A Care Empowerment Program Using Virtual Reality for Family Caregivers of People With Dementia

Tzu Chi University

Status: Completed

Conditions: Dementia Family Caregiver

Treatments: Other: care empowerment program; Other: Routine family support

Study type: Interventional

Funder types: Other

Identifiers

NCT05475002

YLH-IRB-11104

Details and patient eligibility

About

This study aims to evaluate a care empowerment program using virtual reality on dementia knowledge, attitude, self-efficacy in managing BPSD, empathy and caregiver burden of family caregivers of people with dementia.

Full description

The majority of patients with dementia live at home and cared by their families in Taiwan. Most of family caregivers have limited knowledge and care skills of dementia, therefore they experience great stress and caregiver burden which may have negative impact on their physical and mental health.

This two-group randomised controlled trial aims to evaluate a care empowerment program using virtual reality on dementia knowledge, attitude, care self-efficacy in managing BPSD, empathy and caregiver burden of family caregivers of people with dementia.

The intervention group will receive the Care Empowerment Program, which consists of dementia care e-books and virtual reality-based dementia activities, in addition to the routine dementia care manual and family support group.

The control group will only receive routine dementia care manual and family support group with no dementia virtual reality activity.

Both groups will be assessed for their dementia knowledge, attitudes, self-efficacy in managing BPSD, empathy and caregiver burden at baseline, month 3, and 4.

Enrollment: 92 patients

Sex: All

Ages: 20 to 90 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• age 20 to 90 years,
• Taiwanese nationality,
• have provided care for relatives with dementia or cognitive impairment for at least three months,
• have a mobile phone or tablet and regular access to the internet,
• provide informed consent to participate in the study.

Exclusion criteria

• family members who do not meet the inclusion criteria,
• can not provide informed consent.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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92 participants in 2 patient groups

Intervention group

Experimental group

Description:

care empowerment program

Treatment:

Other: care empowerment program

Control group

Active Comparator group

Description:

routine family support

Treatment:

Other: Routine family support