- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05502419
Effects of Neural Slump Mobilization in Addition to Conventional Physical Therapy in Low Back Pain
August 14, 2022 updated by: Foundation University Islamabad
Low back pain is amongst the most prevalent musculoskeletal conditions worldwide.This condition has a significant impact on the person's quality of life by effecting their various activities of daily living.
As of 2017 it remains the leading cause of years lived with disability.Various management strategies are used for the treatment of low back pain.
In the recent years neurodynamic techniques are being used for the treatment of low back pain.
Escpecially, patients of low back pain who have neural mechanosensitivity may benefit from neural mobilization techniques.
Slump stretching is a neurodynamic technqiue which is used to improve the mobility of dural tissue.Different studies have shown postive results of slump stretching in patients of low back pain.
However no such study has investigated the role of slump stretching in improving range of motiion in low back pain patients.So this study aims to investigate the the effect of slump stretching in low back pain patients specially on low back Low back pain is amongst the most prevalent musculoskeletal conditions worldwide.This condition has a significant impact on the person's quality of life by effecting their various activities of daily living.
As of 2017 it remains the leading cause of years lived with disability.Various management strategies are used for the treatment of low back pain.
In the recent years neurodynamic techniques are being used for the treatment of low back pain.
Escpecially, patients of low back pain who have neural mechanosensitivity may benefit from neural mobilization techniques.
Slump stretching is a neurodynamic technqiue which is used to improve the mobility of dural tissue.Different studies have shown postive results of slump stretching in patients of low back pain.
However no such study has investigated the role of slump stretching in improving range of motiion in low back pain patients.So this study aims to investigate the the effect of slump stretching in low back pain patients specially on low back
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
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
-
Rawalpindi, Punjab, Pakistan, 46000
- Fauji Foundation Hospital
-
-
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 44 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients aged 18-44 years
- Both males and females
- Persons with low back pain with a positive slump test
- Patients with a NPRS intensity of at least 5
Exclusion Criteria:
- Patients with signs or symptoms of nerve root involvement
- Pregnant females, patients with history of spinal surgery, patients of spondylolistheis, spinal stenosis and disc herniation.
- Patients with serious spinal conditions infection, tumors, osteoporosis, spinal fracture
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 |
|---|---|
|
Active Comparator: conventional physical therapy
|
Moist heat with hydro collator pack, Maitland Mobilization for Lumbar spine, Therapeutic exercise: Core stability exercises
|
|
Experimental: conventional physical therapy with slump stretching
|
Moist heat with hydro collator pack, Maitland Mobilization for Lumbar spine, Therapeutic exercise: Core stability exercises
Slump stretching will be performed with the patient in the long sitting position with the patient's feet against the wall to assure the ankle remained in 0 degree dorsiflexion.
The therapist will apply over pressure to the cervical spine flexion to the point where the patient's symptoms will be reproduced.
The position will be held for 30 s.
A total of 5 repetitions will be completed.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
ROM
Time Frame: 2 weeks
|
Range of motion will be measured with gravity based inclinometer.
One inclinometer will be placed on T12 spinous process and the second inclinometer will be placed on S1 spinous process of participant.
The patient is asked to perform forward flexion, extension and lateral flexion, The range of motion is recorded by subtracting the value on lower inclinometer from upper inclinometer.
|
2 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Back Pain
Time Frame: 2 weeks
|
Back Pain will be measured via Numeric Pain Rating Scale.
A higher score will signify higher level of pain.
|
2 weeks
|
|
Physical Function
Time Frame: 2 weeks
|
Repeated sit to stand test will be used to assess the physical function of the participant
|
2 weeks
|
|
Disability
Time Frame: 2 weeks
|
Disability will be assessed via Pain Disability Index.
A higher score signifies poor outcome
|
2 weeks
|
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 1, 2022
Primary Completion (Anticipated)
January 1, 2023
Study Completion (Anticipated)
February 1, 2023
Study Registration Dates
First Submitted
August 10, 2022
First Submitted That Met QC Criteria
August 14, 2022
First Posted (Actual)
August 16, 2022
Study Record Updates
Last Update Posted (Actual)
August 16, 2022
Last Update Submitted That Met QC Criteria
August 14, 2022
Last Verified
August 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FUI/CTR/2022/8
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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