Effects of Early Cardiopulmonary Rehabilitation in Patients With Acute Decompensated Heart Failure

NCT ID: NCT07155421

Last Updated: 2025-12-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-11-10

Study Completion Date

2025-12-31

Brief Summary

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Acute decompensated heart failure (ADHF) is a severe condition characterized by rapid deterioration of cardiac function, leading to impaired oxygen delivery and multi-organ dysfunction. ADHF often results in reduced physical and respiratory capacity, greater dependence on oxygen support, difficulty performing daily activities, and prolonged hospital stays. In recent years, early exercise-based cardiopulmonary rehabilitation (CPR) has been introduced as part of heart failure management. Evidence suggests that early CPR improves overall health and cardiac function in heart failure patients. However, data regarding its effects in ADHF remain limited. While some studies indicate that early CPR enhances physical function, its impact on respiratory parameters and clinical outcomes is less well established.

Cardiopulmonary rehabilitation is a multidisciplinary program designed to promote physical, psychological, and social recovery in patients with cardiovascular and pulmonary diseases. It includes exercise training, education, psychosocial support, and behavioral strategies. Early CPR specifically aims to improve cardiovascular and respiratory functions in heart failure patients. Initiating CPR in the early phase of ADHF may accelerate recovery, strengthen cardiopulmonary function, shorten hospitalization, and improve quality of life.

This study aims to evaluate the effects of early CPR on functional capacity, hemodynamic parameters, and respiratory parameters in patients with ADHF.

Detailed Description

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Conditions

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Heart Failure

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Early cardiopulmonary rehabilitation group

Exercise-based cardiopulmonary rehabilitation will be applied to this group during the hospital stay every day for 3 times a day.

Group Type EXPERIMENTAL

Early Cardiopulmonary Rehabilitation

Intervention Type OTHER

An individualized CPR program including positioning, deep breathing exercises (diaphragmatic and segmental breathing exercises), pursed-lip breathing exercises, breathing exercises using incentive spirometry, and progressive mobilization exercises (in-bed range of motion exercises, sitting, standing, and walking exercises)

Routine in-hospital care

Intervention Type OTHER

Routine in-hospital care for acute decompansated heart failure

Control Group

Routine in-hospital care will be applied to this group.

Group Type OTHER

Routine in-hospital care

Intervention Type OTHER

Routine in-hospital care for acute decompansated heart failure

Interventions

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Early Cardiopulmonary Rehabilitation

An individualized CPR program including positioning, deep breathing exercises (diaphragmatic and segmental breathing exercises), pursed-lip breathing exercises, breathing exercises using incentive spirometry, and progressive mobilization exercises (in-bed range of motion exercises, sitting, standing, and walking exercises)

Intervention Type OTHER

Routine in-hospital care

Routine in-hospital care for acute decompansated heart failure

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients hospitalized with a diagnosis of acute decompensated heart failure
* Being clinically stable

Exclusion Criteria

* Having diagnosed pulmonary, neurological, renal, liver, gastrointestinal, orthopedic or oncological pathologies
* Having cardiomyopathy or congestive pericarditis
* Recent heart surgery in the past 6 months
* New or suspected thromboembolic event
* Presence of open wounds, ulcerations or major dermatological diseases in the lower extremities
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istanbul University - Cerrahpasa

OTHER

Sponsor Role collaborator

Saglik Bilimleri Universitesi

OTHER

Sponsor Role collaborator

Yeditepe University

OTHER

Sponsor Role collaborator

Izmir Bakircay University

OTHER

Sponsor Role lead

Responsible Party

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Melih Zeren

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Istanbul University- Cerrahpasa, Cardiology Institute

Istanbul, , Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Central Contacts

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Kiymet Muammer, PT, PhD

Role: CONTACT

+90 552 2058527

Facility Contacts

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Kiymet Muammer, PT, PhD

Role: primary

+90 552 20585

Other Identifiers

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bakircaymzeren09

Identifier Type: -

Identifier Source: org_study_id

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