Effectiveness of McKenzie and Trochanteric Belt With CT Therapy to Reduce Pain and Dysfunction of SI Joint

May 16, 2023 updated by: Muhammad Naveed Babur, Superior University

Effectiveness of McKenzie Exercises and Trochanteric Belt With Conventional Physical Therapy to Reduce Pain and Dysfunction of SI Joint in Pregnant Women

To determine the effectiveness of McKenzie exercises and trochanteric belt with conventional physical therapy to reduce pain and dysfunction of Sacroiliac joint (SIJ) in pregnant women

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

to findout the effectiveness of exercises in pregnant women

Study Type

Interventional

Enrollment (Anticipated)

40

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 Contact

Study Locations

  • Pakistan
      • Lahore, Pakistan
        • Recruiting
        • • General Hospital. • Chaudhary Muhammad Akram Teaching and Research Hospital, University of Lahore Teaching Hospital, Shadman Medical Center, Services Hospital, Bahria International Hospital

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:

  • Pregnant patients with sacroiliac joint pain are included and participant patients with age group 18- to 35
  • low back pain due to sacroiliac joint who suffer from sever pain during sitting and during positioning change when stand from sitting position are included

Exclusion Criteria:

  • Patients with age group of below 18 years and above 35 years
  • Patients with disease of coagulopathy
  • systemic infection
  • skin infection over sacroiliac joint patients with history of allergies to injected medications.
  • Patients with psoriasis
  • inflammatory bowel disease
  • peripheral arthritis
  • Women with UTI complications are excluded.
  • Women with respiratory issues are also excluded

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: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: McKenzie exercise
Behavioral: McKenzie exercise
routine simple McKenzie exercise
Other: Trochanteric belt
Diagnostic test: Trochanteric belt
Trochanteric belt with conventional physical therapy

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
feature of Visual analogue scale to check pain and feature PSFS to check Movement of joints
Time Frame: 6 Months
Pre and Post interventions using VAS, PDFS
6 Months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Superior University

Investigators

  • Study Chair: Abdul Wahab, Superior Uni

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)

April 1, 2023

Primary Completion (Anticipated)

June 1, 2023

Study Completion (Anticipated)

August 31, 2023

Study Registration Dates

First Submitted

March 18, 2023

First Submitted That Met QC Criteria

May 16, 2023

First Posted (Actual)

May 18, 2023

Study Record Updates

Last Update Posted (Actual)

May 18, 2023

Last Update Submitted That Met QC Criteria

May 16, 2023

Last Verified

May 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • DPT/Batch-Fall18/524

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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