- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05404152
Evaluation of Cognitive Impairment in the Elderly Admitted to Nursing Homes
June 29, 2022 updated by: MARIA ELENA MOSQUERA LOSADA, Universidad de Murcia
This research aims at analysing the profile of the elderly with cognitive impairment (IC) and inquiring about the mental illnesses that cause cognitive impairment of a population (elderly admitted to nursing homes with a high incidence).
Study Overview
Status
Completed
Detailed Description
The objectives of these studies are to determine the presence of IC and the profile of users who suffer from it in 8 nursing homes in the province of Pontevedra of new admission in 2017, as well as the identification of the frequency of underdiagnosis in the filiation of the mental pathology that causes IC and if that underdiagnosis is related to the presence of doctors or nurses specialists in geriatrics.
Sociodemographic, clinical (with special relevance in cognitive assessment and the presence of mental disorders) and functional variables will be analyzed.
In addition to providing information that can improve the DC early detection as well as the scarcity of studies in this field, the importance of this research is justified by developing treatment guidelines for people with IC in the future
Study Type
Observational
Enrollment (Actual)
390
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Murcia, Spain
- UMurcia
-
-
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
60 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
- Elderly without cognitive assessment at admission
- Existence of doubts about the presence of IC
Description
Inclusion Criteria:
- Vounteer
- Elderly Admitted to Nursing homes
- From 60 years old
Exclusion Criteria:
- Elderly without cognitive assessment at admission
- Existence of doubts about the presence of IC
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
- Observational Models: Other
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
---|
Ederly
Elderly Admitted to Nursing homes
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Study of Evaluation of Cognitive Impairment. MEC o MMSE <24 points or diagnosis of Neurocognitive disorder
Time Frame: Two years
|
Two years
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Statistical correlation of CI with educational level.
Time Frame: Two years
|
Two years
|
Other Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Causes underdiagnosis of IC affiliation and Mental illnesses that cause IC
Time Frame: Two years
|
Two years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: MARIA ELENA MOSQUERA LOSADA, MSc in Nursing, Universidad de Murcia
- Study Director: ANTONIA GOMEZ-CONESA, PhD, PT, Universidad de Murcia
- Study Director: RAMON GONZALEZ CABANACH, PhD, University of A Coruna
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)
December 31, 2021
Primary Completion (Actual)
April 1, 2022
Study Completion (Actual)
May 1, 2022
Study Registration Dates
First Submitted
May 30, 2022
First Submitted That Met QC Criteria
May 30, 2022
First Posted (Actual)
June 3, 2022
Study Record Updates
Last Update Posted (Actual)
July 5, 2022
Last Update Submitted That Met QC Criteria
June 29, 2022
Last Verified
May 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CIE/UM22
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Yes
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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