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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06442124
Other study ID # P.T-REC-012/005149
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 12, 2024
Est. completion date June 30, 2024

Study information

Verified date June 2024
Source Ahram Canadian University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

PURPOSE: This study will be conducted to investigate the effect of BMI on gluteus maximum activity in adulthood with sacroiliac dysfunction BACKGROUND: Sacroiliac joint (SIJ) pain is pain arising from SIJ structures and SIJ dysfunction (SIJD) generally refers to aberrant position or movement of SIJ structures . An estimated 15-30% of all low back pain cases are due to SIJ pain The present study will be conducted to add a new information to the body of knowledge of physical therapy profession as it will investigate the effect of BMI on gluteus maximum activity in adulthood with sacroiliac dysfunction HYPOTHESES: . •There will be no effect of BMI on gluteus maximum activity in adulthood with sacroiliac dysfunction RESEARCH QUESTION: - Do BMI has an effect on gluteus maximum activity in adulthood with sacroiliac dysfunction?


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date June 30, 2024
Est. primary completion date June 20, 2024
Accepts healthy volunteers No
Gender All
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - adulthood with sacroiliac dysfunction - Their ages will range from 20-40 years old. - Their BMI will be less than 20- 30kg/m2. - All of them suffer from mild to moderate degree of sacroiliac pain. - The subjects complain from sacroiliac pain for 1 month ago Exclusion Criteria: - Exclusion criteria were a history of any of the following condition: - inflammatory diseases or any rheumatic disorders, - a history of vertebral fractures - surgical spinal fixation. - •any neurological disorders like MS

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Electromyography (EMG)
The present study will be conducted to add a new information to the body of knowledge of physical therapy profession as it will investigate the effect of BMI on gluteus maximum activity recorded by EMG in adulthood with sacroiliac dysfunction

Locations

Country Name City State
Egypt Ahram Canadian university Giza

Sponsors (1)

Lead Sponsor Collaborator
Ahram Canadian University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary gluteus maximum muscle activity measured by Electromyography (EMG) up to 8 weeks
Primary weight and height will be combined to report BMI in kg/m^2) up to 8 weeks
Primary visual analogue scale for pain up to 8 weeks
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