Health-Related Quality of Life in Patients With Systemic Lupus Erythematosus:Focusing on Fibromyalgia
1 other identifier
observational
300
0 countries
N/A
Brief Summary
Systemic lupus erythematosus (SLE) patients show a high prevalence of fibromyalgia though rates vary considerably from one study to another (from 8.2% to 45%). Although fibromyalgia can bring out the disability in daily life, the majority of previous reports only ascertained no significant association between the presence of fibromyalgia and the severity of SLE. It is necessary to make unremitting effort to reduce the mortality and life-threatening disease flare-up due to SLE disease itself. Additionally, we think that physicians need to pay more attention to improve health-related quality of life (HRQoL) in the patients with SLE. HRQoL could be influenced by various factors such as depression, fibromyalgia, disease duration, disease activity and etc. To improve the HRQoL in SLE patients, it might be the clinically important and constructive theme to investigate that which is the most important factor among the fibromyalgia, depression, sleep quality, SLE activity and SLE duration. The objective of this study is to evaluate the degree of contribution of fibromyalgia for reduced HRQoL and to identify the status of managing fibromyalgia in Korean patients with SLE.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2013
Typical duration for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2013
CompletedFirst Submitted
Initial submission to the registry
January 17, 2013
CompletedFirst Posted
Study publicly available on registry
January 21, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2015
CompletedFebruary 2, 2017
January 1, 2017
2.3 years
January 17, 2013
January 31, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
EuroQoL (EQ-5D)
1 year
Eligibility Criteria
* Patients : 150 women age 30 to 60 years with SLE * Control subjects : age, sex matched control subject (150 subjects) * Patients : First visit and second visit after an interval of six months * Control subjects : baseline only
You may qualify if:
- Woman between 30 and 60 years of age, inclusive
- Have a diagnosis of Systemic lupus erythematosus according to the 1997 updated American college of Rheumatology criteria for classification of systemic lupus erythematosus
You may not qualify if:
- Patients were excluded if they had had a history of head injury that led to unconsciousness
- Have unstable disease necessitating an increase in prednisone dose or the addition of another immunosuppressive medication
- Have a current malignancy
- Have a history of or current evidence of substance abuse (drug or alcohol) problem within the previous 2 years
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
January 17, 2013
First Posted
January 21, 2013
Study Start
January 1, 2013
Primary Completion
May 1, 2015
Study Completion
November 1, 2015
Last Updated
February 2, 2017
Record last verified: 2017-01