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Enrolling by invitation NCT06934759

Impact and Lived Experience of Parents of a Child With a Large or Giant Congenital Melanocytic Nevus

— Observational Congenital Melanocytic Nevi Congenital Melanocytic Nevus Parent Psychology, Social

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: No Intervention: Observational Cohort.
Who it may be relevant to
Registry conditions: Congenital Melanocytic Nevi, Congenital Melanocytic Nevus, Parent, Psychology, Social. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Impact and Lived Experience of Parents of a Child With a Large or Giant Congenital Melanocytic Nevus (PANGEA Study) : A National Qualitative Study

Overview

The goal of this observational study is to describe the experiences of parents at the birth of a child with a large or giant congenital melanocytic nevus through semi-structured interviews, and to identify potential intervention strategies to improve their care and support.

Interventions

  • Other No Intervention: Observational Cohort
    There is no intervention

Primary outcome measures

  • Results of the Semi-Structured Interviews with Parents [Time frame: Socio-demographic data and interview transcripts will be collected during the semi-structured interviews (lasting between 30 minutes and 1 hour), thus at a single time point (Day 1). No follow-up is required.]

Eligibility criteria

Inclusion criteria

  • Aged 18 years or older
  • Willing to participate in a semi-structured interview
  • Has received full information about the research and has not objected to participating or to the use of their data
  • Able to understand and speak French
  • Parent of a child under 18 years of age

Exclusion criteria

  • Under 18 years of age
  • Not willing to participate
  • Currently under legal protection (e.g., guardianship or curatorship)
  • Cognitive and/or psychological impairments preventing participation in a semi-structured interview
  • Poor understanding and/or expression of the French language
  • Parent of a child over 18 years of age

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

France · 1 center
  • Centre Hospitalier Régional Universitaire de Nancy — Nancy

Identifiers

NCT: NCT06934759 · 2024PI238

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗