- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05239247
Effects of Eldoa Versus Meckenzie Exercise on Non-specific Low Back Pain Patients
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Federal
-
Islamabad, Federal, Pakistan, 44000
- Rawal General And Dental Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Gender (Female)
- Age (40-69)
- NPRS (Grade <3)
- Chronic pain (more than or equal to 3 months)
- Restricted ROM
- Lumbar straightening
Exclusion Criteria:
- Any other orthopedic or neurological condition of hip or lumbar spine.
- sign and symptoms of lower motor neuron disease.
- Current use of medication prescribed for pain.
- Radiculopathy.
- malignancy.
- Fracture.
- Lumbar trauma.
- Disc pathology
Study Plan
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 |
|---|---|
|
Experimental: Mckenzie extension exercise
|
Hot pack applied on lumbar region for (ten minute). Mckenzie extension exercise performed 02 sets of 05 repetitions with 45 second hold and 15 sec rest between each set once a day. TENS is applied on lumbar region for (ten minutes). |
|
Experimental: Eldoa stretch technique
|
Hot pack applied on lumbar region for (ten minute). Eldoa stretch performed 02 sets of 05 repetitions with 45 second hold and 15 second rest between each set once a day. TENS is applied on lumbar region for (ten minutes). |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
lumbar ROM by inclinometer.
Time Frame: 12 days
|
Flexion 60 Extension 25 Left Lat Flex 25 Right Lat Flex 25
|
12 days
|
|
Lumbar Posture by flexicurve ruler.
Time Frame: 12 days
|
Excessive lordosis (EL) is over 75°, normal lordosis (NL) is 40°, hypo-lordosis (HL) is in the 20°
|
12 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
pain on Numeric pain rating scale.
Time Frame: 12 days
|
Changes from baseline, Pain was measured through Numeric pain rating scale.It comprises of a continuous scale of 10cm line.0 to 1 represent no pain, 1 to 3 represent mild pain ,4 to 6 represent moderate pain, 7 to 10 represent severe pain.
|
12 days
|
|
functional outcome by Oswestry low back pain disability questionnaire.
Time Frame: 12 days
|
0% to 20%: minimal disability: The patient can cope with most living activities.
Usually no treatment is indicated apart from advice on lifting sitting and exercise.
21%-40%: moderate disability: The patient experiences more pain and difficulty with sitting, lifting and standing.
Travel and social life are more difficult and they may be disabled from work.
Personal care, sexual activity and sleeping are not grossly affected and the patient can usually be managed by conservative means.
41%-60%: severe disability: Pain remains the main problem in this group but activities of daily living are affected.
These patients require a detailed investigation.
61%-80%: crippled: Back pain impinges on all aspects of the patient's life.
Positive intervention is required.
81%-100%:These patients are either bed-bound or exaggerating their symptoms
|
12 days
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Muniba Shamshad
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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