ISRCTN10276613
Completed
未知
Improving the oral healTh of Older People In Care homes: a feasibility study (TOPIC)
niversity College London0 sites119 target enrollmentApril 17, 2020
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Oral health
- Sponsor
- niversity College London
- Enrollment
- 119
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
2021 Protocol article in https://pubmed.ncbi.nlm.nih.gov/34215322/ (added 05/07/2021)
Investigators
Eligibility Criteria
Inclusion Criteria
- •Care home providers in London and Northern Ireland will be recruited using the following eligibility criteria:
- •1\. Care homes will require to have a minimum of 20 residents (as approximately half are expected to be edentate)
- •Residents in the recruited care homes will be screened to determine whether they meet the eligibility criteria:
- •1\. Over the age of 65 years
- •2\. Dentate or partially dentate
- •3\. Full\-time resident in care facility
Exclusion Criteria
- •The exclusion criteria for the care homes will be:
- •1\. Have high\-dependency units and end\-of\-life care
- •The exclusion criteria for the residents will be:
- •1\. Residents who are receiving end\-of\-life or palliative care
- •2\. Residents with severe cognitive impairment (6\-CIT score of 10 or higher)
- •A trained dental examiner will screen the participants for eligibility using a screening questionnaire covering the above criteria. Participants will also be asked the Six\-item Cognitive Impairment Test (6\-CIT) in order to assess their level of cognitive function. Residents with normal cognitive function (6\-CIT score of 0\-7\) and those with mild cognitive impairment (6\-CIT score of 8\-9\) will be included in the study, while those with severe cognitive impairment (6\-CIT score of 10 or higher) will be excluded. As cognitive function tends to fluctuate in this population, we will attempt the 6\-CIT screening test at different days and times on residents identified with severe cognitive impairment in order to identify potential time periods that would facilitate higher inclusion of participants in the study.
Outcomes
Primary Outcomes
Not specified
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