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Идёт набор NCT06528158

Speech Groups for Children Living With a Sibling Who Suffers From Anorexia Nervosa

Наблюдательное Anorexia Nervosa

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: sibling group.
Кому может быть актуально
Состояния в реестре: Anorexia Nervosa. Базовые параметры: 8 лет — 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Франция
Следующий шаг
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Официальное название

Sibling Group for Children and Teenagers Living With a Sibling Who Suffers From Anorexia Nervosa: a Pilot Acceptability Study

Обзор

Anorexia nervosa (AN) is a complex mental disease with a huge impact on the patient's siblings life and well-being. Based on literature, group interventions for siblings of children suffering from a chronic disease could provide an effective support. A few have been studied, and even fewer exist for siblings of children with AN.

Подробное описание

AN has a significant impact on nuclear family (parents and siblings). An emerging literature highlights the need for a particular attention to siblings. Despite this evidence, research and clinical applications still lack in this area. Indeed, most of health services in AN offer support for patients, family, parents, but only few specific support for siblings, although positive outcomes of sibling group interventions were reported in other somatic and psychic disabilities.

Noting the gap between the need and the lack of specific support, the study hypothesis is that the poor diffusion of these interventions in AN might result from a low acceptability. The study propose to explore acceptability to adapt and improve group intervention for siblings of children and teenagers receiving care for anorexia nervosa.

The study is a mixed-method pilot study assessing the acceptability of a group intervention by including a maximum of 24 siblings of children suffering from AN, aged from 8 to 18, across three group sessions, each consisting of 4 meetings. All participants will be invited to fulfill two different auto-questionnaires about their quality of life (before and after group session) and the intervention's acceptability (after group session).

Quantitative data will be complemented with qualitative data, collected from individual semi-structured interviews with a targeted sampling among group participants.

Вмешательства

  • Другое sibling group
    The group will be based on a systemic model and led by two child psychiatrists trained in family and multi-family therapy, who will not subsequently be involved in the data analysis. It will consist of 4 sessions of 1h30, spread over a period of 2 months, with a maximum of 8 participants per session. The first 3 sessions will be spaced 15 days apart, and the last session will take place 3 weeks apart from the third session. The characteristics of the group (frequency, duration, number of sessio

Первичные конечные точки

  • Group ACCEPTABILITY [Срок оценки: after attending group sessions, maximum 3 months after baseline]
Вторичные конечные точки (2)
  • Impact of the groups on quality of life [Срок оценки: baseline]
  • impact of the groups on quality of life [Срок оценки: after attending group sessions, maximum 3 months after baseline]

Критерии участия

  • inclusion criteria : Sibling presenting a DSM (Diagnostic and Statistical Manual)-5 of Mental Disorders diagnosis of AN, and engaged in inpatient or outpatient healthcare
  • exclusion criteria :
  • (1) Opposition from the participant and/or from their legal representatives.
  • (2) Non-fluent French speaker
  • (3) Clinical presentation not compatible with the group sessions

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Дизайн исследования

Модель наблюдения
Другое

Центры проведения

Франция · 1 центр
  • UH Toulouse — Toulouse

Идентификаторы

NCT: NCT06528158 · RC31/24/0181

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗