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Effect of Plyometric Exercises on Improving Cardiorespiratory Endurance in Undergraduate Students

Not Applicable
Conditions
sedentary young population.
Registration Number
IRCT20230122057183N1
Lead Sponsor
Muhammad Institute of Medical and Allied Sciences, Multan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
40
Inclusion Criteria

Adults 18-30 years of age
Gender (Male and Female)
People with low or moderate physical activity (international Physical Activity Questionnaire)
People with no health problems like hypertension and bones or muscles related problems (PARQ-Questionnaire)
People having BMI ranging between 19-23 or over (South-Asian BMI scale)

Exclusion Criteria

?Any recent fractures
People with loss of hearing, sight and other senses
Hemodynamically unstable patients
People having undergone surgery within last 6 weeks
People with any physical disability
Cognitive impairments
Refusal to give consent approval

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cardiorespiratory Endurance by Shuttle Run Test. Timepoint: Before Intervention, after 3rd week and 6th week of intervention. Method of measurement: Cardiorespiratory Endurance will be checked by shuttle run test.
Secondary Outcome Measures
NameTimeMethod
Muscle Strength. Timepoint: Before intervention, 3rd week and 6th week of intervention. Method of measurement: Manual Muscle Testing.;Heart Rate. Timepoint: Before intervention, 3rd week and 6th week of intervention. Method of measurement: Pulse Oximeter.;Blood Pressure. Timepoint: Before intervention, 3rd week and 6th week of intervention. Method of measurement: sphygmomanometer.;Respiratory Rate. Timepoint: Before intervention, 3rd week and 6th week of intervention. Method of measurement: Manually by placing fingers under nose.;Oxygen Saturation. Timepoint: Before intervention, 3rd week and 6th week of intervention. Method of measurement: Pulse Oximeter.;Quality of LIfe. Timepoint: Before intervention, 3rd week and 6th week of intervention. Method of measurement: SF-8 Questionnaire.
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