Skip to content

Identification of Vulnerability Factors in the Course of Pemphigus Patients

Identification of Vulnerability Factors in the Course of Pemphigus Patients - SHS Pemphigus Clinical Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02237313
Acronym
SHS-Pemphigus
Enrollment
48
Registered
2014-09-11
Start date
2015-04-20
Completion date
2017-07-03
Last updated
2026-02-05

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

Conditions

Dermatological Disease, Pemphigus

Keywords

psychological support, therapeutic education, vulnerability of patients

Brief summary

The bullous pemphigoid treatment is based on corticosteroids continued for several years. Pemphigus causes some patients a psychological impact and sometimes major vulnerability that can occur not only at diagnosis but also at later stages of disease progression. Our hypothesis is that these episodes of vulnerability may be under four kinds of factors that may be connected to the plurality of the history of these patients, and the resources they can mobilize throughout this experience, generating inequality in management and "work" around the disease.

Detailed description

The originality of the project lies in its multidisciplinary approach (dermatology, psychology, sociology). No such study has yet been carried out in the pemphigus who has been the subject of a very small number of works in sociology or psychology. The only studies are studies of quality of life with no longitudinal follow-up. The perspective of qualitative and quantitative data, sociological and psychological approaches, should allow more innovative and adapted to the medico-social and psychological care of patients with pemphigus approaches. The purpose of this study is to identify the determinants leading to moments of vulnerability in the course of patients with pemphigus in order to be able to offer preventive or corrective actions to improve the experience of the disease.

Interventions

BEHAVIORALpsychological support and therapeutic education program

Sponsors

University Hospital, Rouen
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER

Eligibility

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

Inclusion criteria

* Patient major * Patients with pemphigus vulgaris, diagnosed on a combination of: 1. clinical signs and 2. histological image above basal epithelial detachment with intra acantholysis, 3. direct immunofluorescence showing deposition of Immunoglobulin G and / or C3 to the surface of keratinocytes * Join a social security scheme * patient has been informed and have signed consent to participate in the study

Exclusion criteria

* Person placed under judicial protection, * Patient without liberty by administrative or judicial decision, * Patient participating in another trial for the duration of monitoring.

Design outcomes

Primary

MeasureTime frameDescription
analysis of vulnerability factors12 monthsevaluation of : perception by the patient of misdiagnosis, perception of a possible difference in assessment of the severity of his illness between himself and healthcare professionals, patient behavior in relation to available information sources, and the influence of information gathered on the illness experience, Patient trajectory during the diagnostic phase using individual interview and questionnaire

Secondary

MeasureTime frameDescription
analysis of vulnerability factors6 monthsevaluation of : perception by the patient of misdiagnosis, perception of a possible difference in assessment of the severity of his illness between himself and healthcare professionals, patient behavior in relation to available information sources, and the influence of information gathered on the illness experience, Patient trajectory during the diagnostic phase using individual interview and questionnaire
assessment of anxiety, uncertainty, fear, coping strategies12 monthsassessment of anxiety, uncertainty, fear, coping strategies using individual interview and questionnaire

Countries

France

Contacts

PRINCIPAL_INVESTIGATORPascal Joly, Professor

University Hospital, Rouen

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026