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CompletedNCT07440810Updated Feb 27, 2026

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

An interventional study of Blood Flow restriction + Low Load resistance training and Low load Resistance training in Sports Physical Therapy, sponsored by Riphah International University. Completed at 1 site in Pakistan. Open to male participants aged 18 Years to 30 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-27.

Sponsored by Riphah International University · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 1 year 3 months after the study started (first participant enrolled Nov 2024, registered Feb 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
Male
01

Study summary

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

Read the 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

02

Conditions studied

  • Sports Physical Therapy

Keywords

  • Low load Resistance training
  • Blood flow restriction
  • Fast Bowlers
03

In context

Lead sponsor

Riphah International University is the lead sponsor of 2,133 studies on the registry; 633 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
24 participants (actual)

Study arms

  • 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

    Other: Blood Flow restriction + Low Load resistance training

  • 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.

    Other: Low load Resistance training

Interventions

  • OtherBlood Flow restriction + Low Load resistance training

    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.

  • OtherLow load Resistance training

    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

06

What researchers measure

Primary outcomes

  1. Arm circumference

    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

    Time frame: 6 weeks

  2. 1 Repetition maximum

    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.

    Time frame: 6 weeks

  3. Medicine Ball Throw test

    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.

    Time frame: 6 weeks

07

Study locations

1 site
  • Paklions International Cricket Academy
    Lahore, Punjab Province 54000, Pakistan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07440810
Lead sponsor
Riphah International University
Responsible party
Sponsor
First posted
Feb 27, 2026
Start date
Nov 21, 2024
Primary completion
Sep 15, 2025
Completion
Nov 15, 2025
Last update
Feb 27, 2026

Study contacts

Javaria Basharat, DPT
principal investigator · Riphah International University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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