Fibromyalgia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Men and women; age 18 years or older; diagnosed with fibromyalgia (American College of Rheumatology 2016 criteria) or chronic pain; not currently participating in another rehabilitation program
Exclusion criteria
Exclusion criteria: Pregnancy or breastfeeding; pain of oncological origin; uncontrolled metabolic disorder; individuals presenting simultaneously with fibromyalgia and other chronic pain from a cause other than fibromyalgia; individuals with any physical or psychological condition that limits communication with the research team or the full application of the intervention protocol
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluate the progression of pain intensity measured using the Numeric Rating Scale (NRS) at the beginning and end of the study;Evaluate the progression of pressure pain thresholds in the upper trapezius, hand, lumbar spine, and knee measured using pressure algometry at the beginning and end of the study;Evaluate the progression of catastrophizing measured using the Pain Catastrophizing Scale (PCS) at the beginning and end of the study;Evaluate the progression of kinesiophobia measured using the Tampa Scale of Kinesiophobia (TSK-11) at the beginning and end of the study | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluate the progression of hypervigilance measured using the Pain Vigilance and Awareness Questionnaire (PVAQ-9) at the beginning and end of the study;Evaluate the progression of pain interference measured using the Brief Pain Inventory, Spanish Form (BPI-SF) at the beginning and end of the study | — |
Countries
Chile
Contacts
Universidad San Sebastián