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

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

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06269263
Acronym
Pilot-CRHF
Enrollment
30
Registered
2024-02-21
Start date
2024-02-29
Completion date
2025-04-30
Last updated
2026-05-06

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

Conditions

Heart Failure

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

Interventions

Guided by physiotherapists, patients will receive different trainings regrading endurance/balance/resistance,/coordination at home

Sponsors

University of Leipzig
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Pilot study of home-based cardiac rehabilitation

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Percentage of patients completing the programAfter 12 weeksPercentage of patients completing the program

Secondary

MeasureTime frameDescription
Quality of life by KCCQAfter 12 weeksQoL measured by Kansas City Cardiomyopathy Questionnaire (KCCQ). KCCQ measures in values from 0 to 100 with higher values indicating better quality of life
Exercise capacityAfter 12 weeksExercise capacity measured by 6-minutes walk test

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 7, 2026