- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06548334
The Effectiveness of Lumber Regression Technique on Disc Bulge Randomized Control Trial
August 7, 2024 updated by: Muhammad Naveed Babur, Superior University
Lumbar disc bulges lead to considerable pain and disability in affected individuals, with current interventions lacking consistency of outcomes.
The lumbar regression method offered a hopeful, noninvasive option.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
this study was proposed to evaluate its efficacy in improving accessary lower limb flexibility and reducing functional disability and pain management.
To provide evidence about its effectiveness and help with clinical practice, this study aimed to improve patient outcomes in subjects having lumbar disc bulges.
Study Type
Interventional
Enrollment (Actual)
22
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
- Nemat Hospital & Heart Center, Manga Mandi
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Individuals with a diagnosis of Disc bulge confirmed by MRI.
- Between 18 and 65 years of age.
- Chronic low back pain from the last 3 months
- A stable treatment environment that allows intervention.
- Ability to understand and follow course directions.
- Willingness to give informed consent
Exclusion Criteria:
- Spondylolisthesis
- Spondylosis
- Vertebral fracture
- Lack of ava
- Further research interventions.
- Unstable medical condition
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: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Advanced Physiotherapy
|
The physiotherapist used the regression techniques for 1 hour of session 2 times for 8 weeks.
The caudal component involved the spinous process of the treated segment touching the therapist's hand and not applying force as though mobilising the segment at grade 2. These were applied if there is a suspected case of a posterolateral disc prolapse where the aim is to increase the diameter of the foramen and decrease the tension exerted on the nerve root.
Applied posteroanterior was used to distract the anterior intervertebral end plate and to approximate the posterior end plates so as to pull back the protruded nuclear material by creating a negative pressure.
|
|
Active Comparator: Conventional Physiotherapytechniques
|
In traditional physiotherapy, the patient underwent two sessions per week for eight weeks.
Each session lasted one hour and included 20minutes of TENS treatment.
The flexibility exercises consisted of hamstring stretches and single and double knee-to-chest stretches.
The strengthening exercises were partial sit-ups, quadruped lifts, and double leg hold; pelvic tilts were performed with 10-15 repetitions, each held for 20-30 seconds and repeated three times.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Roland Morris disability questionnaire
Time Frame: 12 Months
|
The Roland-Morris low back pain and disability questionnaire (RMD) was utilised to evaluate the quality of life prior to and following the completion of the treatment.
This questionnaire has demonstrated strong validity and reliability.
The score is measured on a scale of 0 to 24, and percentage scores were calculated for each participant.
Greater scores indicate a greater level of disabilities.
Its sensitivity is 95%, and its specificity is 69%.
|
12 Months
|
|
Straight Leg Raise
Time Frame: 12 months
|
The normal angle for an SLR is from 0-35 degrees, which signifies the least amount of strain.
Stretched from 35-70 degrees, sciatic nerve root stretching is achieved, and possible problems such as herniated disc or radiculopathy may be evidenced.
70- 90 degrees reflect highest normal flexibility: it may be related to hip joint pathology or some other conditions which are not a result of nerve injury.
During both the first evaluation and the final therapy, the SLR was assessed using a digital inclinometer (clinometer) installed on a Techno Camon 20 Android phone.
The digital inclinometer has been found to exhibit high levels of reliability and validity
|
12 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)
October 1, 2023
Primary Completion (Actual)
April 1, 2024
Study Completion (Estimated)
September 30, 2024
Study Registration Dates
First Submitted
August 7, 2024
First Submitted That Met QC Criteria
August 7, 2024
First Posted (Actual)
August 12, 2024
Study Record Updates
Last Update Posted (Actual)
August 12, 2024
Last Update Submitted That Met QC Criteria
August 7, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- MSRSW/Batch-Fall22/736
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
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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