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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04467229
Other study ID # APHP200623
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date July 6, 2020
Est. completion date September 30, 2020

Study information

Verified date July 2020
Source Assistance Publique - Hôpitaux de Paris
Contact Alexandra LOISEL, PH
Phone 01 71 73 85 47
Email loisel.alexandra@aphp.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date September 30, 2020
Est. primary completion date September 30, 2020
Accepts healthy volunteers No
Gender All
Age group 10 Years to 18 Years
Eligibility 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:

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

Study Design


Intervention

Behavioral:
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.

Locations

Country Name City State
France Centre de la douleur et de la migraine-Hôpital Trousseau Paris

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Screening questionnaire score A new Screening questionnaire elaborated beforehand by the study will be answered by patients in order to detect psychological suffering in chronically painful adolescents The screening questionnaire consists in 10 items (yes/no response format) Baseline visit
Secondary Hospital Anxiety and Depression (HAD) score Patients complete a Hospital Anxiety and Depression (HAD) scale questionnaire Baseline visit
Secondary Pediatric Pain Screening Tool (PPST) score Patients complete a Pediatric Pain Screening Tool questionnaire Baseline visit
Secondary Participants feedback Focus group questions will provide descriptions of patients' experiences with the questionnaire up to 3 months upon recuitment
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