Skip to content

Effectiveness of an Observational Unit at St. Olavs Hospital

An Open Randomized Trial of the Effectiveness of an Observational Unit at St. Olavs Hospital

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01092234
Enrollment
105
Registered
2010-03-24
Start date
2010-03-31
Completion date
2011-03-31
Last updated
2017-10-02

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

Conditions

Emergency Patients

Keywords

Observational units, Length of stay (LOS), Readmission

Brief summary

The trial is designed to evaluate the effectiveness of a newly established Observational unit at St. Olavs Hospital in terms of readmission rates, compared to the provision of care in normal/traditional units for defined diagnosis and medical problems.

Detailed description

Observational units are thought to be more efficient than traditional ward units, but the evidence is scarce. The trial will in a randomized fashion evaluate the study hypothesis at an organizational level and not confined to specific diagnosis. The hypothesis to be tested is to confirm or reject the equal effectiveness of an Observational unit compared to a traditional ward for organizing in-hospital care.There are established eligibility and exclusion criteria based on clinical experience. Endpoint is length of stay and readmission within 30 days. In addition the study will give information on the use of diagnostic and treatment resources used and collect some basic demographic variables.

Interventions

OTHERTraditional ward

provision of care in a traditional unit/ward.

OTHEROrganizational change

Observational unit (new organizational unit) for organizing in-hospital care

Sponsors

St. Olavs Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Caregiver)

Eligibility

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

Inclusion criteria

* Emergency admitted patients only * All patients on the list (appendix 1) with a tentative length of stay \< 24 hours * Predicted stay of less than 24 hours * Willingness and able to sign a informed consent

Exclusion criteria

* Emergency admitted patients with life threatening illnesses * Patients with a tentative length of stay \> 24 hours based on the summary of medical and logistical considerations e.g. need of major - surgery, infections with prolonged infusions of antibiotics. * Unwillingness to sign a informed consent * By discretion of the physician/surgeon * Readmission of any reason in the study period (within 30 days)

Design outcomes

Primary

MeasureTime frameDescription
Length of stay (LOS)1 yearLength of hospital stay in hours

Secondary

MeasureTime frameDescription
Readmission within 30 days30 daysReadmission to hospital for any reason within 30 calender days

Countries

Norway

Outcome results

None listed

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