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Effects of Lower Limb Resistance Band Exercises in Phase 1 Cardiac Rehabilitation

Not Applicable
Completed
Conditions
Cardiovascular Diseases
Interventions
Other: Lower Limb Resistance Band Exercises
Other: Routine Phase 1 cardiac rehabilitation
Registration Number
NCT06319651
Lead Sponsor
Riphah International University
Brief Summary

This study will be randomized controlled trial with non-probability purposive sampling. Study conducted among post CABG patients. Sample size will be 56, 28 in each group. Outcome will be measured by using 6 minute walk test, Spirometry (FVC, FEV1/FVC and PEF), Functional Independence Measure.

Detailed Description

This study will be randomized controlled trial with non-probability purposive sampling. Study conducted among post CABG patients. Descriptive analysis will be applied. Data will be collected from Rehmatul lil Alameen Institute of cardiology Lahore. Sample size will be 56, 28 in each group. In addition to the routine Phase 1 cardiac rehabilitation for experimental group the exercise protocol consisted of 10 minutes of warm up, elastic band strength exercise protocol (30 minutes) and cool down (5 minutes) so that an exercise session lasted about 45-50 minutes, exercise will performed circularly 2 sets, 10 repetition with a 2 minute rest after each cycle and monitored the performance of exercise for 6 days. Resisted band exercise are Extending thighs, Closing thighs, Opening thighs, Bending thighs, Dorsiflexion, Plantarflexion. For control group routine Phase 1 cardiac rehabilitation only. Outcome will be measured by using 6 minute walk test, Spirometry (FVC, FEV1/FVC and PEF), Functional Independence Measure.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
56
Inclusion Criteria
  • Age 35 to 60
  • Female and Male both
  • Hemodynamic stable patients
  • Arrhythmias or angina not present
  • Post elective sternotomy surgery
  • Post extubating
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Exclusion Criteria
  • Chronic obstructive pulmonary disease
  • Neurological Sequelae
  • Neuromuscular disease
  • Emergency or off pump surgery
  • Surgical re-intervention
  • Patient who remained on mechanical ventilation longer than 24 hours
  • Patient who had a baseline partial pressure of oxygen (PaO2) less than 75 mmHg and partial pressure of carbon dioxide (PCO2) 45 mmHg
  • Patients who had history of respiratory tract infection within a period of three months
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Experimental GroupLower Limb Resistance Band ExercisesIn addition to the routine Phase 1 cardiac rehabilitation, Resistance Exercises * Extending thighs * Closing thighs * Opening thighs * Bending thighs * Bending ankles * Ankle opening
Routine Phase 1 cardiac rehabilitationRoutine Phase 1 cardiac rehabilitationRoutine Phase 1 cardiac rehabilitation only.
Experimental GroupRoutine Phase 1 cardiac rehabilitationIn addition to the routine Phase 1 cardiac rehabilitation, Resistance Exercises * Extending thighs * Closing thighs * Opening thighs * Bending thighs * Bending ankles * Ankle opening
Primary Outcome Measures
NameTimeMethod
Forced vital capacity (FVC)6 Days

Forced vital capacity (FVC) is the amount of air that can be forcibly exhaled from your lungs after taking the deepest breath possible. It's measured by spirometry

6 Minute Walk Test6 Days

The 6 Minute Walk Test is a sub-maximal exercise test used to assess aerobic capacity and endurance. The distance covered over a time of 6 minutes is used as the outcome by which to compare changes in performance capacity

FEV1/FVC ratio6 Days

The FEV1/FVC ratio is the ratio of the forced expiratory volume in the first one second to the forced vital capacity of the lungs. The normal value for this ratio is above 0.75-85. It's measured by spirometry

Forced expiratory volume (FEV1)6 Days

Forced expiratory volume (FEV1) calculates the amount of air that a person can force out of their lungs in 1 second. It's measured by spirometry

Functional Independence Measure6 Days

The Functional Independence Measure (FIM) is an instrument that was developed as a measure of disability for a variety of populations and is not specific to any diagnosis. The FIM instrument Includes measures of independence for self-care, including sphincter control, transfers, locomotion, communication, and social cognition.

Is an 18-item, seven-level, ordinal scale intended to be sensitive to changes over the course of a comprehensive inpatient medical rehabilitation program.

Uses the level of assistance an individual needs to grade functional status from total independence to total assistance).

The tool is used to assess a patient's level of disability as well as a change in patient status in response to rehabilitation or medical intervention.

FIM 3 levels.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Rehmatul lil Alameen Institute of cardiology

🇵🇰

Lahore, Punjab, Pakistan

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