NCT06406907

Brief Summary

Effects of short duration blood flow restriction training on musculoskeletal and performance outcomes.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
68

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Nov 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 6, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

May 9, 2024

Completed
6 months until next milestone

Study Start

First participant enrolled

November 2, 2024

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 8, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 8, 2025

Completed
Last Updated

November 24, 2025

Status Verified

November 1, 2025

Enrollment Period

8 months

First QC Date

May 6, 2024

Last Update Submit

November 18, 2025

Conditions

Keywords

Blood flow restrictionSurface EMGReactive strength indexAbdominal muscles

Outcome Measures

Primary Outcomes (7)

  • Thigh Muscles Ultrasound Assessment

    Subject lying in supine position. 50% of thigh length was measured from ASIS to mid patella. Ultrasound measurements of muscle thickness of bilateral rectus femoris, and vastus intermedius were performed.

    2 weeks

  • Abdomen Muscles Ultrasound Assessment

    Subject lying in supine position. The images of bilateral, transverse abdominis, internal oblique and external oblique were taken by placing the probe transversely in the mid-axillary line, between the subcostal line and the iliac crest 15 cm lateral to the umbilicus. For the rectus abdominis examination, the probe was placed transversely 3 cm lateral to the umbilicus.

    2 weeks

  • Thigh Muscles Strength Assessment

    Subject sitting on a table unsupported. Knee in 75° flexion. Dynamometer was fixed with the table with the help of a strap the other end of the strap was fixed with subject's leg just above the ankle joint. Patient performed MVC for 5 seconds. First 2 seconds submaximal effort. Last 3 seconds maximum effort. 3 trials. 2 mins break between the trails.

    2 weeks

  • Abdominal Muscles Strength Assessment

    Subject stood in a custom made frame. Knee slightly bent. Heels on the mark so it is standardized for all subjects. Knees and thighs secured and tightened with belt. Chest harness placed and connected to the dynamometer belt. Subject was positioned in 17.5° trunk flexion. Trunk angle checked with goniometer. Patient performed MVC for 5 seconds. First 2 seconds submaximal effort. Last 3 seconds maximum effort. 3 trials. 2 mins break between the trails.

    2 weeks

  • Thigh Muscles Electromyography Assessment

    Subject sitting on a table unsupported. Knee in 75° flexion. For quadriceps muscles the electrodes were placed approximately half the distance between the knee and the iliac spine.Patient performed MVC for 5 seconds. First 2 seconds submaximal effort. Last 3 seconds maximum effort. 3 trials. 2 mins break between the trails.

    2 weeks

  • Abdominal Muscles Electromyography Assessment

    Subject stood in a custom made frame. Knee slightly bent. Heels on the mark so it is standardized for all subjects. Knees and thighs secured and tightened with belt. Chest harness placed and connected to the dynamometer belt. Subject was positioned in 17.5° trunk flexion. For rectus abdominis the electrodes were placed 3 cm lateral to the umbilicus. For external oblique the electrodes were placed 15 cm lateral to the umbilicus. Patient performed MVC for 5 seconds. First 2 seconds submaximal effort. Last 3 seconds maximum effort. 3 trials. 2 mins break between the trails.

    2 weeks

  • Jump Assessment

    Subjects were standing 2 meters away from the mobile stand. My jump 3 mobile app was used for assessment. For jump assessment the mobile was fixed on a stand and placed in front of the subject.

    2 weeks

Secondary Outcomes (2)

  • Delayed Onset Muscle Soreness Assessment

    2 weeks

  • Rating of Perceived Exertion Scale

    2 weeks

Study Arms (5)

High Frequency Blood Flow Restriction Training Group

EXPERIMENTAL

Subjects allocated to this group performed squat exercise 6 days per week for 2 weeks with B Strong blood flow restriction cuffs, with the pressure set at 300mmHg of mercury for arm and 350mmHg of mercury for thigh and 30% of 1RM.

Other: High Frequency Blood Flow Restriction Training Group

Low Frequency Blood Flow Restriction Training Group

EXPERIMENTAL

Subjects allocated to this group performed squat exercise 3 days per week for 2 weeks with B Strong blood flow restriction cuffs, with the pressure set at 300mmHg of mercury for arm and 350mmHg of mercury for thigh and 30% of 1RM.

Other: Low Frequency Blood Flow Restriction Training Group

High Frequency Blood Flow Restriction Training Instability Group

EXPERIMENTAL

Subjects allocated to this group performed squat exercise 6 days per week for 2 weeks with B Strong blood flow restriction cuffs, with the pressure set at 300mmHg of mercury for arm and 350mmHg of mercury for thigh and 30% of 1RM on instability pneumatic discs.

Other: High Frequency Blood Flow Restriction Training Instability Group

Low Frequency Blood Flow Restriction Training Instability Group

EXPERIMENTAL

Subjects allocated to this group performed squat exercise 3 days per week for 2 weeks with B Strong blood flow restriction cuffs, with the pressure set at 300mmHg of mercury for arm and 350mmHg of mercury for thigh and 30% of 1RM on instability pneumatic discs

Other: Low Frequency Blood Flow Restriction Training Instability Group

Control Group

SHAM COMPARATOR

The subjects of this group performed squat exercise 6 days a week but without BFR. Pneumatic cuff will be wrapped around the thigh of the subjects but it would not be inflated. The subjects of this group performed squat exercise 6 days a week but without BFR. Pneumatic cuff were applied to the most proximal part of the thighs and arms but were not inflated.

Other: Control Group

Interventions

Subjects allocated to this group performed squat exercise 6 days per week for 2 weeks with B Strong blood flow restriction cuffs, with the pressure set at 300mmHg of mercury for arm and 350mmHg of mercury for thigh and 30% of 1RM. Blood flow restriction cuffs were applied to the most proximal part of the thighs and arms. Each subject performed 75 repetitions in total across 4 sets of squats in the order of 30-15-15-15. Rest between sets was 30 sec. Subjects were instructed to tummy tuck while performing the exercise.

High Frequency Blood Flow Restriction Training Group

Subjects allocated to this group performed squat exercise 3 days per week for 2 weeks with B Strong blood flow restriction cuffs, with the pressure set at 300mmHg of mercury for arm and 350mmHg of mercury for thigh and 30% of 1RM. Blood flow restriction cuffs were applied to the most proximal part of the thighs and arms. Each subject performed 75 repetitions in total across 4 sets of squats in the order of 30-15-15-15. Rest between sets was 30 sec. Subjects were instructed to tummy tuck while performing the exercise.

Low Frequency Blood Flow Restriction Training Group

Subjects allocated to this group performed squat exercise 6 days per week for 2 weeks with B Strong blood flow restriction cuffs, with the pressure set at 300mmHg of mercury for arm and 350mmHg of mercury for thigh and 30% of 1RM on instability pneumatic discs. Blood flow restriction cuffs were applied to the most proximal part of the thighs and arms. Each subject performed 75 repetitions in total across 4 sets of squats in the order of 30-15-15-15. Rest between sets was 30 sec. Subjects were instructed to tummy tuck while performing the exercise.

High Frequency Blood Flow Restriction Training Instability Group

Subjects allocated to this group performed squat exercise 3 days per week for 2 weeks with B Strong blood flow restriction cuffs, with the pressure set at 300mmHg of mercury for arm and 350mmHg of mercury for thigh and 30% of 1RM on instability pneumatic discs. Blood flow restriction cuffs were applied to the most proximal part of the thighs and arms. Each subject performed 75 repetitions in total across 4 sets of squats in the order of 30-15-15-15. Rest between sets was 30 sec. Subjects were instructed to tummy tuck while performing the exercise.

Low Frequency Blood Flow Restriction Training Instability Group

The subjects of this group performed squat exercise 6 days a week but without BFR. Pneumatic cuff were applied to the most proximal part of the thighs and arms but were not inflated. Each subject performed 75 repetitions in total across 4 sets of squats in the order of 30-15-15-15. Rest between sets was 30 sec. Subjects were instructed to tummy tuck while performing the exercise.

Control Group

Eligibility Criteria

Age18 Years - 30 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Sedentary males (\< 2.5h/week physical activity) or \< 300 METs per week (36)
  • Age 18-30 years
  • BMI between 18.5-29.9
  • Free from any lower-limb pain or injury
  • No previous experience with BFRT
  • Ankle brachial index values between 0.9-1.4
  • Not doing regular strength training of lower limb in the past 6 months
  • No strenuous physical activities 72h before and during the study period
  • Non-smokers

You may not qualify if:

  • Any injuries of the musculoskeletal system that could prevent the participants from training or testing
  • Any use of medication and/or supplements (e.g., protein powder, vitamins, creatine, NSAIDs, etc.)
  • Peripheral arterial disease
  • Diabetes and hypertensive patients

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Riphah International University

Islamabad, 44000, Pakistan

Location

MeSH Terms

Interventions

Control Groups

Intervention Hierarchy (Ancestors)

Epidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

Study Officials

  • Asghar Khan

    asghar.khan@riphah.edu.pk

    STUDY CHAIR
  • Waqar Ahmed Awan, PhD

    Riphah International University

    STUDY CHAIR
  • Saad Rauf, PhD*

    Riphah International University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 6, 2024

First Posted

May 9, 2024

Study Start

November 2, 2024

Primary Completion

July 8, 2025

Study Completion

July 8, 2025

Last Updated

November 24, 2025

Record last verified: 2025-11

Data Sharing

IPD Sharing
Will not share

Locations