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Impact of External Workplace Violence on the Occupational Well-being of Healthcare Workers

3. november 2026 opdateret af: Consorci Sanitari de l'Alt Penedès i Garraf

Impact of External Occupational Violence on Healthcare Professionals and Organizations: a Multicenter Cross-sectional Study

The goal of this observational study is to learn whether external workplace violence (violence by patients, relatives, or companions) is associated with poorer occupational well-being in healthcare workers aged 18 years or older who have regular face-to-face contact with patients or their families. The main questions it aims to answer are:

  • Do healthcare workers who have experienced external workplace violence in the past 12 months report more negative effects of work (somatization, exhaustion, and alienation) than those who have not?
  • How common is external workplace violence, what types occur (physical, verbal, symbolic, digital, or economic), and how intense are they?
  • Is external workplace violence associated with working conditions and organizational practices? Researchers will compare healthcare workers who have experienced external workplace violence with those who have not to see if their occupational well-being scores differ.

Participants will complete a single anonymous online survey about their experience of workplace violence, their occupational well-being, their working conditions, and the measures they consider most effective to reduce violence.

Studieoversigt

Status

Rekruttering

Detaljeret beskrivelse

This multicenter cross-sectional study will be conducted in seven healthcare organizations with different profiles. Participants will be randomly selected from the staff census of each center, stratified by area or department, and invited to complete an anonymous online survey hosted on the REDCap platform of the sponsor. The survey includes the collateral effects dimension of the General Occupational Well-being Questionnaire (cBLG; somatization, exhaustion, and alienation scales; total score 13-91), 22 items of the Working Conditions Questionnaire (cCT; score 0-220), 6 ad hoc items on organizational practices (score 0-60), self-reported workplace violence in the past 12 months by type and intensity, and sociodemographic and occupational variables.

The primary analysis will compare mean collateral effects scores between workers with and without external workplace violence using Student's t test, followed by multivariable analyses adjusted for sex, age group, professional category, care setting, work shift, type of contract, and seniority. Subgroup analyses by sex, professional category, and center, and a dose-response analysis by violence intensity, are planned.

Undersøgelsestype

Observationel

Tilmelding (Anslået)

442

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

  • Navn: Noemí Casaponsa
  • Telefonnummer: 43197 0034938960025
  • E-mail: recerca@csapg.cat

Studiesteder

    • Barcelona
      • Barcelona, Barcelona, Spanien
        • Rekruttering
        • Hospital Clinic
        • Kontakt:
        • Ledende efterforsker:
          • Marta Hage
      • Barcelona, Barcelona, Spanien
        • Rekruttering
        • Sistema d'Emergències Mèdiques de Catalunya
        • Kontakt:
        • Ledende efterforsker:
          • Mireia Campos
      • Calella, Barcelona, Spanien
        • Rekruttering
        • Corporació de Salut del Maresme i la Selva
        • Kontakt:
        • Ledende efterforsker:
          • Sergio Bujaldón
      • Terrassa, Barcelona, Spanien
        • Rekruttering
        • Consorci Sanitari de Terrassa
        • Kontakt:
        • Ledende efterforsker:
          • Clara Romero
      • Vilafranca del Penedès, Barcelona, Spanien
        • Rekruttering
        • Consorci Sanitari de l'Alt Penedès i Garraf
        • Kontakt:
        • Ledende efterforsker:
          • Genís Cervantes
      • Vilafranca del Penedès, Barcelona, Spanien
        • Rekruttering
        • Institut Català de Salut Àrea Penedès
        • Kontakt:
        • Ledende efterforsker:
          • Alberto Domínguez
    • Girona
      • Girona, Girona, Spanien
        • Ikke rekrutterer endnu
        • Institut d'Assistència Sanitària
        • Kontakt:
        • Ledende efterforsker:
          • María Cruz Rodríguez

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Prøveudtagningsmetode

Sandsynlighedsprøve

Studiebefolkning

Active healthcare workers of the participating centers whose work involves direct and regular contact with external users (patients, relatives, or companions), including clinical, technical, auxiliary, and administrative or front-desk staff

Beskrivelse

Inclusion Criteria:

  • Aged 18 years or older
  • At least 12 months of employment at the study center
  • Active healthcare worker whose work involves direct and regular contact with external users (patients, relatives, or companions), defined as at least one face-to-face interaction on 2 or more days in a typical working week

Exclusion Criteria:

  • Refusal to participate in the study

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Observationsmodeller: OTHER
  • Tidsperspektiver: CROSS_SECTIONAL

Kohorter og interventioner

Gruppe / kohorte
Healthcare workers with external workplace violence

Workers who self-report at least one episode of external workplace violence (physical, verbal, symbolic, digital, or economic) in the past 12 months

Healthcare workers without external workplace violence

Workers who report no episodes of external workplace violence in the past 12 months

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Collateral effects of work (occupational well-being)
Tidsramme: At survey completion (single time point)

Sum of the somatization (5 items), exhaustion (4 items), and alienation (4 items) scales of the collateral effects dimension of the General Occupational Well-being Questionnaire (cBLG; Blanch et al.). Total score range: 13 to 91; higher scores indicate greater deterioration of occupational well-being.

At survey completion (single time point)

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

24. februar 2026

Primær færdiggørelse (Anslået)

31. december 2026

Studieafslutning (Anslået)

31. december 2026

Datoer for studieregistrering

Først indsendt

3. november 2026

Først indsendt, der opfyldte QC-kriterier

3. november 2026

Først opslået (Faktiske)

9. november 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

9. november 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

3. november 2026

Sidst verificeret

1. november 2026

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

JA

IPD-planbeskrivelse

IPD (without personal identification data) could be shared by requirement from other researchers after the end of the study, and only for research purposes and previous approval of promotor center of the study (CSAPG). Anyway, Spanish and European Union legal policy about data protection will strictly be followed (IPD will not be transferred outside European Union).

IPD-delingstidsramme

After publication of main results of the study

IPD-delingsadgangskriterier

IPD will be shared only for scientific research purposes and following the Spanish and European Union normative law about data protection. The requirements will be directed to the IP of the study. The IP will evaluate the request to verify and evaluate the data that is requested and the purposes for which it is requested. Next, the IP will transfer the request to the promotor center the study for the final decision.

IPD-deling Understøttende informationstype

  • STUDY_PROTOCOL

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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