non-specific cervical pain. Myalgia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with non-specific cervical pain- Aged between 35-55 years old No major acute or associated pathologies Agreement of participation in the study 85% of attendance to the therapeutical sessions Treatment continuity No current pain medication- Complete assessment sessions
Exclusion criteria
Exclusion criteria: Patients with acute cervical pain Major acute or associated pathologies Disagreement of participation in the study Less than 85% of attendance to the therapeutic sessions Discontinuity of treatment Current pain medication Incomplete assessment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of life. Timepoint: before intervention and 4 weeks after intervention. Method of measurement: We ill use a Health related quality of life questionnaire - it is a self administered questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| The second outcome is intensity of pain. Timepoint: one assessment before intervention and final assessment after 4 weeks. Method of measurement: VAS scale. | — |
Countries
Romania
Contacts
University of Oradea