Cross Training Effects on Flexibility, Endurance and Speed

February 23, 2026 updated by: Riphah International University

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

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

52

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 Locations

    • Punjab Province
      • Lahore, Punjab Province, Pakistan, 54000
        • Pakistan Sports Board

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:

  • 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

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: 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.
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
Baseline, 4 weeks and 8 weeks
Agility t Test
Time Frame: Baseline, 4 weeks and 8 weeks
Agility t Test for measuring speed
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

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

Investigators

  • Principal Investigator: Muhammad Tayyab Malik, DPT, Riphah International University

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)

July 30, 2024

Primary Completion (Actual)

January 30, 2025

Study Completion (Actual)

January 30, 2025

Study Registration Dates

First Submitted

February 23, 2026

First Submitted That Met QC Criteria

February 23, 2026

First Posted (Actual)

February 27, 2026

Study Record Updates

Last Update Posted (Actual)

February 27, 2026

Last Update Submitted That Met QC Criteria

February 23, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • REC/RCR&AHS/24/0441

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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