- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04896190
The Relationship Between Q Angle and Quadriceps Muscle Activation on Dynamic Balance in Women (Quadriceps)
May 20, 2021 updated by: merve yilmaz menek, Istanbul Medipol University Hospital
The quadriceps angle (Q angle) is significant for the lower extremity alignment.
Anatomical alignment of Q angle is related to Quadriceps muscle strength.
Women have consistently been found to have larger Q angles than men and are more often affected due to patellofemoral problems.
Quadriceps muscle activation and lower extremity alignment affect musculoskeletal health in women.The aim of this study wa s to determine the relationship between Q angle and quadriceps muscle activation on dynamic balance in women.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Objective: To determine the relationship between Q angle and quadriceps muscle activation on dynamic balance in women.
Design: Correlational Study.
Setting: University.
Participants: Forth women will be included in the study.
Interventions: Q angle in standing and supine positions, quadriceps muscle activation, static and dynamic balance and functionality were measured.
Main Outcome Measurements: Q angle will measured with a tape measure; muscle activation will measured with Surface Electromyography (EMG) static balance will measured with Flamingo Balance Test (FBT); dynamic balance will measured with ProKin 252 Techno Body device; and, functionality will measured with Short Form Musculoskeletal Assessment (SFMA).
Before the evaluation of EMG amplitude on dynamic balance position, the Q angle will measured in supine and standing positions.
The EMG signals collected by measuring the muscle activation of the Vastus Medialis and Vastus Lateralis during dynamic balance position on the ProKin device will recorded.
Study Type
Interventional
Enrollment (Actual)
40
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 Locations
-
-
-
Istanbul, Turkey
- İstanbul Medipol University
-
-
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
19 years to 25 years (ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- The inclusion criteria were being women, being aged 19-25, and not having musculoskeletal or neurological problems.
Exclusion Criteria:
- Exclusion criteria were having an operation in the past year, taking medicine related to lower limb problems, persistent pain and discomfort of the lower extremity.
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: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Experimental group
Before the evaluation of EMG amplitude on dynamic balance position, the Q angle was measured in supine and standing positions.
The EMG signals collected by measuring the muscle activation of the Vastus Medialis and Vastus Lateralis during dynamic balance position on the ProKin device were recorded.
Q angle evaluations, static and dynamic balance and functional status of all participants were evaluated.
|
Evaluation of Q angle, Quadriceps muscle activation, static and dynamic balance and functionality of all individuals was done.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Q angle evaluation
Time Frame: 5 minutes
|
The Q angle was measured with a standard universal goniometer.
It was measured by drawing a line from the Anterior Superior Iliac Spine to the center of the patella and a second line from the center of the tibial tubercle to the center of the patella.
|
5 minutes
|
|
Electromyographic (EMG) measurements
Time Frame: 15 minutes
|
EMG biofeedback is a device that detects neuromuscular contractions and provides feedback signals to the subject.
During the ProKin 252 Techno Body balance system, Vastus Medialis and Vastus Lateralis muscles activity levels were recorded at 1000-Hz sample data-regulating Surface EMG device and analyzed using the Biometrics Datalog (UK) system.
|
15 minutes
|
|
Dynamic Balance Evaluation
Time Frame: 15 minutes
|
Dynamic balance was evaluated by ProKin 252 Techno Body balance device.
The participants were taken to the balance platform on the right foot with their eyes open, after determining the reference interval and setting the test time as 30 seconds.They were instructed to stay balanced on the platform
|
15 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Static Balance Evaluation
Time Frame: 5 minutes
|
Static balance was assessed with Flamingo Balance Test (FBT) in open and closed eyes conditions.The subjects stood on the beam which was 50 cm long, 5 cm in height and 3 cm wide.
Then the instructor started the stopwatch and the subjects tried to stand in this position for one minute.
When the time was over, the subjects' attempts after they fell were counted and this score was recorded
|
5 minutes
|
|
Functionality Assessment
Time Frame: 5 minutes
|
The functional status of subjects was evaluated with the Short Musculoskeletal Function Assessment Questionnaire (SMFA).
|
5 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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)
January 15, 2019
Primary Completion (ACTUAL)
February 13, 2021
Study Completion (ACTUAL)
February 15, 2021
Study Registration Dates
First Submitted
May 13, 2021
First Submitted That Met QC Criteria
May 20, 2021
First Posted (ACTUAL)
May 21, 2021
Study Record Updates
Last Update Posted (ACTUAL)
May 21, 2021
Last Update Submitted That Met QC Criteria
May 20, 2021
Last Verified
May 1, 2021
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- merveyilmaz
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
I will publish my manuscript about this study, so researchers can access my individual participant's daha with this way.
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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