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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04585360
Other study ID # 2019-A01819-48
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date October 10, 2020
Est. completion date February 15, 2021

Study information

Verified date August 2020
Source Assistance Publique - Hôpitaux de Paris
Contact Nicolas NN NOEL, MD PhD
Phone + 33 1 45 21 27 57
Email nicolas.noel@aphp.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The psychoBehçet'study is aimed at evaluating the psychological and neurocognitive symptoms in 25 consecutive patients followed for Behçet's disease. This is a monocentric, observational, non interventional study.


Description:

Patients will be evaluated during a day-care facility for Behçet's disease activity together with evaluation of anxiety and depression symptoms (SCL90-R and MINI assessments), fatigue (MFI) and quality of life (SF36).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 25
Est. completion date February 15, 2021
Est. primary completion date February 15, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult male or female

- Regular follow-up in the internal medicine department of Bicetre hospital

- Diagnosed with Behçet's disease

Exclusion Criteria:

- Refusal to participate in the study

- Poor command of the French language

- Patients under legal protection

- Pregnant woman

Study Design


Related Conditions & MeSH terms

  • Behcet Syndrome
  • Behçet's Disease, neuroBehcet, Anxiety, Depression, Tiredness

Intervention

Other:
Questionnaires evaluating anxiety and depression symptoms, tiredness, and quality of life
Realization of specific questionnaires evaluating: psychiatric symptoms (self-assessment according to the SLC-90R questionnaire and hetero-assessment by the internist doctor of the center according to the M.I.N.I. questionnaire) fatigue (Multidimensional Fatigue Inventory (MFI-20), French version, in self-assessment) quality of life (SF36 self-assessment questionnaire)

Locations

Country Name City State
France Internal medecine department Le Kremlin-Bicetre Val De Marne

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary SCL90-R questionnaire Anxiety/depression symptoms questionnaire Inclusion visit
Secondary MINI questionnaire Anxiety/depression symptoms questionnaire Inclusion visit
Secondary MFI questionnaire Tiredness assessment Inclusion visit
Secondary SF36 questionnaire Quality of life Inclusion visit
Secondary BSAS/BDCAF evaluation Behçet's disease activity Inclusion visit