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

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

Status

Enrolling by invitation

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06934759

Acronym

PANGEA

Enrollment

Registered

2025-04-18

Start date

2025-12-01

Completion date

2026-08-31

Last updated

2025-12-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Keywords

parents, congenital melanocytic nevus, congenital melanocytic nevi, psychology, lived experience

Brief summary

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

OTHERNo Intervention: Observational Cohort

There is no intervention

Study design

Observational model

COHORT

Time perspective

CROSS_SECTIONAL

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame	Description
Results of the Semi-Structured Interviews with Parents	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.	Analysis of the interview transcripts = verbatim analysis Individual semi-structured interviews will be conducted via videoconference, with an estimated duration of 30 minutes to 1 hour. An interview guide has been developed to define the key dimensions to be explored. Each interview will be audio-recorded using a voice recorder and then fully transcribed. The interviews will undergo a thematic content analysis to identify meaningful patterns (nodes of meaning) within participants' narratives, using an inductive approach. A double coding will be performed by two investigators on five interviews to strengthen the thematic framework. The remaining interviews will be coded by a single investigator

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026