Blood Flow Technique Effect on the Muscle Mechanics

March 1, 2025 updated by: Melis Destan, Okan University

Kan Akımı Kısıtlayıcı Egzersizin Kas Mekanikleri Üzerine Akur Etkisi

This study will be a study in which we take measurements with the myotonPRO device to determine whether the resistant exercises performed without the blood flow restrictive technique and with the blood flow restrictive technique affect the biceps muscle of the participants, who were divided into groups by randomization method after determining the 1 max repetition you can lift.

Study Overview

Status

Not yet recruiting

Conditions

Study Type

Observational

Enrollment (Estimated)

57

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

Sampling Method

Non-Probability Sample

Study Population

generally college students

Description

Inclusion Criteria:

  • Being a healthy male or female volunteer between 18 and 35 (who has not participated in any resistance training program for at least 6 months).
  • Being right-hand dominant according to the results of the Edinburgh Handedness Inventory.

Exclusion Criteria:

  • Having a history of biceps musculoskeletal injury.
  • Having any condition that prevents participation in resistance exercise.
  • Having cardiovascular disease.
  • Using medication for blood pressure control.

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

Cohorts and Interventions

Group / Cohort
progressive resistance exercise group with bfr (%80)
Participants in this group will perform progressive resistance exercises with 80% blood flow restriction (BFR) exposure, while muscle mechanical properties will be monitored and recorded during the process.
progressive resistance exercise group with bfr (%20)
Participants in this group will perform progressive resistance exercises with 20% blood flow restriction (BFR) exposure, while muscle mechanical properties will be monitored and recorded during the process.
Non-Blood Flow Restriction Group
Participants in this group will perform progressive resistance exercises without applying the blood flow restriction (BFR) technique, while muscle mechanical properties will be monitored and recorded during the process."

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
muscle mechanics test
Time Frame: Single assessment at baseline and one, two and three days after with measurement
Single assessment at baseline and one, two and three days after with measurement

Collaborators and Investigators

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

Sponsor

Okan 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 (Estimated)

March 3, 2025

Primary Completion (Estimated)

April 5, 2025

Study Completion (Estimated)

May 1, 2025

Study Registration Dates

First Submitted

February 28, 2025

First Submitted That Met QC Criteria

March 1, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

March 1, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2024-34

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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