Extending the Validation of SCREEN to Persons Living With Dementia or in Retirement Homes
NCT ID: NCT04675229
Last Updated: 2025-07-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ENROLLING_BY_INVITATION
600 participants
OBSERVATIONAL
2022-09-25
2025-08-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
SCREEN and other nutrition and health measures will be completed in 600 older adults (300 living in retirement homes with or without MCI-D, and 300 living with MCI-D in the community). SCREEN will be completed twice to determine reliability, and persons with MCI-D will have their results compared to those of a caregiver who completes it on their behalf. A dietitian's assessment and rating of nutrition risk will be used as the gold-standard to determine validity.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Preventing Malnutrition Among Older Adults
NCT05860140
Assessment of DeMentia Nutrition Intervention Needs Among Care Recipients and carEgivers
NCT05536830
Frailty Rehabilitation
NCT03824106
Elucidation of Sensory Characteristics and Food Preferences in the Elderly
NCT02873858
The Effect of Nutrition Follow up After Hospital Discharge in Undernourished Elderly
NCT01345032
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
SCREEN is the leading nutrition risk tool for community-living seniors and is the logical choice for use in those with MCI-D and/or living in retirement residences. However, it has not been validated in these groups. It cannot be assumed that the existing validation in cognitively well older adults living in their own homes can translate to these two vulnerable groups. As well, one question on grocery shopping needs to be changed to accommodate persons living in retirement homes. This study is also timely with the recent update of Canada's Food Guide and recommendations to increase protein intake to mitigate frailty. Two questions on SCREEN need to be modified to adapt the new language on protein foods used in the new Food Guide. This study will undertake the validation and reliability testing of SCREEN, considering these minor revisions, in 600 older adults (community-dwelling older adults with MCI-D and those living in retirement homes with or without MCI-D). Validation of SCREEN for these populations will ensure that a single tool can be used in all older adults living in community and retirement settings. Specifically, understanding at what point a person with MCI-D is no longer a reliable informant for completing SCREEN will help with identification when a caregiver should complete the questionnaire. This is why the Montreal Cognitive Assessment is used, as it provides discrete scores differentiating mild cognitive impairment from dementia. The results of this study will have significant impact on practice by allowing, for the first time, confidence in the identification of nutrition risk in these under-served groups in Canada. There is an urgent need for this research. Early identification of nutrition risk and its subsequent management has the potential to advance our health care system by promoting the prevention of frailty and its consequences. This study will have a meaningful impact in the 'real world' setting of primary and community care for older adults in Canada and worldwide, by providing a feasible, validated and useful nutrition risk tool.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
CROSS_SECTIONAL
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* potential participants with MCI-D will have a caregiver who either lives with the participant or is in daily contact OR
* potential participants have subjective complaint - MoCA used to confirm cogntive change OR
* Retirement home participants will have lived in their residence for a minimum of 3 months
* read and communicate in English
* provide written consent or assent for persons MCI-D; caregiver written consent required if participant with cognitive change unable to provide
Exclusion Criteria
* do not speak or read English
* live outside of the geographic boundaries of this study (i.e., \> 45 km from Kitchener/Waterloo or London).
55 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Canadian Institutes of Health Research (CIHR)
OTHER_GOV
University of Waterloo
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Heather Keller
Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Heather Keller
Role: PRINCIPAL_INVESTIGATOR
U Waterloo
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Heather Keller
Guelph, Ontario, Canada
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ORE#42827
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.