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Auto-immune Diseases and Quality of Life

Qualitative Study of the Consequences of Auto-immune Diseases on Quality of Life

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02855840
Acronym
QUALIMAIRAU
Enrollment
77
Registered
2016-08-04
Start date
2015-03-02
Completion date
2017-03-31
Last updated
2017-10-10

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

Conditions

Quality of Life, Systemic Auto-immune Diseases

Brief summary

Systemic lupus erythematous (SLE), systemic sclerosis (Ssc) and inflammatory myopathy (IM) are rare diseases, whose prevalence is estimated at 43, 15 and 10 cases, respectively, for 100 000 inhabitants in France. These diseases belong to the group of auto-immune diseases and require specialized follow-up in an expert centre. The repercussions of SLE, Ssc and IM on the everyday life of patients are heavy, and notably linked to skin involvement, to diminished functional capacities and psychological problems. The vast majority of these diseases concern middle-aged, professionally-active individuals, for whom the socio-professional repercussions are major and too often neglected. The aim of this study is to analyse the consequences of auto-immune diseases on quality of life. Current quality of life questionnaires are not suitable, and do not reveal the reality of the situation and its different nuances. In this research, the quality of life of patients will be envisaged through their everyday lives. How do these patients construct the social reality of the disease? How do they perceive their health status and their social situation? How do they organize their everyday lives around the disease: work, leisure, relationships with their entourage... ?

Interventions

OTHERcompletion of the quality of life questionnaire

Sponsors

Centre Hospitalier Universitaire Dijon
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* For all patients: * Patients aged 18 to 75 years * Patients able to understand written and spoken French * Patients who have been given oral and written information about the research For patients with SLE: \- SLE defined by American College of Rheumatology (ACR) 1997 criteria For patients with systemic sclerosis: \- SSc according to the Leroy or American Rheumatism Association (ARA) criteria For patients with IM: \- IM according to the Trojanov criteria

Exclusion criteria

* Refusal to take part in the study * Cognitive/psychological status incompatible with interviews

Design outcomes

Primary

MeasureTime frame
semi-directive individual interviews in the 3 groups of patientsday one

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026