- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07606040
Low Back Pain and Hamstring-to-Quadriceps Strength Ratio in Military Personnel (LBP-H/Q ratio)
Association Between Low Back Pain and Hamstring-to-Quadriceps Strength Ratio in Lithuanian National Defence Volunteer Forces Personnel
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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LT
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Kaunas, LT, Lithuania, 44221
- Department of health promotion and rehabilitation
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- The study participants consisted of a targeted population of Lithuanian National Defence Volunteer Forces personnel
Exclusion Criteria:
- Individuals with a clinically diagnosed low back pain disorder or acute episodes of low back pain were excluded
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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Military personnel
Targeted population of Lithuanian National Defence Volunteer Forces personnel
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Low back pain prevalence
Time Frame: Baseline
|
Participants were asked whether they had experienced low back pain during the past 12 months (yes/no).
Participants who responded "yes" were classified into the low back pain group.
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Baseline
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Low back pain intensity
Time Frame: Baseline
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LBP intensity was assessed using the Visual Analogue Scale (VAS, 0-10) , where 0 - no pain, and 10 - worst imaginable pain.
|
Baseline
|
|
Low back pain duration
Time Frame: Baseline
|
Participants were asked to indicate LBP duration.
LBP pain duration was classified as acute (<3 months) or chronic (≥3 months)
|
Baseline
|
|
Muscle strength peak torque
Time Frame: Baseline
|
Muscle strength was assessed using the Biodex System 4 isokinetic dynamometer. Participants were instructed to avoid vigorous physical activity 24 hours before testing and refrain from eating for at least 2 hours prior to assessment. A 10-minute warm-up on a cycle ergometer (50-60 W) and light dynamic exercises were performed before testing. Participants were seated with the backrest at 85° and hip flexion at 90°. The dynamometer axis was aligned with the lateral femoral epicondyle, and the lower leg was secured 2-3 cm above the ankle. The range of motion was set from 70° knee flexion to full extension. The trunk and tested limb were stabilized using straps. Testing included 5 repetitions at 60°/s and 10 repetitions at 120°/s, with a 30-second rest interval between sets. Prior to testing, participants performed 3-5 familiarization repetitions. Peak torque normalized to body weight (Nm/kg) was recorded. |
Baseline
|
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Average torque
Time Frame: Baseline
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Was measured in Nm
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Baseline
|
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Muscle power
Time Frame: Baseline
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in W
|
Baseline
|
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Body weight
Time Frame: Baseline
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Measured in kg
|
Baseline
|
|
Body height
Time Frame: Baseline
|
Measured in meters
|
Baseline
|
|
Age
Time Frame: Baseline
|
Measured in years
|
Baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Previous injuries
Time Frame: Baseline
|
Participants were asked whether they had lumbar or lower limb injuries during the past 12 months that could influence the results (yes / no).
|
Baseline
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Lithuanian Sports University31
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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