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Clinical Trials/NCT06442540
NCT06442540
Recruiting
Not Applicable

Effects of Intra Muscular Electrotherapy Combined With Manipulative Therapy in Patients With Sacral Torsion

Foundation University Islamabad1 site in 1 country32 target enrollmentJuly 15, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sacroiliac Joint Dysfunction
Sponsor
Foundation University Islamabad
Enrollment
32
Locations
1
Primary Endpoint
Pain Intensity
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

This study is a randomised controlled trial and the purpose of this study is to determine the effect of intra muscular electrotherapy combined with manipulative therapy in terms of pain, mobility, range of motion, and disability."

Detailed Description

The purpose of this study is to determine the effect of intra muscular electrotherapy combined with manipulative therapy in terms of pain, mobility, range of motion, and disability in patients with sacral torsion." (age : 22-44 years ) 1. Numeric pain rating scale 2. Inclinometer Lumbar Flexion 3. Oswestry Disability Questionairre 4. Goniometer SLR ROM Data will be collected before and after the intervention protocol for each participant. Data collection procedure: Participants of interest would be approached and explained about the research. Informed written consent will be taken. Pre and post intervention scores will be recorded.

Registry
clinicaltrials.gov
Start Date
July 15, 2023
End Date
June 20, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Pain Intensity

Time Frame: 4 weeks

Numeric Pain Rating Scale (NPRS): ICC (0.93-0.96) It has a scale of 0-10 or 0-100 points and can be given verbally or in writing

Lumbar ROM

Time Frame: 4 weeks

Lumbar ROM will be measured using Inclinometer

SLR ROM

Time Frame: 4 weeks

SLR ROM will be measured using Goniometer

Level of Disability

Time Frame: 4 Weeks

Oswestry disability questionairre

Study Sites (1)

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