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Pilot Study for the Investigation of the functional ability of the SmartPointer (SP) demonstrator for the eldery under laboratory conditions. SmartPointer (SP) laboratory study

Pilot Study for the Investigation of the functional ability of the SmartPointer (SP) demonstrator for the eldery under laboratory conditions. SmartPointer (SP) laboratory study - SPL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00017474
Enrollment
34
Registered
2019-09-06
Start date
2020-01-06
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

R26

Interventions

Group 1: Prior to the study written consent is requested from each participant. The research question will be answered by using a mixed-medthod-design. The subjects will be randomly assigned to two gr

Sponsors

Charité - Universitätsmedizin Berlin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Elderly aged 60 and above without physical impairments and with limitations in mobility (use of a walker, wheelchair, walking stick or similar). Written informed consent and participant information sheet.

Exclusion criteria

Exclusion criteria: Elderly aged 59 or younger, severe cognitive impairment MMSE <24, presence of legal care taker, recent surgery on the dominant hand which will make the execution of gestures with the remote not possible or just under severe pain. Tremor or arthrosis in the dominant Hand, elderly with severe limitations of vision, so that the light of the remote cannot be recognised, elderly with red-green impairment (dyschromatopsia)

Design outcomes

Primary

MeasureTime frame
The following validated questionnaires will be used -Mini Mental State Examination (MMSE) (Fol-stein et al., 1975) - Questionnaire technology commitment (Neyer et al., 2012) - system usability scale - SUS (Bangor et al., 2008)

Secondary

MeasureTime frame
It will be investigated, to what extent external factors influence the gesture recognition by login data, video recordings of the executed gestures and an additional self developed protocol whereby it will be recorded if an executed gesture is correctly being recognized by the detector and transformed into the right action (operation targeted device). Thereby an action can be visualized by green (working)/red (not working) lights on the device.

Countries

Germany

Contacts

Public ContactCornelia Eicher

Forschungsgruppe Geriatrie

cornelia.eicher@charite.de030450553345

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026