- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05421871
Comparison of Spinal Stabilization Exercises Vs Maitland Mobilization Along With Laser Therapy
June 14, 2022 updated by: Muhammad Naveed Babur, Superior University
Comparison of Spinal Stabilization Exercises Vs Maitland Mobilization Along With Laser Therapy in Non-Specific Low Back Ache
Comparison of Spinal Stabilization Exercises Vs Maitland Mobilization Along with Laser Therapy in Non-Specific Low Back Ache
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Comparison of Spinal Stabilization Exercises Vs Maitland Mobilization Along with Laser Therapy for finding the better method for the treatment of Non-Specific Low Back Ache
Study Type
Interventional
Enrollment (Anticipated)
52
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 Contact
- Name: Areeba Touseef, DPT
- Phone Number: +923349867317
- Email: areebatoseef@gmail.com
Study Locations
-
-
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Lahore, Pakistan
- Al-Zahra Medical complex Johar town, Laser spine center Model town, Laser spine center Johar town.
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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
18 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Both male and female within the age range of 18-60 years.
- Visual analogue scale that scores 3 and higher.
- Non radiating low back pain
Exclusion Criteria:
- Patients with a history of spinal diseases and injury
- Spinal stenosis
- Degenerative changes
- Neuropathy
- Intervertebral disc collapse.
- Spinal discectomy
- Spinal laminectomy
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: Diagnostic
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Spinal Stabilization Exercises
Spinal Stabilization Exercises technique
|
Spinal Stabilization Exercises technique
|
|
Experimental: Maitland Mobilization Along With Laser Therapy
Maitland Mobilization Along With Laser Therapy technique
|
Maitland Mobilization Along With Laser Therapy technique
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Spinal Stabilization Exercises in Non-Specific Low Back Ache
Time Frame: 6 Months
|
26 participants with the exercises include double knee to chest, single knee to chest, pelvic tilting,bridging and hamstring muscle stretching.(2)
The stabilization exercises will be performed for 25 minutes.
The patients will be educated on correct posture and starting positions for their exercises.
Roland-Morris disability questionnaire to check the ovelall condition.
|
6 Months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Maitland Mobilization Along with Laser Therapy in Non-Specific Low Back Ache
Time Frame: 6 Months
|
26 participants with the most commonly used Maitland technique is central posterior-anterior mobilization in which the therapist will perform 4 sets of mobilization for 30 seconds in grade I which will be administered to the three spinous processes around the most painful areas which will be followed by grade II with a rest interval of 30 seconds.
Roland-Morris disability questionnaire to check the ovelall condition.
|
6 Months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Anticipated)
June 1, 2022
Primary Completion (Anticipated)
August 1, 2022
Study Completion (Anticipated)
November 1, 2022
Study Registration Dates
First Submitted
May 5, 2022
First Submitted That Met QC Criteria
June 14, 2022
First Posted (Actual)
June 16, 2022
Study Record Updates
Last Update Posted (Actual)
June 16, 2022
Last Update Submitted That Met QC Criteria
June 14, 2022
Last Verified
June 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DPT/Batch-Fall17/509
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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