Exploring Patient Reported Outcomes in Inherited Ichthyosis

Sponsor
Maastricht University Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT06123091
Collaborator
(none)
20
1
15
1.3

Study Details

Study Description

Brief Summary

The goal of this observational study is to learn about the presence of extracutaneous manifestations in patients with congenital ichthyosis.

The main question it aims to answer is:
  • Do patients with congenital ichthyosis experience extracutaneous manifestations?

Participants will fill in questionnaires in which the investigators will explore whether patients experience extracutaneous manifestations, and if so what these manifestations entail. Examples of such questions are whether patients experience (joint) pain or whether they experience hindrance due to their complaints.

Condition or Disease Intervention/Treatment Phase
  • Other: Questionnaires with patient reported outcome measures

Detailed Description

There is only limited knowledge about extracutaneous manifestations in patients with congenital ichthyosis. With this study, the investigators aim to identify extracutaneous manifestations with questionaires based on patient reported outcomes.

Secondary research questions include:
  • What is the prevalence of joint complaints in patients with congenital ichthyosis

  • What is the influence of ichthyosis on the quality of life patients experience

Furthermore, the investigators aim to discover knowledge gaps in current patient management and possible areas of improvement in patient care towards healthcare professionals.

Study Design

Study Type:
Observational
Anticipated Enrollment :
20 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Exploring Patient Reported Outcomes in Inherited Ichthyosis
Actual Study Start Date :
Sep 1, 2023
Anticipated Primary Completion Date :
Oct 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Congenital ichthyosis patients

Questionnaires

Other: Questionnaires with patient reported outcome measures
Questionnaires to gain insight of the prevalence of extracutaneous manifestations and the impact of the disease on the quality of life.

Outcome Measures

Primary Outcome Measures

  1. Extracutaneous manifestations in general [Day 1]

    Evaluation of possible extracutaneous manifestations patients with congenital ichthyosis exhibit. This is measured by a questionnaire the investigators have composed. The questions entail patient reported outcomes on their general health and the health issues patients experience due to ichthyosis.

Secondary Outcome Measures

  1. Prevalence of joint complaints measured by the Psoriasis Epidemiology Screening Tool [Day 1]

    Prevalence of joint complaints measured by the Psoriasis Epidemiology Screening Tool (PEST). The higher the total score, the more joint complaints patients with congenital ichthyosis experience.

  2. Prevalence of joint complaints measured by the Early Arthritis Recognition Clinic questionnaire [Day 1]

    Prevalence of joint complaints measured by the Early Arthritis Recognition Clinic (EARC) questionnaire. The higher the total score, the more joint complaints patients with congenital ichthyosis experience.

  3. Prevalence of joint complaints Early Arthritis for Psoriatic patients questionnaire [Day 1]

    Prevalence of joint complaints measured by the Early Arthritis for Psoriatic patients (EARP) questionnaire. The higher the total score, the more joint complaints patients with congenital ichthyosis experience.

  4. Prevalence of joint complaints measured by the Clinical Arthritis Rule questionnaire [Day 1]

    Prevalence of joint complaints measured by the Clinical Arthritis Rule (CARE) questionnaire. The higher the total score, the more joint complaints patients with congenital ichthyosis experience.

  5. Impact of ichthyosis on quality of life [Day 1]

    Evaluation of quality of life measured by the Dermatology Life Quality Index (DLQI) questionnaire. Scores range from 0-30, where a higher score indicates that the skin disease has a bigger influence on their quality of life.

  6. Impact of ichthyosis on quality of life measured by Skindex-29 [Day 1]

    Evaluation of the quality of life of patients with congenital ichthyosis measured by the Skindex-29 questionnaire. Scores ranging from >25 and >44, where a higher score indicates that the skin disease has a bigger influence on their quality of life.

  7. Prevalence of itch complaints [Day 1]

    Evaluation of possible extracutaneous manifestations patients with congenital ichthyosis exhibit. This is measured by a numeric rating scale (NRS) of itch. The higher the outcome, the more itch patients experience

  8. Prevalence of pain complaints [Day 1]

    Evaluation of possible extracutaneous manifestations patients with congenital ichthyosis exhibit. This is measured by a numeric rating scale (NRS) of pain. The higher the outcome, the more pain the patients experience

Eligibility Criteria

Criteria

Ages Eligible for Study:
16 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 16 years and older

  • Clinically and genetically confirmed congenital ichthyosis

Exclusion Criteria:
  • <16 years of age

  • Not able to read Dutch

  • Not able to fill in questionnaires online or in print

Contacts and Locations

Locations

Site City State Country Postal Code
1 Maastricht University Medical Centre + Maastricht Netherlands 6229HX

Sponsors and Collaborators

  • Maastricht University Medical Center

Investigators

  • Principal Investigator: Antoni C Gostynski, MD, PhD, Maastricht UMC+

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Maastricht University Medical Center
ClinicalTrials.gov Identifier:
NCT06123091
Other Study ID Numbers:
  • METC2023-0122-A-1
First Posted:
Nov 8, 2023
Last Update Posted:
Nov 8, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 8, 2023