- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07438730
Cross Training Effects on Flexibility, Endurance and Speed
Effects of Cross Training on Flexibility, Endurance and Speed Among Sprinters
CrossFit is one form of Resistance Exercise that is recognized as a high-intensity program that combines elements of mobility, technique, and strength and has seen increasing popularity in recent years. CrossFit workouts often incorporate Olympic lifts and elements of gymnastic exercises using handstands and rings. A large part of CrossFit workouts also consists of the "workout of the day" or "WOD," where workouts are performed for the best time or performed in the "as many rounds as possible" style and are completed in a group environment, with some workouts performed as a shared workload. The social nature of CrossFit, in addition to the annual 'CrossFit Games', which include national qualifying workouts and regional competitions, is what has led to CrossFit being described as the "Sport of Fitness". Competitors who complete all workouts and rank high enough will progress to the next stage of the competition. Regardless of which stage, it is expected that each workout will consist of a set of challenges that will require some combination of strength, power, endurance, and/or sport-specific skill.
By examining the effects of cross-training on flexibility, endurance, and speed, this study aims to provide a comprehensive understanding of how a diversified training regimen can contribute to the overall athletic development of sprinters. The findings could lead to improved training strategies that enhance performance and longevity in the sport.
Study Overview
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Punjab Province
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Lahore, Punjab Province, Pakistan, 54000
- Pakistan Sports Board
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age 18 to 30 years.
- Young sprinters (only male)
- Participants volunteered to participate in the study.
- Recreational sprinters.
Exclusion Criteria:
• Systemic disease e.g anemia, SLE and multiple sclerosis.
- Neuro-musculoskeletal disease e.g muscular dystrophy.
- Respiratory problems e.g bronchitis, COPD and asthma.
- Cardiovascular disease e.g coronary heart disease, aortic disease and stroke.
- Sprinters with history of any past surgical intervention related to orthopedic injuries.
- Sprinters with any current episode of low back pain for 3 months.
- Sprinters with history of musculoskeletal injuries.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Group A
will be the control group with conventional training including 4-5 repetitions of squats, 2-3 repetitions of 20 seconds low intensity running exercise per session 3 times a week followed by 8 weeks.
|
|
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Experimental: Group B
Group B will include cross training protocol with cycling, 8-10 repetitions of low lunges, 4-5 repetitions of cobra pose, 4-5 repetitions of 40 seconds maximum running at 80-100% HR max followed by 20 seconds of walking for 20 minutes exercise per session 3 times a week followed by 8 weeks.
|
Cross training protocol with cycling, 8-10 repetitions of low lunges, 4-5 repetitions of cobra pose, 4-5 repetitions of 40 seconds maximum running at 80-100% HR max followed by 20 seconds of walking for 20 minutes exercise per session 3 times a week followed by 8 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sit and reach test
Time Frame: Baseline, 4 weeks and 8 weeks
|
Sit and reach test for flexibility
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Baseline, 4 weeks and 8 weeks
|
|
Agility t Test
Time Frame: Baseline, 4 weeks and 8 weeks
|
Agility t Test for measuring speed
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Baseline, 4 weeks and 8 weeks
|
|
Yo-Yo Intermittent test
Time Frame: Baseline, 4 weeks and 8 weeks
|
Yo-Yo Intermittent test for measuring endurance
|
Baseline, 4 weeks and 8 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Muhammad Tayyab Malik, DPT, Riphah International University
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/RCR&AHS/24/0441
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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