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Dementia and Storytelling in Vietnam

Digital Storytelling to Promote Early Dementia Diagnosis in Rural Vietnam

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07431528
Enrollment
100
Registered
2026-02-24
Start date
2026-10-01
Completion date
2027-10-31
Last updated
2026-02-24

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

Conditions

Alzheimer Dementia (AD)

Keywords

Storytelling intervention, mHealth, Early detection, Rural health, Vietnam

Brief summary

This project aims to improve knowledge regarding Alzheimer's dementia and related dementias (ADRD) among older adults and their caregivers in Vietnam and promote the early diagnosis of ADRD using a digital storytelling intervention.

Detailed description

This study will develop and test a Digital Storytelling intervention to improve older adults' and caregivers' knowledge of ADRD and to facilitate early diagnosis in rural areas of Vietnam. The Digital Storytelling Intervention includes interactive multimedia modules for motivating behavior change and improving knowledge and attitudes toward ADRD among older adults and their caregivers through the power and voices of patients with mild to moderate ADRD, older persons with cognitive concerns, and their caregivers. Mobile Health technology (Computerized Intervention Authoring System - CIAS) will be used to deliver the intervention.

Interventions

Participants will receive a digital storytelling intervention featuring narratives from older adults with mild to moderate Alzheimer's disease and related dementias (ADRD) and their caregivers who have successfully managed the condition. The stories highlight the benefits of early ADRD diagnosis and strategies for managing diagnostic and care-related challenges. The intervention will be delivered at baseline and biweekly thereafter for three months via CIAS, with didactic "Learn More" modules provided following the stories.

Participants will receive basic information about Alzheimer's disease and related dementias (ADRD), issued by the Vietnam Ministry of Health (usual care), at baseline and at Month 3.

Sponsors

University of Massachusetts, Worcester
Lead SponsorOTHER
Alzheimer's Association
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Subject)

Intervention model description

Cluster randomized controlled trial

Eligibility

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

Inclusion criteria

* Older adults (age ≥ 60 years) residing in one of the four participating communities (communities in rural areas of Phu Tho province with minimum distance of 10 km between participating communities) * Concern about mild cognitive impairment expressed by the participant, caregiver, or healthcare provider, with no formal screening for ADRD * Ability and willingness to provide informed consent * Caregivers of eligible participants will be invited to participate after providing written consent.

Exclusion criteria

* Current participation in another ADRD study * Severe cognitive impairment as evaluated by study co-investigators * Enrollment in palliative care or diagnosis of a terminal illness * Previous exposure to digital storytelling modules * Prior participation in the digital storytelling development.

Design outcomes

Primary

MeasureTime frameDescription
Intervention Feasibility: Participant Recruitment and RetentionBaseline, Month 3, Month 6Feasibility will be assessed using recruitment and retention records, including the number of participants approached, reasons for ineligibility or refusal, and study completion rates.
Intervention Engagement: Interaction Records from CIASMonth 3, Month 6Engagement will be assessed using the number of videos watched.
Intervention Engagement: Exit InterviewMonth 6Information on participants' experiences with the intervention will be collected through exit interviews.
Intervention Acceptability: System Usability Scale (SUS)Month 3, Month 6SUS is a 10-item, 5-point Likert scale for subjective assessment of usability. The SUS scores range from 0 to 100. A score of \> 50 indicates that the technology-based interventions are acceptable.
ADRD Knowledge: Dementia Knowledge Assessment Scale (DKAS)Baseline, Month 3, Month 6DKAS is a 25-item scale that evaluates dementia knowledge. Total scores range from 0 to 50, with higher scores indicating greater knowledge.
Attitudes: Dementia Attitude Scale (DAS)Baseline, Month 3, Month 6DAS is a 20-item, 7-point Likert scale assessing attitudes toward dementia and people living with dementia. Items are summed, with selected items reverse-coded as appropriate, to calculate a total score (range: 20-140). Higher scores indicate more positive attitudes.

Secondary

MeasureTime frameDescription
ADRD Screening/DiagnosisMonth 3, Month 6Rates of ADRD screening and diagnosis will be obtained via interviews and through review of participants' medical records by trained study staff. The diagnosis will be reviewed and confirmed by the study co-investigators (physicians).
Quality of Life: SF-12Baseline, Month 3, Month 6The SF-12 is a 12-item scale that assesses health-related quality of life across physical and mental well-being domains. Scores can range from 0 to 100, with higher scores indicating better quality of life.
Self-Care: The Self-Care of Chronic Illness Inventory (SC-CII)Baseline, Month 3, Month 6SC-CII is a 29-item scale assessing self-care behaviors across three domains: self-care maintenance, self-care monitoring, and self-care management. Scores range from 0 to 100, with higher scores indicating better self-care.

Countries

Vietnam

Contacts

CONTACTHoa Nguyen, PhD
hoa.nguyen@umassmed.edu508-856-8999
CONTACTDeogwoon Kim, PhD
deogwoon.kim13@umassmed.edu
PRINCIPAL_INVESTIGATORHoa Nguyen, PhD

University of Massachusetts, Worcester

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026