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Gluteus Maximus Versus Gluteus Medius Strength On Back Muscles Performance In Patients With Sacroiliac Dysfunction

Primary Purpose

Sacroiliac Joint Dysfunction

Status
Not yet recruiting
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Glutes maximus strength protocol
Gluteus medius strength program
Corrective Exercises
Ultrasound
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sacroiliac Joint Dysfunction

Eligibility Criteria

25 Years - 40 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Age from 25-40 years. Patients with chronic lumbopelvic pain (more than 12 weeks) and clinical test positive for SIJD. The pain distribution and tenderness on palpation under the posterior superior iliac spine (PSIS) are reliable signs that the SIJ is the source of pain. Complaint of unilateral pain rather than bilateral pain is also considered more likely to be coming from an SIJ. Patients willing and able to participate in an exercise program safely and without cognitive impairments that would limit their participation. Exclusion Criteria: Neurological disorder, psychosomatic disorder Tumor. Infection condition. Recent surgeries. Pregnancy. Back pain referred from organic cause. Osteoporosis and bone disease (induced or idiopathic).

Sites / Locations

  • Outpatient clinic faculty of physica therapy cairo university

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Glutes maximus Strengthening group

Glutes Medius Strengthening group

Conventional treatment group

Arm Description

Twenty patients received Strengthening exercises for Glutes maximus muscle and conventional physical therapy (corrective exercises and ultrasound).

Twenty patients received Strengthening exercises for Glutes medius muscle and conventional physical therapy (corrective Exercises and therapeutic ultrasound (US).

Twenty Patients received conventional therapy (corrective exercises and ultrasound).

Outcomes

Primary Outcome Measures

Assessing the change in the peak torque of back muscles
By using isokinetic dynamometer, and the unit of of measurement will be (Kg).
Assessing the change in pain threshold
by using Traditional pressure algometers are ideal for measuring pressure pain threshold (PPTs) of superficial muscles and bony landmarks. Pressure pain threshold has been defined as the lowest stimulus intensity at which a subject perceives mechanical pain
Assessing the change in Functional ability level
By using Modified Oswestry Disability Questionnaire (MODQ). The Oswestry Low Back Pain Disability Questionnaire Arabic version will be used to measure disability caused by low back pain in the general population. It consists of 10 questions each consisting of six alternatives. Every question is scored from 0-5 and a percentage are formulated as a result of the sum of the scores.
Assessing the change in pain intensity
By using visual analogue scale (VAS). This scale will be used to measure the intensity of pain. It has been graded as a 10-cm line, which was used for measuring the intensity of perceived pain. In this scale, zero represents the absence of pain, 1-3 shows mild pain, 4-6 denotes moderate pain, and 7-10 indicates severe pain

Secondary Outcome Measures

Full Information

First Posted
March 17, 2023
Last Updated
March 30, 2023
Sponsor
Cairo University
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1. Study Identification

Unique Protocol Identification Number
NCT05809206
Brief Title
Gluteus Maximus Versus Gluteus Medius Strength On Back Muscles Performance In Patients With Sacroiliac Dysfunction
Official Title
Gluteus Maximus Versus Gluteus Medius Strength On Back Muscles Performance In Patients With Sacroiliac Dysfunction
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
April 10, 2023 (Anticipated)
Primary Completion Date
June 15, 2023 (Anticipated)
Study Completion Date
August 15, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo 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 be conducted to compare between the effect of glutes maximus and glutes medius muscles strength on back muscle performance in patients with Sacroiliac joint dysfunction.
Detailed Description
The purposes of this study are: To investigate the effect of Gluteus maximus strengthening exercises and Gluteus medius strengthening exercises on back pain in patient with Sacroiliac joint dysfunction To investigate the effect of Gluteus maximus strengthening exercises and Gluteus medius strengthening exercises on back muscle performance in patients with Sacroiliac joint dysfunction To investigate the effects of Gluteus maximus strengthening exercises and Gluteus medius strengthening exercises on function in patient with Sacroiliac joint Dysfunction

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sacroiliac Joint Dysfunction

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Glutes maximus Strengthening group
Arm Type
Experimental
Arm Description
Twenty patients received Strengthening exercises for Glutes maximus muscle and conventional physical therapy (corrective exercises and ultrasound).
Arm Title
Glutes Medius Strengthening group
Arm Type
Experimental
Arm Description
Twenty patients received Strengthening exercises for Glutes medius muscle and conventional physical therapy (corrective Exercises and therapeutic ultrasound (US).
Arm Title
Conventional treatment group
Arm Type
Active Comparator
Arm Description
Twenty Patients received conventional therapy (corrective exercises and ultrasound).
Intervention Type
Other
Intervention Name(s)
Glutes maximus strength protocol
Intervention Description
The subjects attended physical therapy two times. Per week for a total of 10 visits. Each session lasted approximately 30 minutes. In the first five sessions, subjects performed the following exercises to strengthen the gluteus maximus: bilateral bridge, unilateral bridge, and non-weight-bearing hip extension in prone with the knee flexed at 90 degrees. In the next five sessions, abduction and external rotation in a quadruped ("fire hydrant" exercise) and weight-bearing hip extension (known as "deadlift" exercise) were added. Each exercise was performed for 10 repetitions. Elastic resistance was added to the fire hydrant, hip extension in prone and dead lift exercises to allow each subject to perform at a 10-repetition maximum. The resistance for each subject was adjusted weekly as needed. The exercise program was performed under direct supervision only during the physical therapy sessions.
Intervention Type
Other
Intervention Name(s)
Gluteus medius strength program
Intervention Description
Strengthening exercises for Gluteus Medius subdivisions: The anterior GMED exercise: side lying abduction exercise The middle GMED exercise: wall press Exercise The posterior GMED exercise: was the pelvic drop exercise
Intervention Type
Other
Intervention Name(s)
Corrective Exercises
Intervention Description
The following low back corrective exercises were given: To stretch the tight lower back muscles: Seated Forward Bend and Full Squat held for 5 sec and Repeated for 3 times, once a day. To strengthen the weak lower abdomen: Draw in and Reverse Crunch 3 seconds, repeated 5 times, once a day. To stretch the tight hip flexors: held for 10-15 seconds repeated 5 times on both legs, once a day. To stretch the tight quadriceps: held for 3 seconds, repeated 5 times on each side, once a day. To strengthen weak hamstrings: Kick Butts 2 sec, repeated 8 times, once a day.
Intervention Type
Device
Intervention Name(s)
Ultrasound
Intervention Description
US was administered in continuous mode at PSIS with patient in prone lying position, with a frequency of 1 MHz and intensity of 0.8 W/cm2 for 5 minutes every alternating day
Primary Outcome Measure Information:
Title
Assessing the change in the peak torque of back muscles
Description
By using isokinetic dynamometer, and the unit of of measurement will be (Kg).
Time Frame
at baseline and after 5 weeks of intervention
Title
Assessing the change in pain threshold
Description
by using Traditional pressure algometers are ideal for measuring pressure pain threshold (PPTs) of superficial muscles and bony landmarks. Pressure pain threshold has been defined as the lowest stimulus intensity at which a subject perceives mechanical pain
Time Frame
at baseline and after 5 weeks of intervention
Title
Assessing the change in Functional ability level
Description
By using Modified Oswestry Disability Questionnaire (MODQ). The Oswestry Low Back Pain Disability Questionnaire Arabic version will be used to measure disability caused by low back pain in the general population. It consists of 10 questions each consisting of six alternatives. Every question is scored from 0-5 and a percentage are formulated as a result of the sum of the scores.
Time Frame
at baseline and after 5 weeks of intervention
Title
Assessing the change in pain intensity
Description
By using visual analogue scale (VAS). This scale will be used to measure the intensity of pain. It has been graded as a 10-cm line, which was used for measuring the intensity of perceived pain. In this scale, zero represents the absence of pain, 1-3 shows mild pain, 4-6 denotes moderate pain, and 7-10 indicates severe pain
Time Frame
at baseline and after 5 weeks of intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age from 25-40 years. Patients with chronic lumbopelvic pain (more than 12 weeks) and clinical test positive for SIJD. The pain distribution and tenderness on palpation under the posterior superior iliac spine (PSIS) are reliable signs that the SIJ is the source of pain. Complaint of unilateral pain rather than bilateral pain is also considered more likely to be coming from an SIJ. Patients willing and able to participate in an exercise program safely and without cognitive impairments that would limit their participation. Exclusion Criteria: Neurological disorder, psychosomatic disorder Tumor. Infection condition. Recent surgeries. Pregnancy. Back pain referred from organic cause. Osteoporosis and bone disease (induced or idiopathic).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Reham Abd El-Moneim
Phone
+201006722789
Email
Rehamgomma.88@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Reham Abd El-Moneim
Organizational Affiliation
Cairo University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Outpatient clinic faculty of physica therapy cairo university
City
Dokki
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Gluteus Maximus Versus Gluteus Medius Strength On Back Muscles Performance In Patients With Sacroiliac Dysfunction

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