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Therapeutic Education Using an Internet Application in Hereditary Ichthyosis (e-ETPichtyose)

T

Toulouse University Hospital

Status

Completed

Conditions

Ichthyosis

Treatments

Other: Therapeutic patient education program

Study type

Interventional

Funder types

Other

Identifiers

NCT03641261
RC31/16/8765

Details and patient eligibility

About

The main purpose is to evaluate the feasibility (global use) of a therapeutic patient education program using a specific web application in patients with hereditary ichthyosis.

Enrollment

42 patients

Sex

All

Ages

15 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient with hereditary ichthyosis, according to the classification established during the 2009 consensus conference
  • Who has given his informed consent form
  • Who is affiliated to a social security system

Exclusion criteria

  • Patient who has already participated in a therapeutic patient education program for the hereditary ichthyosis
  • Unable to connect or use a computer tool
  • Impossibility to be present at the only face-to-face session
  • Patient who is not available for the collective educational session
  • Patient with little or no motivation to follow a therapeutic patient education program (motivation evaluated by the educational team by phone call before inclusion)
  • Patient not mastering the French language
  • Person under legal protection (guardianship, curators or safeguard of justice)

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

42 participants in 1 patient group

Therapeutic Patient Education program
Experimental group
Description:
All included patients will follow a Therapeutic Patient Education program dedicated to the hereditary ichthyosis and using a web application, WebIchtyose
Treatment:
Other: Therapeutic patient education program

Trial contacts and locations

1

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Central trial contact

Isabelle Dreyfus, PharmD; Juliette Mazereeuw-Hautier, MD

Data sourced from clinicaltrials.gov

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