- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05163821
Pilot of a New Cognitive Assessment Tool for Detecting Dementia in the Migrant Somali Population
December 15, 2023 updated by: Sophie Jeffery, Greater Manchester Mental Health NHS Foundation Trust
Aims
- The investigators want to find out if the tool that they have made to assess memory and thinking in Somali elders ( the 'MSCAT') is acceptable to that community and practical to administer and score.
- The public will benefit from this research because it seeks to enhance reliability of diagnosis of dementia, thus access to support and treatment for people from an ethnic minority group experiencing memory problems.
Background
- The investigators are a group of staff from the Memory Assessment Service in Manchester. There are currently no suitable tests for dementia for people from Somalia.
- Research evidence tells us there are many reasons why the tools that used now are not working. This includes: differences in culture and ways of life that are very different to a British born person who has lived in the UK for all of their life.
- Somali people find out at a later stage if they have dementia resulting in delayed treatment/support.
- This research supports the government's promise to improve the pathway to a diagnosis of dementia for minority groups.
Design and methods
- 10 participants
- The investigators will compare the assessment tool (MSCAT) that the team have developed to the Addenbrookes Cognitive Examination III tool that is typically used.
- Participants will be seen at an agreed location (e.g. home, mosque or GMMH trust site). They will meet a Somali speaking researcher to do both tests on 2 appointments and discuss how they found the tests afterwards.
- The investigators will check participants understanding of the research before they agree to take part. Verbal and written information will be provided.
Public involvement
- The local Somali community helped advise on the creation of the new MSCAT assessment tool.
- The investigators will write project information for participants in Somali and English.
Dissemination of results
• Professional conference presentations and publications
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
12
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
-
-
-
Manchester, United Kingdom, M13 9WL
- Greater Manchester Mental Health NHS Trust
-
-
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
50 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
Somali-born migrants in UK
Description
Inclusion Criteria:
- The participants will all be Somali-born migrants, over the age of 50, living in the UK.
Exclusion Criteria:
- Exclusion criteria will include the presence of dementia, current delirium, or inability to complete the tasks due to visual/hearing/physical impairment
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 |
---|---|
Participants
Somali migrants in UK, aged over 50.
|
Cognitive screen for dementia
Cognitive screen for dementia
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Qualitative feedback on completing the cognitive screens
Time Frame: Immediately after completing the screen
|
Interview
|
Immediately after completing the screen
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
January 8, 2022
Primary Completion (Actual)
December 4, 2023
Study Completion (Actual)
December 4, 2023
Study Registration Dates
First Submitted
December 7, 2021
First Submitted That Met QC Criteria
December 7, 2021
First Posted (Actual)
December 20, 2021
Study Record Updates
Last Update Posted (Estimated)
December 18, 2023
Last Update Submitted That Met QC Criteria
December 15, 2023
Last Verified
December 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- x503s
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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