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Construction and Application of a Management Plan for Depressive Symptoms and Readmission in Patients with Chronic Heart Failure Based on Acceptance and Commitment Therapy

Construction and Application of a Management Plan for Depressive Symptoms and Readmission in Patients with Chronic Heart Failure Based on Acceptance and Commitment Therapy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117604
Enrollment
Unknown
Registered
2026-01-27
Start date
2025-07-07
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Heart Failure

Interventions

control group:The control group received routine care provided by the Department of Cardiology at their respective intervention centers. Upon discharge, patients received routine discharge guidance, w
intervention group:Implement the HeartACT intervention program on the basis of routine care

Sponsors

Tianjin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Meeting the diagnostic criteria of the "2018 Chinese Guidelines for the Diagnosis and Treatment of Heart Failure"; 2. Not receiving other treatments such as surgery during the treatment period; being conscious and having normal cognitive function; 3. Aged > 18 years old; 4. Classified as Grade ?-? by the New York Heart Association (NYHA); 5. Predicted to be at high risk of 30-day readmission for patients with chronic heart failure (assessment tool: Web Calculator for Predicting 30-day Readmission Risk in Patients with Chronic Heart Failure); 6. Having no prior professional psychological education before admission; 7. Having complete clinical data and being able to independently complete relevant questionnaires; 8. Signing the informed consent form and voluntarily participating in this study.

Exclusion criteria

Exclusion criteria: 1. Patients with other heart diseases; 2. Patients with acute exacerbation of CHF caused by new-onset acute coronary syndrome, malignant arrhythmia, etc.; 3. Patients with liver or kidney function diseases; 4. Patients with progressive neurological deficits (such as progressive muscle weakness, paresthesia, etc.); 5. Patients with confirmed mental and psychological disorders who are receiving psychological treatment; 6. Patients with a history of drug or alcohol dependence; 7. Patients currently participating in other studies.

Design outcomes

Primary

MeasureTime frame
Depression Score;readmission rate;

Secondary

MeasureTime frame
Anxiety Score;Psychological flexibility;Degree of cognitive fusion;sleep quality;

Countries

China

Contacts

Public ContactXiaoying Zang

Tianjin Medical University

xiaoyingzang@163.com+86 189 2069 7750

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026