跳至主要内容
临床试验/NCT06797180
NCT06797180Enrolling By Invitation不适用

Effectiveness of Virtual Reality-Based Educational Intervention in Enhancing Caregiving Competence for Managing Agitated Behaviors in Dementia Residents: A Randomized Controlled Trial

Mackay Medical College2 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2023年5月31日最近更新:

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
120
试验地点
2
主要终点
Change in caregiving ability scores before intervention to post-intervention and follow-up.

研究概览

简要总结

This study aims to develop and evaluate the effectiveness of a VR-based educational intervention designed to improve the dementia caregiving abilities of formal caregivers in residential care homes. The intervention focuses on enhancing caregivers' knowledge and skills in managing behavioral symptoms of dementia through immersive VR scenarios, group discussions, and evidence-based management strategies, with the goal of better equipping them to provide high-quality care for residents with dementia.

详细描述

Background:

Agitated behaviors, such as aggression, care resistance, and wandering, are common in dementia and present significant challenges for formal caregivers in long-term care (LTC) facilities. These behaviors often stem from unmet needs, such as pain, discomfort, or communication barriers, contributing to caregiver stress and reduced care quality. Virtual reality (VR) technology offers an immersive, first-person experience that enables caregivers to better understand triggers of agitated behaviors, empathize with residents' experiences, and improve their caregiving abilities.

Purpose:

This study aims to develop and evaluate the effectiveness of a VR-based educational intervention for formal caregivers in residential care homes. Specifically, the study compares two groups: (1) an experimental group receiving both a 100-minute behavioral and psychological symptom (BPSD) foundational education and an additional 100-minute VR training program, and (2) a control group receiving only the 100-minute BPSD foundational education. The study evaluates three outcomes: (1) dementia care competence, (2) confidence in caregiving, and (3) self-reported frequency of BPSD assessment and management at pre-intervention, post-intervention, and two-week follow-up.

Methods:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Participant, Care Provider)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 18 years or older.
  • Able to communicate in Mandarin or Taiwanese.
  • A formal caregiver of individuals with dementia.
  • At least one month of work experience in the residential care facility.

排除标准

  • Caregivers who do not meet the above inclusion criteria.
  • Individuals who are unable or unwilling to provide informed consent.

结局指标

主要结局

Change in caregiving ability scores before intervention to post-intervention and follow-up.

时间窗: Data will be collected before the intervention (baseline), immediately post-intervention (after training), and at follow-up (two weeks after the intervention).

Caregiving ability was measured using the Dementia Competence Scale for Acute Care (DCS) developed by Yang, Yang, Hsiao, Kuo, and Wang (2021). This scale includes three subscales: 13 items on knowledge, 11 items on attitudes, and 9 items on skills. The Cronbach's α values for the knowledge, attitude, and skills subscales were 0.88, 0.94, and 0.85, respectively. The test-retest reliability, as measured by the intraclass correlation coefficient (ICC), was 0.82 for the overall scale, with 0.87 for the knowledge subscale, 0.64 for the attitude subscale, and 0.74 for the skills subscale.

Confidence in assessing and managing BPSD

时间窗: Data will be collected before the intervention (baseline), immediately post-intervention (after training), and at follow-up (two weeks after the intervention).

Confidence in assessing BPSD (Behavioral and Psychological Symptoms of Dementia) and in effectively managing BPSD was evaluated using a 5-point scale, ranging from "very unconfident" to "very confident."

次要结局

  • Change in frequency of assessment and management of BPSD before intervention to post-intervention and follow-up.(Data will be collected before the intervention (baseline), at 1 week post-intervention, and at follow-up (two weeks after the intervention).)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Chin-Tsung Shen

The Office of Research and Development

Mackay Medical College

研究点 (2)

Loading locations...

相似试验