Muscle Energy Technique and Kinesiotaping in Mechanical Sacroiliac Joint Dysfunction

June 17, 2020 updated by: Asir John Samuel

Efficacy of Muscle Energy Technique and Kinesiotape Application in Addition to Other Physiotherapeutic Intervention in Patients With Mechanical Sacroiliac Joint Dysfunction

Background:

Mechanical sacroiliac joint dysfunction is associated with pain and stiffness which can later on gives restriction of overall motion. Total 60% of the body weight is mainly received by the sacroiliac joint and it is related with pelvis and lower extremity. Due to Bio- mechanical alteration muscles around the joint area get weakened.Muscle energy technique helps to improve body's normal function by giving strength as well as decrease pain and stiffness and Kinesiotaping also helps to stabilize the joint structure by giving more functional benefit.

Aim:

The Aim of the study is to evaluate the efficacy of Muscle energy technique & Kinesiotaping in addition to other physio-therapeutic intervention in patients with Mechanical Sacroiliac joint Dysfunction.

Methods:

This study is a randomized clinical trial and subjects will recruit on the basis of inclusion criteria. Age group between 30 to 50 years of mechanical sacroiliac joint dysfunction patients will be taken. Any pathological condition like inflammation of sacroiliac joint and fracture of pelvic bone will be excluded. Patient will be randomized on the basis of SNOSE method. After randomization in two equal group treatment will be given and data will be analyzed separately. One Experimental group will receive Muscle energy technique and conventional physiotherapy and another experimental group will receive Kinesiotaping and conventional physiotherapy. Modified Oswestry Disability Index helps to evaluate functional limitation associated with Mechanical Sacroiliac joint Dysfunction.

Data Analysis:

Normality of the collected data will be established by Shapiro wilk test. Based on the normality, descriptive statistics data will be expressed as mean± standard deviation or median and intra-quartile range. Within group comparison will be calculated by paired-t test or Wilcoxon Signed Rank test and between group comparison will be done through Independent-t test or Mann-Why U test. P value will be set at significance level(0.05).

Study Overview

Detailed Description

  1. Introduction:

    Mechanical Sacroiliac joint dysfunction (SIJD) is the most common source of low back pain and affects 70-85% adults. It is also associated with groin & buttock pain and sometime also leg pain. Non discogenic pain can also be occur due to dysfunction around Sacroiliac Joint. Sacroiliac joint dysfunction also called as pelvic girdle pain (PGP), which arises from several intra-articular structures, anterior sacroiliac ligament, posterior sacroiliac ligament, articular cartilages. Sacroiliac joint pain is one of the common sources of mechanical low back pain. This may lead to bio-mechanical alteration in structure around pelvis.Where as Muscle Energy Technique(MET) involves physiological response of the antagonists of a muscle which has been isometrically contracted. Mainly MET is a soft tissue manipulation which include force generated by the patient may be maximum muscle contraction are twitch of the muscle. Where as functional stability as well as mobility can be achieved by Kinesiotape application.

    1.1: Problem statement:

    Mainly sacroiliac joint dysfunction associated with altered arthokinematics due to muscle weakness. Kinesiotaping and MET will be helpful if they are used with conventional physiotherapy. Thus there is need to find out the efficacy of MET and Kinesiotaping in addition to conventional physiotherapy in patients with mechanical SIJD.

    1.2:Purpose of the study:

    The purpose of the study is to find out the efficacy of MET and Kinesiotaping in addition to conventional physiotherapy in patients with mechanical sacroiliac joint dysfunction.

    1.3: Objectives of the study:

    1.3.1:To determine the effect of MET and Kinesiotaping in addition to conventional physiotherapy in patients with Mechanical Sacroiliac joint Dysfunction. 1.3.2:To compare the effect of MET &Kinesiotaping in patients with Mechanical Sacroiliac joint dysfunction.

  2. Procedure:

The study will be a Two group pre test post test Randomized clinical trial. The study protocol has been approved from the Institutional Ethics Committee of Maharishi Markandeshwar Deemed to be University.

MET Application: MET will be used with conventional treatment in Experimental Group 1. MET will be applied for posterior and anterior in-nominate and for weakened muscles like piriformis.

Here patient will be asked to apply 20% force against therapist force and hold that contraction for 10 seconds with 3-5 repetitions.The treatment will be given for 3 times a week and continued for 4 weeks.

Kinesiotaping will be given with conventional physiotherapy in Experimental Group 2. In this group KT will be applied to piriformis muscle and Sacroiliac joint (SIJ).

For piriformis application patient will be in side lying position where the effected leg will be placed uppermost with hip in flexion, adduction, and internal rotation and Y strips will be used & treatment will be given for 4 weeks with 3 alternative days in a week.

Conventional Physiotherapy will be given in both the groups. Before going for intervention Hydrocollator pack will be given in both the groups for at least 15 minutes.

Study Type

Interventional

Enrollment (Actual)

30

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 Locations

    • Haryana
      • Ambala, Haryana, India, 133207
        • Maharishi Markandeshwar Hospital, Mullana

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

28 years to 48 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Pain in the low back, buttock and groin area
  • Restricted Sacroiliac joint motion as tested by clinical tests (Standing Flexion & Sitting Flexion test)
  • Leg pain more than 4 weeks but less than 1 year

Exclusion Criteria:

  • Inflammation in sacroiliac joint like sacroilitis
  • Pregnancy
  • Pelvic bone Fractures
  • Metallic implants (endoprostheses) in pelvis
  • Malignancy
  • Inflammatory bowel disease

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Muscle Energy Technique and Conventional Physiotherapy
Muscle Energy Technique will be given with conventional physiotherapy for 3 days per week and will be continue for 4 weeks, where each session of Muscle Energy Technique will be repeated for 3-5 repetitions.

Muscle energy technique will be given in two different position. For anterior in- nominate rotation and posterior in- nominate rotation patient position will be in supine lying position.

For weakened muscle,piriformis application the patient should be side-lying position, close to the edge of the table, affected side uppermost, both legs flexed at hip and knee.

The therapists stand facing the patient at hip level,then patient should be close enough to the edge of the table for the therapist to stabilize the pelvis against his trunk. The angle of hip flexion should not exceed 60°, and then places one hand on the contralateral ASIS to prevent pelvic motion, while the other hand is placed against the lateral flexed knee as this is pushed into resisted abduction to contract piriformis.

Isometric contraction should be hold for 3-5 second and that particular method will be repeated for 7-10 times.

Hydro-collator pack will be used superior to the affected area for at-least 15 minute to reduce the stiffness. Hydocollator pack will be wrap twice with a thick towel and then it will be placed to the affected part.
Experimental: Kinesiotaping and Conventional Physiotherapy
Kinesiotape application will be given with conventional physiotherapy for 3 days per week and will be continue for 4 weeks
Hydro-collator pack will be used superior to the affected area for at-least 15 minute to reduce the stiffness. Hydocollator pack will be wrap twice with a thick towel and then it will be placed to the affected part.

Kinesiotaping will be applied to piriformis muscle and Sacroiliac joint (SIJ). This tape will be applied in I shape to both sides of the spine from sacrum to Anterior Superior Iliac Spine. For SIJ taping same 5 cm KT tape will be used, it will be applied from below posterior sacroiliac spine to opposite side. Here patient should be in standing position.

For Piriformis application patient will be in side lying position where the affected leg will be placed uppermost with hip in flexion, adduction, and internal rotation , then the application will be performed. The base of the tape will be placed over contralateral part of sacrum and then make a Y strip with no tension will be attached over the greater trochanter of femur.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Digitalized Pain Pressure Algometer
Time Frame: 2 weeks
It is an important tool for measuring pain pressure threshold level
2 weeks
Hand Held Dynamometer
Time Frame: 2 weeks
It is useful tool for calculating muscle strength of lower extremity
2 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Modified Oswestry Disability Index
Time Frame: 2 weeks

It is an extremely important tool used to measure a patients permanent functional disability. The total score ranges from 0-50. For each section total possible score is 5.

0-20%- Minimal disability 20-41%-Moderate disability 41-60%-Severe disability 61-80%-Crippled 81-100%-Bed bound

2 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Manisha Sarkar, BPT, (MPT), Department of Musculoskeletal Physiotherapy, MMIPR

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Shinde M, Jagtap V. Effect of Muscle Energy Technique and Mulligan Mobilization in Sacroiliac Joint Dysfunction. Glob J Res Anal. 2018;(3):79-81.
  • Society TK, Therapy P, Journal T, Therapy KP, Ther KP, Scholar G, et al. The effects of spinal decompression therapy on pain and disability in patients with chronic low back pain. J Korean Phys Ther. 2017;29(6).

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)

September 1, 2019

Primary Completion (Actual)

March 18, 2020

Study Completion (Actual)

March 19, 2020

Study Registration Dates

First Submitted

May 1, 2019

First Submitted That Met QC Criteria

May 4, 2019

First Posted (Actual)

May 7, 2019

Study Record Updates

Last Update Posted (Actual)

June 18, 2020

Last Update Submitted That Met QC Criteria

June 17, 2020

Last Verified

June 1, 2020

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • MMDU/IEC/1370
  • U1111-1232-1305 (Other Identifier: UTN by WHO International Clinical Trial Registry Platform)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

It is not yet decided

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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