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

Sponsor
Riphah International University (Other)
Overall Status
Completed
CT.gov ID
NCT05076136
Collaborator
(none)
64
1
2
11.6
5.5

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Regional treatment
  • Other: Standard physiotherapy treatment
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
64 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Comparison of Regional Manual Therapy and Standard Physical Therapy Intervention in Females With Sacroiliac Joint Pain.
Actual Study Start Date :
Nov 24, 2019
Actual Primary Completion Date :
Oct 10, 2020
Actual Study Completion Date :
Nov 10, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Regional treatment

Group A was given regional treatment with baseline treatment protocol

Other: Regional treatment
In reginal treatment patients were given physiotherapy exercises and manual therapies on hip joint as well as on surrounding areas of hip joint such as lumber area and sacroiliac joint.

Active Comparator: Standard physiotherapy treatment

Group B was given standard physiotherapy treatment with baseline protocol

Other: Standard physiotherapy treatment
In this treatment patients were given just hip joint mobilizations and quadriceps and hamstrings stretching.

Outcome Measures

Primary Outcome Measures

  1. NPRS [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.

  2. Oswestry low back disability questionnaire [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

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 50 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Bajwa hospital Lahore Punjab Pakistan 57000

Sponsors and Collaborators

  • Riphah International University

Investigators

  • Study Chair: Tasneem Shahzadi, Mphil, Riphah international university Lahore

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Riphah International University
ClinicalTrials.gov Identifier:
NCT05076136
Other Study ID Numbers:
  • REC/RCRS/20/1017
First Posted:
Oct 13, 2021
Last Update Posted:
Oct 13, 2021
Last Verified:
Sep 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 13, 2021