Blood Flow Technique Effect on the Muscle Mechanics
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Biceps, Muscle Rigidity. Basic parameters: 18 years — 25 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Kan Akımı Kısıtlayıcı Egzersizin Kas Mekanikleri Üzerine Akur Etkisi
Overview
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.
Primary outcome measures
- muscle mechanics test [Time frame: Single assessment at baseline and one, two and three days after with measurement]
Eligibility criteria
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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06861699 · 2024-34