Informations générales (source: ClinicalTrials.gov)

NCT04014543 Statut inconnu
Assessing the Quality of Life of Caregivers and Before and After the Position of Gastronomy
Interventional
N/A
Assistance Publique Hopitaux De Marseille (Voir sur ClinicalTrials)
janvier 2019
octobre 2020
29 juin 2024
The goal of this reasearch project is to study the quality of life of caregivers and children with generic questionnaires, validated and used in other pathologies and chronic diseases of the child. This will allow reproducibility and comparisons to other populations, general or other chronic diseases (acute leukemias ...) This is to conduct a pilot study, preliminary to the construction of a larger study, longitudinal with several evaluation times.
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Etablissements

Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données
Assistance Publique Hopitaux de Marseille - 13354 - Marseille - France Alexandre Fabre En recrutement Contact (sur clinicalTrials)

Critères

Tous
Inclusion Criteria:

Child:

- 1 month to 17 years old;

- Accepting to participate in the study;

- Having a pathology requiring enteral nutrition in the long term exclusive or mixed;

- Having the programming of the insertion of percutaneous gastrostomy in the
multidisciplinary pediatric ward.

Helping :

- Parent or representative of the parental authority of a child meeting the inclusion
criteria above;

- Accepting to participate in the study;

- Having the ability to comply with the protocol requirements (in particular:
understanding and speaking French).

- Siblings:

- 8 to 17 years old;

- Accepting to participate in the study;

- Having the ability to comply with the requirements of the protocol (understanding
and speaking French, presenting no sensory, motor, cognitive or severe chronic
illness);

- Living in the same home as the sick child.



Child:

- Refusing to participate in the study;

- Surgical, radiological or emergency gastrostomy.

Helping :

- Inability to comply with study protocol, or investigator uncertainty about
willingness or ability to comply with protocol requirements;

- Refusing to participate in the study.

- Siblings:

- Refusing to participate in the study.