Fibromyalgia Clinical Trial
Official title:
Development of Predictive Models Based on Artificial Intelligence for the Analysis of the Psychosocial Profile of the Patient With Fibromyalgia on Pain and Severity of the Disease.
The primary goal of this research project is to develop different prediction models in fibromyalgia disease through the application of machine learning techniques and to assess the explainability of the results. As specific objectives the research project intends: to predicting Fibromyalgia severity of patients based on clinical variables; to assess the relevance of social-psycho-demographic variables on the fibromyalgia severity of the patients; to predict the pain suffered by the patients as well as the impact of the fibromyalgia on patient's life; to categorize fibromyalgia group of patients depending on their levels of Fibromyalgia severity.
Status | Not yet recruiting |
Enrollment | 150 |
Est. completion date | November 2021 |
Est. primary completion date | November 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Age between 18 and 65 years. - Fullfilled the 2010 American Collegue of Rheumathology criteria for fibromyalgia. - Understanding of spoken and written Spanish. Exclusion Criteria: - Diagnosed psychiatric pathology. - Rheumatic pathology not medically controlled. - Neurological pathologies that make evaluations difficult. |
Country | Name | City | State |
---|---|---|---|
Spain | Hospital General Nuestra Señora del Prado | Talavera De La Reina | Toledo |
Lead Sponsor | Collaborator |
---|---|
University of Castilla-La Mancha |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pain intensity | It will be measured with a visual analog scale (VAS) of 100 millimeters in length. The subject has to indicate the level ofpain he feels, being 0 the absence of pain and 100 the maximum imaginable. | Baseline. | |
Primary | Disease severity. | It will be measured using the Polysymptomatic Distress Scale (PDS) (or Fibromyalgia Severity Scale), composed of the sum of the following two scales:
Widespread Pain Index (WPI): Questionnaire in which a total of 19 body areas are represented. The subject has to mark the regions where the pain appears. It represents a measure of the extent of pain, with a maximum score of 19 points. Symptom Severity Scale (SSS): Questionnaire that measures the severity of the symptoms associated with fibromyalgia, such as fatigue, non-restorative sleep, cognitive problems, headaches, abdominal pain or cramps and depression. It represents a measure of somatic and non-somatic symptoms of fibromyalgia, with a maximum score of 12 points. |
Baseline. | |
Primary | Referred pain area after suprathreshold pressure stimulation. | A pressure algometer (Force Ten™, Wagner Instruments, USA) will be used. It will be performed on the infraspinatus muscle (point equidistant between the midpoint of the spine of the scapula, the inferior angle of the scapula and the midpoint of the medial border of the scapula) at a constant suprathreshold pressure (20% above the pressure pain threshold) for 60 seconds.
After the stimulation, the subject should draw the induced pain area on a digital bodychart using the Navigate Pain application (Navigate Pain, Aalborg University, Denmark). |
Baseline. | |
Secondary | Fibromyalgia Impact Quality-of-Life. | It will be measured with the version adapted to the Spanish of the Fibromyalgia Impact Questionnaire (FIQ). | Baseline. | |
Secondary | Anxiety. | The version adapted to Spanish from the State Scale (STAI-ES) of the State-Trait Anxiety Inventory (STAI) will be used. | Baseline. | |
Secondary | Pain catastrophizing. | The Spanish version of the Pain Catastrophizing Scale (PCS) will be used. | Baseline. | |
Secondary | Depression. | The adaptation to the Spanish of Beck Depression Inventory II will be used. | Baseline. |
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