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Elder-friendly Approaches to the Surgical Environment (EASE) Study

Elder-friendly Approaches to the Surgical Environment - Implementation of an Elder Friendly Surgical Unit

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02233153
Acronym
EASE
Enrollment
723
Registered
2014-09-08
Start date
2014-04-30
Completion date
2017-12-31
Last updated
2018-10-19

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

Conditions

General Surgery

Keywords

Senior, Elderly, Acute Care, Emergency Surgery

Brief summary

The aim of this study is to examine the impact implementing an elder-friendly surgical unit has on post-operative complications, mortality and quality of life for patients ≥ 65 years old who have undergone emergency surgical care.

Detailed description

The investigators hypothesize that the elder-friendly surgical unit will reduce in-hospital complications and mortality in a cost-effective manner, for this at risk population. Specific elder-friendly interventions include: 1. Locate all elderly surgical patients on one nursing unit 2. Interdisciplinary team-based care 3. Elder-friendly evidence-informed practices including: comfort rounds with early mobilization, delirium prevention/management, optimal nutrition and prevention of post-operative complications 4. Early and interdisciplinary discharge management This is a prospective, before-after study with a concurrent control group. Four senior patient groups will be followed:

Interventions

OTHERElder-Friendly Surgical Unit

Sponsors

Alberta Innovates Health Solutions
CollaboratorOTHER
University of Alberta
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* All patients \> 65 years old admitted for Acute care and Emergency Surgery * Received acute abdominal surgery

Exclusion criteria

* Elective general surgery cases * Nursing home resident requiring full nursing care \[dependency in 3 or more activities of daily living \] * Palliative surgery \[surgery with the primary intention of improving quality of life or relieving symptoms caused by advancing non-curative disease\] * Multi-system trauma * Patients from out of province or transferred from another inpatient service or hospital

Design outcomes

Primary

MeasureTime frameDescription
Post-Operative complicationsDuring initial in-hospital stay (0-12 weeks on average)Includes a) intensive care unit admission (includes respiratory failure, cardiac arrest or septic shock), b) vascular complications (myocardial infarction, stroke, deep venous thrombosis, pulmonary embolism), c) serious infections (pneumonia, intra-abdominal abscess, urinary tract infection, deep wound infection or infected decubitus ulcer) or d) protracted delirium (≥48 hours)
DeathDuring initial in-hospital stay (0-12 weeks on average)

Secondary

MeasureTime frameDescription
Post-discharge complications or health-events requiring re-admissionWithin 30 days post-discharge
Cost per quality-adjusted life year6 months post-dischargeBoth direct and indirect study participant costs

Other

MeasureTime frameDescription
Health Related Quality of Life6 weeks and 6 months post-dischargeIncluding: EQ-5D questionnaire, SF-12 Questionnaire
Functional Status (Frailty)6 weeks post-dischargeIncluding: Edmonton Frail Scale, and Timed Up-and-Go Test

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026