ArmeoSenso - Home Therapy and Assessment for Patients With Arm Impairments Based on Wearable Movement Sensors

NCT ID: NCT02098135

Last Updated: 2015-09-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

14 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-11-30

Study Completion Date

2015-09-30

Brief Summary

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stroke, spinal cord injury, rehabilitation, home therapy, upper limb, arm, virtual reality, interia sensor,

* Trial with medical device

Detailed Description

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Conditions

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Stroke Spinal Cord Injury

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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ArmeoSenso

The ArmeoSenso system is an easy to set up and use upper limb rehabilitation system for the home environment. It consists of a motion capture system based on wearable sensors in combination with a personal computer as well as a therapy software that provides an ergonomic user interface, therapy games and automated assessments.

Group Type EXPERIMENTAL

ArmeoSenso

Intervention Type DEVICE

Virtual realty therapy with a touchscreen computer and movement sensors, over 42 days.

Interventions

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ArmeoSenso

Virtual realty therapy with a touchscreen computer and movement sensors, over 42 days.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* 18 years old
* Stroke or spinal cord injury in prehistory
* Motor deficits of the upper limb (s)
* Lifting the paretic arm against gravity possible AND
* Minimum amount of movement in the horizontal plane of 20 x 20 cm
* Ability and willingness to participate in the study

Exclusion Criteria

* Severe aphasia
* Severe dementia
* Severe depression
* Relevant restriction of vision, which can not be compensated by aids (eg hemianopia)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Zurich

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Andreas Luft, Prof MD

Role: PRINCIPAL_INVESTIGATOR

University Hospital Zurich, Division of Neurology

Locations

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University Hospital Zurich, Divison of Neurology

Zurich, Canton of Zurich, Switzerland

Site Status

Countries

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Switzerland

References

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Wittmann F, Held JP, Lambercy O, Starkey ML, Curt A, Hover R, Gassert R, Luft AR, Gonzenbach RR. Self-directed arm therapy at home after stroke with a sensor-based virtual reality training system. J Neuroeng Rehabil. 2016 Aug 11;13(1):75. doi: 10.1186/s12984-016-0182-1.

Reference Type DERIVED
PMID: 27515583 (View on PubMed)

Other Identifiers

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2013-0182

Identifier Type: -

Identifier Source: org_study_id

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