Mulligan's Mobilization and Proprioceptive Neuromuscular Facilitation Technique in Sacroiliac Joint Dysfunction
Primary Purpose
SACROILIAC JOINT DYSFUNCTION
Status
Recruiting
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
Mulligan Mobilization
PNF
Sponsored by
About this trial
This is an interventional treatment trial for SACROILIAC JOINT DYSFUNCTION focused on measuring Mulligan Mobilization, Proprioceptive Neuromuscular Facilitation, Contract Relax, Sacroiliac joint Dysfunction
Eligibility Criteria
Inclusion Criteria:
Age 20 to 35 years
- Both genders
- Subjects with positive provocation test ( Faber's test\Patricks test, Gaenslen test, distraction test, compression test, sacral thrust test)
- Subjects with positive innominate test ( Stork Test\Gillet Test)
- Subjects who agree to fill the informed consent
Exclusion Criteria:
Pregnant women
- Presence of neurological signs
- Patient with ankylosis spondylosis.
- Patient has been diagnosed by disease other than SIJ dysfunction
- Patients having any congenital posture problem or previous surgery
- SLR less than 45 degree
- Patient having any mental problem or reduced cognitive ability
Sites / Locations
- Govt. Hospital DHQRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Mulligan Mobilization
PNF Technique
Arm Description
Treatment will be given with frequency of 3 sets with 10 repetitions on sacroiliac joint 3 times a week for 6 weeks
Three sets of stretching of each muscle will be performed for each position with the frequency of 3 times a week for 6 weeks.
Outcomes
Primary Outcome Measures
Numeric Pain Rating scale
The most common validated tool for assessment of pain in clinical tests is the numeric pain rating score (NPRS), a 10-point scale where 0 indicates no pain and 10 indicates severe pain
Modified Oswestry Disability Questionnaire
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 questionnaire consists of 10 items addressing different aspects of function. Each item is scored from 0 to 5, with higher values representing greater disability. The total score is multiplied by 2 and expressed as a percentage
Secondary Outcome Measures
Full Information
NCT ID
NCT05356650
First Posted
April 26, 2022
Last Updated
April 26, 2022
Sponsor
Riphah International University
1. Study Identification
Unique Protocol Identification Number
NCT05356650
Brief Title
Mulligan's Mobilization and Proprioceptive Neuromuscular Facilitation Technique in Sacroiliac Joint Dysfunction
Official Title
Comparative Effects of Mulligan's Mobilization and Proprioceptive Neuromuscular Facilitation Technique on Pain and Disability in Patients With Sacroiliac Joint Dysfunction: A Randomised Controlled Trail
Study Type
Interventional
2. Study Status
Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 15, 2022 (Actual)
Primary Completion Date
August 15, 2022 (Anticipated)
Study Completion Date
September 15, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Riphah International University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study will aim to compare the effects of mulligan mobilization and PNF on pain and disability with patients of SIJ dysfunction and will be helpful for clinical physiotherapist to choose more effective treatment protocol for patients as there are fewer researches on comparison of these techniques.
Detailed Description
The sacroiliac joint dysfunction syndrome (SIJDS) is an ongoing controversial issue and an important source of low back pain (LBP). It has been emphasized in many studies that the pathologies of sacroiliac joint (SIJ) are a source of pain in the lumbar spine and hip region. The prevalence of SIJDS in patients with chronic mechanical LBP is between 15 and 30% SIJD is a condition in which pain arises from the sacroiliac joint and is caused by the abnormal movement of ilium around the sacrum and abnormal function of the SIJ structures, like ligaments, muscles, capsules. The prevalence of SIJP has been stated to be up to 75% in LBP patients.
Physiotherapy techniques are used to correct SIJ mal-alignment manually by restoring the normal function and balance of lumbar and pelvic muscles and ligaments. Mulligan described the positional fault theory in which articular mal-alignment leads to altered kinematics and eventual dysfunction(2). Proprioceptive neuromuscular facilitation (PNF) is a form of flexibility exercises used to resolve muscle shortening and strain.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
SACROILIAC JOINT DYSFUNCTION
Keywords
Mulligan Mobilization, Proprioceptive Neuromuscular Facilitation, Contract Relax, Sacroiliac joint Dysfunction
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
38 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Mulligan Mobilization
Arm Type
Experimental
Arm Description
Treatment will be given with frequency of 3 sets with 10 repetitions on sacroiliac joint 3 times a week for 6 weeks
Arm Title
PNF Technique
Arm Type
Experimental
Arm Description
Three sets of stretching of each muscle will be performed for each position with the frequency of 3 times a week for 6 weeks.
Intervention Type
Other
Intervention Name(s)
Mulligan Mobilization
Intervention Description
The patient will be in a prone position. With one hand, the physiotherapist will fix the sacrum and place the fingers of her other hand under the anterior superior iliac spine. The therapist then pull the ilium on the sacrum and will instruct the patient to do press-ups. Treatment will be given with frequency of 3 sets with 10 repetitions on sacroiliac joint 3 times a week for 6 weeks
Intervention Type
Other
Intervention Name(s)
PNF
Intervention Description
PNF stretching will be performed using contract-relax techniques of agonists in supine, prone and side-lying. Contract-relax will be applied with a 6-second contraction with 80% force of the maximal isometric contraction on the muscles (iliopsoas, hamstrings and gluteal muscles) and will be followed by a 15-second passive static stretching in the opposite direction of that muscles. Three sets of stretching of each muscle will be performed for each position with the frequency of 3 times a week for 6 weeks.
Patient will be in supine, prone, side lying. Both groups will receive a baseline treatment (Moist Heat Pack for 10 minutes and 10 minutes of Ultrasound (0.75 MHz, continuous wave)
Primary Outcome Measure Information:
Title
Numeric Pain Rating scale
Description
The most common validated tool for assessment of pain in clinical tests is the numeric pain rating score (NPRS), a 10-point scale where 0 indicates no pain and 10 indicates severe pain
Time Frame
3 months
Title
Modified Oswestry Disability Questionnaire
Description
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 questionnaire consists of 10 items addressing different aspects of function. Each item is scored from 0 to 5, with higher values representing greater disability. The total score is multiplied by 2 and expressed as a percentage
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Age 20 to 35 years
Both genders
Subjects with positive provocation test ( Faber's test\Patricks test, Gaenslen test, distraction test, compression test, sacral thrust test)
Subjects with positive innominate test ( Stork Test\Gillet Test)
Subjects who agree to fill the informed consent
Exclusion Criteria:
Pregnant women
Presence of neurological signs
Patient with ankylosis spondylosis.
Patient has been diagnosed by disease other than SIJ dysfunction
Patients having any congenital posture problem or previous surgery
SLR less than 45 degree
Patient having any mental problem or reduced cognitive ability
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nosheen Manzoor
Phone
03236877879
Email
nosheen.manzoor@riphahfsd.edu.pk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nosheen Manzoor
Organizational Affiliation
Riphah International University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Govt. Hospital DHQ
City
Jhang
State/Province
Punjab
ZIP/Postal Code
38000
Country
Pakistan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nosheen Manzoor
Phone
03236877879
Email
Nosheenmanzoor_444@yahoo.com
First Name & Middle Initial & Last Name & Degree
Aisha Waseem
12. IPD Sharing Statement
Plan to Share IPD
No
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Mulligan's Mobilization and Proprioceptive Neuromuscular Facilitation Technique in Sacroiliac Joint Dysfunction
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