Cervical Syndrome Clinical Trial
Official title:
Vacuum Myofascial Therapy Device for Non-specific Neck Pain. A Single Blind Randomized Clinical Trial
Verified date | May 2020 |
Source | University of Cadiz |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study aim to investigate the effects of physium therapy for improving pressure pain thresholds (PPTs), range of motion,Neck Disability Index, the multidimensional health related quality of life (SF-12) and the multidimensional health related quality of life and pain in patients with mechanical neck pain (NP).
Status | Completed |
Enrollment | 38 |
Est. completion date | September 15, 2018 |
Est. primary completion date | August 15, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 60 Years |
Eligibility |
Inclusion Criteria: - Patients of both sexes, - Aged between 20 and 60 years, in an - Active state of pain and diagnosed with a month of evolution. Exclusion Criteria: - Patients who are pregnant, have pacemaker and those Surgically operated cervical spine - - Patients who have been treated with myofascial therapy a month earlier. |
Country | Name | City | State |
---|---|---|---|
Spain | Clínica Pastoriza | El Puerto De Santa María | Cádiz |
Lead Sponsor | Collaborator |
---|---|
University of Cadiz |
Spain,
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The intensity of cervical pain | A 10-point Numerical Pain Rating Scale (NPRS; 0: no pain, 10: maximum pain) will be used to assess the patients' current level of cervical pain, and the worst and lowest level of pain experienced in the preceding week in the cervical area. | Baseline | |
Secondary | The intensity of cervical pain | A 10-point Numerical Pain Rating Scale (NPRS; 0: no pain, 10: maximum pain) will be used to assess the patients' current level of cervical pain, and the worst and lowest level of pain experienced in the preceding week in the cervical area. | Four weeks | |
Secondary | Active cervical range of motion | Measured by goniometer type crom | Baseline and four weeks. | |
Secondary | Pressure pain thresholds in cervical trigger points | Pressure pain thresholds (PPTs) will be measured with a pressure algometer (Baseline, Pain TestTM, Wagner Instruments). The clinimetric properties of this instrument have been evaluated previously. The PPT will the point at which pressure elicited pain and will presented as kilograms per square centimeter. All measurements will be conducted by the same well-trained physician. | Baseline and four weeks | |
Secondary | The multidimensional health related quality of life | Questionnaire SF 12 | Baseline and four weeks | |
Secondary | This questionnaire has been designed to give us information as to how your neck pain has affected your ability to manage in everyday life. | Neck Disability Index | Baseline and four weeks. |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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