- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04522531
Effect of Open Kinetic Chain Shoulder Exercises on Scapulothoracic Muscle Activity on Stable and Unstable Ground
October 29, 2022 updated by: Kübra Canli, Hacettepe University
Exercises used in shoulder rehabilitation compose of open kinetic chain and closed kinetic chain exercises.The force formed on the trunk and legs is transferred to the shoulder in open and closed kinetic chain exercises before shoulder muscles activation.
It was shown that trunk and leg muscle activity changes when they are performed in different ground.
But it is unknown how this alteration effect shoulder muscle activity.
This will be provide a significance approach due to incremented of shoulder muscle activity is important for shoulder rehabilitation setting.
To achieve this aim that is rising of muscle activity, various approach is applied including alteration of ground which individual performed exercise on it.
And, it was shown that closed cinetic chain exercise which performed on different ground change shoulder muscle activity.
However, it is unknown whether alteration of ground effect shoulder muscle activity or not in open cinetic chain exercise.
That's why the aim of this study is to investigate alteration of scapulothoracic shoulder muscle activity in open cinetic chain shoulder exercise which enforced different ground.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
24
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Kübra Canlı
- Phone Number: +90 0312 305 15 76
- Email: canli09@hacettepe.edu.tr
Study Locations
-
-
Sıhhıye
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Ankara, Sıhhıye, Turkey, 06100
- Hacettepe Universty
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Contact:
- Kübra Canlı, MD
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-
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
20 years to 45 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Being healthy
- Right hand dominant
- Ages between 20-45 years
- To be volunteer participate in the study
Exclusion Criteria:
- Having any shoulder pain in current or in the past
- Any previous surgery
- Pain in any part of the body
- Doing regularly a professional sports
- Neurological disease
- Systemic disease
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
- Primary Purpose: Other
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Exercise performed on stabil ground
Open cinetic chain shoulder exercise will performed on stabil ground.
This exercises will be include PNF (flexion-adduction-external rotation pattern), PNF (flexion-abduction-external rotation pattern), scapular plan abduction, external rotation while keeping shoulder in 45 degree abduction.
The weight which used during exercise planned according to individuals body weight: 0-59 kg: 3 kg; 60-69 kg: 4 kg; 70-85 kg: 5Kg.
Exercises will be carried out in 3 phases consisting of concantric, isometric and eccentric phases.
Each phase will be lasted 3 seconds.
The time will be checked by using a metronome.
|
Open cinetic chain shoulder exercise will be performed on BOSU which provides an unstabil ground.
This exercises will be include PNF (flexion-adduction-external rotation pattern), PNF (flexion-abduction-external rotation pattern), scapular plan abduction, external rotation while keeping shoulder in 45 degree abduction.
The weight which used during exercise planned according to individuals body weight: 0-59 kg: 3 kg; 60-69 kg: 4 kg; 70-85 kg: 5Kg.
Exercises will be carried out in 3 phases consisting of concantric, isometric and eccentric phases.
Each phase will be lasted 3 seconds.
The time will be checked by using a metronome.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Muscle recruitment firing
Time Frame: Change from baseline muscle recruitment firing to in 5 minutes after completion of exercise
|
EMG analysis will be performed scapulothoracic muscle including upper trapezius, middle trapezius, lower trapezius and serratus anterior muscle.
EMG sensors will be placed for each muscle according to SENIAM guidlines.
Maximal voluntary isometric contraction will be performed three times for each muscle according to Kendal.
Data will be collected during exercise performance which performed on stabil ground as well as unstabil ground using a BOSU (BOSU, Fitness, LLC, San Diego, CA).
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Change from baseline muscle recruitment firing to in 5 minutes after completion of exercise
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Muscle thickness evaluation
Time Frame: Change from baseline muscle recruitment firing to in 5 minutes after completion of exercise
|
Muscle thickness will be analysed including upper trapezius, middle trapezius, lower trapezius and serratus anterior muscle during resting and each exercise performance.
For muscle thickness evaluation SHMADZU SDU-1200PRO Diagnostic Ultrasound System (Shimadzu, Japan) device will be used.
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Change from baseline muscle recruitment firing to in 5 minutes after completion of exercise
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Anticipated)
March 20, 2023
Primary Completion (Anticipated)
August 20, 2023
Study Completion (Anticipated)
December 20, 2023
Study Registration Dates
First Submitted
August 4, 2020
First Submitted That Met QC Criteria
August 19, 2020
First Posted (Actual)
August 21, 2020
Study Record Updates
Last Update Posted (Actual)
November 1, 2022
Last Update Submitted That Met QC Criteria
October 29, 2022
Last Verified
October 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Hacettepe Universty
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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