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Parenting Concerns in Patients With Cystic Fibrosis (MucoPar)

Expectations and Needs of Patients With Cystic Fibrosis Becoming Parents - Exploratory Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04133246
Acronym
MucoPar
Enrollment
52
Registered
2019-10-21
Start date
2019-09-25
Completion date
2020-12-21
Last updated
2025-11-20

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

Conditions

Cystic Fibrosis

Keywords

cystic fibrosis, parenthood, Psycho-social, Qualitative study

Brief 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

Detailed description

Life expectancy has improved significantly in cystic fibrosis in recent years. From paediatric disease, it has become a disease of the adult, with the emergence of new issues, such as becoming a parent. Parent patients still face the risk of complications and death while their child is still young. However, there is very little data in the literature on parenting in cystic fibrosis. Therefore, the purpose of this study is to explore and collect the perceptions, expectations and needs of CF patients and their spouses about parenting. All patients with children, followed in 2 large adult CF centers, and their spouses will be invited to participate in a 6 to 10-person discussion group (focus group) led by a psychologist. He will ensure that all the participants express themselves and are encouraged to develop their points of view, their divergences and their common points about what constitutes to be a parent. The discussions will be recorded and transcribed. Patients who cannot participate in groups (e.g. patients colonized with Burkholderia cepacia complex) but wish to be included in the study will benefit from an individual interview with the psychologist, also registered and transcribed. A thematic analysis will be carried out from the transcriptions of group contents. For individual interviews, phenomenological interpretative analysis (IPA) will be used. A synthesis of the two analyses will then be done. The collected information should make it possible to develop and propose adapted medico-psycho-social interventions, if necessary, in connection with patient associations.

Interventions

BEHAVIORALFocus group

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

Interview led by the psychologist about the patient's parenthood

Sponsors

URC-CIC Paris Descartes Necker Cochin
CollaboratorOTHER
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

For patients * Have cystic fibrosis * Be a parent and raise or have raised at least one child * Being followed in one of the two adult CF centers participating in the study For CF patients' spouses \- Live with the CF patient participating in the study For both CF patients and spouses * Being an adult (at least 18 y.o.) * Have a good level of French and good speaking skills

Exclusion criteria

* For both CF patients and spouses * Psychiatric pathology (borderline state, bipolarity and other psychotic disorders) * Serious somatic disease not related to cystic fibrosis

Design outcomes

Primary

MeasureTime frameDescription
Identification of themes about parenthood in CF from groups2 yearsby thematic analysis. 8 to 10 focus groups composed of 5 to 10 persons are to be conducted until saturation of themes.

Secondary

MeasureTime frameDescription
Identification of themes about parenthood in CF from individual interviews2 yearsby the IPA method. 20 individual interviews are to be conducted until saturation of themes
Occurrence of themes2 yearsnumber of appearances of each theme, revealed by the 2 analyses, in the group arm on one hand, and in the interview arm on the other hand. The occurrence will provide information on the importance of each theme

Countries

France

Outcome results

None listed

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