Sedentary Behavior Modification, Cardiopulmonary Function & QOL Post Cardiac Surgery Patients.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50-80
SponsorRiphah International University

About this trial

This study aims to investigate randomized controlled trial to evaluate whether reducing sedentary behavior improves recovery in post-cardiac surgery patients. Participants are assigned to either a behavioral intervention that substitutes sitting with light activity or to usual care. Changes in exercise capacity and quality of life are the primary measured outcomes. It is hypothesized that the intervention group will demonstrate superior gains in both physical function and well-being. The results could inform a valuable adjunct to existing cardiac rehabilitation programs.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patient Aged 50-80 years (represents the majority cases)

Natural decline in physical capacity, making them an ideal population for studying these outcomes)

Underwent elective or emergency cardiac surgery (once patient is in ward)/1

Disqualifiers

Those requiring invasive mechanical ventilation

Individuals with significant cognitive impairment affecting consent or compliance

Pregnant women or Lactating Mother

Trial design

Design model

Parallel

Treatments tested in this trial

  • Sedentary Behaviour Modification Protocol

    Other intervention

    structured intervention designed to reduce the total time spent sitting or lying down (excluding sleeping) and to break up long, uninterrupted periods of inactivity. Effective protocols, often guided by the COM-B model (Capability, Opportunity, Motivation, Behaviour), aim to replace sedentary time with light-intensity physical activity (e.g., walking, standing).

  • Standard Cardiac Rehabilitation

    Other intervention

    A 3-12 week outpatient, medically supervised program starting shortly after surgery, focusing on monitored exercise (Treadmill), risk factor modification, and education to safely improve heart function. It involves 1-hour sessions 2-3 times a week, combining aerobic training, light strength training, and lifestyle counseling

Treatment groups

24 Participants
are divided into 2 treatment groups
Group A: Sedentary Behaviour ModificationExperimental treatment 1 intervention
Group B: Standard Cardiac RehabilitationPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Peak Expiratory Flow Rate (PEFR)

peak expiratory flow rates measured through digital spirometer.3 zones of measurements are commonly used to interpret peak flow rates. Normal value of PEFR is 80 to 100%.Green zone indicates 80 to 100% normal peak flow reading, yellow zone indicates 50 to 79 %of normal peak flow readings, and red zone indicates less than 50% of normal peak flow reading.

Time frame
12 weeks
2

Forced Vital Capacity (FVC)

Forced Vital Capacity (FVC) Forced vital capacity (FVC) measured through digital spirometer. If the value of FVC is within 80% of the reference value, the results are considered normal. Changes in FVC from baseline to 3rd week and after 6 weeks day of intervention will be assessed.

Time frame
12 weeks
3

Forced Expiratory volume in 1sec (FEV1)

Forced expiratory volume in 1sec (FEV1) measured through digital spirometer. If the value of FEV1 is within 80% of the reference value, the results are considered normal.

Time frame
12 weeks
4

36-Item Short Form Health Survey

The SF-36 Health Survey is a widely used tool that measures eight scales related to functional and well-being health-related quality of life (HRQOL).

Time frame
12 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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