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Clinical Trials/NCT04527692
NCT04527692
Unknown
Not Applicable

Exploring the Quality of Life of Children/Adolescents in Palliative Settings and That of Their Parents

University Hospital, Toulouse1 site in 1 country320 target enrollmentApril 15, 2020
ConditionsPalliative Care

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Palliative Care
Sponsor
University Hospital, Toulouse
Enrollment
320
Locations
1
Primary Endpoint
Quality of life measure
Last Updated
5 years ago

Overview

Brief Summary

Investigators will propose to each family monitored by the teams to participate in the study (children between 1 and 18 years old, families understanding and speaking a minimum of French).

Semi-directed interviews are organized with children/adolescents and their parents who have agreed to participate in the study. The interviews are conducted by the care teams themselves. Socio-demographic data are collected.

Detailed Description

An information letter will be distributed to the children and parents and their non opposition to their participation will be sought (or assent for the child via a written document adapted to the age) will be systematically requested. Several instruments will be used by the members of the paediatric teams during their routine home or hospital visits to children and their families: the CPOS (Downing 2018), the KINDL (generic questionnaire on quality of life validated for healthy children, Erhart et al. 2009), the QOLLTI-F v.2 (questionnaire on quality of life for parents, Cohen 2007, 2015). The interviews will therefore be semi-directed interviews with children/adolescents and their parents who have agreed to participate in the study. The interviews will be conducted by the care teams themselves. In addition to the CPOS, KINDL and QOOLTI-F, socio-demographic data are collected.

Registry
clinicaltrials.gov
Start Date
April 15, 2020
End Date
November 15, 2022
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Children/adolescents aged 1 to 18 years with a serious illness and requiring follow-up by a regional pediatric palliative care resource team and/or temporarily hospitalized.
  • Having given his non-opposition to his participation.
  • A minor of whom at least one of the two holders of parental authority has given his or her consent to the participation of their child.
  • Child of whom one of the two holders of parental authority has himself agreed to participate in the study.

Exclusion Criteria

  • Children/adolescents at the end of life (imminent death foreseeable).
  • Children/adolescents and their parents who do not understand French.
  • Child or parent under legal protection (guardianship, curatorship).

Outcomes

Primary Outcomes

Quality of life measure

Time Frame: Day 1

Exploring the quality of life of children/adolescents in palliative settings and that of their parents through the development of the Childrens palliative outcome scale.

Secondary Outcomes

  • psychometric measure - KINDL(Day 1)
  • psychometric measure - QOLLTI-F(Day 1)
  • psychometric measure - Children's palliative outcome scale(Day 1)

Study Sites (1)

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