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Suicide, AttemptedS-Urg-QualiNCT05296343

Guidelines for Parental Involvement in the Care of Suicidal Youth

An observational study of Suicide, Attempted and Emergencies, run by University Hospital, Clermont-Ferrand at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 15 to 25 years
Conditions the study is for
Suicide, Attempted, Emergencies
How many people
61 participants
Where
1 siteFrance
Study dates
18 May 2022to 31 Oct 2024
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 15 to 25 years
  • All sexes
  • Child, Adult

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.

Who may be able to join

  • 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
Show all 12Show fewer
  • Working in ED
  • Usually taking care of suicidal youths
  • All the participants
  • French speaking
  • Affiliation to a social security regime
  • Participation agreement

Who cannot join

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

Trial locations and contacts

1 site in 1 country.

France1 site
  • CHU de Clermont-Ferrand

    Clermont-Ferrand, 63000

Other trials in France

About this study

Official title: 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.

Read the 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.

Keywords
Adolescent, Parent, Qualitative study, Guidelines
Medical subject headings
Suicide, Attempted, Emergencies

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT05296343
Study groupRoleWhat they receive
Adolescents and young adultsBoys 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
ParentsOne or the two parents of the included adolescents and young adults
Healthcare professionalsProfessionals working in one emergency departments of the inclusion centers and who usually take care of suicidal adolescents and young adults

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Developing guidelines defining the role of parents in the medical decision and the care of the youths

    Thematic framework summarizing the perspectives of three groups of participants.

    Measured: Day 1

Secondary outcomes (2)
  1. Describing each context of care

    Qualitative description of each of the three context of care (<16y, 16-18y, >18y)

    Measured: Day 1

  2. Describing expectations from each group

    Qualitative description of each of the three participant groups (adolescents and young adults, parents, professionals)

    Measured: Day 1

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Mar 2022
  2. Study start18 May 2022
  3. Primary completion31 Oct 2024
  4. Study completion31 Oct 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
61 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05296343
Sponsor's protocol ID
AOI 2021 LACHAL
Other IDs
2021-A03244-37
Acronym
S-Urg-Quali
Status last verified
Nov 2024
First submitted
14 Mar 2022
Last updated
12 Nov 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Suicide, Attempted and Emergencies, run by University Hospital, Clermont-Ferrand at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 12 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 12 Nov 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Developing guidelines defining the role of parents in the medical decision and the care of the youths (time frame: Day 1). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Nov 2024.

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