Pilot Usability Study to Set Up and Use the Feetsee™ Foot Monitoring Device in Adults With Diabetes
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 20
- 试验地点
- 1
研究概览
简要总结
Single-center, prospective, minimal-risk, non-experimental usability study assessing the setup and use of the FDA-registered (Class I medical device; 510(k)-exempt) Feetsee™ home foot-monitoring system by adults with diabetes in their home environment over 8 weeks.
This study in non clinical, observational pilot usability study conducted under FDA Human Factors and Usability Engineering guidance (2016).
详细描述
Participants will be recruited from outpatient diabetes and podiatry clinics at UT Health San Antonio, an academic medical center. The study itself is conducted as a home-use usability study: after initial training, participants set up and use the Feetsee foot-monitoring system in their own homes, following the US IFU and in-app instructions. Data will be collected via paper/electronic CRFs, patient questionnaires, and Feetsee device/app usage logs (exported to REDCap and secure sponsor databases).
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Males and females aged 18 years or older
- •Clinical diagnosis of Type 1 or Type 2 diabetes
- •At least one palpable foot pulse per feet
- •Possess basic ability to use a smartphone or tablet
- •Have no prior experience with the Feetsee™ system
- •Be willing and able to provide informed consent
排除标准
- •Active foot ulceration at enrollment
- •Active Charcot neuro-osteoarthropathy
- •Severe vascular disease (complete absence of foot pulses)
- •Amputation of more than three toes
- •Active malignancy or immunosuppressive condition
- •Cognitive or physical impairments preventing proper device usage
- •Concurrent participation in another investigational study with contraindicated procedures