- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06082908
Geriatric Syndrome in Nursing Home Residents
June 10, 2025 updated by: Ulkukezbansahin, Giresun University
Predictors of the Disability in Nursing Home Residents: a Descriptive Study
Disability in daily living activities (ADL) is a typical issue among nursing care residents.
The goal of this study was to look at the geriatric syndromes that cause incapacity in nursing home residents.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
More often than not, people who live in nursing homes can't move out.
One of the main reasons they leave their own home is to lose their freedom.
Nursing homes also have a lot of people with geriatric diseases like cognitive impairment, balance problems, urinary incontinence, and disability.
But it's not known what role geriatric syndromes play in ADL impairment.
To come up with good ways to treat geriatric syndromes, which are the main causes of ADL disability in nursing home patients, we need to know more about them.
So, the point of this study was to look into geriatric syndromes that are linked to disability and find out what causes disability in nursing home patients.
Study Type
Observational
Enrollment (Actual)
124
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
-
-
-
Giresun, Turkey, 28000
- Giresun University
-
-
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
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
This cross-sectional study was conducted in nursing homes located in two cities.
Description
Inclusion Criteria:
- age over 65
- staying in a nursing home for at least 12 months
- consent to participate in the study were the inclusion criteria.
Exclusion Criteria:
- people who were mentally unable to answer questions,
- people who were hospitalized
- people who had severe hearing or vision problems that made it hard to communicate
- people who took benzodiazepines or psychotropic drugs that made it hard to walk or balance
- people who had fractures or endoprostheses in any part of their bodies.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
frailty
Time Frame: 5 minute
|
FRAIL includes five items that evaluate ambulation, weight loss, fatigue, diseases, and resistance. Each item receives a value of 0 or 1, for a total score ranging from 0 (best) to 5 (worst). A score of 3 shows frailty, a score of 1-2 indicates prefrailty, and a score of 0 indicates robustness. |
5 minute
|
|
disability
Time Frame: 5 minute
|
The Barthel Index (BI) was used to determine the level of disability in ADL.
The indicator has a maximum total score of 100, indicating that the individual is entirely autonomous in all physical functions.
The lowest possible score is 0; this indicates that the individual is entirely dependent.
|
5 minute
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
sarcopenia
Time Frame: 5 minute
|
The SARC-F questionnaire was used to assess the risk of sarcopenia.
The indicator has a maximum total score of 100, indicating that the individual is entirely autonomous in all physical functions.
The lowest possible score is 0; this indicates that the individual is entirely dependent.
|
5 minute
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: ULKU K SAHIN, PhD, Giresun University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Vermeulen J, Neyens JC, van Rossum E, Spreeuwenberg MD, de Witte LP. Predicting ADL disability in community-dwelling elderly people using physical frailty indicators: a systematic review. BMC Geriatr. 2011 Jul 1;11:33. doi: 10.1186/1471-2318-11-33.
- Jenkins KR, Fultz NH. Functional impairment as a risk factor for urinary incontinence among older Americans. Neurourol Urodyn. 2005;24(1):51-5. doi: 10.1002/nau.20089.
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)
June 1, 2022
Primary Completion (Actual)
December 30, 2022
Study Completion (Actual)
April 25, 2023
Study Registration Dates
First Submitted
October 9, 2023
First Submitted That Met QC Criteria
October 9, 2023
First Posted (Actual)
October 13, 2023
Study Record Updates
Last Update Posted (Actual)
June 13, 2025
Last Update Submitted That Met QC Criteria
June 10, 2025
Last Verified
October 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- Nursing home
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
The datasets generated during and analyzed during the current study are available from the corresponding author on reasonable request.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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