Chronic Pain Clinical Trial
Official title:
Comparison and Effects of Low and High Frequency Percutaneous Electrical Nerve Stimulation on Myofascial Chronic Neck Pain Patients.
Verified date | May 2018 |
Source | Centro Universitario La Salle |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Comparison between high and low frequency percutaneous electrical nerve stimulation as treatment of myofascial chronic neck pain. The main hypothesis is that low frequency treatment will have more hypoalgesic effects than high frequency, and low frequency effects will last longer.
Status | Completed |
Enrollment | 40 |
Est. completion date | April 9, 2018 |
Est. primary completion date | April 9, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Neck pain of more than 6 months of evolution. - Pain level of more than 30 millimeter on the VAS scale. - Active myofascial frigger points on upper trapezius muscle. Exclusion Criteria: - Upper limb radiculopathy. - Recent whiplash. - Cervicogenic dizziness. - Migraine. - Previous cervical surgery. |
Country | Name | City | State |
---|---|---|---|
Spain | CSEU La Salle | Madrid |
Lead Sponsor | Collaborator |
---|---|
Centro Universitario La Salle |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain | Subjective feeling expressed by subjects in the area of discomfort. It will be measured by a Visual Analogue Scale, meaning a score of 0 points/centimiters "no pain" and a score of 10 points/centimiters "unbearable pain". | Changes on pain will be assessed during one month follow up. Baseline will be measured on the first day and one month later pain score will be reassessed. | |
Secondary | Pressure pain threshold | Minimal amount of pressure that induces pain. An algometer will be used to measure pressure pain threshold. Units will be kilograms per square centimeter. The higher the score is, the less sensitive the area will be. | Changes on pain will be assessed during one month follow up. Baseline will be measured on the first day and one month later pain score will be reassessed. | |
Secondary | Neck disability index. | Ten items questionnaire designed to asses the level of pain and self-assessment of cervical disability. The NDI (Spanish version) is composed of 10 questions related to daily functional activities. NDI presents an acceptable reliability with an intraclass correlation coeffcient (ICC) ranging from 0.50 to 0.98. It has been proposed that the clinically important difference required for NDI is seven points. | Pre treatment at the beginning of the study and one month later, on the last of the follow up period. | |
Secondary | kinesiofobia | Eleven items questionnaire designed to asses pain-related fear. TSK-11, Spanish version. | Pre treatment at the beginning of the study and one month later, on the last of the follow up period. |
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