Low Back Pain Clinical Trial
Official title:
Evaluation of the Responsiveness of the Bridge Tests in Subjects With Non-specific Subacute or Chronic Low Back Pain
NCT number | NCT03879031 |
Other study ID # | 1/Bridge |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | March 20, 2019 |
Est. completion date | November 30, 2019 |
Verified date | December 2019 |
Source | University of Bologna |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This observational study aims to investigate the internal responsiveness and external responsiveness of the Bridge Tests (supine bridge test, prone bridge test, and side bridge test) in relation to pain and disability, in subjects with subacute and chronic non-specific low back pain submitted to a physical therapy program.
Status | Completed |
Enrollment | 139 |
Est. completion date | November 30, 2019 |
Est. primary completion date | November 30, 2019 |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Non-specific subacute or chronic low back pain (low back pain from 1 month or more, not related to specific pathologies); - Low back pain, with or without irradiation to the lower limb, noted as =2 on a scale of 0-10; - Good comprehension of written and spoken Italian Language; - Informed consent. Exclusion Criteria: - Acute low back pain; - Specific causes of low back pain (truma, herniated disc, vertebral deformity, fractures, dislocations); - Central or peripheral neurologic signs; - Systemic pathologies; - Rheumatic disorders; - Neuromuscular pathologies; - Tumors; - Cognitive deficits; - Surgical interventions in the last six months prior to the study; - Osteoporosis. |
Country | Name | City | State |
---|---|---|---|
Italy | Policlinico S.Orsola-Malpighi | Bologna | Emilia Romagna |
Lead Sponsor | Collaborator |
---|---|
University of Bologna |
Italy,
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* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in low back pain over time | 0-100 Numerical Rating Scale (NRS) for low back pain. This scale is arranged to measure the amount of perceived lumbar pain, from 0 (= no pain) to 100 (=maximum pain). | Time zero: at baseline - Time one: at the end of the last session of physical therapy treatment (8 weeks after Time zero) | |
Primary | Changes in lumbar disability over time | Oswestry Disability Index - Italian version (ODI-I). This questionnaire measures disability related to low back pain in 10 different domains (Pain Intensity, Personal Care, Lifting, Walking, Sitting, Standing, Sleeping, Sex Life, Social Life, and Traveling). The patients are asked to identify which of six statements in each domain applies to them at the time of evaluation. The sentences are arranged from no impairment (0) to maximum impairment (5). The scores for each domain are added together (range from 0 to 50) and multiplied by 2 which yields a Disability Index Score percent. If not all items are completed, the score is prorated by averaging the items completed and then multiplying it by 10. A Disability Index Score of 0% to 20% corresponds to minimal disability, 21% to 40% to moderate disability, 41% to 60% to severe disability, 61% to 80% crippled, and 81% to 100% indicates a patient that is either bed-bound or exaggerating their symptoms. | Time zero: at baseline - Time one: at the end of the last session of physical therapy treatment (8 weeks after Time zero) | |
Secondary | Changes in Global Perceived Effect (GPS) questionnaire (Italian version) over time | The GPE is composed of one question on a 7-point Likert-type scale, evaluating the subjective self-reported improvement or deterioration after the intervention, from "fully improved" (score 1) to "fully worsened" (score 7). More specificaly, 1=fully improved; 2=much improved; 3=a little improved; 4=no change; 5= a little deterioration; 6=much deterioration; 7=fully worsened. GPE is widely used in the physical therapy literature. | At the end of the last session of physical therapy treatment (8 weeks after Time zero) |
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