- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06625424
Effect of Short Sprint Interval Training With Active Recovery as Compared to Passive Recovery on Anaerobic Capacity in Non-athletic Population
Study Overview
Status
Conditions
Detailed Description
Based on a global health initiative to promote "Exercise is Medicine" strategy by American College of Sports Medicine, designing an exercise prescription which is time efficient, cost-effective, easily performable and has great adherence or compliance is necessary. SIT is a type of Anaerobic training which not only enhances the anaerobic capacity but also the aerobic capacity of an individual as well. Thus SIT plays a crucial role in prevention of the NCDs by maintain and improving CRF. Classic SIT is limited to athletic population therefore this study aims to promote the use of modified SIT training protocol called as SSIT by shortening the sprinting time from 30s to 10s so that non-athletic individuals are able to perform it. Apparently there are lack of field based studies on SIT. Most studies use lab based training performed on treadmill and cycle ergometer which can be expensive and time-consuming, especially when several subjects have to train at the same time. Furthermore no comparison has been made between active and passive recovery in short term sprint interval training in field (a bout of 10 second of less). This study aims to test the novel effects of Short Sprint Interval Training with two different types of recovery method performed on field rather than lab to enhance anaerobic capacity in a short amount of time.
This study would be a single blinded randomized control trial, conducted over a period of 12 months at football ground at F-11/1 Islamabad. Subjects will be selected via non-probability convenience sampling technique, followed by block randomization into two groups, the intervention group A and intervention group B using sealed envelope method. The sample size as calculated by G*Power software will be 38 non -athletic individuals. Informed consent will be taken from individuals selected as per inclusion criteria. Participants then being allocated to one of the 2 groups, will be required to complete a self-reporting demographic form. For training, participants will perform SSIT 3 times a week for a total duration of 02 weeks. Anaerobic capacity of the participants will be measured using running based anaerobic sprint test (RAST) before intervention and after intervention of two weeks. Collected data will then be entered and analyzed on the SPSS software version 23.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Hammad Najam, MS-CPT*
- Phone Number: 0336-9430246
- Email: najam.hammad14@gmail.com
Study Locations
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Punjab
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Rawalpindi, Punjab, Pakistan, 46000
- Recruiting
- Foundation University College of Physical Therapy
-
Contact:
- Furqan Hassan, PhD*
- Phone Number: 0333-4056768
- Email: furqanhassan33@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male and Female young adults ranging from 18-25 Years of age.
- Young adults who perform moderate to vigorous Intensity exercise at least once a week according to IPAQ.
- Those who are cleared for physical activity after screening through PAR-Q.
Exclusion Criteria:
- Young adults having history of any Musculoskeletal, cardiovascular, pulmonary and neurological Disorder.
- Young adults having history of injury in the past 30 days.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Interventional group
Participants in this group will perform short sprint interval training on a flat running track in field. Each lane will be materialized by placing cones 5 m from each other for a total of 30 m on which Subject will perform Short Sprint Interval Training. The instructions will be to travel the greatest distance possible in 10 seconds, making trips of 5, 10, 15 m, etc. Participants of this group will opt for 1 minute of active recovery i.e. they will perform brisk walk between 6 bouts of 10 sec sprint. The duration of the training will be of 2 weeks. |
Participants will perform short sprint interval training on a flat running track in field. Each lane will be materialized by placing cones 5 m from each other for a total of 30 m on which the Subjects will perform Short Sprint Interval Training. The instructions will be to travel the greatest distance possible in 10 seconds, making trips of 5, 10, 15 m, etc. Participants will opt for 1 minute of active recovery i.e. they will perform brisk walk between 6 bouts of 10 sec sprint. The duration of the training will be of 2 weeks. |
|
Active Comparator: Control group
Patients will Participants in this group will perform short sprint interval training on a flat running track in field. Each lane will be materialized by placing cones 5 m from each other for a total of 30 m on which Subject will perform Short Sprint Interval Training. The instructions will be to travel the greatest distance possible in 10 seconds, making trips of 5, 10, 15 m, etc. Participants of this group will opt for 1 minute of passive recovery i.e. they will stay stationary between 6 bouts of 10 sec sprint. The duration of the training will be of 2 weeks. |
Participants will perform short sprint interval training on a flat running track in field. Each lane will be materialized by placing cones 5 m from each other for a total of 30 m on which Subject will perform Short Sprint Interval Training. The instructions will be to travel the greatest distance possible in 10 seconds, making trips of 5, 10, 15 m, etc. Participants will opt for 1 minute of active recovery i.e. they will perform brisk walk between 6 bouts of 10 sec sprint. The duration of the training will be of 2 weeks. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Anaerobic Capacity
Time Frame: 2 weeks
|
Evaluation will be done using field test known as Running Based Anaerobic Sprint Test (RAST)
|
2 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- FUI/CTR/2024/38
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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