A Case Study on the Appication of Integrative Medical Service to Improve Quailty of Life and Pain Management in Patients with Fibromyalgia

Not Applicable

Conditions: Diseases of the musculoskeletal system and connective tissue

Registration Number: KCT0007623

Lead Sponsor: Wonkwang University Hospital

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: ot yet recruiting

Sex: All

Target Recruitment: 2

Inclusion Criteria

1) A patient
1. A patient aged between 20 and 65
2. A patient who has been clinically diagnosed with fibromyalgia by a specialist
3. Based on the 2016 WPI of the American Society of Rheumatology, 7 or more points and 5 or more points of severe severity, and chronic pain lasts at least 3 months
4. Between 3 and 6 points based on the 2016 American Rheumatology Association WPI, 9 points or more for severe severity, and at least 3 months of chronic pain
5. A patient who can read and respond to a questionnaire
6. A patient who understands the purpose of this study and agrees in writing to participate in the study;2) The

2)caregiver of patient.
An caregiver(20 to 65 years old) of a selected patient who voluntarily agreed to participate in this study (a guardian is a trusted adult who takes care of his family or daily life)

Exclusion Criteria

1. A person with a history of major psychiatric disorders such as schizophrenia spectrum disorder, delusional disorder, bipolar disorder, alcohol or substance abuse disorder diagnosed by DSM-5
2. A person with a chronic disease that may affect the results of the study;
3. Those who have participated in other clinical studies within the past month;
4. A person who is unable to communicate normally due to dementia or mild cognitive impairment;
5. Patients with somatoform disorder whose main cause is pain, but whose physical cause is not clear, and whose mental problems are significant.
6. Those who are unable to communicate and have restrictions on reading and writing questionnaires;
7. Any other person who determines that the research manager or research manager will not be able to conduct the research according to the patient's medical condition;

Study & Design

Study Type: Observational Study

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
EQ-5D-5L, EQ-VAS

Secondary Outcome Measures

Name	Time	Method
Severity (SSS), Pain (WPI), Daily Activity Disorder Measurement, Number Pain Rating Scale (NPRS), Core Emotional Accuracy Scale (CSEI-S), Sleep Quality Index, and Mind Room Drawing