Additional Effects of Upper Limb Blood Flow Restriction Training With Low Load Resistance Training in Fast Bowlers

February 23, 2026 updated by: Riphah International University

Additional Effects of Upper Limb Blood Flow Restriction Training With Low Load Resistance Training On Strength, Arm Girth And Power In Fast Bowlers

Additional Effects of Upper Limb Blood Flow Restriction Training With Low Load Resistance Training On Strength, Arm Girth And Power In Fast Bowlers

Study Overview

Detailed Description

Additional Effects of Upper Limb Blood Flow Restriction Training With Low Load Resistance Training On Strength, Arm Girth And Power In Fast Bowlers

Study Type

Interventional

Enrollment (Actual)

24

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
        • Paklions International Cricket Academy

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:

  • Fast bowlers aged 18-30 years
  • At least 2 years of regular training & experience in cricket as fast bowlers
  • Engaging in cricket training at least 3 times a week.

Exclusion Criteria:

  • Serious humerus, forearm and wrist injuries within one week before training
  • Presence of any neurological conditions affecting muscle performance or coordination
  • Use of medications that could influence muscle strength, size or power
  • Currently involved in any other experimental training program for upper limb performance.

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group A
Participants allocated to experimental group took part in low-load resistance training combined with blood flow restriction applied by elastic occlusion wrap. The goal was to improve muscle strength and growth using weights while giving enough stimulus for muscles to adapt. Each session was started with warm-up of light aerobic exercises. After warm-up, BFR was applied using elastic wrap bands. The wrap was applied proximally on the arm following practical BFR methods in the literature
Participants allocated to experimental group took part in low-load resistance training combined with blood flow restriction applied by elastic occlusion wrap. The goal was to improve muscle strength and growth using weights while giving enough stimulus for muscles to adapt. Each session was started with warm-up of light aerobic exercises. After warm-up, BFR was applied using elastic wrap bands. The wrap was applied proximally on the arm following practical BFR methods in the literature.
Experimental: Group B

This group participated in low-load resistance training without any BFR. Participants performed exercises like bicep curls and shoulder presses without applying BFR. Rather, they will lift weights equal to about 30% of their one repetition maximum to keep training light using low-loads.

Similar to BFR group, this group will exercise twice a week for six weeks. This training will include two sets of 15 reps for each exercise with enough rest between them. Without blood flow restriction participants could perform the exercises with normal ROM and easier weight control.

This group participated in low-load resistance training without any BFR. Participants performed exercises like bicep curls and shoulder presses without applying BFR. Rather, they will lift weights equal to about 30% of their one repetition maximum to keep training light using low-loads.

Similar to BFR group, this group will exercise twice a week for six weeks. This training will include two sets of 15 reps for each exercise with enough rest between them. Without blood flow restriction participants could perform the exercises with normal ROM and easier weight control

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Arm circumference
Time Frame: 6 weeks
Arm circumference was measured using a measuring tape at standarized anatomical landmark. The tape was placed around the arm gently.the arm size was recorded to nearest centimeter
6 weeks
1 Repetition maximum
Time Frame: 6 weeks
One repetition maximum test was used to assessed muscle strength. The test involves determining the maximum amount of weight a person can lift for a single repetition of given exercise.
6 weeks
Medicine Ball Throw test
Time Frame: 6 weeks
Upper-limb power was measured using medicine ball throw test. it assessed explosive strength of the arm muscles. The participant throws the ball forward as strongly as possible targeting for maximum distance.
6 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Javaria Basharat, 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)

November 21, 2024

Primary Completion (Actual)

September 15, 2025

Study Completion (Actual)

November 15, 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/24/0475

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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