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Improving quality of life for a patient with fibromyalgia and their caregiver: A protocol for the application of the integrative medical service model

Improving quality of life for a patient with fibromyalgia and their caregiver: A protocol for the application of the integrative medical service model

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0007626
Enrollment
2
Registered
2022-08-09
Start date
2022-08-05
Completion date
Unknown
Last updated
2023-01-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Wonkwang University. Iksan Korean Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: A. Patient 1. Adult men and women aged between 20 and 65 2. Adult men and women aged between 20 and 65 who have been clinically diagnosed with fibromyalgia by a specialistBased on the 2016 WPI of the American Society of Rheumatology, 7 points or more, 5 points or more, and chronic pain lasts at least 3 months 3. Based on the 2016 Rheumatoid Society WPI, between 3 and 6 points, severe severity is 9 points or higher, and chronic pain lasts at least 3 months 4. Those who can read and respond to the questionnaire 5. A person who understands the purpose of this study and agrees in writing to participate in the study; B. his/her caregiverAn adult (aged between 20 and 65) guardian of the selected patient who voluntarily agreed to participate in this study (the guardian is a trusted adult who takes care of his family or daily life)

Exclusion criteria

Exclusion criteria: 1. A person with a history of major psychiatric disorders such as schizophrenia spectrum disorder, delusion disorder, bipolar disorder, alcohol or substance abuse disorder diagnosed by DSM-5 2. Persons with chronic diseases that may affect the results of the study 3. Those who have participated in other clinical studies within the last month; 4. Those who are unable to communicate normally due to dementia or mild cognitive impairment; 5. Patients with somatform disorder whose main complaint 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 study will not be conducted according to the patient's medical condition;

Design outcomes

Primary

MeasureTime frame
EQ-5D-5L, EQ-VAS

Secondary

MeasureTime frame
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

Countries

Korea, Republic of

Contacts

Public ContactWon Bae Ha

Wonkwang University. Iksan Korean Medicine Hospital

ha0530@gmail.com+82-63-859-1114

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026