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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07117058
Acronym
HARMONY-Tool
Enrollment
545
Registered
2025-08-12
Start date
2025-03-18
Completion date
2027-09-01
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Generalized Anxiety, Introspective & Anxiety-Prone Patient, Depression, Anxiety, Survivors of Childhood Cancer

Keywords

anxiety symptoms, childhood cancer, screening, psychological complication

Brief summary

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.

Detailed description

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.

Interventions

DIAGNOSTIC_TESTNew rapid screening tool for anxiety and depressive disorders

New rapid screening tool for anxiety and depressive disorders completed by patient during a regular follow-up consultation

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

Questionnaire completed by patient during a regular follow-up consultation : ONLY for patients 7-14 years old.

Questionnaire completed by patient during a regular follow-up consultation : ONLY for patients 15-25 years old.

Sponsors

Centre Hospitalier Universitaire de Saint Etienne
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
7 Years to 25 Years
Healthy volunteers
No

Inclusion criteria

* 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.

Exclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
New rapid screening tool for anxiety-depressive disordersAt inclusionThis 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)At inclusionOnly for 7-14 years old
HADS (Hospital Anxiety and Depression Scale)At inclusionOnly 15-25 years old

Countries

France

Contacts

CONTACTCLAIRE BERGER, MD
claire.berger@chu-st-etienne.fr(0)4.77.12.79.37
CONTACTLéonie CASAGRANDA, PhD
leonie.casagranda@chu-st-etienne.fr+33(0)477127937
PRINCIPAL_INVESTIGATORCLAIRE BERGER, MD

CHU SAINT-ETIENNE

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026