fibromyalgia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients who visit from June 1, 2019 to June 1, 2020 2. Patients who can obtain written consent from voluntary research participation 3. Patients who are 20 years old or older and younger than 80 years old when obtaining consent 4. Gender: male and female
Exclusion criteria
Exclusion criteria: 1. Women who are pregnant or may be pregnant
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| At the consultation, the pain clinic doctor measures the numeric rating scale, pain disability assessment scale, EuroQol, and Self-Rating Depression Scale on an outpatient basis. | — |
Secondary
| Measure | Time frame |
|---|---|
| Observation and inspection are performed for the following items. Also, we will ask for a response to the questionnaire and use the data for this study. These are activities that go beyond normal practice and are performed for research purposes. 1) Basic patient information: age, gender, medical history, height, weight, etc. 2) Blood test 3) Evaluation items of State trait Anxiety Inventery (STAI), numeric rating scale, Pain disability assessment scale, EuroQol, and Self-Rating Depression Scale measured by the attending physician before and after aromatherapy was performed. 4) Biomarkers in saliva (chromogranin A, cortisol, alpha-amylase) 5) Blood pressure and heart rate 6) Oral medication | — |
Countries
Japan
Contacts
International University of Health and Welfare Shioya Hospital Pharmaceutical department