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

  • Egypt
      • 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
Device: Laser Therapy
High-intensity
Other Names:
  • High power
Other: Traditional exercises
Hamstring and piriformis stretch, plank exercises and bird dog exercise
Placebo Comparator: Group (B)
Placebo LASER with traditional exercises
Other: Traditional exercises
Hamstring and piriformis stretch, plank exercises and bird dog exercise
Other: Placebo laser
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

Kafrelsheikh University

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.

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