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N/A Completed N=60 Randomized Single-blind Supportive Care

A Phone Intervention for Family Dementia Caregivers in Vietnam

Source: ClinicalTrials.gov NCT05481320 ↗
Enrolled (actual)
60
Serious AEs
0.0%
Results posted
Mar 2025
Primary outcomePrimary: Zarit Burden Interview-6 (ZBI-6) — 10.2; 10.6; 8.2; 11.4 score on a scale

Summary

This is a cluster randomized controlled trial to examine the feasibility, acceptability, and preliminary efficacy of the phone version of REACH VN, a psychosocial culturally adapted Alzheimer's family caregiving intervention, to support family caregivers of persons living with dementia in Vietnam.

Outcome Measures

OutcomeResultp-value
PRIMARY
Zarit Burden Interview-6 (ZBI-6)
10.2; 10.6; 8.2; 11.4
SECONDARY
Patient Health Questionnaire-4 (PHQ-4)
4.3; 4.8; 2.2; 5.3

Eligibility Criteria

Inclusion Criteria

  • To be eligible to participate, a family member will need to be the identified adult (i.e., age 18 and above) who is the primary informal (i.e., unpaid family member) caregiver (i.e., the person who provides the most time day-to-day care) to an older adult (i.e., age 60 and above) with dementia living in the community. If the primary caregiver is not available to participate, an alternate family member who provides substantial care (i.e., at least 4 h/day) to an older adult with dementia will be eligible to participate.
  • In addition, caregivers will need to score ≥ 6 on the Zarit Burden Interview-4 (ZBI-4).
  • All participants will be living in clusters in Thach That District, a semi-rural area in Hanoi. Clusters will have a minimum of 3 participants and a maximum of 15 participants.

Exclusion Criteria

  • Caregivers with difficulties in the consent process due to cognitive impairment or severe sensory impairment (i.e., visual, hearing)
  • Caregivers don't have access to phone
  • Individuals who are not yet adults (i.e., infants, children, teenagers)
  • Prisoners
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05481320). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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