Non Pain Contingent Spine Rehabilitation Therapy in Chronic Low Back Pain
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| ClinicalTrials.gov Identifier: NCT04619134 |
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Recruitment Status :
Completed
First Posted : November 6, 2020
Last Update Posted : December 29, 2020
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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 detailed description
| 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 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: NCSR Program
Non Pain Contingent Spinal Rehabilitation
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Other: NCSR Program
flexibility exercise,strengthening exercise,dynamic strengthening exercise,endurance training,counselling session |
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Active Comparator: Conventional Physical therapy
Conventional Physical Therapy
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Other: conventional physical therapy
hot pack,flexibility training,strengthening exercise. |
- 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
- 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
- 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
- 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
- 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
- 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
- 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
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| Ages Eligible for Study: | 35 Years to 65 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
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
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
| Pakistan | |
| Pakistan Railway General Hospital | |
| Rawalpindi, Punjab, Pakistan, 46000 | |
| Principal Investigator: | Maria Khalid, MSOMPT | Riphah International University |
| 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 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Low Back Pain Non Pain Contingent Spine Rehabilitation |
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Back Pain Low Back Pain Pain Neurologic Manifestations |

