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Blandet metodevurdering av et foreldrepsykoedukasjonsprogram i en gruppe for forebygging av selvmordsrisiko (Pepps_Mix)

4. november 2026 oppdatert av: Assistance Publique - Hôpitaux de Paris

The number of emergency consultations for children and adolescents for suicidal ideation and suicide attempts has been rising steadily since 2010, and even more so since 2020. In addition, 30% of children and adolescents who have committed a suicidal act reoffend within the year.

Psycho-education programmes for patients have been shown to be effective in a large number of psychiatric pathologies. The programs of psychoeducation for the caregivers of these patients have them also shown their effectiveness, however to date there is no parental psychoeducation program group, for the prevention of the suicidal risk of children and adolescents, which is validated. The service of child psychiatry at the Robert Debré hospital built a program for this purpose, according to current data from the science and has been offering it for 6 months to parents of patients who consulted for suicidal ideation. Rate this program through the description of its implementation would allow it to be validated, this in a dissemination objective. This validation through a mixed method would also allow us to describe the experience participants in this program and to understand improvements Track.

Studieoversikt

Detaljert beskrivelse

Implementation study: non-randomized, single-center, quasi-experimental study before - after for the evaluation criteria of intermediate effectiveness (effectiveness). Study mixed qualitative-quantitative method for the evaluation of several judgment criteria.

The main objectives is to Evaluate the implementation of a parental psychoeducation program in a group of suicide prevention through parental support for the entire program.

The secondary objectives are to evaluate:

  • reaching the target population (Reach)
  • the intermediate effectiveness of the program
  • the adoption of the program by health professionals
  • the implementation on other dimensions
  • the sustainability of the program

Studietype

Observasjonsmessig

Registrering (Faktiske)

40

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Île-de-France Region
      • Paris, Île-de-France Region, Frankrike, 75019
        • Robert Debré Hospital, Child and adolescent psychiatry department

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Prøvetakingsmetode

Ikke-sannsynlighetsprøve

Studiepopulasjon

Parents of a child under 15 years 6 months old urgently consulted at the Robert Debré hospital for ideas suicidal or attempted suicide

Beskrivelse

Inclusion Criteria:

  • Parent committing to participate in the 4 sessions of the parental psychoeducation prevention program suicide risk (PEPPS program)
  • Parents of children under 15 years and 6 months
  • Parents fluent in French

Exclusion Criteria:

  • Lack of affiliation with a social security scheme or CMU (universal health coverage)
  • Parents under guardianship or curatorship

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Observasjonsmodeller: FAMILY_BASED
  • Tidsperspektiver: PROSPECTIVE

Kohorter og intervensjoner

Gruppe / Kohort
Intervensjon / Behandling
All of the participants

Parents participate in the PEPPS program (Parental psychoeducation program for suicide risk prevention) This is a group family psychoeducation program for parents child under 15 years 6 months having been urgently assessed at Robert University Hospital discharged for suicidal ideation or attempted suicide.

This program is built according to a global model based on:

  • A support program for parents of Resourceful adolescents: parent of adolescents support program not specific to the theme of suicidal risk taking place in 3 to 4 sessions of 2 hours.
  • The global program of the Suicide Prevention Intervention Center at the Children Hospital of Philadelphia which offers a multi-family group intervention (parents and children).
  • The recommendations of the High Authority of Health which recommend an intervention psychoeducation type.

Parents must complete the self-questionnaire WHOQOL-bref after the first and the last session of the Pepps program.

Parents must complete the self-questionnaire Evaluation Inventory - Parent after the last session of the Pepps program.

Parents must complete the quiz of knowledge after the first and the last session of the Pepps program.

Participants - qualitative interview

Semi-structured interviews (qualitative) will be carried out with parents who have followed either all or part of the sessions of the band. The parents interviewed will be chosen based on the wealth of information they will be likely to contribute to the study.The sampling method will follow the "snowball" model, described by Kathy Charmaz. According to this, the characteristics of new participants will be determined according to the results of the analysis of the first interviews until data saturation. We will conclude with the latter when no new information emerges from the data collection.

Parents must complete the self-questionnaire WHOQOL-bref after the first and the last session of the Pepps program.

Parents must complete the self-questionnaire Evaluation Inventory - Parent after the last session of the Pepps program.

Parents must complete the quiz of knowledge after the first and the last session of the Pepps program.

In the month following the last session of the program, the semi-structured interviews (qualitative) will be carried out with parents who have followed either all or part of the sessions of the band.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
implementation of a program parental psychoeducation in prevention groups suicide (program PEPPS).
Tidsramme: Week 5

program membership = Number of parents who have been present at the 4 sessions / Number of parents included (having agreed to participate in the program)

Week 5

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
reaching the target population
Tidsramme: Week 5

number of parents to whom the program has been proposed / number of parents having had a child having consulted for suicidal ideation

Week 5
Intermediate program effectiveness by comparison of levels of parents' responses between the start of program and the end of the last session of the program
Tidsramme: Week 5

level of knowledge about suicidal behavior: degree of certainty a knowledge quiz built for the program

Week 5
Intermediate program effectiveness by comparison of levels of parents' responses between the start of program and the end of the last session of the program
Tidsramme: Week 5

parents' quality of life: score WHOQOL-BREF scale

Week 5
adoption of the program by health professionals
Tidsramme: Week 5

number of emergency professionals offering program for parents / number of emergency professionals treating children having consulted for suicidal ideation

Week 5
Implementation on other dimensions
Tidsramme: Week 5

Number of parents participating in at least a session

Week 5
Implementation on other dimensions
Tidsramme: Week 5

Satisfaction of participating parents: Parent Evaluation self-questionnaire Inventory-Parent Treatment

Week 5
Implementation on other dimensions
Tidsramme: Week 5

Describe the parents' experience participant in the PEPPS program: analysis qualitative (interview)

Week 5
sustainability of the program (Maintenance): Interview
Tidsramme: Week 9

Identify the brakes and levers implementation of the program, in order to identify avenues for improvement and dissemination of psychoeducation program: analysis qualitative

Week 9

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

23. mai 2024

Primær fullføring (Faktiske)

30. juni 2025

Studiet fullført (Faktiske)

31. juli 2025

Datoer for studieregistrering

Først innsendt

4. juli 2024

Først innsendt som oppfylte QC-kriteriene

26. august 2024

Først lagt ut (Faktiske)

28. august 2024

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

6. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

4. november 2026

Sist bekreftet

1. november 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • APHP231318

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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