- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06262763
High-intensity Laser Therapy for Sacroiliac Joint Pain (Girls)
February 14, 2024 updated by: Takwa Mohamed Saied Gado, Kafrelsheikh University
Effect of High Intensity Laser on Sacroiliac Joint Pain In Adult Women
Effect of high intensity laser on sacroiliac joint pain
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
Effect of high laser in reduction of pain and improve functional disability in adult women
Study Type
Interventional
Enrollment (Actual)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Kafr Ash Shaykh, Egypt
- Kafr Al-Sheikh University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- The presence of Pain over the sacroiliac joint with no surgical history.
- Unmarried.
- Tender SIJ on palpation.
- Workers with an average age of 18-30 years.
- Body mass index did not exceed 30 kg/m2.
Exclusion Criteria:
- If they have Infections. .Fracture in and around the SIJ Complex.
- Arthritis of joint.
- Pregnancy. .Smoking girls. .Patient not willing to participate in the study. .Any history of surgery. Lumbar spine disc herniation or back injury. Tumor around the joint.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Group (A)
Laser with traditional exercises
|
High-intensity
Other Names:
Hamstring and piriformis stretch, plank exercises and bird dog exercise
|
Placebo Comparator: Group (B)
Placebo LASER with traditional exercises
|
Hamstring and piriformis stretch, plank exercises and bird dog exercise
Not directed radiation to participant
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain intensity
Time Frame: At the beginning and at after 12 session (1 month)
|
By Visual Analogue Sclae (VAS)
|
At the beginning and at after 12 session (1 month)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pressure pain threshold
Time Frame: At the beginning and at after 12 session (1 month)
|
By pressure algometer
|
At the beginning and at after 12 session (1 month)
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Functional disability
Time Frame: At the beginning and at after 12 session (1 month)
|
By Oswestry index (Arabic version)
|
At the beginning and at after 12 session (1 month)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 3, 2023
Primary Completion (Actual)
April 28, 2023
Study Completion (Estimated)
March 28, 2024
Study Registration Dates
First Submitted
February 6, 2024
First Submitted That Met QC Criteria
February 14, 2024
First Posted (Actual)
February 16, 2024
Study Record Updates
Last Update Posted (Actual)
February 16, 2024
Last Update Submitted That Met QC Criteria
February 14, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HILT for SIJP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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.
Clinical Trials on Sacroiliac Joint Pain
-
SI-BONE, Inc.RecruitingSacroiliac Joint Pain | Sacroiliac Joint Dysfunction | Sacroiliac Disorder | Sacroiliac; FusionUnited States
-
Gaziler Physical Medicine and Rehabilitation Education...RecruitingSacroiliac Joint Somatic Dysfunction | Sacroiliac Joint PainTurkey
-
University Health Network, TorontoCompletedSacroiliac Joint Arthritis Causing Low Back PainCanada
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Logan College of ChiropracticCompletedSacroiliac Joint PainUnited States
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Riphah International UniversityCompletedSacroiliac Joint PainPakistan
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Samar Mimi Mohamed OkbyNot yet recruitingSacroiliac Joint Pain
-
Cairo UniversityCompletedSacroiliac Joint PainEgypt
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Avanos MedicalCompletedSacroiliac Joint PainUnited States
-
Johns Hopkins UniversityMilton S. Hershey Medical Center; United States Naval Medical Center, San Diego and other collaboratorsCompletedSacroiliac Joint PainUnited States
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Cairo UniversityNot yet recruitingPostpartum Sacroiliac Joint Pain
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