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临床试验/NCT07117058
NCT07117058招募中不适用

Validation of a Rapid Screening Tool for Anxiety-depressive Disorders in Children, Adolescents and Young Adults Treated in Oncology. Multicenter Study. Short Title: HARMONY-Tool

Centre Hospitalier Universitaire de Saint Etienne10 个研究点 分布在 1 个国家目标入组 545 人开始时间: 2025年3月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
545
试验地点
10
主要终点
HADS (Hospital Anxiety and Depression Scale)

研究概览

简要总结

In France today, it is estimated that one in every 850 people aged between 20 and 45 is a childhood cancer survivor (CCS), equivalent to around 40,000 to 50,000 people. Some descriptive studies have established that the diagnosis and treatment of cancer can affect psychological health. A French study published by our team in 2015 and 2020 showed that in adulthood, 40% of CCS had anxiety symptoms, a rate significantly higher than that of the general French population (25%). However, although there are validated scales for screening children for psychological disorders (anxiety, depression, etc.), there is no rapid screening tool that can be used routinely by an oncologist during consultations. So, the study aims to develop and validate a short test, which could easily be carried out systematically during follow-up consultations after childhood cancer. It would make it possible to identify people with no psychological complications and, conversely, those in whom further investigation, based on the classic reference scales for assessing psychological disorders, would be relevant.

详细描述

The aim of the HARMONY-Tool study is to develop and validate, using a psychometric method, a rapid screening tool for anxiety-depressive disorders in children, adolescents and young adults cured of childhood cancer.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

年龄范围
7 Years 至 25 Years(Child, Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients diagnosed with pediatric cancer before the age of 18,
  • •Patient whose intensive treatment had ended at least 3 months prior to inclusion,
  • •Patients considered to be in complete remission by the doctor responsible for their treatment,
  • •Patient affiliated to or entitled under a social security scheme,
  • •Patient having received informed information about the study OR the holder(s) of parental authority having received informed information about the study in the case of minors.

排除标准

  • •Refusal to participate expressed by the patient or minor,
  • •Patients whose cancer has relapsed or progressed,
  • •Pregnant women, women in labor, breast-feeding mothers,
  • •Persons deprived of their liberty, hospitalized without consent, hospitalized for purposes other than those of the research,
  • •Adults under legal protection (guardianship) or unable to express their consent.

研究组 & 干预措施

7-10 years old group

Develop and validate, using a psychometric method, a rapid screening tool for anxiety-depressive disorders in children cured of childhood cancer.

干预措施: New rapid screening tool for anxiety and depressive disorders (Diagnostic Test)

7-10 years old group

Develop and validate, using a psychometric method, a rapid screening tool for anxiety-depressive disorders in children cured of childhood cancer.

干预措施: SCARED-R-51 (Screen for Child Anxiety Related Emotional Disorders-Revised) (Diagnostic Test)

11-14 years old group

Develop and validate, using a psychometric method, a rapid screening tool for anxiety-depressive disorders in adolescents cured of childhood cancer.

干预措施: New rapid screening tool for anxiety and depressive disorders (Diagnostic Test)

11-14 years old group

Develop and validate, using a psychometric method, a rapid screening tool for anxiety-depressive disorders in adolescents cured of childhood cancer.

干预措施: SCARED-R-51 (Screen for Child Anxiety Related Emotional Disorders-Revised) (Diagnostic Test)

15-25 years old group

Develop and validate, using a psychometric method, a rapid screening tool for anxiety-depressive disorders in young adults cured of childhood cancer.

干预措施: New rapid screening tool for anxiety and depressive disorders (Diagnostic Test)

15-25 years old group

Develop and validate, using a psychometric method, a rapid screening tool for anxiety-depressive disorders in young adults cured of childhood cancer.

干预措施: HADS (Hospital Anxiety and Depression Scale) (Diagnostic Test)

结局指标

主要结局

HADS (Hospital Anxiety and Depression Scale)

时间窗: At inclusion

Only 15-25 years old

New rapid screening tool for anxiety-depressive disorders

时间窗: At inclusion

This tools is under construction. Items development of this tool is following 3 steps : 1. Identification of dimensions and generation of items : a combination of a deductive method (literature review) and an inductive method (questioning individuals) are used to identify the various dimensions relevant to the early assessment of anxiety and depressive disorders and generate the corresponding items. 2. Content validity : the expert judges method to confirm, supplement, or reduce the initial selection of items are used 3. Response options for content validity : binary response options for questions that are unambiguous are used. This tool will contain a maximum of 7 questions for children aged 6 to 10, 8 questions for adolescents aged 11 to 14 (in particular because of an additional question on the use of addictive substances) and 10 questions for the 15-25 age group (with the possibility of finer dimensions)

SCARED-R-51 (Screen for Child Anxiety Related Emotional Disorders-Revised)

时间窗: At inclusion

Only for 7-14 years old

HADS (Hospital Anxiety and Depression Scale)

时间窗: At inclusion

Only 15-25 years old

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (10)

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