Correlation Between Sacral Angle and Lumbar Range of Motion in Women With Genu Valgum
NCT ID: NCT04377373
Last Updated: 2020-05-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
64 participants
OBSERVATIONAL
2019-04-14
2019-09-05
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Role of Rotational Guided Growth in Management of Increased Femoral Anteversion
NCT06320769
Relationship of Dynamic Knee Valgus With Foot Posture, Pain, and Balance in Chronic Ankle Instability.
NCT07121725
Effects of Lumbopelvic Manipulation on Hip and Knee Neuromuscular Activity
NCT01637480
Temporal Activation of Core Muscles and Vasti in Isolated Patellofemoral Osteoarthritis
NCT04589702
Association Between Chronic Ankle Instability and Sacroiliac Joint Dysfunction
NCT04555083
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
* Screening for genu valgum via postural assessment from frontal view, then measuring the Q angle bilaterally.
* Patients with Q-angle \>20 degress were under the following procedures:
A. Full-Length AP standing X-ray,then the investigators measured the hip-knee angle (the angle between the mechanical axis of the femur and the tibia). It will be obtained by connecting the center of the femoral head to the midpoint of the tibial eminential spine in a line tangential to the femoral condyles, and another line from here to the centre of the trochlea tali.
B-Lumbo-sacral X-ray lateral view was done at the time and the sacral angle was the measured by Ferguson´s technique in degrees using a protractor and this was the sacral angle.
C- During the same session, trunk range of motion was measured by Modified schober test D- Collected data were taken for statistical analysis.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
CROSS_SECTIONAL
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Age ranges from 18-25 years old.
3. BMI ≥ 30 (kg/m2)
Exclusion Criteria
2. lumbar spine fracture
3. Spondylolisthesis
4. Foraminal or extra foraminal lumbar disc herniation
5. spinal tumors, and bone metabolic diseases 6 - Knee surgeries
18 Years
25 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Cairo University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Karima Abdelaty Hassan
Lecturer
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Nasr A. Abdelkader, PhD
Role: PRINCIPAL_INVESTIGATOR
Lecturer,Cairo University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Cairo university
Giza, , Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
P.T.REC/012/002300
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.