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Construction and application of early rehabilitation exercise fear intervention program for patients with acute decompensated heart failure based on PERMA model

Construction and application of early rehabilitation exercise fear intervention program for patients with acute decompensated heart failure based on PERMA model

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116208
Enrollment
Unknown
Registered
2026-01-06
Start date
2025-01-16
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Acute decompensated heart failure

Interventions

Control group:Routine care (including health education, psychological support, and exercise guidance from the Rehabilitation Department)
follow-up via telephone or outpatient visit at one and three months after discharge.
Experimental group:Integrated Care Plan: Routine Care + PERMA-Based Early Rehabilitation Intervention for Exercise Fear in ADHF Patients P (Positive Emotion): Psychoeducation, relaxation training, min

Sponsors

Zunyi Medical University Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >=18 years. 2. Meet the clinical and guideline diagnostic criteria for Acute Decompensated Heart Failure (ADHF). 3. Score > 37 points on the Tampa Scale for Kinesiophobia-Heart (TSK-H) or a validated cardiac-specific fear of movement questionnaire. 4. Normal limb function, classified as New York Heart Association (NYHA) Functional Class II–IV, and in a clinically stable condition. 5. Clinically stable for 24 hours following optimized medical therapy. 6. Ability to independently perform basic activities of daily living prior to hospital admission, including independent walking (with or without assistive devices). 7. Clear consciousness and adequate literacy skills. 8. Absence of psychiatric disorders or cognitive impairment. 9. Provision of informed consent and voluntary participation in the study.

Exclusion criteria

Exclusion criteria: 1.Patients with severe diseases such as respiratory failure, chronic renal failure or tumors; 2.Acute coronary syndrome within 2 days; 3. Chest pain within 8 hours, or combined with mechanical complications; 4. Lethal arrhythmia, high-level atrioventricular block, new-onset atrial fibrillation or atrial flutter; 5. Patients requiring cardiac pacemakers, implantable cardioverter defibrillators (ICD) or ventricular assist devices, or those waiting for heart transplantation within the next 6 months; 6. Death during hospitalization; 7. Severe language expression, hearing, vision or limb function disorders.

Design outcomes

Primary

MeasureTime frame
Degree of kinesiophobia; perceived self-efficacy;quality of life;Readmission Rate;

Secondary

MeasureTime frame
Cardiac function(6-Minute Walk Test,6MWT/NTProBNP Test);Risk of Thrombosis(D-dimer Test);Anxiety (ANX);Depression (DEP);Average Length of Stay (ALOS);

Countries

China

Contacts

Public ContactMei Lu

Zunyi Medical University Affiliated Hospital

562480946@qq.com+86 180 8969 3616

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026