- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07508150
Anthropometric Normalization in Inter-Individual Variability of Comprehensive Isokinetic Strength Assessment (PT)
Role of Anthropometric Normalization in Inter-Individual Variability of Comprehensive Isokinetic Strength Assessment in Healthy Women: A Methodological Study
Study Overview
Status
Conditions
Detailed Description
Accurate normalization of peak torque (PT) is critical for comparing muscle strength across individuals of varying body composition. While body weight (BW) is commonly used, body mass index (BMI) may provide a more stable representation of inter-individual variability. The study aims to compare the effects of BW and BMI normalization on inter-individual variability of trunk, hip, and knee muscle strength in healthy female participants.
Thirty healthy adult females will undergo isokinetic testing of trunk flexors/extensors, hip flexors/extensors/abductors/adductors, and knee flexors/extensors. PT values will be normalized to BW and BMI. Coefficient of variation (CV%) will be calculated for each method to evaluate relative variability.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Azza M Abdelmohsen, professor
- Phone Number: 01145046304
- Email: dr_azzamohammed@yahoo.com
Study Contact Backup
- Name: Azza M, professor
- Phone Number: 01145046304
- Email: dr_azzamohammed@yahoo.com
Study Locations
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Giza, Egypt, 12511
- Faculty of physical therapy, Cairo University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
he absence of any current or prior musculoskeletal injury or pain affecting the trunk, pelvis, or lower extremities within the preceding six months.
- absence of neurological, cardiovascular, or systemic conditions that could influence muscle strength or motor performance.
- a normal BMI relative to their age and sex and were recreationally active without engaging in any structured strength training program targeting the trunk or hip muscles during the three months preceding the study.
- all participants were able to comprehend the study procedures and provide written informed consent.
Exclusion Criteria:
- any history of musculoskeletal injury, surgery, or chronic pain involving the spine, pelvis, hip, knee, or ankle. Individuals with diagnosed neurological disorders, balance impairments, or vestibular conditions were also ineligible.
- cardiovascular, respiratory, or systemic diseases that could affect physical performance or muscle strength were excluded
- a prior history of lower limb or trunk fractures. Individuals engaged in competitive sports or structured resistance training programs targeting the trunk and lower limb muscles within the preceding three months were not included.
- musculoskeletal deformities, leg length discrepancies, or any other condition that could interfere with the testing procedures
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
trunk muscle peak torque
Time Frame: two weeks
|
Isokinetic trunk muscle strength testing
|
two weeks
|
|
hip muscle peak torque
Time Frame: two weeks
|
Isokinetic hip muscle strength testing
|
two weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Azza M, professor, Cairo University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Approved by IRB
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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