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Physical Activity Program on Clinical Output in Heart Failure (Heartfailu)

N

Nigde Omer Halisdemir University

Status

Completed

Conditions

Heart Failure
Nursing Caries

Treatments

Other: Physical activity program

Study type

Interventional

Funder types

Other

Identifiers

NCT05349786
NOHU- Cardiac Nursing

Details and patient eligibility

About

Background: This study was carried out to determine the effect of physical activity program applied to individuals with heart failure on quality of life, functional capacity and mortality risk level.

Objective: The study, which was conducted as a randomized controlled experimental study, was completed with a total of 40 HF patients, 20 of whom were interventions and 20 were controls. A physical activity program lasting at least 30 minutes each session was applied to HF patients in the intervention group, three days a week for three months, and the walks of the patients were followed by a pedometer.

Full description

Background: This study was carried out to determine the effect of physical activity program applied to individuals with heart failure on quality of life, functional capacity and mortality risk level.

Objective: The study, which was conducted as a randomized controlled experimental study, was completed with a total of 40 HF patients, 20 of whom were interventions and 20 were controls. A physical activity program lasting at least 30 minutes each session was applied to HF patients in the intervention group, three days a week for three months, and the walks of the patients were followed by a pedometer. At the same time, a monthly home visit and weekly phone call were made to the patients. No intervention was applied to the patients in the control group, apart from weekly phone calls. All patients were receiving optimal stable HF therapy.

Enrollment

40 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Over 18 years of age,
  • Class I, II, III according to NYHA classification,
  • Without any diagnosis of musculoskeletal deformity or disease that may prevent them from doing physical activity,
  • Hypertension stage 1 and 2,
  • Stable chronic disease processes such as diabetes,
  • Patients whose treatment for these diagnoses has not been changed in the last month,
  • Dyspnea status less than 4-5 degrees according to the Modified Borg Scale,
  • Cognitive competence,
  • At least primary school graduates

Exclusion criteria

  • Known and diagnosed moderate or severe mitral/aortic regurgitation, hypertrophic obstructive cardiomyopathy, uncontrollable arrhythmia (atrial fibrillation etc.), bundle branch block on ECG,
  • Acute myocardial infarction in the last three months,
  • Unstable angina pectoris, pacemaker, valve surgery, coronary artery bypass surgery history, newly diagnosed or suspected thromboembolic event,
  • Diagnosed with cerebrovascular and peripheral vascular insufficiency, other chronic diseases (such as chronic obstructive pulmonary disease, chronic kidney failure, pulmonary emphysema, rheumatic valve disease, cancer diagnosis),
  • Chronic fatigue syndrome

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Intervention Group
Experimental group
Description:
A physical activity program lasting at least 30 minutes each session was applied to HF patients in the intervention group, three days a week for three months. A pedometer was used to visualize the walking performed in the physical activity program and to record reliably. Weekly phone calls and monthly home visits were made to the patients in order to determine the continuation of the medical treatment and walking program used by the patients, to increase their motivation and to detect or intervene in any situation related to the walking program.
Treatment:
Other: Physical activity program
Non-Intervention Group
No Intervention group
Description:
The individuals in the control group, were pre-tested, evaluated at the first, second, and third months, and followed up in the process without any intervention. Patients were reminded that they should continue their routine medical treatment and not start any physical activity program.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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