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Mobile-Phone-Based Psychoeducation for Dementia Caregivers in Vietnam

N

Nguyen Tran To Tran

Status

Completed

Conditions

Depression, Anxiety
Stress

Treatments

Other: Psychoeducation

Study type

Interventional

Funder types

Other

Identifiers

NCT06700551
557-HDDD-DHYD

Details and patient eligibility

About

The goal of this study is to determine whether a mobile phone-based psychoeducational intervention can reduce stress among caregivers of individuals with dementia in Vietnam. The primary research question is: Does the intervention reduce levels of depression, anxiety, and stress among participants? The secondary research question is: Does the intervention increase caregivers' knowledge about dementia, enhance social support, or reduce caregiver burden?

Full description

The study consists of two groups: an intervention group and a control group. Participants in the intervention group will receive psychoeducational content through the Zalo app on their mobile phones. Weekly, they will be provided with a topic related to dementia care, such as daily caregiving, fall prevention, pressure injury prevention and care, self-care, and coping as a caregiver. Levels of depression, anxiety, and stress will be assessed both before and after the intervention. In the control group, participants will continue receiving standard care.

Enrollment

172 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Primary Caregiver Requirement: Participants must have been the primary caregivers of poeple with dementia for at least the past 6 months and plan to continue in this role for the next 6 months of the intervention. Patients with demeentia criteria: Patients must have been diagnosed with dementia for at least 6 months and reside within the community.
  • Language and Education Requirement: Participants must be able to read and understand Vietnamese (with at least a primary education level) and be willing to participate in the study.
  • Smartphone Requirement: Participants must own a smartphone with the Zalo app or be willing to install it (with a brief training session provided for new users).
  • Age Requirement: Participants must be aged 18 years or older.

Exclusion criteria

  • Having any acute diseases or cognitive impairment (screening by Mini-Cog) or
  • Having vision or hearing impairment

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

172 participants in 2 patient groups

Psychoeducation Intervention Group
Experimental group
Description:
In the intervention group, participants will receive interventions through the Zalo app on their mobile phones. Weekly, the investigator will send a topic for participants to learn about. Participants will have the opportunity to ask questions and share their feelings or experiences through the Zalo app.
Treatment:
Other: Psychoeducation
Control group
No Intervention group
Description:
Participants will receive usual care and will not receive any intervention

Trial contacts and locations

1

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Central trial contact

Tran TT Nguyen, MD, MSc; The HN Than, MD, PhD

Data sourced from clinicaltrials.gov

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