Prevalence and Recognition of Cognitive Impairment in Hospitalized Patients: a Flash Mob Study
1 other identifier
observational
757
1 country
1
Brief Summary
The aim of this multicenter, cross-sectional, observational flash mob study is to investigate the prevalence of cognitive impairment in hospitalized elderly aged 65 years or older, and the recognition of cognitive impairment by healthcare professionals.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Sep 2022
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 24, 2022
CompletedFirst Posted
Study publicly available on registry
May 27, 2022
CompletedStudy Start
First participant enrolled
September 21, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 21, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
September 21, 2022
CompletedOctober 24, 2023
October 1, 2023
Same day
May 24, 2022
October 23, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Percentage of hospitalized patients aged 65 years or older with cognitive impairment
Cognitive impairment is measured with the Mini-Cog
Baseline
Percentage of hospitalized patients aged 65 years or older with cognitive impairment that has been recognized by nurses, physicians, both their nurse and physician, and either their nurse or physician
Cognitive impairment is measured with the Mini-Cog
Baseline
Eligibility Criteria
Patient population: Dutch-speaking, hospitalized patients aged ≥ 65 years old. Healthcare professional population: Nurses and physicians who work at participating wards and take care of one or more participating patients.
You may qualify if:
- Dutch-speaking
- Hospitalized
- Age ≥ 65 years old
You may not qualify if:
- Unable to perform the Mini-Cog (e.g. due to visual impairment, severe hearing loss, being too ill, or otherwise unable to speak or write)
- Patients who require medical isolation
- Not willing to participate.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Department of Geriatric Medicine
Groningen, 9700RB, Netherlands
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Barbara C van Munster, Prof. dr.
University Medical Center Groningen, University Center for Geriatric Medicine
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 24, 2022
First Posted
May 27, 2022
Study Start
September 21, 2022
Primary Completion
September 21, 2022
Study Completion
September 21, 2022
Last Updated
October 24, 2023
Record last verified: 2023-10