THE EFFECTIVENESS OF CONGESTIVE HEART FAILURE - CONTINUING CARE PROGRAM (CHF-CCP) ON HEALTH STATUS AND DEPRESSION OF HEART FAILURE PATIENTS AND ANXIETY OF CAREGIVERS

Phase 1

• Conditions: health status and depression in patients after heart failure and caregiver anxiety; CHF-CCP innovation, health status, depression, anxiety

• Registration Number: TCTR20240522003
• Lead Sponsor: DOCTOR OF NURSING SCIENCE PROGRAM

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-05-22
• Last Update Posted: 19 August 2024
• Study Completion: 2024-09-01

Recruitment & Eligibility

• Status: Pending (Not yet recruiting)
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

1 ) Patients with heart failure receiving services at the medical clinic and the heart failure clinic. Following inclusion criteria and exclusion criteria are established to select five patients.
A patient will be included in the study if he/she
1. is 18 years old and older,
2. is diagnosed with heart failure within the past 1 year,
3. is a patient with NYHA Functional Class II-IV,
4. is able to communicate in writing and listening to the Thai language,
5. has no cognitive impairment, measured with a Mini-cog score of > 3,
6. has a Barthel ADL index score of < 11, and
7. has a primary caregiver and can be contacted via smartphone.
2) The primary family caregivers. Of all selected five patients with heart failure, their five primary family caregivers also will be selected: one caregiver per patient. Following inclusion and exclusion criteria are specified to select these caregivers.
A primary family caregiver will be included in the study if he/she
1. is 18 years old or older,
2. is the primary family caregiver taking care of selected patients
with heart failure in the past one year, and
3. is able to be contacted via smartphone.

Exclusion Criteria

A patient will be excluded from the study if
he/she
1.has a history of psychiatric disease
2.has a moderate score anxiety PHQ9 score of greater than or equal to 13 points.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
health status and depression Pretest and the sixth and the eighth week posttests. Six Minute Walk Test, The Kansas City Cardiomyopathy Questionnaire, PHQ9

Secondary Outcome Measures

Name	Time	Method
anxiety Pretest and the sixth and the eighth week posttests. The State Anxiety Inventory