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

Not Applicable

Completed

• Conditions: Stroke; Spinal Cord Injury

• Registration Number: NCT02098135
• Lead Sponsor: University of Zurich

Brief Summary

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

* Trial with medical device

Detailed Description

Not available

Study Timeline

• Study Start: 2013-11
• Study First Submitted: 2014-03-06
• Study First Submitted QC: 2014-03-26
• Study First Posted: 2014-03-27
• Primary Completion: 2014-11
• Status Verified: 2015-09
• Study Completion: 2015-09
• Last Update Submitted: 2015-09-14
• Last Update Posted: 2015-09-15

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 14

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Numbers of participant which can perform the ArmeoSenso - training.	42 days

Secondary Outcome Measures

Name	Time	Method
Improvement in the Arm function	42 days	WMFT (Wolf Motor Function Test), FMA-UL (Fugl-Meyer Assessment - Upper Limb), GRASSP (Graded and Redefined Assessment of Strength, Sensibility and Prehension)

Trial Locations

Locations (1)

University Hospital Zurich, Divison of Neurology; 🇨🇭 Zurich, ZH, Switzerland