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Clinical Trials/DRKS00030209
DRKS00030209
Completed
N/A

Geriatric rehabilitation using a digital training solution: a functional model usability study. - ExerG Usability

Reha Rheinfelden0 sites47 target enrollmentOctober 5, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Primary end-user group: Geriatric in-patients or out-patients (65 years or older) of the Reha Rheinfelden. Secondary end-user group: Therapists of the Reha Rheinfelden (physiotherapist, occupational therapist or sports therapist) working in the area of rehabilitation and prevention, who have experience in the training of elderly people and in geriatric or neurological rehabilitation.
Sponsor
Reha Rheinfelden
Enrollment
47
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 5, 2022
End Date
August 30, 2023
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Primary end\-user: Aged \= 65 years, in\- or outpatient of the Reha Rheinfelden, Walking impairment as defined by Functional Ambulation Categories (category \= 3\), ability to speak and understand German, body height \> 1,60 m.

Exclusion Criteria

  • Primary end\-user: \- Cognitive impairment as defined by a Mini Mental State Examination (MMSE) score of \= 21; \- known cybersickness; \- visual, neurological, cardiorespiratory, psychiatric, or orthopaedic impairments which reduce the person's capability of following the instructions or to play the game; \- recently occurred epileptic seizures (in the past 6
  • months); \-recent surgery/fractures/surgical interventions/joint replacement and malignancy (in the past 6 months); \- impairment of hearing (e.g. verbal communication not possible); \- severe movement pain (\>5 Visual Analogue Scale); \- joint contractures (e.g. shoulder, knee, hip) that could
  • lead to limitations during end\-user evaluation of the
  • ExerCube; \- severe psychiatric illness (e.g., pronounced paranoid states, severe depression).

Outcomes

Primary Outcomes

Not specified

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