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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05691907
Other study ID # FUI/CTR/2023/2
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date February 1, 2023
Est. completion date December 1, 2024

Study information

Verified date January 2023
Source Foundation University Islamabad
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the effects Of Directional Preference Exercises in Comparison to Motor Control Exercises in Patients With Mechanical Low Back Pain


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 40
Est. completion date December 1, 2024
Est. primary completion date December 1, 2024
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Both male & Female patients - Age group 20-60 Years - Diagnosed with mechanical low back pain having pain aggravation in flexion bias Exclusion Criteria: - Lumbar stenosis - Cauda Equina - Spondylolisthesis - Ankylosing Spondylitis - Scoliosis - Leg Length Discrepancy - Muscular Dystrophy - Low back pain from non-musculoskeletal causes - Fracture or traumatic low back pain - Any infection, tumor, spinal surgery, cognitive impairments, or any other rheumatologic disease would be excluded

Study Design


Related Conditions & MeSH terms


Intervention

Device:
THE therapy
THE therapy consisting of: Heating Pad Interferential Therapy
Procedure:
Directional Preference Exercises
Directional Preference Exercises consisting of Mckenzie's extension protocol
Motor Control Exercises
Motor Control Exercises consisting of External limb loading extension protocol

Locations

Country Name City State
Pakistan Foundation University Islamabad
Pakistan Kulsum International Hospital Islamabad

Sponsors (1)

Lead Sponsor Collaborator
Foundation University Islamabad

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Back Pain Pain will be measured using Numeric Pain Rating Scale, on a scale of 1 to 10. higher scores represent poorer outcome. 2 week
Primary Disability Disability will be measured using Roland Morris Disability Questionnaire. Higher scores represent poorer outcome. 2 week
Primary Range of Motion Range of Motion will be measured using inclinometer. Higher scores represent better outcome. 2 week
Primary Sleep Quality Sleep Quality will be measured using Pittsburg Sleep Quality Index. Higher scores represent poorer outcome. 2 week
Primary Postural Stability Index Postural Stability Index will be measured using Biodex Balance System. Higher scores represent poorer outcome. 2 week
Primary Real time Physical Activity Real time Physical Activity will be measured using wearable sensor technology. Higher scores represent better outcome. 2 week
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