Parenting Concerns in Patients With Cystic Fibrosis (MucoPar)

NCT04133246 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2025-11-20

No results posted yet for this study

Summary

The purpose of this study is to explore and collect the perceptions, expectations and needs of CF patients about parenting. This will be done in the context of several small groups of patients led by a psychologist who will ensure that all the participants express themselves; he will encourage them to develop their points of view, their divergences and their common points about what constitutes to be a parent.

The collected information should make it possible to develop and propose adapted medico-psycho-social interventions, if necessary, in connection with patient associations

Conditions

Interventions

BEHAVIORAL

Focus group

Groups of 6 to 10 patients and spouses led by the psychologist about their parenthood lasting 2 hours

BEHAVIORAL

Individual interview

Interview led by the psychologist about the patient's parenthood

Sponsors & Collaborators

  • URC-CIC Paris Descartes Necker Cochin

    collaborator OTHER
  • Assistance Publique - Hôpitaux de Paris

    lead OTHER

Principal Investigators

  • Cécile FLAHAULT, Ph.D · Assistance Publique - Hôpitaux de Paris

  • Dominique HUBERT, MD · Assistance Publique - Hôpitaux de Paris

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-25
Primary Completion
2020-12-21
Completion
2020-12-21

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 NCT04133246 on ClinicalTrials.gov