Chronic Low-back Pain Clinical Trial
Official title:
Interferential Current Treatment Reduces Low Back Pain and Improves Functionality in Patients With Chronic Low Back Pain.
Verified date | April 2023 |
Source | Universidade Federal do Oeste do Para |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
. 24 individuals were evaluated, with low back pain for more than 12 weeks and aged between 12 and 65 years. The current used in the lumbar region of the participants was of the tetrapolar interferential type and the stimulation mode was the automatic vector, carrier of 4,000 HZ, modulation frequency (AMF) of 50 HZ, sweep frequency of SWEEP of 20HZ. The assessment of pain and functionality was performed using the data collection instrument, the Visual Analogue Pain Scale (VAS), Rolland Morris Disability Questionnaire (RMDQ) and the Owestry Disability Questionnaire (ODQ) respectively. The present study demonstrates that treatment with interferential current promotes chemical improvement in participants, which opens up new perspectives on the use of this therapeutic approach.
Status | Completed |
Enrollment | 24 |
Est. completion date | March 15, 2023 |
Est. primary completion date | January 10, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Individuals of both genders - Aged between 18 and 65 years - Voluntarily sought the Clinic's physiotherapy service - Low back pain for more than 12 weeks - Medical request and diagnosis of low back pain with or without pain radiating to the lower limbs - Immunization against COVID 19. - Signature of the free detailed term clarified. (FDTC) Exclusion Criteria: - Physiotherapy treatment carried out in a period equal to or less than 8 weeks before starting the research - Reporting any contraindications inherent to the use of electrotherapy - Participants with fractures or spinal surgery - Involved in a legal medical dispute - Diagnosis of fibromyalgia - Patients with flu-like symptoms during the research period - Participants who have more than 2 (two) absences will be excluded from the research. |
Country | Name | City | State |
---|---|---|---|
Brazil | Luiz Paulo Sobral Pereia | Santarém | Para |
Lead Sponsor | Collaborator |
---|---|
Universidade Federal do Oeste do Para | Fundação Amazônia de Amparo a Estudos e Pesquisas FAPESPA |
Brazil,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Isolated comparative evaluation method, before and after, in the three arms with Application of Rolland Morris Questionnaires | Application of Rolland Morris Questionnaires before and after intervention, this questionnaires assesses mild and moderate pain and disability | 12 months | |
Primary | Isolated comparative evaluation method, before and after, in the three arms, Application of Owestry Questionnaire | Application of Owestry Questionnaire before and after intervention, this questionnaires evaluates more severe disabilities | 12 months | |
Primary | Isolated comparative evaluation method, before and after, in the three arms, Application analogue visual score for pain | Application analogue visual score for pain before and after intervention, evaluates the level of pain according to the patient's reference | 12 months |
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