- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05352360
Comparison of Pilates Exercises Verses Muscle Energy Techniques Along With Kinesio Taping in Non-Specific Low Back Pain
April 24, 2022 updated by: Muhammad Naveed Babur, Superior University
To Compare the effects of Pilates Excercises versus muscle energy technique along with kinesiotaping in non specific low back pain.
Study Overview
Status
Enrolling by invitation
Intervention / Treatment
Detailed Description
This study will help to compare the effects of pilates Exercises with kinesiotaping and on other hand the effects of muscle energy technique with kinesiotaping for improving pain, disability and Range of Motion in patient with non specific low back pain.
By combining these interventions, time consumption for treatment and disability among community due to low back pain will be reduced.
This treatment will be effective for participants for improving function, movement of joints and muscle to manage and treat low back pain.
The combination of treatment will be more effective to relief non specific low back pain.
The targeted population of 18-40 years old and most of them are having occupational related low back pain or due to bad posture, study will have an impact in improving and managing the low back pain in such population.
Study Type
Interventional
Enrollment (Anticipated)
42
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
-
-
Punjab
-
Lahore, Punjab, Pakistan
- Chaudhary Muhammad Akram Teaching and research hospital, Jinnah Hospital Lahore and Mayo Hospital Lahore
-
-
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
14 years to 36 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Subjects of both genders should present with non-specific low back pain and between 18 and 40 years of age.(21)
- Could maintain their standing posture independently for _>30s.
- Patient having enough physical autonomy to participate in the physical activities required by the study.
- The patient having a visual analog scale (VAS) score of equal to or >3 will be included.(16).
Exclusion Criteria:
- A history of spinal surgery, compression fracture, spondylolisthesis, or sciatica, ongoing pregnancy, experiencing hypertension, cardiovascular disease, diabetes mellitus, liver disease, renal disease, rheumatoid arthritis, or other rheumatologically related pathologies (8).
- Those taking corticosteroids 2 weeks before recruitment.
- Hypersensitivity to the tape(6).
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: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Pilates Exercises with kinesiotaping
|
Exercises with Kinesio Taping
|
|
Experimental: Muscle energy technique with kinesiotaping
|
Exercises with Kinesio Taping
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pilates Exercises Verses Muscle Energy Techniques Along with Kinesio Taping
Time Frame: 6 Months
|
Comparison of both type of exercises for Non-Specific Low Back Pain
|
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 (Actual)
March 31, 2022
Primary Completion (Anticipated)
June 1, 2022
Study Completion (Anticipated)
September 1, 2022
Study Registration Dates
First Submitted
April 14, 2022
First Submitted That Met QC Criteria
April 24, 2022
First Posted (Actual)
April 28, 2022
Study Record Updates
Last Update Posted (Actual)
April 28, 2022
Last Update Submitted That Met QC Criteria
April 24, 2022
Last Verified
April 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DPT/Batch-Fall17/517
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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