Intergenerational Reminiscence and Digital Storytelling
Intergenerational Connections: Reminiscence and Digital Storytelling to Improve Social and Emotional Well-being of Older Adults With ADRD
1 other identifier
interventional
206
1 country
1
Brief Summary
The goal of this clinical trial is to develop and test how reminiscence offered by trained young adult volunteers using a digital storytelling (DST) platform may help older persons with Alzheimer's disease and related dementias (ADRD) to improve their social and emotional well-being. The main questions it aims to answer are:
- 1.Whether is this reminiscence and DST based intervention effective in improving social and emotional well-being of older adults with ADRD?
- 2.Whether do young adult participants improve their social and emotional well-being as well as knowledge and attitudes towards aging after participating this study?
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable alzheimer-disease
Started Apr 2021
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
Study Start
First participant enrolled
April 15, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 11, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
August 30, 2022
CompletedFirst Submitted
Initial submission to the registry
July 14, 2023
CompletedFirst Posted
Study publicly available on registry
August 9, 2023
CompletedAugust 9, 2023
August 1, 2023
1.3 years
July 14, 2023
August 7, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Quality of life of older adults
Older adults' quality of life will be measured using the Quality of Life-Alzheimer's Disease (QoL-AD). Thirteen items will be asked with each rated by a scale of 1-4 (poor, fair, good, or excellent). Sum scores will be calculated for final analysis with a potential range of 13-52. The higher the QoL-AD score, the better is the quality of life.
up to 6 months
Affect of older adults
Positive affect (PA) and negative affect (NA) of older adults will be conducted with Positive and Negative Affect Schedule (PANAS). Ten positive and Ten negative emotions will be asked using a 5-point scale. Sum scores will be calculated with higher scores indicating more PA and NA respectively, with potential range of 10-50 for each sum score.
up to 6 months
Resilience of older adults
Resilience of older adults will be measured using the Brief Resilience Scale (BRS). Six items will be asked and each item ranges from 1 (low resilience) to 5 (high resilience). Total scores will be calculated for final analysis with a potential range of 6-30. The higher the sum score, the more resilience of older adults.
up to 6 months
Loneliness of older adults
Loneliness will be measured by the De Jong Gierveld Loneliness Scale. Six items will be asked, each is measured with a 5 Likert scale. High sum scores indicate great loneliness with a potential range of 6-30.
up to 6 months
Secondary Outcomes (3)
Loneliness of young adult
up to 6 months
Knowledge of ADRD
up to 6 months
Attitudes toward aging
up to 6 months
Other Outcomes (1)
To qualitatively evaluate the usefulness of this intervention from the perspectives of the selected Dyads
interview will last for up to 60 minutes
Study Arms (2)
Reminiscence with digital storytelling
EXPERIMENTALOlder adults in the intervention group will receive 10 sessions of life-review or reminiscence discussion with the trained young adult volunteers (1-1.5 hours each week for 10 weeks). At the end of the study, they create a digital storybook based on their previous discussion.
Social wellness with scrapbook or journal
SHAM COMPARATOROlder adults in the control group will have general social wellness discussion with the young adult volunteers. At the end of the study, they will create a journal/scrapbook.
Interventions
The older and young adult participants will be randomly assigned into the intervention (reminiscence) or control (social wellness) groups and then be randomly matched as dyads within each group. Older adults in the intervention group will receive 10 sessions of life-review with the trained young adult volunteers (1-1.5 hours each week for 10 weeks). During weeks 1-6, a life history interview will be carried out with different themes in each week: major turning points in life (W1), family history (W2), life/career accomplishments (W3), history of loves and hates (W4), stress experiences (W5), and meaning and purpose of life (W6). During weeks 7-10, the dyads will develop the DST together using tablets already owned by the UTA School of Social Work. The contents of sessions 7-10 will be structured as: outline/script, plan and storyboard (W7), film and record (W8), evaluate, integrate and finalize (W9), and publish/share (W10).
Older adults in the control group will have general social wellness discussion with the young adult volunteers, instead of structured reminiscence guidelines. The topics are: diet and health (week 1); exercise/activity and health (week 2); emotions and health (week 3); religious/spiritual practices and health (week 4); family/friend relationships and health (week 5); and social activities/engagement and health (week 6). For weeks 7-10, instead of DST, the young adult volunteer will work with the older adult to create an unstructured, non-digital record of the social visit related to wellness in later life (e.g. wellness scrapbook/journal).
Eligibility Criteria
You may qualify if:
- are aged 65 years or older;
- have cognitive impairment measured by Ascertain Dementia 8 screening scale;
- have decisional capacity as measured by the University of California, San Diego Brief Assessment of Capacity to Consent (UBACC) ;
- are not participating any other research protocol currently;
- can speak and understand English.
You may not qualify if:
- participating in another trial or intervention;
- have health issues that prevent them from participating in the study for 3 months;
- cannot commit to be available for the full 10 weeks of intervention.
- age 18-30 years old;
- currently enrolled as a student at UTA when the study is conducted;
- can commit to be available for the full 10 weeks of the intervention.
- not current UTA student in the time of the study;
- have health issues or limited availability that prevent them from participating for the entire 10 weeks of intervention.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The University of Texas at Arlington
Arlington, Texas, 76019, United States
Related Publications (1)
Xu L, Fields NL, Daniel KM, Cipher DJ, Troutman BA. Reminiscence and Digital Storytelling to Improve the Social and Emotional Well-Being of Older Adults With Alzheimer's Disease and Related Dementias: Protocol for a Mixed Methods Study Design and a Randomized Controlled Trial. JMIR Res Protoc. 2023 Sep 7;12:e49752. doi: 10.2196/49752.
PMID: 37676706DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor
Study Record Dates
First Submitted
July 14, 2023
First Posted
August 9, 2023
Study Start
April 15, 2021
Primary Completion
August 11, 2022
Study Completion
August 30, 2022
Last Updated
August 9, 2023
Record last verified: 2023-08
Data Sharing
- IPD Sharing
- Will not share