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MindMate: A Study of a Reminder System for People With Dementia

Primary Purpose

Dementia

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
MindMate
Sponsored by
NHS Greater Glasgow and Clyde
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Dementia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • NHS Greater Glasgow and Clyde

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

5 week baseline

6 week baseline

7 week baseline

Arm Description

5 week baseline data collection followed by 6 week MindMate intervention

6 week baseline data collection followed by 6 week MindMate intervention

7 week baseline data collection followed by 6 week MindMate intervention

Outcomes

Primary Outcome Measures

Memory
Number of target events the participant remembered to complete

Secondary Outcome Measures

Acceptability
Unified Theory of Acceptance and Use of Technology (UTAUT) questionnaire

Full Information

First Posted
September 19, 2016
Last Updated
November 2, 2018
Sponsor
NHS Greater Glasgow and Clyde
Collaborators
University of Glasgow
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1. Study Identification

Unique Protocol Identification Number
NCT02908997
Brief Title
MindMate: A Study of a Reminder System for People With Dementia
Official Title
MindMate: A Single Case Experimental Design Study of a Reminder System for People With Mild Dementia
Study Type
Interventional

2. Study Status

Record Verification Date
November 2018
Overall Recruitment Status
Completed
Study Start Date
January 17, 2017 (Actual)
Primary Completion Date
July 31, 2018 (Actual)
Study Completion Date
July 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NHS Greater Glasgow and Clyde
Collaborators
University of Glasgow

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dementia

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
3 (Actual)

8. Arms, Groups, and Interventions

Arm Title
5 week baseline
Arm Type
Experimental
Arm Description
5 week baseline data collection followed by 6 week MindMate intervention
Arm Title
6 week baseline
Arm Type
Experimental
Arm Description
6 week baseline data collection followed by 6 week MindMate intervention
Arm Title
7 week baseline
Arm Type
Experimental
Arm Description
7 week baseline data collection followed by 6 week MindMate intervention
Intervention Type
Other
Intervention Name(s)
MindMate
Intervention Description
A dementia-specific mobile reminding application
Primary Outcome Measure Information:
Title
Memory
Description
Number of target events the participant remembered to complete
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Acceptability
Description
Unified Theory of Acceptance and Use of Technology (UTAUT) questionnaire
Time Frame
Change from baseline to 6 week post-intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jonathan Evans, BSc DClinPsy PhD
Organizational Affiliation
University of Glasgow
Official's Role
Principal Investigator
Facility Information:
Facility Name
NHS Greater Glasgow and Clyde
City
Glasgow
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

MindMate: A Study of a Reminder System for People With Dementia

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