Skip to main content
OpenTrials
Completed

NCT Number: NCT04755608

The Effect of Low-Intensity Resistance Exercise Training

It was to compare the effect of low-load resistance training with blood flow restriction (LL-BFR) and high-intensity resistance training (HI-RT) on muscle strength, endurance and volume, functional performance, and delayed onset muscle soreness (DOMS).

The study included 13 young women. It is a controlled study designed for individuals to perform two different exercise protocols unilaterally. The persons were randomly allocated into two groups as LI- BFR (Group I, n = 13) and HI-RT (Group II, n = 13). Both groups received training for 6 weeks and 3 days a week. Blood flow restriction was performed only in group I.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–26 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University and Health Sciences Physical Therapy and Rehabilitation

Istanbul, Uskudar, 34668, Turkey (Türkiye)

About this study

Both sides triceps muscle thickness, triceps and biceps strength and endurance, functional performances (upper extremity Y balance test (UQYBT)), delayed-onset muscle soreness (DOMS) were evaluated before and after training.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Between the ages of 18-26,
  • Do not have a chronic disease history and do not use medication,
  • Female individuals were included.

Exclusion criteria

  • People who made resisted exercise in the last 6 months,
  • Smoker,
  • BMI above 30 kg / m2,
  • Individuals with hypertension were excluded.

Treatment and study plan

Low Intensity Exercises with Blood Flow Restriction

Other

In the exercise protocol, people exercised resistance between 20% and 30% of 1 MaxRepetition with free weight. In addition, blood flow was restricted in 70% of the arterial occlusion pressure of the individual with the help of a cuff during exercise.

High Intensity Resistant Exercise

Other

People included in the study did resistance exercise with free weight at 70-80% of 1 MT.

Primary outcomes

  1. triceps muscle thickness

    Time frame: 6 weeks

    Triceps brachial (TB) long head thickness was measured using the Esaote mylab C series ultrasound device.

  2. triceps and biceps strength

    Time frame: 6 weeks

    Triceps brachial muscle strength was evaluated with an isokinetic dynamometer (Cybex HUMAC / NORM, CSMI, 2004). Isometric muscle strength measurement was performed at the beginning and end of the study at angular velocities of 0-150 ° elbow range, 60 ° / s (strength measurement)

  3. triceps and biceps endurance

    Time frame: 6 weeks

    Triceps brachial muscle strength was evaluated with an isokinetic dynamometer (Cybex HUMAC / NORM, CSMI, 2004). Isometric muscle strength measurement was performed at the beginning and end of the study at angular velocities of 0-150 ° elbow range, 180 ° / s (endurance measurement).

  4. functional performances

    Time frame: 6 weeks

    Upper Extremity Y Balance Test

  5. delayed-onset muscle soreness

    Time frame: 6 weeks

    Visual Analog Scale

Sponsors and collaborators

Lead sponsor

Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey

Other

Registry information

Official study title

The Effect OfF Low-Intensity Resistance Exercise Training Combined With Blood Flow Restruction On Triceps Brachii Muscle Volume And Performance

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Feb 16, 2021
Registry last updated
Feb 16, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.