iPad Technology for HOME Rehabilitation in Patients After Stroke: iHOME Acute/Chronic
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 29
- 试验地点
- 6
- 主要终点
- Total "dose" of intervention received as a proportion of the scheduled time
研究概览
简要总结
A pilot randomized, two parallel group study comparing an iPad software game application versus standard care in post-stroke patients.
Study hypothesis: Tablet PC technology using the iPad is a feasible and potentially efficacious tool which has the potential to promote fine motor recovery of the upper extremity after stroke.
详细描述
The standard one hour of out-patient rehabilitation is insufficient in providing the repetitive intense training required for rehabilitation of fine motor recovery. There are also limited interventions are available for home use after discharge from a rehabilitation centre. Hence, there is now a need to determine the feasibility of innovative strategies for home use, to cover the gap after discharge from rehabilitation institutions.
iHOME is an original, low cost, potentially high impact intervention to fulfil this gap. If proven to be effective, the use of tablet technology has a broad range of potential outcomes and benefits. The anticipated public benefit is for stroke patients to be able to potentially employ the iPad, an accessible technological device, as an expansion of rehabilitation in an in-home setting.
iHOME is a pilot randomized controlled trial with a blinded outcome assessment. The trial is subdivided into iHOME Acute and iHOME Chronic, where patients have had a stroke less than 3 months or more than 6 months ago, respectively, at the time of randomization. Participants will be randomly allocated in a 1:1 ratio to the interventions arms (i.e. the investigational and control group).
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
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patient has provided written consent prior to entry into the study
- •Males or females, 18 - 85 years of age
- •Evidence of ischemic or hemorrhagic stroke confirmed by CT or MRI head scan
- •Patient with onset of symptoms less than 3 months (for iHOME Acute) or patient more than 6 months (for iHOME Chronic) at the time of randomization
- •Measurable deficit of the upper extremity ≥3 according to the Chedoke McMaster scale e.g. participants should be able to touch their chin and contralateral knee to be eligible (for iHome Acute), or measurable deficit of the upper extremity ≥4 according to the Chedoke McMaster scale e.g. participants should be able to touch their chin and contralateral knee to be eligible (for iHome Chronic)
- •Functional independence prior to present stroke (mRS = 0-1)
- •Patient is alert, medically stable according to the treating physician and able to follow simple verbal commands
排除标准
- •Patient had stroke onset more than 3 months ago (for iHOME Acute) or patient had stroke onset less than 6 months ago (for iHOME Chronic)
- •Inability to follow verbal commands or having global aphasia
- •Severe illness with life expectancy less than 3 months
- •Uncontrolled hypertension, unstable angina, or recent myocardial infarction
- •History of seizures
- •Participation in another clinical trial involving rehabilitation or investigational drug
- •Unable to comply with the protocol
- •Patient has any condition(s) that would warrant exclusion from the study
- •Any medical condition that might confound the interpretation of results or put the patient at risk
研究组 & 干预措施
Standard/ Usual Care
Patients may receive outpatient rehabilitation as required as part of usual/standard care. No experimental intervention will be given to this group.
干预措施: Standard/ Usual Care (Other)
iPad Intervention
Patients randomized to the iPad arm will be instructed to self-administer 20 minutes of game sessions per day for 10 days over a 2 week (14 day) period.
干预措施: iPad Intervention (Other)
结局指标
主要结局
Total "dose" of intervention received as a proportion of the scheduled time
时间窗: 10 days over a 2 week period
The maximum total dose of intervention is 200min (20 min/day x 10 days). A 70% received intervention (≥140 min) from the total scheduled time will be considered successful. This will be measured by the amount of time the patient uses the application (this data is stored in the application).
次要结局
- Efficacy in fine motor function skills(3 business days after final study intervention session)