Skip to content

More Effective Violence Risk Management - eDASA+APP FI

More Effective Violence Risk Management for Psychiatric Wards - eDASA+APP FI

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06342531
Acronym
eDASA+APP FI
Enrollment
26
Registered
2024-04-02
Start date
2024-06-01
Completion date
2026-12-31
Last updated
2025-04-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Violence

Keywords

violence risk assessment, DASA, Dynamic Appraisal of Situational Aggression, mental health nursing, EPIC, electronic health records, violence risk management, inpatient psychiatric care, coercive measures, clinical decision support system, CDSS, co-design, nurse-patient collaboration

Brief summary

The main goal of this study is to evaluate if the Finnish version of eDASA+APP (electronic Dynamic Appraisal of Situational Aggression + Aggression Prevention Protocol), a clinical decision support system (CDSS), has an impact on reducing workplace violence, use of coercive measures and increasing nurses' job satisfaction in adult psychiatric inpatient care.

Detailed description

The study includes three phases: 1) exploring attitudes of nurses and nurse managers towards validated tools, violence risk assessment and management, 2) a pre-implementation including a co-design process of the eDASA+APP to ensure optimal integration and adaptation to local context and integration into the local EPIC based EHR system together with relevant stakeholders (health care staff and expert-by-experience), and 3) a quasi-experimental implementation study to evaluate the impact of the intervention (eDASA+APP FI).

Interventions

BEHAVIORALeDASA+APP FI

A CDSS for nurses to assist in their daily short-term violence risk assessment and management, is integrated into an EPIC-based EHR system.

Sponsors

Helsinki University Central Hospital
CollaboratorOTHER
University of Turku
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Intervention model description

A pre-post design (quasi-experimental), a cluster design

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* adult psychiatric wards

Exclusion criteria

* psychiatric wards specialized only for the care of people with intellectual disabilities, wards providing care for both adults and underaged patients (eating disorder units)

Design outcomes

Primary

MeasureTime frameDescription
Workplace violencePre-post (3 months)Violence experienced by healthcare staff in the wards, routinely collected data

Secondary

MeasureTime frameDescription
Coercive measuresPre-post (3 months)Routinely monitored and collected by the wards according to the Finnish Mental Health Act
Job satisfactionPre-post (3 months)Nurses yearly job satisfaction survey will be used (Nurse Engagement Survey (NESplus))

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026