Coping Strategies, Loneliness, and Resilience in Patients With Dermatosis

NCT07640373 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 375

Last updated 2026-06-10

No results posted yet for this study

Summary

The European Society for Dermatology \& Psychiatry (ESDaP) studies the connection between the skin and the mind. Two previous studies of this type were conducted in 13 and 15 European countries, respectively. The first study assessed the psychological impact of skin diseases (anxiety, depression, sleep disorders), and the second analyzed feelings of stigma, stress, and body dysmorphic disorder (an abnormal perception of one's body).

In this study, new psychological variables will be examined: coping strategies, loneliness, and resilience.

A total of 23 centers will participate in the ESDaP3 study, located in 15 European countries (Austria, France, Germany, Hungary, Italy, North Macedonia, the Netherlands, Norway, Poland, Spain, Sweden, Switzerland, Turkey, and the United Kingdom).

The aim of this study is to examine coping strategies, loneliness, and resilience among patients with a skin condition. Coping strategies refer to the various ways a person uses to manage a difficult or stressful situation. Resilience refers to a person's ability to cope with difficult situations, adapt to changes or challenges, and regain a sense of balance despite obstacles. Other factors will be assessed: sleep, anxiety and depression, and quality of life. A questionnaire will be given to your potential partner to assess the impact of the skin condition on their life at this time.

At the study's sole French site, Brest University Hospital, 250 patients with a skin condition and 125 people without a skin condition will be enrolled.

Conditions

  • Skin Disease
  • Skin Disorder
  • Skin Condition
  • Inflammatory Skin Conditions
  • Autoimmune Skin Diseases
  • Cancerous Skin Conditions
  • Genetic Skin Conditions

Interventions

OTHER

Questionnaires

* Coping strategies: Brief COPE questionnaire (dispositional format) * Loneliness: UCLA Loneliness Scale (ULS-8) * Resilience: Brief Resilience Scale (BRS) * Sleep: Insomnia Severity Index Questionnaire (ISI) * Anxiety: Generalized Anxiety Disorder 2 (GAD-2) * Depression: Patient Health Questionnaire-2 (PHQ-2) * Quality of life: Dermatology Life Quality Index (DLQI) * Well-being: Skin Well-Being Scale * Impact of dermatosis on the partner: FROM-16

Sponsors & Collaborators

  • University of Graz

    collaborator OTHER
  • Justus-Liebig University Gießen Medical Center

    collaborator UNKNOWN
  • Szeged University

    collaborator OTHER
  • University of Skopje

    collaborator OTHER
  • University of Amsterdam

    collaborator OTHER
  • University of Stavanger

    collaborator OTHER
  • University of Bergen

    collaborator OTHER
  • Wroclaw Medical University

    collaborator OTHER
  • University of Rzeszow

    collaborator OTHER
  • Universidade do Algarve

    collaborator OTHER
  • Universidad de Zaragoza

    collaborator OTHER
  • University of La Laguna

    collaborator OTHER
  • Malmö University

    collaborator OTHER
  • Lund University

    collaborator OTHER
  • Karolinska Institutet

    collaborator OTHER
  • Sisli Hamidiye Etfal Training and Research Hospital

    collaborator OTHER
  • Cardiff University

    collaborator OTHER
  • University Hospital Muenster

    collaborator OTHER
  • Leiden University Medical Center

    collaborator OTHER
  • The Royal London Hospital, UK

    collaborator UNKNOWN
  • University Hospital, Brest

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-07-31
Primary Completion
2029-07-31
Completion
2029-10-31

Countries

  • France

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07640373 on ClinicalTrials.gov