Guidelines for Parental Involvement in the Care of Suicidal Youth (S-Urg-Quali)

March 24, 2022 updated by: University Hospital, Clermont-Ferrand

Developing Guidelines for Parental Involvement in the Emergency Care of Suicidal Adolescents and Young Adults: a Qualitative Study

Parents occupy a central place in the emergency care of suicidal adolescents and young adults. However, from 15 to 25yo, three different administrative situations exist in France:

  • <16yo: admission to a child ED by a team trained to receive the youngest patients.
  • 16-18yo: admission to an adult ED by team devoted to adult care, no exit without parents' authorization.
  • >18yo: admission to an adult ED by team.

Laying on qualitative observational protocol and a Delphi approach, this study will explore the perspective of adolescents and young adults following a suicidal attempt, the perspective of their parents, and the perspective of their healthcare professionals to build guidelines for parental involvement in care of suicidal youths.

Study Overview

Status

Not yet recruiting

Detailed Description

Suicide is the second leading cause of death among 15-25 year olds, with the highest rate of hospitalization for SC of any age group. The psychopathology of suicidal behavior in adolescents and young adults (AYA) is homogeneous: risk factors, precipitating factors, representations. Parents occupy a central place in care. They are i) involved in the care decision; ii) actively involved in care; and ii) a source of motivation for trust and adherence to care.

However, if the psychopathology of suicidal crisis is homogeneous, the transition between pediatric and adult care implies very different management in the emergency department (ED). In France, three situations can be described:

  • <16yo: admission to a child ED by a team trained to receive the youngest patients.
  • 16-18yo: admission to an adult ED by team devoted to adult care, no exit without parents' authorization.
  • >18yo: admission to an adult ED by team devoted to adult care, no right to contact the parents in case of patient opposition.
  • Before 16 years of age: admission to the children's UAS, care by a team trained to receive the youngest patients.
  • 16-18 years: admission to the adult UAS, care by adult professionals, clinical and legal particularities of care for minors.
  • After 18 years old: admission to adult UAS, legal constraints of the adult care setting.

The objectives of this qualitative observational study is to build guidelines for the involvement of the parents in the care in these three situations.

The study will include adolescents and young adults from the three situations, their parents and the professionals who take care of them. Individual semi-structured interviews will be organized to collect their experiences. Qualitative analyses will be conduct, following Interpretative Phenomenological Analysis. A pre-approved guideline will be construct and a Delphi approach will be conducted to approved the final version of the guideline.

Study Type

Observational

Enrollment (Anticipated)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Clermont-Ferrand, France, 63000
        • CHU de Clermont-Ferrand
        • Principal Investigator:
          • Jonathan Lachal

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

15 years to 25 years (Child, Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Any adolescent and young adult admitted to an Emergency Department (ED) in one of the inclusion center following a suicidal act or considered as such by the medical team. Their parents; healthcare professionals working in ED of the inclusion centers.

Description

Inclusion Criteria:

Adolescents and Young adults

  • Admitted to an Emergency Department (ED) following a suicidal act or considered as such by the medical team

Parents

  • Parents of the included youths >18y

Healthcare professionals

  • >18y
  • Working in ED
  • Usually taking care of suicidal youths

All the participants

  • French speaking
  • Affiliation to a social security regime
  • Participation agreement

Exclusion Criteria:

All the participants

  • Present an acute somatic or psychiatric disease which may hinder the well organization of the interview

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Adolescents and young adults
Boys and girls from 15 to 25 years old admitted to an Emergency Department (ED) following a suicidal act or considered as such by the medical team
Parents
One or the two parents of the included adolescents and young adults
Healthcare professionals
Professionals working in one emergency departments of the inclusion centers and who usually take care of suicidal adolescents and young adults

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Developing guidelines defining the role of parents in the medical decision and the care of the youths
Time Frame: Day 1
Thematic framework summarizing the perspectives of three groups of participants.
Day 1

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Describing each context of care
Time Frame: Day 1
Qualitative description of each of the three context of care (<16y, 16-18y, >18y)
Day 1
Describing expectations from each group
Time Frame: Day 1
Qualitative description of each of the three participant groups (adolescents and young adults, parents, professionals)
Day 1

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jonathan Lachal, University Hospital, Clermont-Ferrand

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

May 1, 2022

Primary Completion (Anticipated)

May 1, 2023

Study Completion (Anticipated)

May 1, 2023

Study Registration Dates

First Submitted

March 14, 2022

First Submitted That Met QC Criteria

March 24, 2022

First Posted (Actual)

March 25, 2022

Study Record Updates

Last Update Posted (Actual)

March 25, 2022

Last Update Submitted That Met QC Criteria

March 24, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • AOI 2021 LACHAL
  • 2021-A03244-37 (Other Identifier: ANSM)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Emergencies

3
Subscribe