- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05059964
Circuit Training and Aerobic Exercise Among Sedentary Elderly Population
Comparison of Circuit Training and Aerobic Exercise on Cardiopulmonary Fitness Among Sedentary Elderly Population
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Khyber Pakhtunkhwa
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Upper dir, Khyber Pakhtunkhwa, Pakistan, 18000
- District Headquarter Hospital - Upper Dir
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Participants meeting the below criteria, shall be recruited in the study.
- Sedentary elderly people (Can perform 6 MWT without complication)
- Sedentary elderly population
- No regular exercise or gym activity since last 6 months
Exclusion Criteria:
- Already trained (any gym activity or regular exercise)
- Diagnosed cardiopulmonary disease
- Diabetes
- Any neurological complication
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Circuit Training program
circuit training for 4 weeks
|
The 4 weeks Circuit Training program, it will be of 3 times per week. Each CT workout includes 6 stations per circuit Training. Before the training period, all participants underwent an exercise familiarization session to ensure proper execution of technique. The 6 stations will be included as 40 lb. carry for 100 ft., 3-min stair climb, 45 s plank pose, 20 lb. carry with a fast walk for 100 ft., right and left single leg stands for as long as balance was maintained, and a 15 lb. carry up and down 30 stairs |
|
Active Comparator: Continuous aerobic exercise Group
aerobic exercise for 4 weeks
|
Continuous aerobic exercise Frequency 3 time per week Intensity 50% of Heart rate reserve Type continuous aerobic exercise Time 40 minutes
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
6 min walk test: Distance (meters)
Time Frame: 4th Week
|
Changes from the baseline, 6 min walk test (6 MWT) was used to measure Functional capacity.
It is a sub maximal exercise test which can aid in assessing functional capacity of patients with cardiopulmonary diseases, in this test we find out the maximum distance in meters which an individual covers in 6 min without any support.
|
4th Week
|
|
Step test
Time Frame: 4th Week
|
The Step Test is designed to measure a person's aerobic fitness. Participants step up and down, on and off an aerobics- type step for THREE minutes to increase heart rate and to evaluate the heart's recovery rate during the minute immediately following the step test exercise. Changes from the baseline to 4th week. for Age 56-65 heart rate recovery rate in beats per minute fit score: Excellent< 89, Above Average 90-100, Average 101-111, Below Average 112-122, Poor > 123 |
4th Week
|
|
Forced Expiratory Volume in 1 second (FEV1)
Time Frame: 4th Week
|
Changes from the Baseline, the digital spirometer is used in clinical setting to analyze Forced Expiratory Volume in 1 second FEV1 in Liters
|
4th Week
|
|
Forced vital Capacity (FVC)
Time Frame: 4th week
|
Changes From the Baseline, the digital spirometer is used in clinical setting to analyze Forced vital Capacity in Liters
|
4th week
|
|
Peak Expiratory Flow (PEF)
Time Frame: 4th week
|
Changes from the Baseline, the digital spirometer is used in clinical setting to analyze peak expiratory flow PEF in Liter/second.
|
4th week
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/01086 Ataur Rahman
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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