- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05185882
The Effect of Different Focusing Methods on Muscle Activity
November 7, 2022 updated by: Emre Serdar Atalay, Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey
The Effect of Different Focusing Methods on Muscle Activity During The Single Leg Squat Movement
The aim of this study is to compare the effects of different focusing methods on muscular activity
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
After the first data collecting ( Demographic data, Inclusion criteria) surface electromyography EMG evaluations will be taken from 6 muscles( Vastus Medialis, Rectus Femoris, Vastus Lateralis, Biceps Femoris, Semitendinosus, Gluteus Medius).
These recordings will be taken in 3 different circumstances: 1- Without a focusing method 2- With an external focus and 3- With an internal focus
Study Type
Observational
Enrollment (Actual)
16
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
-
-
İ̇stanbul
-
Ankara, İ̇stanbul, Turkey
- Emre Serdar Atalay
-
-
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
16 years to 23 years (Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Healthy Volunteers
Description
Inclusion Criteria:
- Being between the ages of 18-25
- Having a Body Mass Index between 18.5-24.9
Exclusion Criteria:
- Having trauma/surgery involving the lower extremity in the last 6 months or having any disorder affecting hip and knee muscle function
- Foot Posture Index score not being between 0 and +5
- Hamstring Flexibility- Sit and Reach Test score greater than +5 cm
- Restricted ankle dorsiflexion angle (It will be expected to be at least 5 degrees more than neutral)
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
- Observational Models: Case-Only
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
1
|
Single leg squat exercise in different circumstances
|
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, Vastus Lateralis, Rectus Femoris, Biceps Femoris, Semitendinosus and Gluteus Medius Muscles in 3 conditions in a row(Without a focusing method, With an internal focus, With an external focus
|
Procedure (During the intervention)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Foot Posture Index
Time Frame: Baseline, for inclusion criteria
|
Evaluations of Foot by inspection
|
Baseline, for inclusion criteria
|
Sit and Reach Test
Time Frame: Baseline, for inclusion criteria
|
Assessment of hamstring flexibility
|
Baseline, for inclusion criteria
|
Gluteus Medius Muscle Dynamometer Assessment
Time Frame: Baseline, for inclusion criteria
|
Assessment of Gluteus Medius Strength
|
Baseline, for inclusion criteria
|
Ankle Dorsi Flexion Goniometer Assessment
Time Frame: Baseline, for inclusion criteria
|
Assessment of Dorsiflexion
|
Baseline, for inclusion criteria
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Emre Serdar Atalay, PhD, Saglik Bilimleri Universitesi
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)
September 20, 2022
Primary Completion (Actual)
October 4, 2022
Study Completion (Actual)
October 4, 2022
Study Registration Dates
First Submitted
December 4, 2021
First Submitted That Met QC Criteria
January 10, 2022
First Posted (Actual)
January 11, 2022
Study Record Updates
Last Update Posted (Actual)
November 8, 2022
Last Update Submitted That Met QC Criteria
November 7, 2022
Last Verified
November 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021-388
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
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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