The evaluation of questionnaires to improve treatment of acute pain in the Emergency Department

Feasibility, usability and Measurement properties of Patient Reported Outcome Measures (PROMs) related to acute pain in the Emergency Department - OPTIMIZED-1 study

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON57480

Enrollment

200

Registered

2025-02-06

Start date

2025-04-28

Completion date

Unknown

Last updated

2026-06-08

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

Conditions

Pain

Interventions

APS-POQ-RED, BPI-SF, EQ-5D-5L, OBAS, QoR-15

Eligibility

Age

16 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Adult patients = 18years - NRS or VAS for pain of 4/10 or greater (at arrival to the ED) - Acute pain for less than 6 weeks  - Informed consent obtained.

Exclusion criteria

Exclusion criteria: -Intoxicated with alcohol or drugs. - Self-inflicted injury. - Cognitive impairment - Unable to give consent. - Triaged into the most urgent category (Manchester Triage System or Dutch Triage Standard)

Design outcomes

Primary

Measure	Time frame
For objective 1: NRS, APS-POQ-RED, BPI-SF, EQ-5D-5L, OBAS, QoR-15, and Patient Global Impression of Change (PGIC) and satisfaction. For objective 2: Time to complete PROM, time to discuss PROM with healthcare professional, an overview of facilitators and barriers for implementation of PROMs in the ED, usability and experience from surveys.	—

Countries

Netherlands

Contacts

Public ContactA Top

Leids Universitair Medisch Centrum

optimized_SEH@lumc.nl071 526 9111

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jun 11, 2026