The Effect of Low-Intensity Resistance Exercise Training

Sponsor
Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey (Other)
Overall Status
Completed
CT.gov ID
NCT04755608
Collaborator
(none)
13
1
2
8
1.6

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Low Intensity Exercises with Blood Flow Restriction
  • Other: High Intensity Resistant Exercise
N/A

Detailed Description

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
13 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Self Controlled Randomised TrialSelf Controlled Randomised Trial
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
The Effect OfF Low-Intensity Resistance Exercise Training Combined With Blood Flow Restruction On Triceps Brachii Muscle Volume And Performance
Actual Study Start Date :
Dec 1, 2019
Actual Primary Completion Date :
Aug 1, 2020
Actual Study Completion Date :
Aug 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Low Intensity Blood Flow Restriction Group

Other: Low Intensity Exercises with Blood Flow Restriction
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.

Active Comparator: High Intensity Resistant Training Group

Other: High Intensity Resistant Exercise
People included in the study did resistance exercise with free weight at 70-80% of 1 MT.

Outcome Measures

Primary Outcome Measures

  1. triceps muscle thickness [6 weeks]

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

  2. triceps and biceps strength [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 [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 [6 weeks]

    Upper Extremity Y Balance Test

  5. delayed-onset muscle soreness [6 weeks]

    Visual Analog Scale

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 26 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University and Health Sciences Physical Therapy and Rehabilitation İstanbul Uskudar Turkey 34668

Sponsors and Collaborators

  • Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey

Investigators

  • Principal Investigator: Yunus Emre Tütüneken, MSc, Istinye University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Emre Serdar Atalay, Assist. Prof., Saglik Bilimleri Universitesi
ClinicalTrials.gov Identifier:
NCT04755608
Other Study ID Numbers:
  • 46418926-19-138
First Posted:
Feb 16, 2021
Last Update Posted:
Feb 16, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Emre Serdar Atalay, Assist. Prof., Saglik Bilimleri Universitesi
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 16, 2021