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Clinical Trials/NCT05347537
NCT05347537
Completed
Not Applicable

Effects of Mulligan's Mobilization With and Without Clamshell Exercise on Pain, Disability and Quality of Life in Patients With Sacroiliac Joint Dysfunction

Riphah International University1 site in 1 country36 target enrollmentApril 27, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sacroiliac Joint Somatic Dysfunction
Sponsor
Riphah International University
Enrollment
36
Locations
1
Primary Endpoint
1. NPRS
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Sacroiliac joint dysfunction is the changing of joint structure (ligaments, muscles and cartilage) that cause impairments and movement restrictions. It is one of the primary sources of low back pain among female population and often misdiagnosed. Almost 15-30% patients are suffering from sacroiliac joint dysfunction who presented with the complaint of low back pain. The aim of the study is to determine the effect of mulligan's mobilization with and without clamshell exercise on pain, disability and quality of life in patients with sacroiliac joint dysfunction.

Detailed Description

A Randomized controlled trial will be conducted at Fatima Memorial Hospital Physiotherapy Clinic \& Boston Physiotherapy and wellness Clinic through consecutive sampling technique on 32 patients which will be allocated through simple random sampling through sealed opaque enveloped into group A \& group B. Group A will be treated with only mulligan's mobilization with movement at the frequency of 3 sets with 10 repetitions 3 times/ week without the clamshell exercise. Group B will be treated with mulligan's mobilization with movement and clamshell exercises. Outcome measures will be conducted through pain, disability and quality of life questionnaire after 6 weeks. Data will be analyzed during SPSS software version 21. After assessing normality of data by Shapiro Wilk test, it will be decided either parametric or non-parametric test will be used within a group or between two groups.

Registry
clinicaltrials.gov
Start Date
April 27, 2022
End Date
October 15, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Male and female between the ages of 20 to 50 years with positive Leslett's criteria.
  • Sacroiliac pain of sub-acute level with the duration of 4 weeks

Exclusion Criteria

  • Spondylosis
  • Lumbar canal stenosis
  • Spondylolisthesis
  • Pervious spinal surgery
  • Congenital postural deformities and
  • Lumbar disc herniation
  • Pelvic bone fractures

Outcomes

Primary Outcomes

1. NPRS

Time Frame: follow up at 6th week

Patient level of pain was assessed using this scale. This scale ranges from 0 to 10. 0 indicates "no pain" and 10 indicates "worst pain"

2. Oswestry Disability index (NDI)

Time Frame: follow up at 6th week

It comprises 10 items, 7 related with daily activities, 2 related to pain , 1 related to concentration. Each item scores from 0 to 5. Total score is expressed as percentage with higher scores related to greater disability.

Euro Quality of life (EQ-5D)

Time Frame: follow up at 6th week

Quality of life will be checked by Euro Quality of life (EQ-5D) Health Related Quality of Life Question.

Study Sites (1)

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