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

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

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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