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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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02908997
Enrollment
3
Registered
2016-09-21
Start date
2017-01-17
Completion date
2018-07-31
Last updated
2018-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dementia

Brief summary

A study to investigate the effectiveness of a reminder tool application at increasing performance on memory tasks in people with mild dementia

Detailed description

Background Memory difficulties are a core feature of dementia. These include difficulties remembering to do something at a specific time and place in the future (Prospective Memory). Although a range of electronic prospective memory aids currently exist (e.g. Neuropage), the evidence supporting their use among the dementia population remains limited. Mindmate is a recently developed mobile application that aims to support individuals with a diagnosis of dementia, improving self-management skills and quality of life. Aims This study will explore the effectiveness of MindMate reminder alerts delivered to a smart phone or tablet computer as a memory aid for people with a diagnosis of Mild Dementia. Method Three participants with a diagnosis of dementia, who are considered to be in the early stages and who report everyday prospective memory difficulties, will be recruited from Older People Community Mental Health teams within Greater Glasgow and Clyde. The participants will own a smart phone or tablet and will be living with a partner or family member who will also participate in the study. During the initial baseline phase, the partner or family member will monitor the number of pre defined tasks the participant remembered and forgot. The partner or family member will record this information on a weekly monitoring form and this phase will last between five to seven weeks. This will be followed by a five-week intervention phase where MindMate reminder alerts will be sent to the participant's phone or tablet. Again, tasks that require remembering will be identified prior to the intervention phase, and family members or carers will monitor their success on a form. Results will be analysed using visual inspection and Tau-U analysis. Applications This study will provide information on the effectiveness of a form of assistive technology at supporting people with a dementia, which could improve quality of life of those with a diagnosis.

Interventions

OTHERMindMate

A dementia-specific mobile reminding application

Sponsors

University of Glasgow
CollaboratorOTHER
NHS Greater Glasgow and Clyde
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Memory6 weeksNumber of target events the participant remembered to complete

Secondary

MeasureTime frameDescription
AcceptabilityChange from baseline to 6 week post-interventionUnified Theory of Acceptance and Use of Technology (UTAUT) questionnaire

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026