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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04619901
Other study ID # 2017_14
Secondary ID 2018-A01226-49
Status Recruiting
Phase
First received
Last updated
Start date February 12, 2020
Est. completion date March 2023

Study information

Verified date January 2023
Source University Hospital, Lille
Contact Laurent Storme, MD,PhD
Phone 03 20 44 61 99
Email laurent.storme@chru-lille.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Palliative care is now an accepted principle in most maternity and neonatology wards, however not much is known about its psychological and social consequences on families. Some children continue their life after a palliative care decision has been taken. In France, quality of life and the neuro-developmental evolution of newborns who continue their life after a palliative care decision has been taken, have never been studied.


Recruitment information / eligibility

Status Recruiting
Enrollment 34
Est. completion date March 2023
Est. primary completion date March 2023
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Father and/or Mother of a child, who is alive or not, for whom a decision of palliative care has been made in the neonatal period - Under the care of one of the Level 3 Maternity Centers in the North and Pas-de-Calais departments (Arras, Lens, Lille, Valenciennes) since 2018 - Written consent of the two legal guardians of the child allowing the collection of data concerning the child - Written consent of the parent(s) participating to this study by completing the parental questionnaires Exclusion Criteria: - Medico-legal complaint underway - Parents who do not understand French - Parents or children who are under legal protection (guardianship, curatorship) - Parents or children who are not Social Security beneficiaries

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Semi-structured interviews
Exploring the psychological and social impact on parents of a palliative care decision concerning their child in the neonatal period
Questionnaire
Assessing the neuro-developmental evolution of children and understanding the determinants of the psychological and social impact of palliative care decisions on parents
following Scales
Scales : Hospital Anxiety and Depression, Intolerance to Uncertainty, and Brief COPE.

Locations

Country Name City State
France CH ARRAS Arras
France CH LENS Lens
France Hop Jeanne de Flandre Chu Lille Lille
France CH Valenciennes Valenciennes

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Semi Structured interview Parents : Exploring the psychological and social impact of the palliative care decision 2 hours semi structured interviews will be done to describe the psychological and social impact a decision of palliative care concerning their newborn infant has on parents. 24 months after palliative care decision
Secondary Ages and Stages Questionnaire (ASQ) - Clinical Examination of Child Child : Neuro-Developmental Assessment 24 months after palliative care decision
Secondary Semi Structured Interview Parents : Determinants of the psychological and social impact of the palliative care decision 24 months after palliative care decision
Secondary Hospital Anxiety and Depression Scale (HADS) Parents :Psychometric Measure of Anxiety and Depression The scale allows to detect anxiety and depression using 14 items rated from 0-3. 24 months after palliative care decision
Secondary Intolerance to Uncertainty Scale (EEI) Parents : Psychometric Measure of Intolerance to Uncertainty This questionnaire contains 27 items measuring emotions, cognitions and behaviours in ambiguous situations, the consequences of being uncertain and attempts to control the future.Items are rated on a Likert scale from 1 ("Not at all matching") to 5 ("Very matching"). The total share is obtained by adding the items. 24 months after palliative care decision
Secondary Brief COPE Parents : Psychometric Measure of Coping Strategies The Brief-COPE is a 28 item self-report questionnaire withs scoring and interpretation: Positive reframing / Planning/ Humor / Religion/Self-blame 24 months after palliative care decision