Effect of Animation-Based Digital Education on Risk Knowledge and Frailty in Older Adults
The Impact of a Digital Training Model Developed Using Animation Technique on Risk Knowledge Level and Frailty Among Older Adults
With the global aging trend, the management of geriatric risks faced by older adults and the effectiveness of health education for this population are gaining increasing importance. Literature indicates that health education for older adults, when delivered through methods that support individual engagement and the use of digital tools, yields more effective results in terms of learning and behavior change. This doctoral study aims to evaluate the effect of a digital education model, structured based on the Health Belief Model and developed using branching scenario animation technique, on geriatric risk knowledge level and frailty status among older adults residing in nursing homes.
The study will be conducted as a randomized controlled trial in three nursing homes in Istanbul, with measurements at baseline (T0), immediately post-intervention (T1), 1-month follow-up (T2), and 3-month follow-up (T3). Based on power analysis, 66 participants will be randomly assigned to intervention and control groups (33 per group) using block randomization. The intervention group will receive scenario-based digital animation education developed on the Vyond platform and structured according to the theoretical components of the Health Belief Model. The control group will receive standard care during the study period and will be offered the same digital animation education after completion of all assessments (post 3-month follow-up).
The primary outcome is geriatric risk knowledge level, assessed using an interactive digital game called "Knowledge Wheel." Secondary outcomes include frailty status, measured by the Edmonton Frail Scale, and technology acceptance. Changes in knowledge and frailty levels measured through assessment tools will reveal the short- and medium-term effects of the education. Thus, the model's impact on health-related behavior change in older adults will be comprehensively evaluated.
The unique aspect of this study is that it will be one of the first experimental studies to implement an interactive scenario-based digital education model in older adults. The findings are expected to contribute to the development of age-friendly health education models.
研究概览
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:ELIF PAKLACI YORMAZ, MSc
- 电话号码:+9021261010
- 邮箱:elif.paklaci@gmail.com
研究联系人备份
- 姓名:BESEY OREN, PhD
- 电话号码:+90 216 777 8 777
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Aged 65 years or older
- Ability to speak and understand Turkish
- Minimum literacy level (able to read and write)
- Mini-Mental State Examination (MMSE) score ≥ 24
- No visual or auditory impairment, or ability to compensate for such impairments with assistive devices
- Ability to interact with digital devices such as smartphones or tablets at a basic level
Exclusion Criteria:
- Diagnosis of cognitive impairment or dementia
WITHDRAWAL CRITERIA:
- Participants will be withdrawn from the study if:
- Serious health problems occur during any phase of the study or death occurs
- Perception or compliance problems are identified during sessions
- The participant fails to attend at least one educational session
学习计划
研究是如何设计的?
设计细节
- 主要用途:预防
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Intervention Group
Participants will receive branching scenario-based digital animation education developed using Vyond platform and structured according to Health Belief Model components. The education addresses geriatric health risks including falls, malnutrition, polypharmacy, and cognitive decline through interactive scenarios. Assessments will be conducted at baseline (T0), immediate post-intervention (T1), 1-month follow-up (T2), and 3-month follow-up (T3). |
An interactive digital education program developed on Vyond animation platform, based on Health Belief Model framework. The program includes branching scenarios on geriatric health risks (falls, nutrition, medication safety, cognitive health, social engagement). Participants make choices within scenarios and receive personalized feedback. Each session lasts approximately 30-45 minutes. The intervention uses interactive storytelling to enhance engagement and knowledge retention among older adults. |
|
无干预:Control Group
Participants will receive standard nursing home care during the study period. No additional educational intervention will be provided during the study. The same digital animation education will be offered after completion of all assessments (post 3-month follow-up). Assessments will be conducted at baseline (T0), T1, T2, and T3 time points. |
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Geriatric Risk Knowledge Level
大体时间:Measured at baseline (T0), immediately post-intervention (T1), 1-month follow-up (T2), and 3-month follow-up (T3) - approximately 4 months total
|
Change in knowledge score related to geriatric health risks (falls, medication management, nutrition, cognitive health, social engagement) assessed using an interactive digital game called "Knowledge Wheel". The assessment evaluates participants' understanding of risk factors, prevention strategies, and health-promoting behaviors based on Health Belief Model components. |
Measured at baseline (T0), immediately post-intervention (T1), 1-month follow-up (T2), and 3-month follow-up (T3) - approximately 4 months total
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Frailty Status
大体时间:Measured at baseline (T0), immediately post-intervention (T1), 1-month follow-up (T2), and 3-month follow-up (T3) - approximately 4 months total
|
Change in frailty level measured by the Edmonton Frail Scale (EFS). The scale assesses nine domains: cognition, general health status, functional independence, social support, medication use, nutrition, mood, continence, and functional performance. Scores range from 0-17, with higher scores indicating greater frailty. |
Measured at baseline (T0), immediately post-intervention (T1), 1-month follow-up (T2), and 3-month follow-up (T3) - approximately 4 months total
|
合作者和调查者
调查人员
- 首席研究员:ELIF PAKLACI YORMAZ, MSc、Saglik Bilimleri Universitesi
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
Individual participant data will not be shared due to privacy protection regulations under Turkish Personal Data Protection Law (KVKK) and institutional ethics committee restrictions. The study involves vulnerable population (older adults in nursing homes) with sensitive health information. Aggregate results and findings will be disseminated through peer-reviewed publications and conference presentations.
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