NCT05984732

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. 1.Whether is this reminiscence and DST based intervention effective in improving social and emotional well-being of older adults with ADRD?
  2. 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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
206

participants targeted

Target at P75+ for not_applicable alzheimer-disease

Timeline
Completed

Started Apr 2021

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 15, 2021

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 11, 2022

Completed
19 days until next milestone

Study Completion

Last participant's last visit for all outcomes

August 30, 2022

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

July 14, 2023

Completed
26 days until next milestone

First Posted

Study publicly available on registry

August 9, 2023

Completed
Last Updated

August 9, 2023

Status Verified

August 1, 2023

Enrollment Period

1.3 years

First QC Date

July 14, 2023

Last Update Submit

August 7, 2023

Conditions

Keywords

ADRDDSTreminiscenceolder adultyoung adult volunteerRCT

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

EXPERIMENTAL

Older 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.

Behavioral: Reminiscence with digital storytelling

Social wellness with scrapbook or journal

SHAM COMPARATOR

Older 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.

Behavioral: Social wellness with scrapbook or journal

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).

Reminiscence with digital storytelling

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).

Social wellness with scrapbook or journal

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)

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

Location

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.

MeSH Terms

Conditions

Alzheimer Disease

Condition Hierarchy (Ancestors)

DementiaBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesTauopathiesNeurodegenerative DiseasesNeurocognitive DisordersMental Disorders

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

Locations