Memory and Attention Disorders and Malnutrition in Hospital Setting

June 7, 2018 updated by: Tampere University Hospital

Prevalence of Memory and Attention Disorders and Malnutrition in Hospitalized Older Adults (Muistitoimintojen ja Tarkkaavaisuuden häiriöiden ja Vajaaravitsemuksen Yleisyys iäkkäillä Sairaalahoidossa Olevilla Potilailla [Finnish])

This is a cross-sectional observational study that investigates the prevalence of memory disorders, attention disorders (suggesting delirium), and malnutrition in hospitalized older adults (aged 70 years or over) in a tertiary care centre, using rapid screening toos (Six-item screener for memory disorders, Months of the Year Backwards Test for delirium, and NRS-2002 and Mini Nutritional Assessment Short Form for malnutrition).

Study Overview

Study Type

Observational

Enrollment (Actual)

151

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

70 years and older (Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

All patients born in 1946 or earlier hospitalized in somatic wards.

Description

Inclusion Criteria:

  • Hospitalized in Tampere University Hospital (excl. psyciatry, pediatrics, ICU)
  • Able to communicate in Finnish

Exclusion Criteria:

  • Unable to communicate because of unconciuousness, critical health status, or communication difficulties
  • Having a (surgical) procedure at the time of data collection

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Patients aged 70 or over
Patients eligible for the study will undergo screening for memory disorders, attention disorders, and malnutrition
Screening for memory disorders, attention disorders, and malnutrition, using Six-Item Screener, Months of the Year Backwards Test, and NRS-2002 and MNA-SF, respectively.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prevalence of memory disorders
Time Frame: day of recruitment
Abnormal result in Six-Item Screener
day of recruitment
Prevalence of attention disorders
Time Frame: day of recruitment
Abnormal result in Months of the Year Backwards Test
day of recruitment
Prevalence of malnutrition and risk of malnutrition
Time Frame: day of recruitment
Abnormal result based on nutritional status screening tools
day of recruitment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Esa Jämsen, MD, PhD, Consultant

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2016

Primary Completion (Actual)

December 31, 2016

Study Completion (Actual)

May 31, 2018

Study Registration Dates

First Submitted

August 9, 2017

First Submitted That Met QC Criteria

August 14, 2017

First Posted (Actual)

August 17, 2017

Study Record Updates

Last Update Posted (Actual)

June 8, 2018

Last Update Submitted That Met QC Criteria

June 7, 2018

Last Verified

June 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • Ger1-16

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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