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Effect of Blood Flow Restriction Technique on Delayed Onset Muscle Soreness

Effect of Blood Flow Restriction Technique on Pain, Muscle Tone and Strength in Delayed Muscle Soreness

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06389747
Enrollment
15
Registered
2024-04-29
Start date
2024-04-24
Completion date
2024-06-15
Last updated
2024-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain Intensity

Keywords

pain, muscle strength, muscle tonus

Brief summary

The aim of our study is to determine and evaluate the effects of blood flow restriction technique on pain, biomechanical properties and strength of the muscle in delayed onset muscle pain in healthy individuals. A Double Blind, Randomized Controlled, prospective study was planned.

Detailed description

All participants will be taken into the DOMS creation protocol. Participants will then be divided into 80% intensity BFR and 20% intensity Blood Flow Restriction technique (BFR) groups and will be included in an exercise protocol accompanied by BFR application.

Interventions

OTHERBFR technique

For BFR application, Airbands brand, wireless, automatic training cuffs will be used. During application, it will be ensured that the device module faces forward and the cuff will be fixed in the correct position by wrapping the band around the metal ring. There will be a space between the skin and the cuff that can fit two fingers. The cuff will then be paired via Bluetooth with the Airbands app installed on the phone. BFR cuffs will be placed proximal to the biceps brachii muscle and pressure will be applied. The cuff will be inflated to automatically detect limb pressure. BFR application with 80% pressure to one group of participants and 20% pressure to the other group will be applied simultaneously with the exercise.

Sponsors

Istanbul University - Cerrahpasa
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

participants and assessors will be blind to different intensity BFR groups.

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy individuals between the ages of 18-35 (who have not participated in any resistance training program for at least 6 months)

Exclusion criteria

* Having a previous musculoskeletal system injury * Having a condition that prevents resistance exercise * Having cardiovascular disease * Using medication for blood pressure control

Design outcomes

Primary

MeasureTime frameDescription
myoton2 monthsit will be used for assessment of muscle tonus and biomechanic properties, scores are changin according to different parameters.
dynamometer2 monthsit will be used for assessment of myscle strength, lower scores indicate that the situation is getting worse.
Visual analog scale2 monthsit will be used for assessment of pain intensity, It is scored between 0-10, and higher scores indicate that the situation is getting worse.
dolorimeter2 monthsit will be used for assessment of pain thresold pressure, lower scores indicate that the situation is getting worse.

Countries

Turkey (Türkiye)

Contacts

Primary ContactGamze Aydın, PhD
gmzetsn@gmail.com+905377600256

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026