MindMate: A Study of a Reminder System for People With Dementia
MindMate: A Single Case Experimental Design Study of a Reminder System for People With Mild Dementia
1 other identifier
interventional
3
1 country
1
Brief Summary
A study to investigate the effectiveness of a reminder tool application at increasing performance on memory tasks in people with mild dementia
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jan 2017
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 19, 2016
CompletedFirst Posted
Study publicly available on registry
September 21, 2016
CompletedStudy Start
First participant enrolled
January 17, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 31, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
July 31, 2018
CompletedNovember 6, 2018
November 1, 2018
1.5 years
September 19, 2016
November 2, 2018
Conditions
Outcome Measures
Primary Outcomes (1)
Memory
Number of target events the participant remembered to complete
6 weeks
Secondary Outcomes (1)
Acceptability
Change from baseline to 6 week post-intervention
Study Arms (3)
5 week baseline
EXPERIMENTAL5 week baseline data collection followed by 6 week MindMate intervention
6 week baseline
EXPERIMENTAL6 week baseline data collection followed by 6 week MindMate intervention
7 week baseline
EXPERIMENTAL7 week baseline data collection followed by 6 week MindMate intervention
Interventions
A dementia-specific mobile reminding application
Eligibility Criteria
You may qualify if:
- has a diagnosis of Mild Dementia, according to International Classification of Diseases (ICD) 10 Criteria
- has received the diagnosis from a psychiatrist
- owns a smart phone or tablet
- has a family member/partner/carer who is willing to monitor memory aid use
- has capacity to consent to being involved in the research
- is reporting memory difficulties that are affecting them in daily life
You may not qualify if:
- visual or auditory difficulties which cannot be corrected through the use of appropriate aids
- has a pre-existing neurological or severe psychiatric problem (e.g. bipolar disorder, psychosis)
- has a diagnosis of dementia that is considered to be in the moderate to severe stages
- those whose first language is not English
- those with a diagnosed or suspected developmental learning disability
- those who are currently using online or electronic memory aids
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- NHS Greater Glasgow and Clydelead
- University of Glasgowcollaborator
Study Sites (1)
NHS Greater Glasgow and Clyde
Glasgow, United Kingdom
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jonathan Evans, BSc DClinPsy PhD
University of Glasgow
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 19, 2016
First Posted
September 21, 2016
Study Start
January 17, 2017
Primary Completion
July 31, 2018
Study Completion
July 31, 2018
Last Updated
November 6, 2018
Record last verified: 2018-11
Data Sharing
- IPD Sharing
- Will not share