Auriculoterapia e Massagem for Neck Pain and Quality of life improvement
Not Applicable
- Conditions
- eck PainC10.597.617.576
- Registration Number
- RBR-9tkt8z
- Lead Sponsor
- Escola de Enfermagem da Universidade de São Paulo
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Data analysis completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Pain score equal or greater than 5 by the Visual Analogue Scale; age between 20 and 55 years
Exclusion Criteria
Paresthesia; decreased strength; anti-inflammatory drugs; analgesics and muscle relaxants; cervical spine surgeries;
inflammation and or infection in treated regions;tissue damage in the external ear or cervical and thoracic region
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Expected event: reduction of cervical pain in the period of 1 month according to the Visual Analog Pain Scale, from the observation of a variation of at least 30% in the pre and post intervention measurements for the two practices, massage and auriculotherapy. ;Event achieved: reduction of cervical pain in the period of 1 month, according to the Analog visual Pain Scale, of a 46% variation in auriculotherapy and 60% in massage, in pre and post intervention measurements. The measurements were performed one week pre intervention and one week post intervention.
- Secondary Outcome Measures
Name Time Method Expected event: increase in quality of life in the physical and mental domains, in the period of 1 month, according to the 12-Item Short-Form Health Survey, from the observation of a variation of at least 15% in pre and post intervention measurements for Two practices, massage and auriculotherapy. ;Event achieved: increased quality of life in the mental domain in the period of one month, according to 12-Item Short-Form Health Survey, a 21% variation in auriculotherapy and 19% in massage, in pre and post intervention measurements. The measurements were performed one week pre intervention and one week post intervention.