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SmartRoll - Development of a smart walker for mobility in clinical settings

SmartRoll - Development of a smart walker for mobility in clinical settings - SmartRoll

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00036747
Enrollment
60
Registered
2025-04-30
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-10-06

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

Conditions

The study examines the requirements of carers, physiotherapists and geriatric patients for a smart rollator, as well as the readiness of these groups for technology and patients' fear of falling.

Interventions

Group 1: The present research and development project ‘SmartRoll - Development of a smart rollator for mobility in a clinical setting’ is a prospective procedure in a mixed-methods design. The planned

Sponsors

Medizinische Fakultät der Martin-Luther-Universität Halle-Wittenberg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - German or English speaking, - Ability to give consent (no court supervision), - Persons who can walk at least 20 metres independently and can therefore be described as walkable

Exclusion criteria

Exclusion criteria: - People with impaired cognition (test: DemtTect =8 points), - People in the end-of-life phase as assessed by carers or by themselves, - Persons with amputated extremities, - Persons who are not sufficiently resilient (= NYHA III), - People after spinal surgery, - People with severely impaired hearing, speech or language skills.

Design outcomes

Primary

MeasureTime frame
The demonstrator of the smart walker for use in clinical settings has been developed to Technological Readiness Level (TRL 6) after two years of project work.

Secondary

MeasureTime frame
- Realisable range of functions defined and detailed planning of the technical development plan completed, - Functional model (individual functionalities) is available for practical testing by user groups, - Demonstrator (with several functionalities) is available for practical testing by user groups, - Demonstrator with new mechanical structure is available for clinical testing; pilot concept can be implemented in a clinical setting, - Clinical trials completed, demonstrator optimised.

Countries

Germany

Contacts

Public ContactRené Schwesig

Medizinische Fakultät der Martin-Luther-Universität Halle-Wittenberg

rene.schwesig@uk-halle.de+49 345 557 1317

Outcome results

None listed

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