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The objective of this study is to validate the prototype of the WeTakeCare- system in the real environment (=end users homes) and is embedded in Work-Package 4 (validation and evaluation) with the following main tasks:
T4.1. Definition of methodologies and protocols T4.2. First validation: concept assessment T4.3. Second validation: functional assessment T4.4. Third validation: real environment T4.5. Final check
Within the validation phase III of our project the investigators want to validate the contents of our fitness and information software WeTakeCare with the target group: elderly and their unprofessional caregivers. It runs on the Microsoft Kinect-System, which is authorised in Switzerland, and is in accordance with the prescribing information. The fitness- and information software contains information about strategies and devices which are available in case an older person is not able to perform the everyday movements in a safe and easy way.
Aim of the training and information software is to support elderly to stay independent from others help as long as possible. The mentioned software is not a medical or therapeutical treatment or a medical or therapeutical product. Performed exercises or presented information are highly regarded in the interest of safety and protection of the participants, and serves to prevent physical restrictions or damage .
There is only minimal risk or burden for the participants; the contents of the intervention itself (training of basic motor skills, instruction of strategies and the use of assistive devices to (partly) compensate restrictions in ADL performance, enablement of caregivers) are a standard in rehabilitation of elderly.
The investigators expect the start of the third validation in October 2015.
Full description
General study design and justification of design
Type of study: Validation of the prototype of the fitness- and information Software: WeTakeCare (pilot test) in a pre- post design, no comparators
Duration:
Population to be studied: Healthy elderly (aged 50+) with mild to moderate restrictions in the performance of ADL and their caregivers Number of participants: Involvement of a total of 20 couples in Switzerland. Incorporating 2-5 couples in the first month to allow detection and resolution of any problem.
Study phases
Within the pretesting phase possible participants are screened to validate the cognitive status as well as the physical condition to include only elderly and caregivers which have a benefit from participation.
STUDY INTERVENTION (SPIRIT #11) 8.1 Identity of Investigational Products (treatment / medical device) (ICH/E6 6.2.1, 6.4.2, 6.4.4; AGEK Checklist 2, item 3) Enrolled participants will get the technical appliances and support with the installation of the gadgets. (Kinect I (Microsoft-Kinect) and if necessary an appropriate Laptop) Occupational therapists will give a comprehensive instruction to the system, which also includes clarification of safety precautions.
The participants are free to use the system within their everyday life whenever they want.(Alone or together with their caregivers.)
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Elderly and caregivers
Exclusion criteria
Elderly
Medical restrictions or instability such as
high risk of falling
Severe restrictions in ADL performance
living in a care facility
receiving professional care
Primary purpose
Allocation
Interventional model
Masking
13 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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