Effects of a Video-based mHealth Program for the Homebound Older Adults: A Pilot Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 68
- 试验地点
- 2
- 主要终点
- Self-efficacy will be measured by general self-efficacy scale
研究概览
简要总结
Homebound older adults are among the highest users in health care systems. The high use of health care services is related to their physical limitations compounded by complex health and social care needs. Homebound older adults can be difficult to reach because they seldom participate and engage in community services due to their functional limitations, which leaves their health needs largely unrecognized at an earlier stage. This study tries to bring this group of older adults to the providers' attention and design a health-social oriented self-care mHealth program and subject it to empirical testing.
详细描述
Methods/Design The SPIRIT statement was used as a guideline for this protocol paper. Study design and setting This is a single-blinded, two-armed randomized controlled trial. The research assistant who collects the data is blinded, but the subjects and the health care providers who are involved in the intervention are not. This study is supported by five community centers. The centers are widely scattered across Hong Kong, which helps to maximize the generalizability effect of this program.
Participants and recruitment strategy, and randomization The leaders of the community centers will help draw up lists of potential subjects. Simple random sampling with a fixed sample size will be employed to recruit subjects. The inclusion criteria of this study are (1) being aged 60 or over, (2) going outdoors less than once a week in the last six months, (3) living within the service area of a participating community center, and (4) ability to use a smartphone. The exclusion criteria are (1) being diagnosed with dementia, (2) inability to hear, see or communicate, (3) being bed-bound, (4) having an active psychiatric illness with recent hospital admission within the last six months, (5) living within an area with no internet coverage, and (6) being already engaged in other mHealth programs.
Potential subjects will be approached and invited to participate in the study. A consent form will be signed once the subject agrees to participate. The random assignment schedule, generated using the computer software Research Randomizer, will be compiled by a research team member who is not involved in subject recruitment. The group assignments will be put in a sealed envelope and revealed sequentially at the time of randomization. The research assistant, after successfully recruiting a subject, will call the research team member for the random assignment. The research team member who has no knowledge of the identity of the subject will make the assignment based on computer numbers ('1' = video-based mHealth program; '2' = control group).
Interventions A three-month program will be designed in this study. There will be two groups involved in this study, described as follows.
Intervention group This group of participants will receive a video-based mHealth program that includes two main elements: 1) nurse case management supported by a social service team, and 2) individual-specific video messages covering self-care topics delivered via smartphone.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- 60 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •people who are aged 60 or above
- •go outdoor less than once per week in current 6 months
- •living within the service area of community centre
- •using smartphone
排除标准
- •diagnosed with dementia
- •unable to hear, see or communicate
- •bed-bound
- •active psychiatric illness with recent hospital admission within last 6 months
- •living within an area with no internet coverage
- •already engaged in other mHealth programs
结局指标
主要结局
Self-efficacy will be measured by general self-efficacy scale
时间窗: Change from Baseline score of general self-efficacy scale at 3 months
measured by the general self-efficacy scale. The score is from 10-40, higher the better.
次要结局
- instrumental activity of daily living(Change from Baseline score of Lawton Instrumental activity of daily living scale at 3 months)
- emergency department attendance(Change from Baseline attendance at 3 months)
- medication adherence(Change from Baseline score of adherence to refills and mediaction scale at 3 months)
- Activity of daily living will be measured by Barthel index scale(Change from Baseline score of Barthel index at 3 months.)
- depression(Change from Baseline score of geriatric depression scale at 3 months)
- Health service utilisation(Change from Baseline attendance at 3 months)
- general well-being of individual(Change from Baseline score of physical and mental components at 3 months)
- general out-patient attendance(Change from Baseline attendance at 3 months)
研究者
Arkers, Wong
Assistant professor
The Hong Kong Polytechnic University
