Digital Reminiscence for People With Dementia (DTR)
Primary Purpose
Dementia
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
DRT Intervention
Sponsored by

About this trial
This is an interventional treatment trial for Dementia focused on measuring dementia, reminiscence therapy, touch screen technology, digital reminiscence therapy
Eligibility Criteria
Inclusion Criteria:
- People who have been clinically diagnosed with dementia determined by psychiatrist in the selected care homes. The diagnosis will be recorded in their care home notes.
- People who are residents in the designated care home and they are anticipated to be resident in the care home for the coming year.
- People who have the capacity to understand and consent to participate in the study (including those who can consent in the moment), OR they will have a consultee who can be approached for their assent if they are not able to consent in the moment but meet the eligibility criteria.
Exclusion Criteria:
- People who are deemed too unwell to participate determined by care home staff.
- People with a diagnosis of an additional psychiatric disorder other that those identified in the inclusion criteria (e.g. schizophrenia, MDD) determined by care home staff.
Sites / Locations
- University of Nottingham
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
DRT Intervention
Arm Description
Intervention: Individual digital reminiscence therapy programme.
Outcomes
Primary Outcome Measures
Feasibility of the digital reminiscence therapy for PwD
Assessed by recruitment rate
Secondary Outcome Measures
Acceptability of the digital reminiscence therapy for PwD
Assessed by qualitative interview data - analysis will determine participant enjoyment of the intervention, barriers to programme use, and reasons for non-adherence and attrition
Adherence to intervention
Assessed by adherence rate (number of sessions completed)
Study attrition
Assessed by % lost to attrition
Explore whether outcome measures are sensitive to change - for memory
Pre-post changes in Arabic Version of Saint-Louis-University-Mental-Status (SLUMS; Abdelrahman & El Gaafary, 2014) it is a 30-point, 11 questions. The maximum score is 30 points.
Cut-off scores based on high School Education:
21-26 = Mild Neurocognitive Impairment, 1-20 = Dementia.
Less than High School Education:
20-24 = Mild Neurocognitive Impairment, 1-19 = Dementia.
Explore whether outcome measures are sensitive to change - for quality of life
Older People's Quality of Life Questionnaire (OPQOL-brief-13; Bowling et al., 2012) Each of the 13 items is scored from 1 to 5. The items are summed for a total OPQOL-Brief, then positive items are reverse coded, so that higher scores represented higher QoL.
Explore whether outcome measures are sensitive to change - for anxiety and depression
Arabic version of Hospital Anxiety and Depression Scale (Arabic HADS; Al Aseri et al., 2015) it comprises 7 questions for anxiety and 7 questions for depression. each subscale is ranged from 0 to 3. Cut-off scores for both is 8 separately; 8-10: mild, 11-14: moderate, 15-21: severe.
Explore whether outcome measures are sensitive to change - for communication
Holden Communication Scale for Persons with Dementia (HCS; Strøm et al., 2016). it includes 12 items. each subscale is scored from 0 to 4. The total scores range from 0-48 and the higher score the more difficulties.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03429686
Brief Title
Digital Reminiscence for People With Dementia
Acronym
DTR
Official Title
The Use of Digital Technology in Reminiscence Work With People With Dementia in Jordanian Care Homes: A Feasibility Study
Study Type
Interventional
2. Study Status
Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
November 28, 2017 (Actual)
Primary Completion Date
February 28, 2018 (Actual)
Study Completion Date
February 28, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Nottingham
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to explore the feasibility and acceptability of a digital reminiscence therapy (DRT) intervention for people with dementia (PwD). The objectives of this study include:
To determine whether DTR can be delivered as planned in the care of PwD in Jordanian care homes.
To determine whether DTR is acceptable/tolerable to PwD and care home staff in Jordanian care homes
To identify the most appropriate outcome measures to evaluate the delivery of DRT to PwD in Jordanian care homes to be used in a subsequent definitive trial.
Detailed Description
Reminiscence Therapy has been shown to be beneficial for people with dementia. The aim of this research is to develop and evaluate the feasibility of a digital application to aid reminiscence for people with dementia.
This study proposes to design an application, based upon reminiscence therapy, which can act as storage for personal and communal 'positive memories' in a range of media types. This includes pictures, videos and audio.
The target for this application is people with dementia and their staff caregivers. The study aims to recruit 40-50 participants (40 PwD and 10 staff caregivers). This research will look at the requirements for developing and evaluating a mobile application to see whether it might be used to aid reminiscence for people with dementia. Additionally, this research will ensure whether this digital reminiscence therapy can be delivered and accepted as planned in the care of people with dementia in Jordanian care homes. The acceptance of this digital reminiscence therapy will be assessed by using semi-structured interviews with approximately 15 people with dementia and staff care-givers. Quantitative measures will be used before and after the intervention to explore whether certain outcomes are sensitive to change. These outcomes include memory, communication, anxiety, depression, and quality of life.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dementia
Keywords
dementia, reminiscence therapy, touch screen technology, digital reminiscence therapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
A single group pre-post intervention feasibility study with process evaluation. Data will be collected from residents and staff in Jordanian care homes through questionnaires, from care home records, and qualitative interviews.
Masking
None (Open Label)
Allocation
N/A
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
DRT Intervention
Arm Type
Experimental
Arm Description
Intervention: Individual digital reminiscence therapy programme.
Intervention Type
Other
Intervention Name(s)
DRT Intervention
Other Intervention Name(s)
Digital Reminiscence Therapy Intervention
Intervention Description
The digital reminiscence therapy intervention will run 12 sessions twice per week, for six weeks, for up to an hour at a time (this will depend on the participant's ability and willingness to participate). The sessions of reminiscence therapy will be culturally appropriate and based on the key stages in the life which most people will have experienced. These sessions are individual, face-to-face sessions.
Primary Outcome Measure Information:
Title
Feasibility of the digital reminiscence therapy for PwD
Description
Assessed by recruitment rate
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Acceptability of the digital reminiscence therapy for PwD
Description
Assessed by qualitative interview data - analysis will determine participant enjoyment of the intervention, barriers to programme use, and reasons for non-adherence and attrition
Time Frame
3 months
Title
Adherence to intervention
Description
Assessed by adherence rate (number of sessions completed)
Time Frame
3 months
Title
Study attrition
Description
Assessed by % lost to attrition
Time Frame
3 months
Title
Explore whether outcome measures are sensitive to change - for memory
Description
Pre-post changes in Arabic Version of Saint-Louis-University-Mental-Status (SLUMS; Abdelrahman & El Gaafary, 2014) it is a 30-point, 11 questions. The maximum score is 30 points.
Cut-off scores based on high School Education:
21-26 = Mild Neurocognitive Impairment, 1-20 = Dementia.
Less than High School Education:
20-24 = Mild Neurocognitive Impairment, 1-19 = Dementia.
Time Frame
3 months
Title
Explore whether outcome measures are sensitive to change - for quality of life
Description
Older People's Quality of Life Questionnaire (OPQOL-brief-13; Bowling et al., 2012) Each of the 13 items is scored from 1 to 5. The items are summed for a total OPQOL-Brief, then positive items are reverse coded, so that higher scores represented higher QoL.
Time Frame
3 months
Title
Explore whether outcome measures are sensitive to change - for anxiety and depression
Description
Arabic version of Hospital Anxiety and Depression Scale (Arabic HADS; Al Aseri et al., 2015) it comprises 7 questions for anxiety and 7 questions for depression. each subscale is ranged from 0 to 3. Cut-off scores for both is 8 separately; 8-10: mild, 11-14: moderate, 15-21: severe.
Time Frame
3 months
Title
Explore whether outcome measures are sensitive to change - for communication
Description
Holden Communication Scale for Persons with Dementia (HCS; Strøm et al., 2016). it includes 12 items. each subscale is scored from 0 to 4. The total scores range from 0-48 and the higher score the more difficulties.
Time Frame
3 months
10. Eligibility
Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
People who have been clinically diagnosed with dementia determined by psychiatrist in the selected care homes. The diagnosis will be recorded in their care home notes.
People who are residents in the designated care home and they are anticipated to be resident in the care home for the coming year.
People who have the capacity to understand and consent to participate in the study (including those who can consent in the moment), OR they will have a consultee who can be approached for their assent if they are not able to consent in the moment but meet the eligibility criteria.
Exclusion Criteria:
People who are deemed too unwell to participate determined by care home staff.
People with a diagnosis of an additional psychiatric disorder other that those identified in the inclusion criteria (e.g. schizophrenia, MDD) determined by care home staff.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Holly Blake, Dr
Organizational Affiliation
University of Nottingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Nottingham
City
Nottingham
ZIP/Postal Code
NG7 2UH
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Digital Reminiscence for People With Dementia
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