Early Detection of Mental Disorders in Adolescents With Chronic Pain: Creation of a Screening Tool for Use by the General Practitioner

NCT ID: NCT04467229

Last Updated: 2020-07-10

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-07-06
• Study Completion Date: 2020-09-30

Brief Summary

This research aims to create a tool for detection of mental health disorders in adolescents with chronic pain. The first part is testing a screening questionnaire and comparing in with existing questionnaires. The second part involves two focus group with the adolescents aimed at recording their perception of the questionnaire.

Detailed Description

First part : creation of a screening tool. After detailed interviews with chronic pain experts and bibliographic research, a screening tool for mental disorders in chronically painful adolescents has been designed for use by the general practitioner. This tool is composed of 10 questions, making up a score of 10 points. The tool will be compared to two screening tools used in different clinical contexts, the HAD scale and the RPPS scale, in order to determine a positivity threshold. There is only one center participating in the research, the Centre de la Douleur et de la migraine de l'hôpital Trousseau (Trousseau Hospital Pain Center). Parents' consent is required for participation. For this assessment, the adolescents (between 10 and 18 years old) that see a doctor at the Centre de la douleur, will be asked to fill up the questionnaires in the waiting room. The filling of the questionnaire takes a few minutes. At the end of the appointment, the doctor will read the questionnaire to check that all elements have been addressed during the appointment.

Second part : focus group on the questionnaire: 5 to 10 adolescents will participate in a discussion group lead by a paediatrician and a psychologist from the Centre de la Douleur de Trousseau. Two groups will be organized, the length of the group discussion being one hour. These focus groups will explore the adolescents' perception of the questionnaire and of different elements of the screening. The group will undergo full transcription. The verbatim will be anonymous and will be analysed through qualitative methods.

The data will help designing a guidebook for the clinician explaining the main points in screening for mental disorders in chronic pain adolescent patients.

A validation study for the screening tool will be eventually carried out after the completion of this preliminary study.

Conditions

Chronic Pain; Mental Disorder

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

Focus group with chronically painful adolescents

Adolescents with chronic pain

Group Type: EXPERIMENTAL

Focus group

Intervention Type: BEHAVIORAL

5 to 10 adolescents will participate in a discussion group lead by a paediatrician and a psychologist from the Centre de la Douleur de Trousseau. Two groups will be organized, the length of the group discussion being one hour. These focus groups will explore the adolescents' perception of the questionnaire and of different elements of the screening. The group will undergo full transcription. The verbatim will be anonymous and will be analysed through qualitative methods.

Interventions

Focus group

5 to 10 adolescents will participate in a discussion group lead by a paediatrician and a psychologist from the Centre de la Douleur de Trousseau. Two groups will be organized, the length of the group discussion being one hour. These focus groups will explore the adolescents' perception of the questionnaire and of different elements of the screening. The group will undergo full transcription. The verbatim will be anonymous and will be analysed through qualitative methods.

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• patient from 10 to 18 years old
• chronic pain (existing for more than 3 months or longer than tissue repair time)
• first consultation in the service
• Collection of the written consent of the holders of parental authority and agreement of the adolescent
• Adolescents able to understand the questionnaire and the purpose of the study
• Affiliation to a social security scheme or beneficiary

Exclusion Criteria

• Decompensated physical or psychological pathology requiring urgent medical treatment
• Heavy psychological pathology preventing the adolescent's understanding of the study
• Patient benefiting from State Medical Aid

• Minimum Eligible Age: 10 Years
• Maximum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Alexandra LOISEL

Role: PRINCIPAL_INVESTIGATOR

Assistance Publique - Hôpitaux de Paris

Locations

Centre de la douleur et de la migraine-Hôpital Trousseau

Paris, , France

Countries

France

Central Contacts

Alexandra LOISEL, PH

Role: CONTACT

loisel.alexandra@aphp.fr

01 71 73 85 47

Barbara TOURNIAIRE, ph

Role: CONTACT

barbara.tourniaire@aphp.fr

01 71 73 89 19

Facility Contacts

Alexandra LOISEL, PH

Role: primary

loisel.alexandra@aphp.fr

01 71 73 85 47

Barbara TOURNIAIRE, PH

Role: backup

barbara.tourniaire@aphp.fr

01 71 73 89 19

Other Identifiers

APHP200623

Identifier Type: -

Identifier Source: org_study_id