Skip to main content
Clinical Trials/NCT05076136
NCT05076136
Completed
Not Applicable

Comparison of Regional Manual Therapy and Standard Physical Therapy Intervention in Females With Sacroiliac Joint Pain.

Riphah International University1 site in 1 country64 target enrollmentNovember 24, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sacroiliac; Sprain (Strain)
Sponsor
Riphah International University
Enrollment
64
Locations
1
Primary Endpoint
NPRS
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The SIJ has long been considered an important source of low back pain because of the empirical finding that treatment targeting the SIJ can relieve pain.This study was be a Randomized Clinical Trail conducted at Riphah Rehabilitation Centre Lahore. The study was be completed within the time duration of Six months. Purposive sampling technique was be used. Sample size is calculated by using the G power 3.1. The sample size of 64 patients was be taken in this study to find the comparison of regional manual therapy and standard physiotherapy intervention in females with sacroiliac joint pain. Patients was be divided into two groups.. Patients was be divided into two groups. Group A was be treated with regional manual therapy. In regional manual therapy patients was be given mobilization to lumber region and SIJ, pelvic floor exercises and core strengthening exercises and Group B was be treated with standard physiotherapy in which patients was be given SIJ mobilization and Straight leg raise. Both groups was receive transcutaneous electrical nerve stimulator and heating pad as a common treatment protocol. Numeric pain rating scale (NPRS) and oswestry low back disability questionnaire was be used as Data collecting tools. Two session of treatment per week for eight weeks was be given. Data was be analyzed on SPSS 21.

Registry
clinicaltrials.gov
Start Date
November 24, 2019
End Date
November 10, 2020
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Females with sacroiliac joint pain
  • Age: 20 to 50 years

Exclusion Criteria

  • Patients withany red flag signs i.etumor, fracture, metabolic diseases, rheumatoid arthritis, prolonged history of steroids use, etc.
  • Females with sciatica
  • Females with radiating pain

Outcomes

Primary Outcomes

NPRS

Time Frame: Eight week

The NPRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain.

Oswestry low back disability questionnaire

Time Frame: Eight week

The Oswestry Disability Index (also known as the Oswestry Low Back Pain Disability Questionnaire) is an extremely important tool that researchers and disability evaluators use to measure a patient's permanent functional disability. The test is considered the 'gold standard' of low back functional outcome tools

Study Sites (1)

Loading locations...

Similar Trials