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Not yet recruiting NCT07062900

Low Intensity Physical Activity in Congestive Heart Failure Patients Among Different BMI

No phase Interventional Heart Failure

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Low-Intensity Physical Activity, usual care.
Who it may be relevant to
Registry conditions: Heart Failure. Basic parameters: 45 years — 70 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Pakistan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Effects of Low Intensity Physical Activity on Functional Capacity Quality of Life and Psychological Well Being in Congestive Heart Failure Patients Among Different BMI

Overview

This study examined the effects of low-intensity physical activity on functional capacity, quality of life, and psychological well-being in congestive heart failure patients with varying BMI. Forty patients were divided into intervention and control groups. The intervention group followed an 8-week physical activity program, while the control group received usual care. Results showed significant improvement in walk distance, quality of life, and depression scores in the intervention group. The study concludes that low-intensity physical activity effectively improves health outcomes in heart failure patients across different BMI categories.

Detailed description

This randomized controlled trial explored the effects of low-intensity physical activity on functional capacity, quality of life, and psychological well-being in patients with congestive heart failure across different BMI categories. A total of forty patients were selected and randomly assigned to either an intervention group or a control group. The intervention group participated in an eight-week structured low-intensity physical activity program, while the control group continued with usual care without additional physical activity. Various assessment tools were used to evaluate outcomes, including the 6-minute walk test to measure functional capacity, the Kansas City Cardiomyopathy Questionnaire to assess quality of life, and the Hospital Anxiety and Depression Scale to evaluate psychological well-being. The results demonstrated that although both groups showed some improvement, the intervention group experienced significantly greater gains in all measured outcomes. The 6-minute walk distance increased, KCCQ-12 scores improved notably, and depressive symptoms reduced significantly in the intervention group compared to the control. The study concluded that low-intensity physical activity is an effective and feasible intervention to enhance physical and mental health in congestive heart failure patients, irrespective of their BMI category.

Interventions

  • Behavioral Low-Intensity Physical Activity
    This includes a structured and progressive 8-week physical activity program involving: Gentle walking Portable pedal exerciser Low-intensity resistance exercises (e.g., resistance bands, seated leg press, hip circles) Supervised sessions with warm-up and cool-down components
  • Behavioral usual care
    Standard Medical Management: Participants continued with their prescribed medications and routine clinical follow-ups for congestive heart failure as directed by their healthcare providers.

Primary outcome measures

  • 6-Minute Walk Test (6MWT) [Time frame: 8 weeks]
  • Kansas City Cardiomyopathy Questionnaire (KCCQ-12) [Time frame: 8 weeks]
  • Hospital Anxiety and Depression Scale (HADS) [Time frame: 8 weeks]

Eligibility criteria

Inclusion criteria

  • Hospitalized Congestive heart failure patients
  • Age 45-70
  • Diagnosed with CHF
  • BMI all ranges
  • Severely underweight: BMI<16 kg/m2
  • Underweight: BMI≥ 16 kg/m2 and <18.5 kg/m2
  • Normal weight BMI≥18.5 kg/mg2 and <25kg/m2
  • Overweight: BMI ≥25kg/m2 and<30 kg/m2
  • Obese: BMI≥30 kg/m2
  • Willing to participate in physical activity program

Exclusion criteria

  • Musculoskeletal or neurological disorders
  • Severe COPD or other respiratory diseases
  • Cognitive impairment
  • Cardiac catheter related surgery, valvular surgery within past 6 month
  • Recent Lung embolis
  • Lung cancer
  • Participants in other clinical trial or intervention study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

Pakistan · 1 center
  • Arjumand — Lahore

Identifiers

NCT: NCT07062900 · REC/RCR&AHS/24/0360

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗