- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05420675
Different Arm Positions During Single Leg Squat
August 31, 2022 updated by: Gökhan Karakaş, Hacettepe University
Vastus Medialis Muscle Activation During Single Leg Squat Performed With Arm Position Variations in Healthy Participants
The aim of this study is to compare the effects of different arm positions on muscle activity during single leg squat.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The aim of our study is to examine the effect of different positions of the arms on lower extremity muscle activations during Single Leg Squat (SLS).
This prospective cross sectional study included single leg squat test assessments in different arm positions: 1) Arms free, 2) Arms flexed 90 degrees, 3) Hands on hip, 4) Arms across the chest.
Inclusion criteria were being a young adult (20-30 years old), physical activity level of at least 4 on the Tegner Activity Scale, and volunteering to participate in the study.
Those with a history of lower extremity injury in the last 1 year will be excluded from the study.
Our study will contribute to distinguishing SLS variations for clinicians and researchers and choosing the appropriate SLS for evaluation and treatment.
Study Type
Observational
Enrollment (Actual)
20
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Ankara, Turkey
- Hacettepe University, Faculty of Physical Therapy and Rehabilitation, Department of Physiotherapy and Rehabilitation
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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 30 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Healthy Volunteers
Description
Inclusion Criteria:
- Being between the ages of 20-30
- Physical activity level of at least 4 on the Tegner Activity Scale,
Exclusion Criteria:
- History of lower extremity injury in the last 1 year
- Central or peripheral vestibular disorders
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Surface Electromyography
Time Frame: Procedure (During the intervention)
|
Surface EMG evaluations of Vastus Medialis in 4 conditions in a row (1) Arms free, 2) Arms flexed 90 degrees, 3) Hands on hip, 4) Arms on crossed shoulders.
|
Procedure (During the intervention)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Gözde Yağcı, Assoc.Prof., Hacettepe University Faculty of Physical Therapy and Rehabilitation
- Principal Investigator: Semra Topuz, Prof., Hacettepe University Faculty of Physical Therapy and Rehabilitation
- Principal Investigator: Gökhan Karakaş, M.Sc., Hacettepe University Faculty of Physical Therapy and Rehabilitation
- Principal Investigator: Alev Doğan, M.Sc., Hacettepe University Faculty of Physical Therapy and Rehabilitation
- Principal Investigator: Ali Yalçın, M.Sc., Hacettepe University Faculty of Physical Therapy and Rehabilitation
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 (ACTUAL)
June 8, 2022
Primary Completion (ACTUAL)
July 15, 2022
Study Completion (ACTUAL)
August 1, 2022
Study Registration Dates
First Submitted
June 11, 2022
First Submitted That Met QC Criteria
June 11, 2022
First Posted (ACTUAL)
June 15, 2022
Study Record Updates
Last Update Posted (ACTUAL)
September 2, 2022
Last Update Submitted That Met QC Criteria
August 31, 2022
Last Verified
August 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- GO22-582
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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.