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Clinical Trials/NCT06269263
NCT06269263
Active, not recruiting
Not Applicable

Pilot Study to Determine Feasibility of Home-based Cardiac Rehabilitation in Patients With Chronic Heart Failure (Pilot-CRHF)

University of Leipzig1 site in 1 country30 target enrollmentFebruary 29, 2024
ConditionsHeart Failure

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Heart Failure
Sponsor
University of Leipzig
Enrollment
30
Locations
1
Primary Endpoint
Percentage of patients completing the program
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

The proposed study will determine the willingness of patients for participation. Furthermore, the assessment of tests to identify eligible patients and the type of exercise intervention that goes along with a high patient compliance is crucial. Also, more information about possible factors preventing patients from participating is required. Therefore, if the patient is willing to participate, the investigators will assess patients' medical history, medication and QoL as well as parameters of routine diagnostics (i.e. echocardiography, laboratory testing, MRI). Following, while the in-patient stay due to cardiac decompensation, the investigators will conduct several assessment-tests to determine the physical status, the exercise capacity and the cognitive function. Moreover, physiotherapists will instruct the patients in the exercise program. After discharge from the hospital, physiotherapist will visit the patient at home to instruct them again in the exercises. Then, the patients will conduct the program on their own for a period of 12 weeks. During the exercise period, a doctoral student will visit the patients at home every 3 weeks to check whether they are doing the exercises correctly and to determine whether there are any problems with the program. After the exercise period of 12 weeks, the baseline characteristics will be assessed again at the University Hospital Leipzig.

Detailed Description

See above

Registry
clinicaltrials.gov
Start Date
February 29, 2024
End Date
March 10, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
University of Leipzig
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Chronic heart failure irrespective of the ejection fraction
  • Recent history of acute cardiac decompensation leading to hospitalization

Exclusion Criteria

  • Patients not willing to participate
  • Patients with orthopedic diseases limiting their mobility
  • Cognitive diseases that hinder adequate participation in the opinion of the investigator
  • Inpatient rehabilitation.

Outcomes

Primary Outcomes

Percentage of patients completing the program

Time Frame: After 12 weeks

Percentage of patients completing the program

Secondary Outcomes

  • Quality of life by KCCQ(After 12 weeks)
  • Exercise capacity(After 12 weeks)

Study Sites (1)

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