Lumbar Pain Clinical Trial
NCT number | NCT02815358 |
Other study ID # | 923.642 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | June 2016 |
Est. completion date | November 2016 |
Verified date | June 2019 |
Source | Federal University of Health Science of Porto Alegre |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study aims to verify the effects of a segmental stabilization exercise program on the anticipatory postural adjustment of subjects with chronic lumbar pain. The effects will be assessed by means of superficial electromyography focused on the registry of the onset of multifidius and deltoid (anterior and posterior) activity during a repetitive shoulder flexion/extension.
Status | Completed |
Enrollment | 40 |
Est. completion date | November 2016 |
Est. primary completion date | September 2016 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - women aged between 18 and 65 years old - chronic lumbar pain (at least 3 months) - average pain intensity of =3 on a 10-point scale Exclusion Criteria: - presence of red flags (i.e.,tumor, known fractures, diagnosed inflammatory joint disease, etc); - history of back surgery - pregnancy - less than 3 months of therapeutic treatment (physiotherapy) for low back pain |
Country | Name | City | State |
---|---|---|---|
Brazil | Federal University of Health Sciences of Porto Alegre | Porto Alegre | Rio Grande Do Sul |
Lead Sponsor | Collaborator |
---|---|
Federal University of Health Science of Porto Alegre |
Brazil,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Anticipatory Postural Adjustment by means of Electromyography | Assessed by means of superficial electromyography | change from pre to post-treatment (8 weeks) | |
Secondary | Disability level via the Oswestry Low Back Pain Questionnaire | change from pre to post-treatment (8 weeks) | ||
Secondary | Fear of pain and avoidance of physical activity via the Fear-avoidance beliefs Questionnaire | change from pre to post-treatment (8 weeks) | ||
Secondary | Prognosis or risk of poor clinical outcome via the STarT Back Screening Tool | change from pre to post-treatment (8 weeks) | ||
Secondary | Pain level via visual analogue scale | change from pre to post-treatment (8 weeks) |
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