Try the modernized ClinicalTrials.gov beta website. Learn more about the modernization effort.
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Non Pain Contingent Spine Rehabilitation Therapy in Chronic Low Back Pain

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04619134
Recruitment Status : Completed
First Posted : November 6, 2020
Last Update Posted : December 29, 2020
Sponsor:
Information provided by (Responsible Party):
Riphah International University

Brief Summary:

The aim of study is to determine effects of non pain contingent spine rehabilitation in chronic low back pain.A Randomized controlled trial will be conducted at Railway general hospital.

Sample size will be 32.Participants will be divided in two groups, 16 participants in group A will receive Non pain contingent spine rehabilitation (NCSR) therapy and 16 Group B will receive conventional physical therapy. The study duration will be six months. Purposive non probability sampling technique will be applied.


Condition or disease Intervention/treatment Phase
Low Back Pain Other: NCSR Program Other: conventional physical therapy Not Applicable

Show Show detailed description

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 32 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Official Title: Effects of Non Pain Contingent Spine Rehabilitation Therapy in Chronic Low Back Pain
Actual Study Start Date : December 1, 2019
Actual Primary Completion Date : December 20, 2020
Actual Study Completion Date : December 20, 2020

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: NCSR Program
Non Pain Contingent Spinal Rehabilitation
Other: NCSR Program
flexibility exercise,strengthening exercise,dynamic strengthening exercise,endurance training,counselling session

Active Comparator: Conventional Physical therapy
Conventional Physical Therapy
Other: conventional physical therapy
hot pack,flexibility training,strengthening exercise.




Primary Outcome Measures :
  1. Visual Analog Scale [ Time Frame: 6th week ]
    Visual analogue scale (VAS) is a simple and frequently used method for the assessment of variations in intensity of pain. The VAS consists of a 10cm horizontal line with the words "no pain" and "worst pain" at the line's end. VAS is a reliable and valid tool to reliable and valid tool to measure pain intensity measure pain intensity. Changes from the baseline will be measured and at 4th week and then at 6th week

  2. Functional Disability: Oswestry Disability Index [ Time Frame: 6th week ]
    The Oswestry Disability Index (ODI) is one of the most commonly used outcome measures for the evaluation and treatment of LBP and it is valid, reliable. Changes from the baseline will be measured and at 4th week and then at 6th week


Secondary Outcome Measures :
  1. Lumbar Range of Motion [ Time Frame: 6th week ]
    Bubble Inclinometer. Changes from the baseline will be measured and at 4th week and then at 6th week

  2. Shirado test: to assess isometric endurance of trunk flexors [ Time Frame: 6th week ]
    To evaluate "flexor endurance" Patient in supine position asked to raise the lower extremities with 90 degrees flexion at hip and knee joint and also maintain cervical flexion, maintain this position for at least 5 minutes. Changes from the baseline will be measured and at 4th week and then at 6th week

  3. Ito test: to evaluate isometric endurance of trunk extensors [ Time Frame: 6th week ]
    To measure "extensor endurance" patient in prone position holding sternum off the treatment table and a small pillow below abdomen to decrease lordosis; and maintaining cervical flexion with pelvic stabilization and gluteal contraction maintain this position for 5 minutes. Changes from the baseline will be measured and at 4th week and then at 6th week

  4. Lifting endurance [ Time Frame: 6th week ]
    Progressive Iso inertial lifting evaluation(PILE). Changes from the baseline will be measured and at 4th week and then at 6th week

  5. Fear Avoidance Belief Questionnaire [ Time Frame: 6th week ]
    Fear Avoidance Belief Questionnaire (FABQ). Changes from the baseline will be measured and at 4th week and then at 6th week



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   35 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patient with non-specific chronic low back pain(>3months)

Exclusion Criteria:

  • Spinal surgery
  • Compression Fracture
  • Disc Herniation
  • Cauda equina
  • Pregnancy
  • Cancer
  • Progressive neurological disorder
  • Any Psychological disorder

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04619134


Locations
Layout table for location information
Pakistan
Pakistan Railway General Hospital
Rawalpindi, Punjab, Pakistan, 46000
Sponsors and Collaborators
Riphah International University
Investigators
Layout table for investigator information
Principal Investigator: Maria Khalid, MSOMPT Riphah International University
Publications:

Layout table for additonal information
Responsible Party: Riphah International University
ClinicalTrials.gov Identifier: NCT04619134    
Other Study ID Numbers: REC/00673 Fariha Altaf
First Posted: November 6, 2020    Key Record Dates
Last Update Posted: December 29, 2020
Last Verified: December 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Riphah International University:
Low Back Pain
Non Pain Contingent Spine Rehabilitation
Additional relevant MeSH terms:
Layout table for MeSH terms
Back Pain
Low Back Pain
Pain
Neurologic Manifestations