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Correlation Between Posterior Oblique Sling Activation and Contralateral Glenohumeral Stability in Low Back Pain

CompletedNCT05050695
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

Objective: This study will be conducted to investigate the relationship between the amplitude of posterior oblique sling muscles; ipsilateral gluteus maximus (GM) and contralateral latissmus Dorsi (LD), and the amount of anterior translation of humeral head (ATHH) of the contralateral glenohumeral joint (GHJ) in subjects with unilateral chronic low back pain (CLBP) during ipsilateral prone knee extension (PHE) test. Methods: The study will be conducted on thirty subjects (15 patients with CLBP and 15 healthy subjects). Ipsilateral GM and contralateral LD amplitude will be recorded by surface EMG during PHE of the limb at the painful side and correlated to ATHH of contralateral GHJ as measured by ultrasonography. Hypothesis: There won't be a significant relationship between the amplitude of posterior oblique sling muscles (GM and contralateral LD) during PHE for the ipsilateral leg and the amount of ATHH of the contralateral GHJ in patients with unilateral CLBP.

Study details

Official title
Relationship Between Lumbopelvic Muscles Activity and Ultrasonographic Measurement of Contralateral Anterior Humeral Translation in Chronic Unilateral Low Back Pain
Sponsor
Shaimaa Ramadan Ibrahim Abdul-ghani El Deab
Organization
Cairo University
Start date
2021-10-04
Primary completion
2022-01-25
Sex
All
Age range
from 20 Years to 50 Years
Results posted
No results posted in this snapshot
Countries
Egypt
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria for CLBP group: 1. Patients age between 20-50yrs 2. Patients with chronic low back pain (pain \> 3 months). 3. Patients with unilateral symptoms (facet, disc, SIJ dysfunction) will be referred by an orthopedic physician with or without referral to the leg. Inclusion Criteria for the healthy control group: 1\. matched controls in terms of age, weight, height, and BMI. Exclusion Criteria for both groups: 1. History of shoulder pain 3 months ago. 2. History of any shoulder pathology. 3. Congenital pathology affecting the spine or shoulder. 4. Any neurological disorder. 5. Non-mechanical LBP (e.g., fracture, malignancy, infection) 6. Difficulty performing the PHE task because of weakness in the GM or the test provokes pain. 7. BMI 30 or higher as fat tissue may decrease the ability to measure surface EMG activity

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05050695