BARRIERS TOWARDS PHYSICAL ACTIVITY

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age40-60
SponsorBahria University

About this trial

A cross-sectional study of 323 cardiac patients aged 40 to 60 will be carried out at PNS Shifa and the National Institute of Cardiovascular Diseases. Data will be gathered using surveys and evaluated with SPSS software. The results are likely to show considerable differences in barrier frequency across demographic groups, offering insights into targeted treatments.

Understanding these limitations is critical for establishing successful physical activity regimens, improving heart health, and, eventually, lowering rehospitalization rates. The findings will help to develop specific approaches to overcome these challenges and encourage regular physical exercise among cardiac patients.

Objectives:

1. To identify and categorize the specific barriers to physical activity faced by cardiac patients. 2. To analyze how these barriers differ among various demographic groups (e.g., age, gender). 3. To examine how barriers to physical activity vary according to clinical characteristics.

Methodology:

Using a cross sectional study design, data data was collected from NICVD hospital and PNS shifa hospital by providing questionnaires to patient having cardiac disease. The questionnaires comprises of close ended questions.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

1. Heart patients who have been diagnosed with a cardiovascular condition for more than six months.

Disqualifiers

Existence of musculoskeletal disorders that might affect their physical activity levels.

Neurological conditions that could hinder exercise participation or influence responses to surveys.

Chronic illnesses such as diabetes or irritable bowel syndrome that could interfere with the barriers evaluated in the study.

Trial population

cardiac patients

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Questionnaire and Physical Exam

    Other intervention

    Cardiac Self-Efficacy Scale (CSES) 36-Item Short Form Survey (SF-36) Symptom Distress Scale (SDS)

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

risk factors

We will recurit cardiac patients with the questioonare for the risk factors and reasons not to engage in physical activity

Time frame
2 weeks

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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