- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05532839
Self-paced High-intensity Interval Training and Moderate Intensity Continuous Training in Young Adults
Effects of Self-paced High-intensity Interval Training and Moderate Intensity Continuous Training on the Physical Performance and Psychophysiological Responses in Recreationally Active Young Adults
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Recreational activities are those in which you genuinely engage with others to have fun and relax in your leisure time. This includes activities that require physical activity as well as connections and play with others. They are not activities that you can finish totally on your alone; while you can try to do some with your own, you will miss out on the enjoyment of doing that with others
High-intensity interval training is a training that cycles between high bursts of activity and predetermined times of less intensive exercise or rest period. The therapy lasted 6 weeks, and HIIT comprised of two 12-24 × 30 second high-intensity runs separated by thirty seconds of relaxation.
Moderate-intensity continuous training consists of periods followed by 50 minutes of exercise- bicycling, running, jogging, marching, paddling, etc. - at a recorded frequency of 70-75 percent maximal heart rate. The MICT ran continuously for 24-48 minutes. From the day of the six weeks intervention strategies, the mentioned assays were conducted: Yo-Yo Intermittent Recovery Test level 1, repeated sprint ability , sprint test, alter of way test which is t drill, and physical activity enjoyment scale and shuttle run. Through these trainings, individuals in both groups must follow the old their balanced meal.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Lahore, Punjab, Pakistan
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Lahore, Lahore, Punjab, Pakistan, Pakistan, 54782
- Sadia Afzaal Sukhera
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Both genders was included in our study.
- Participants of age of 16 to 35 years were included.
- Included those participants who were playing sports such as cricket, football, basketball and tennis and their training workload of less than three training units per week and less than one eight minutes, also doing core strength training, also doing cardio trainings and group exercise, from the last two years.
Exclusion Criteria:
- Adults who were having history of any trauma from last 6 month were excluded.
- SOB or any other cardiopulmonary disease.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: High intensity interval training
High-intensity interval training is a training that cycles between high bursts of activity and predetermined times of less intensive exercise or rest period.
|
The therapy lasted 6 weeks, and HIIT comprised of two 12-24 × 30 second high-intensity runs separated by thirty seconds of relaxation.
|
|
Experimental: Moderate intensity continuous interval training
Moderate-intensity continuous training consists of periods followed by 50 minutes of exercise - bicycling, running, jogging, marching, paddling, etc. - at a recorded frequency of 70-75 percent maximal heart rate.
|
The MICT ran continuously for 24-48 minutes.
From the day of the six weeks intervention strategies, the mentioned assays were conducted: Yo-Yo Intermittent Recovery Test level 1, repeated sprint ability , sprint test, alter of way test which is t drill, and physical activity enjoyment scale and shuttle run.
Through these trainings, individuals in both groups must follow the old their balanced meal.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Yo-Yo Intermittent Recovery Test level 1 (YYIRTL-1)
Time Frame: 3 months
|
To assess an athlete's capacity to undertake high-intensity aerobic activities continuously
|
3 months
|
|
Repeated sprint ability (RSA)
Time Frame: 3 months
|
Sprint test of 10-30 meters to improve and uphold maximal exertion through consecutive sprints
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3 months
|
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Change of direction test (T-drill)
Time Frame: 3 months
|
It includes forward, sideways, and revers movements
|
3 months
|
|
Training rating of perceived exertion (RPE)
Time Frame: 3 months
|
It is based on the physical experiences a human has during physical exercise, such as elevated heart rate, increase breathing or respiratory rate, increased perspiration, and muscular tiredness.
|
3 months
|
|
Physical activity enjoyment scale (PACES)
Time Frame: 3 months
|
It is an 18-item scale that examines physical activity pleasure by simply asking to score "how you feel right here about the physical activity you've been performing
|
3 months
|
|
Shuttle run test (PACER)
Time Frame: 3 months
|
The thirty feet agility Shuttle Run is indeed an agility assessment wherein the opponent sprints switch between different line segments as rapidly as feasible, trying to pick up wooden blocks for a distance travelled of 8 m. main goal: this is a way of measuring of power and speed
|
3 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Muhammad Sanaullah, MS, Study Principal Investigator
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
Other Study ID Numbers
- REC/RCR & AHS/22/0415
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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