Effect of Short Sprint Interval Training With Active Recovery as Compared to Passive Recovery on Anaerobic Capacity in Non-athletic Population

October 2, 2024 updated by: Foundation University Islamabad
Short Sprint Interval Training (SSIT) is a modified form of Sprint Interval Training (SIT) defined as "small bouts of supramaximal exercise with recovery periods between them to increase peak oxygen uptake in spite of having a less amount of exercise volume". SSIT was developed so that non- athletic population could also perform a training which was originally designed for athletes to increase anaerobic capacity. The benefit of this type of exercise is that it is time efficient and yields the result in short amount of time as compared to other type of exercises due to its vigorous nature. Moreover this sort of training is mostly performed in lab setting rather than on field, therefore the aim of this study is to determine the effect of short sprint interval training in a field with active recovery as compared to passive recovery on anaerobic capacity in non-athletic population.

Study Overview

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

Interventional

Enrollment (Estimated)

38

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Punjab
      • Rawalpindi, Punjab, Pakistan, 46000
        • Recruiting
        • Foundation University College of Physical Therapy
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 15, 2024

Primary Completion (Estimated)

January 1, 2025

Study Completion (Estimated)

February 1, 2025

Study Registration Dates

First Submitted

October 1, 2024

First Submitted That Met QC Criteria

October 2, 2024

First Posted (Actual)

October 3, 2024

Study Record Updates

Last Update Posted (Actual)

October 3, 2024

Last Update Submitted That Met QC Criteria

October 2, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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