- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03252054
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
Status
Completed
Conditions
Intervention / Treatment
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.
Sponsor
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
Additional Relevant MeSH Terms
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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