High-intensity Laser Therapy for Sacroiliac Joint Pain

Sacroiliac Joint Pain Clinical Trial

— Girls  

Official title:

Effect of High Intensity Laser on Sacroiliac Joint Pain In Adult Women

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT06262763
• Other study ID #: HILT for SIJP
• Status: Active, not recruiting
• Phase: N/A
• Start date: January 3, 2023
• Est. completion date: March 28, 2024

Study information

• Verified date: February 2024
• Source: Kafrelsheikh University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Effect of high intensity laser on sacroiliac joint pain

Description:

Effect of high laser in reduction of pain and improve functional disability in adult women

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 30
• Est. completion date: March 28, 2024
• Est. primary completion date: April 28, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 30 Years

Eligibility

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.

Related Conditions & MeSH terms

• Arthralgia
• Sacroiliac Joint Pain

Intervention

Device:
• Laser Therapy
High-intensity

Other:
• Traditional exercises
Hamstring and piriformis stretch, plank exercises and bird dog exercise
• Placebo laser
Not directed radiation to participant

Locations

Country	Name	City	State
Egypt	Kafr Al-Sheikh University	Kafr Ash Shaykh

Sponsors (1)

Lead Sponsor	Collaborator
Kafrelsheikh University

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Functional disability	By Oswestry index (Arabic version)	At the beginning and at after 12 session (1 month)
Primary	Pain intensity	By Visual Analogue Sclae (VAS)	At the beginning and at after 12 session (1 month)
Secondary	Pressure pain threshold	By pressure algometer	At the beginning and at after 12 session (1 month)