Prevalence and Recognition of Cognitive Impairment in Hos... | NCT05395559

Studies
Prevalence and Recognition of Cognitive Impairment in Hospitalized Patients: a Flash Mob Study

NCT05395559

Sponsor

University Medical Center Groningen

Status

Completed

Last Update Posted

Oct 24, 2023Actual

Enrollment

757Actual

Phase

Not provided

Conditions

Cognitive Impairment
Dementia
Alzheimer Disease
Delirium

Interventions

Not provided

Countries

Netherlands

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Oct 2023

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Sep 21, 2022Actual

Primary Completion Date

Sep 21, 2022Actual

Completion Date

Sep 21, 2022Actual

First Submitted Date

May 24, 2022

First Submission Date that Met QC Criteria

May 24, 2022

First Posted Date

May 27, 2022Actual

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Oct 23, 2023

Last Update Posted Date

Oct 24, 2023Actual

Sponsor/Collaborators Module

Responsible Party, by Official Title

Sponsor

Lead Sponsor

University Medical Center GroningenOTHER

Collaborators

Name	Class
ZonMw: The Netherlands Organisation for Health Research and Development	OTHER
Health∼Holland, Topsector Life Sciences & Health	UNKNOWN

Oversight Module

Has Data Monitoring Committee (DMC)

Is FDA Regulated Drug

Is FDA Regulated Device

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

Not provided

FDAAA801 Violation

Not provided

Description Module

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.

Detailed Description

Not provided

Design Module

Study Type

Observational

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Target Follow-Up Duration

Not provided

Phases

Not provided

Interventional Study Design

Allocation

Not provided

Intervention Model

Biospecimen

No data available

No data is available for this block.

Enrollment

757Actual

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
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

Secondary Outcomes

Not provided

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Dutch-speaking
Hospitalized
Age ≥ 65 years old

Exclusion Criteria:

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.

Accepts Healthy Volunteers

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

65 Years

Maximum Age

Not provided

Standard Ages

Older Adult

Study Population

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.

Sampling Method

Probability Sample

Contacts/Locations Module

Central Contacts

Not provided

Overall Officials

Name	Affiliation	Role
Barbara C van Munster, Prof. dr.	University Medical Center Groningen, University Center for Geriatric Medicine	Principal Investigator

Locations

Facility	Status	City	State	ZIP	Country	Contacts
University Department of Geriatric Medicine		Groningen		9700RB	Netherlands

Condition Browse Module

MeSH Terms

ID	Term
D060825	Cognitive Dysfunction
D003704	Dementia
D000544	Alzheimer Disease
D003693	Delirium

Ancestor Terms

ID	Term
D003072	Cognition Disorders
D019965	Neurocognitive Disorders
D001523	Mental Disorders
D001927	Brain Diseases

Browse Leaves

Not provided

Browse Branches

Not provided