from less than 0 to 1.0, with higher scores representing higher health utility.

Secondary Outcome Measures

Change from baseline in patients' unscheduled health service visits due to heart-related problems at immediately post-intervention
Patients' report of the total number of unscheduled readmission and emergency visits due to heart-related problems in either a / public hospital(s) and/or a private hospital(s)
Change from baseline in patients' unscheduled health service visits due to heart-related problems at three-month post-intervention
Patients' report of the total number of unscheduled readmission and emergency visits due to heart-related problems in either a / public hospital(s) and/or a private hospital(s)
Change from baseline in patients' CHF self-care behavior at immediately post-intervention
The European Heart Failure Self-care Behavior Scale (EHFScBS) will be used for patients to evaluate their self-care behavior. EHFScBS is a 12-item 5-point Likert scale with a score ranging from 0 to 60, a lower score represents a higher level of self-care behaviors.
Change from baseline in patients' CHF self-care behavior at immediately post-intervention
The European Heart Failure Self-care Behavior Scale (EHFScBS) will be used for patients to evaluate their self-care behavior. EHFScBS is a 12-item 5-point Likert scale with a score ranging from 0 to 60, a lower score represents a higher level of self-care behaviors.
Change from baseline in patients' smoking status at immediately post-intervention
Patients' report of not having/ having smoked and the estimated amount of cigarette consumed (if applicable) for the past one week.
Change from baseline in patients' smoking status at three-month post-intervention
Patients' report of not having/ having smoked and the estimated amount of cigarette consumed (if applicable) for the past one week.
Change from baseline in patients' alcohol status at immediately post-intervention
Patients' report of not having/ having alcohol drinking and the estimated amount of alcohol consumed (if applicable) for the past one week.
Change from baseline in patients' alcohol status at three-month post-intervention
Patients' report of not having/ having alcohol drinking and the estimated amount of alcohol consumed (if applicable) for the past one week.
Change from baseline in caregivers' perceived care burden at immediately post-intervention
The Zarit Caregiver Burden Interview (ZBI) will be used for caregivers to evaluate perceived care burden. ZBI is a 22-item 5-point Likert scale with a score ranging from 0 to 88, a lower score indicates less care burden.
Change from baseline in caregivers' perceived care burden at three-month post-intervention
The Zarit Caregiver Burden Interview (ZBI) will be used for caregivers to evaluate perceived care burden. ZBI is a 22-item 5-point Likert scale with a score ranging from 0 to 88, a lower score indicates less care burden.
Change from baseline in participants' anxiety symptoms at immediately post-intervention
The General Anxiety Disorder Scale (GAD) will be used for caregivers and patients. The GAD consists of 7 item 4-point Likert scale. The score of each scale ranges from 0 to 21, with a lower score indicating a lower level of anxiety.
Change from baseline in participants' depressive symptoms at immediately post-intervention
The Patient Health Questionaire (PHQ) will be used for caregivers and patients. The PHQ consists of 9 item 4-point Likert scale. The score of each scale ranges from 0 to 27, with a lower score indicating a lower level of depression.
Change from baseline in participants' anxiety symptoms at three-month post-intervention
The General Anxiety Disorder Scale (GAD) will be used for caregivers and patients. The GAD consists of 7 item 4-point Likert scale. The score of each scale ranges from 0 to 21, with a lower score indicating a lower level of anxiety.
Change from baseline in participants' depressive symptoms at three-month post-intervention
The Patient Health Questionaire (PHQ) will be used for caregivers and patients. The PHQ consists of 9 item 4-point Likert scale. The score of each scale ranges from 0 to 27, with a lower score indicating a lower level of depression.
Change from baseline in participants' perspective taking at immediately post-intervention
The perspective taking subscale from the Interpersonall Reactivity Index (IRI) will be used for caregivers and patients. Chinese version of the perspective taking subscale is a 5-item 5-point Likert scale with a score ranging from 5 to 25, a lower score represents a lower tendency for perspective taking.
Change from baseline in participants' perspective taking at three-month post-intervention
The perspective taking subscale from the Interpersonall Reactivity Index (IRI) will be used for caregivers and patients. Chinese version of the perspective taking subscale is a 5-item 5-point Likert scale with a score ranging from 5 to 25, a lower score represents a lower tendency for perspective taking.
Change from baseline in participants' psychological flexibility at immediately post-intervention
The Comprehensive Assessment of Acceptance and Commitment Therapy Processes (CompACT) will be used for caregivers and patients.CompACT is an 18-item 5-point Likert scale with a score ranging from 18 to 90, a lower score represents a lower level of psychological flexibility.
Change from baseline in participants' psychological flexibility at three-month post-intervention
The Comprehensive Assessment of Acceptance and Commitment Therapy Processes (CompACT) will be used for caregivers and patients.CompACT is an 18-item 5-point Likert scale with a score ranging from 18 to 90, a lower score represents a lower level of psychological flexibility.
Change from baseline in participants' relationship functioning at immediately post-intervention
The Dyadic Adjustment Scale-7(DAS-7) will be used for caregivers and patients.DAS-7 is a 7-item 6-point Likert scale with a score ranging from 0 to 36, a lower score represents less positive relationship quality.
Change from baseline in participants' relationship functioning at three-month post-intervention
The Dyadic Adjustment Scale-7(DAS-7) will be used for caregivers and patients.DAS-7 is a 7-item 6-point Likert scale with a score ranging from 0 to 36, a lower score represents less positive relationship quality.
Change from baseline in participants' generic health-related quality of life at immediately post-intervention
The visual analog scale (VAS) of EuroQol Group 5-Dimension questionnaire (EQ-5D-5L) will be used to evaluate participants' perceived health, the score ranges from 0 to 100 with 100 being better.
Change from baseline in participants' generic health-related quality of life at three-month post-intervention
The visual analog scale (VAS) of EuroQol Group 5-Dimension questionnaire (EQ-5D-5L) will be used to evaluate participants' perceived health, the score ranges from 0 to 100 with 100 being better.
Change from baseline in participants' self-compassion at immediately post-intervention
The Self-compassion Scale (SCS) will be used for caregivers and patients.SCS is an 12-item 5-point Likert scale with a score ranging from 12 to 60, a lower score represents a lower level of self-compassion.
Change from baseline in participants' self-compassion at three-month post-intervention
The Self-compassion Scale (SCS) will be used for caregivers and patients.SCS is an 12-item 5-point Likert scale with a score ranging from 12 to 60, a lower score represents a lower level of self-compassion.

Full Information

First Posted
May 26, 2021
Last Updated
February 10, 2023
Sponsor
The Hong Kong Polytechnic University
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1. Study Identification

Unique Protocol Identification Number
NCT04917159
Brief Title
Acceptance and Commitment Therapy for Patients With Chronic Heart Failure and Their Caregivers on Their Quality of Life
Official Title
Effectiveness of Acceptance and Commitment Therapy on the Health-related Quality of Life in Patients With Chronic Heart Failure and Their Family Caregivers: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
June 10, 2022 (Actual)
Primary Completion Date
January 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Hong Kong Polytechnic 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
This study is to examine whether group-based Acceptance and Commitment Therapy in the patient-caregiver dyads with Chronic Heart Failure is effective in improving dyadic health-related quality of life, dyadic psychological symptoms, caregiver burden, the rate of patient's readmission, and patient's self-care behavior in comparison with those dyads receiving health education over three-month post intervention.
Detailed Description
Chronic heart failure (CHF) is a complex progressive debilitating illness characterized by high morbidity and mortality with unpredictable course and frequent hospital readmissions. Patients with CHF are often old with comorbid impaired psychosocial functioning, and worse health-related quality of life (HRQoL), which generate unavoidable increased dependence on their family caregivers at home. The family caregivers often bear physical and psychological challenges with declined HRQoL, maintaining interdependent relationships with their care recipient when participating in CHF self-management. Dyadic interventions delivered to the patients along with their family caregivers are successful to facilitate patients' self-management to reduce patients' hospital readmission rates and improve HRQoL for both patients and their caregivers post-discharge in the context of chronic disease management. However, little attention has been paid to this vulnerable group. It is noteworthy that a transdiagnostic psychological approach, Acceptance and Commitment Therapy (ACT), aiming to promote psychological flexibility, has demonstrated an ability to break through the psychological barriers to meaningful living among clinical and non-clinical populations. Existing evidence shows promising improvements of ACT on HRQoL in both patients with chronic illness and the family caregivers of the patients with childhood illness. Such evidence implies that ACT in the patient-caregiver dyads may be beneficial for HRQoL and other health outcomes for both patients with CHF and their family caregivers. However, little has been done to address these concerns in mainland China. A pilot testing was to evaluate the feasibility of recruiting participants at the clinical setting and the acceptability of group-based ACT to patient-caregiver dyads with CHF. Then, a pragmatic, single-center, two-arm, parallel (in 1:1 ratio) randomized controlled trial (RCT) will be performed to examine the effects of acceptance and commitment therapy in patient-caregiver dyads with CHF. Eligible patient-caregiver dyads will be randomly assigned to either the intervention group or the control group. Assessments will be conducted before the intervention, immediately post-intervention, and 3-month post-intervention by blind outcome assessors. The ACT intervention will be delivered by two facilitators and continually supervised by an experienced ACT researcher.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Heart Failure
Keywords
Chronic heart failure, Acceptance and Commitment Therapy, Patient-caregiver dyads, Health-related quality of life, Randomized controlled trial

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
ACT Group
Arm Type
Experimental
Arm Description
The ACT intervention was structured to take place over one month on a weekly basis via Tencent's VooV platform. Each roughly 2-hour session will consist of a group-based ACT (1.5 hours) and a brief health education talk on CHF self-management (0.5 hours). Each training session will serve about 4-8 dyads. In addition, each participant will receive one set of session handouts on CHF education, ACT skills, and a homework assignment.
Arm Title
HE group
Arm Type
Active Comparator
Arm Description
The participants of the control group will receive four weekly 2-hour sessions of structured health education on CHF self-management over four consecutive weeks via Tencent's VooV platform, delivered by a registered nurse. Each session will includea a review of the previous session (except the first session), a CHF education talk and a Q&A section to evaluate the participant's understanding of the key concepts. Each session will be offered to 4-8 patient-caregiver dyads. In addition, each participant will receive session handouts on the main topic related to CHF self-management and homework assignments.
Intervention Type
Behavioral
Intervention Name(s)
ACT (Acceptance and Commitment Therapy) plus brief CHF education
Intervention Description
The participants will identify their values and clarify their alternative behavior, exploring their thoughts and feelings, and finding ways to meet their own and their family member's needs. The rational bond between the patient and his/her family caregiver will be emphasized. In addtion, the contents of brief CHF education are based on the latest national clinical practice guideline for CHF, including symptoms monitoring, medication adherence, fluid and salt restriction, smoking cessation, alcohol consumption, and physical activity maintenance.
Intervention Type
Behavioral
Intervention Name(s)
HE (Health Education)
Intervention Description
The educational contents are based on the latest national clinical practice guideline for CHF. Besides the basic information on CHF education provided in intervention group, the contents of CHF education also include definition of CHF, epidemiology, diagnosis, comorbidity, and CHF treatment. ACT components are not covered.
Primary Outcome Measure Information:
Title
Change from baseline in patients' CHF specific health-related quality of life at immediately post-intervention
Description
The short-form Kansas City Cardiomyopathy Questionnaire (KCCQ-12) will be used for patients. KCCQ-12 is a 12-item instrument with a score of 0-100, a lower score indicates a poorer quality of life.
Time Frame
Baseline and post-intervention immediately
Title
Change from baseline in patients' CHF specific health-related quality of life at 3-month post-intervention
Description
The short-form Kansas City Cardiomyopathy Questionnaire (KCCQ-12) will be used for patients. KCCQ-12 is a 12-item instrument with a score of 0-100, a lower score indicates a poorer quality of life.
Time Frame
Baseline and three-month post-intervention
Title
Change from baseline in patients' generic health-related quality of life at immediately post-intervention
Description
The five-dimensional descriptive system of the EuroQol Group 5-Dimension questionnaire (EQ-5D-5L) will be used to evaluate generic health-related quality of life for patients. The scores range from less than 0 to 1.0, with higher scores representing higher health utility.
Time Frame
Baseline and post-intervention immediately
Title
Change from baseline in patients' generic health-related quality of life at three-month post-intervention
Description
The five-dimensional descriptive system of the EuroQol Group 5-Dimension questionnaire (EQ-5D-5L) will be used to evaluate generic health-related quality of life for patients. The scores range from less than 0 to 1.0, with higher scores representing higher health utility.
Time Frame
Baseline and three-month post-intervention
Title
Change from baseline in caregivers' health-related quality of life at immediately post-intervention
Description
The five-dimensional descriptive system of the EuroQol Group 5-Dimension questionnaire (EQ-5D-5L) will be used to evaluate generic health-related quality of life for caregivers. The scores range from less than 0 to 1.0, with higher scores representing higher health utility.
Time Frame
Baseline and post-intervention immediately
Title
Change from baseline in caregivers' health-related quality of life at three-month post-intervention
Description
The five-dimensional descriptive system of the EuroQol Group 5-Dimension questionnaire (EQ-5D-5L) will be used to evaluate generic health-related quality of life for caregivers. The scores range from less than 0 to 1.0, with higher scores representing higher health utility.
Time Frame
Baseline and three-month post-intervention
Secondary Outcome Measure Information:
Title
Change from baseline in patients' unscheduled health service visits due to heart-related problems at immediately post-intervention
Description
Patients' report of the total number of unscheduled readmission and emergency visits due to heart-related problems in either a / public hospital(s) and/or a private hospital(s)
Time Frame
Baseline and post-intervention immediately
Title
Change from baseline in patients' unscheduled health service visits due to heart-related problems at three-month post-intervention
Description
Patients' report of the total number of unscheduled readmission and emergency visits due to heart-related problems in either a / public hospital(s) and/or a private hospital(s)
Time Frame
Baseline and three-month post-intervention
Title
Change from baseline in patients' CHF self-care behavior at immediately post-intervention
Description
The European Heart Failure Self-care Behavior Scale (EHFScBS) will be used for patients to evaluate their self-care behavior. EHFScBS is a 12-item 5-point Likert scale with a score ranging from 0 to 60, a lower score represents a higher level of self-care behaviors.
Time Frame
Baseline and post-intervention immediately
Title
Change from baseline in patients' CHF self-care behavior at immediately post-intervention
Description
The European Heart Failure Self-care Behavior Scale (EHFScBS) will be used for patients to evaluate their self-care behavior. EHFScBS is a 12-item 5-point Likert scale with a score ranging from 0 to 60, a lower score represents a higher level of self-care behaviors.
Time Frame
Baseline and three-month post-intervention
Title
Change from baseline in patients' smoking status at immediately post-intervention
Description
Patients' report of not having/ having smoked and the estimated amount of cigarette consumed (if applicable) for the past one week.
Time Frame
Baseline and post-intervention immediately
Title
Change from baseline in patients' smoking status at three-month post-intervention
Description
Patients' report of not having/ having smoked and the estimated amount of cigarette consumed (if applicable) for the past one week.
Time Frame
Baseline and three-month post-intervention
Title
Change from baseline in patients' alcohol status at immediately post-intervention
Description
Patients' report of not having/ having alcohol drinking and the estimated amount of alcohol consumed (if applicable) for the past one week.
Time Frame
Baseline and post-intervention immediately
Title
Change from baseline in patients' alcohol status at three-month post-intervention
Description
Patients' report of not having/ having alcohol drinking and the estimated amount of alcohol consumed (if applicable) for the past one week.
Time Frame
Baseline and three-month post-intervention
Title
Change from baseline in caregivers' perceived care burden at immediately post-intervention
Description
The Zarit Caregiver Burden Interview (ZBI) will be used for caregivers to evaluate perceived care burden. ZBI is a 22-item 5-point Likert scale with a score ranging from 0 to 88, a lower score indicates less care burden.
Time Frame
Baseline and post-intervention immediately
Title
Change from baseline in caregivers' perceived care burden at three-month post-intervention
Description
The Zarit Caregiver Burden Interview (ZBI) will be used for caregivers to evaluate perceived care burden. ZBI is a 22-item 5-point Likert scale with a score ranging from 0 to 88, a lower score indicates less care burden.
Time Frame
Baseline and three-month post-intervention
Title
Change from baseline in participants' anxiety symptoms at immediately post-intervention
Description
The General Anxiety Disorder Scale (GAD) will be used for caregivers and patients. The GAD consists of 7 item 4-point Likert scale. The score of each scale ranges from 0 to 21, with a lower score indicating a lower level of anxiety.
Time Frame
Baseline and post-intervention immediately
Title
Change from baseline in participants' depressive symptoms at immediately post-intervention
Description
The Patient Health Questionaire (PHQ) will be used for caregivers and patients. The PHQ consists of 9 item 4-point Likert scale. The score of each scale ranges from 0 to 27, with a lower score indicating a lower level of depression.
Time Frame
Baseline and post-intervention immediately
Title
Change from baseline in participants' anxiety symptoms at three-month post-intervention
Description
The General Anxiety Disorder Scale (GAD) will be used for caregivers and patients. The GAD consists of 7 item 4-point Likert scale. The score of each scale ranges from 0 to 21, with a lower score indicating a lower level of anxiety.
Time Frame
Baseline and three-month post-intervention
Title
Change from baseline in participants' depressive symptoms at three-month post-intervention
Description
The Patient Health Questionaire (PHQ) will be used for caregivers and patients. The PHQ consists of 9 item 4-point Likert scale. The score of each scale ranges from 0 to 27, with a lower score indicating a lower level of depression.
Time Frame
Baseline and three-month post-intervention
Title
Change from baseline in participants' perspective taking at immediately post-intervention
Description
The perspective taking subscale from the Interpersonall Reactivity Index (IRI) will be used for caregivers and patients. Chinese version of the perspective taking subscale is a 5-item 5-point Likert scale with a score ranging from 5 to 25, a lower score represents a lower tendency for perspective taking.
Time Frame
Baseline and post-intervention immediately
Title
Change from baseline in participants' perspective taking at three-month post-intervention
Description
The perspective taking subscale from the Interpersonall Reactivity Index (IRI) will be used for caregivers and patients. Chinese version of the perspective taking subscale is a 5-item 5-point Likert scale with a score ranging from 5 to 25, a lower score represents a lower tendency for perspective taking.
Time Frame
Baseline and three-month post-intervention
Title
Change from baseline in participants' psychological flexibility at immediately post-intervention
Description
The Comprehensive Assessment of Acceptance and Commitment Therapy Processes (CompACT) will be used for caregivers and patients.CompACT is an 18-item 5-point Likert scale with a score ranging from 18 to 90, a lower score represents a lower level of psychological flexibility.
Time Frame
Baseline and post-intervention immediately
Title
Change from baseline in participants' psychological flexibility at three-month post-intervention
Description
The Comprehensive Assessment of Acceptance and Commitment Therapy Processes (CompACT) will be used for caregivers and patients.CompACT is an 18-item 5-point Likert scale with a score ranging from 18 to 90, a lower score represents a lower level of psychological flexibility.
Time Frame
Baseline and three-month post-intervention
Title
Change from baseline in participants' relationship functioning at immediately post-intervention
Description
The Dyadic Adjustment Scale-7(DAS-7) will be used for caregivers and patients.DAS-7 is a 7-item 6-point Likert scale with a score ranging from 0 to 36, a lower score represents less positive relationship quality.
Time Frame
Baseline and post-intervention immediately
Title
Change from baseline in participants' relationship functioning at three-month post-intervention
Description
The Dyadic Adjustment Scale-7(DAS-7) will be used for caregivers and patients.DAS-7 is a 7-item 6-point Likert scale with a score ranging from 0 to 36, a lower score represents less positive relationship quality.
Time Frame
Baseline and three-month post-intervention
Title
Change from baseline in participants' generic health-related quality of life at immediately post-intervention
Description
The visual analog scale (VAS) of EuroQol Group 5-Dimension questionnaire (EQ-5D-5L) will be used to evaluate participants' perceived health, the score ranges from 0 to 100 with 100 being better.
Time Frame
Baseline and post-intervention immediately
Title
Change from baseline in participants' generic health-related quality of life at three-month post-intervention
Description
The visual analog scale (VAS) of EuroQol Group 5-Dimension questionnaire (EQ-5D-5L) will be used to evaluate participants' perceived health, the score ranges from 0 to 100 with 100 being better.
Time Frame
Baseline and three-month post-intervention
Title
Change from baseline in participants' self-compassion at immediately post-intervention
Description
The Self-compassion Scale (SCS) will be used for caregivers and patients.SCS is an 12-item 5-point Likert scale with a score ranging from 12 to 60, a lower score represents a lower level of self-compassion.
Time Frame
Baseline and post-intervention immediately
Title
Change from baseline in participants' self-compassion at three-month post-intervention
Description
The Self-compassion Scale (SCS) will be used for caregivers and patients.SCS is an 12-item 5-point Likert scale with a score ranging from 12 to 60, a lower score represents a lower level of self-compassion.
Time Frame
Baseline and three-month post-intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Patient-caregiver dyads will be recruited as units if both are eligible as listed below. Patient Inclusion Criteria: 18 years or older a confirmed diagnosis of Chronic Heart Failure (CHF) according to international guidelines with New York Heart Association (NYHA) functional classification I to III has been hospitalized in the past one year able to nominate a primary family caregiver (if two or more family members where the primary caregivers of the patient, the one who had the highest average contact hours with the patient) can understand and communicate in Chinese can access Tencent VooV Meeting via smartphone for attending the intervention Exclusion Criteria: has a documented medical history of psychiatric illness, dementia, and life-threatening, such as end-stage renal failure, severe pulmonary disease and respiratory disease has cognitive impairment evaluated with a score of 0-2 on the Mini-Cog scale living in a nursing home Caregiver Inclusion Criteria: 18 years or older can understand and communicate in Chinese have been providing care to the patient for more than 14 hours per week for at least three consecutive months can access Tencent VooV Meeting via smartphone for attending the intervention Exclusion Criteria: paid caregivers has a documented medical history of psychiatric illness, dementia, and life-threatening, such as end-stage renal failure, severe pulmonary disease and respiratory disease has cognitive impairment evaluated with a score of 0-2 on the Mini-Cog scale
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yim Wah Mak, PhD
Phone
(852) 2766-6421
Email
yw.mak@polyu.edu.hk
First Name & Middle Initial & Last Name or Official Title & Degree
Xuelin zhang, MN
Phone
(852)5631 8179
Email
19084064r@connect.polyu.hk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yim Wah Mak, PhD
Organizational Affiliation
School of Nursing, The Hong Kong Polytechnic University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Taihe Hospital
City
Shiyan
State/Province
Hubei
ZIP/Postal Code
430000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shouxia Chai, MSN
Phone
17764139581
Email
jiezhixia@163.com

12. IPD Sharing Statement

Learn more about this trial

Acceptance and Commitment Therapy for Patients With Chronic Heart Failure and Their Caregivers on Their Quality of Life

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