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

N/AEnrolling By InvitationNCT06934759

Central Hospital, Nancy, France30 enrolled

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.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Congenital Melanocytic Nevi Congenital Melanocytic Nevus Parent Psychology, Social

Interventions

No Intervention: Observational CohortOTHER

There is no intervention

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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

Locations (1)

Centre Hospitalier Régional Universitaire de Nancy

Nancy, France, France

Outcomes

Primary Outcomes

Results of the Semi-Structured Interviews with Parents

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

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.

Data from ClinicalTrials.gov

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