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INTERACTION, Monitoring of Stroke Patients in Hospital and Home Environment (INTERACTION)

This study is currently recruiting participants.
Verified October 2017 by University of Zurich
Sponsor:
ClinicalTrials.gov Identifier:
NCT02118363
First Posted: April 21, 2014
Last Update Posted: October 25, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Collaborators:
University of Twente
University of Pisa
Roessingh
XSens technologies B.V.
Smartex S.r.l.
Information provided by (Responsible Party):
University of Zurich
  Purpose
Clinical assessment and monitoring of balance and arm function in stroke patients with sensor based measurement, in clinical and home environment.

Condition
Stroke

Study Type: Observational
Study Design: Observational Model: Case-Control
Time Perspective: Prospective
Official Title: Proof of Concept Study of the INTERACTION Technology, Monitoring of Stroke Patients in Hospital and Home Environment

Resource links provided by NLM:


Further study details as provided by University of Zurich:

Primary Outcome Measures:
  • proof of concept [ Time Frame: 3 month ]

Estimated Enrollment: 15
Study Start Date: April 2014
Estimated Study Completion Date: December 2017
Estimated Primary Completion Date: December 2017 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 99 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
subakut or chronic stroke patients
Criteria

Inclusion Criteria:

  • Age: 18 or above
  • Previous Stroke in the personal history
  • Able to walk 10 meters. A walking aid (unilateral or bilateral) is permitted
  • Able to walk without special shoes
  • Able to raise the arm against gravity
  • Able to read and understand questionnaires and able to execute commands
  • Able and willing to participate in the study
  • Singed Informed Consent

Exclusion Criteria:

  • Contraindications on ethical grounds (vulnerable persons)
  • known or suspected non-compliance, drug or alcohol abuse,
  • Severe aphasia
  • Severe dementia
  • Severe depression
  • Relevant medical disease or increased risk of rehospitalization
  • Severe sensory deficits
  • Severe neglect
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02118363


Contacts
Contact: Andreas Luft, Prof +41 44 255 8806 andreas.luft@usz.ch
Contact: Jeremia Held +41 44 255 8806 jeremia.held@uzh.ch

Locations
Switzerland
Cereneo Recruiting
Vitznau, Switzerland, 6354
Contact: Andreas Luft, Prof.    +41 41 399 67 00    andreas.luft@usz.ch   
Principal Investigator: Jeremia Held         
Sponsors and Collaborators
University of Zurich
University of Twente
University of Pisa
Roessingh
XSens technologies B.V.
Smartex S.r.l.
  More Information

Additional Information:
Responsible Party: University of Zurich
ClinicalTrials.gov Identifier: NCT02118363     History of Changes
Other Study ID Numbers: 13101
seventh framework programme ( Other Grant/Funding Number: 287351 )
First Submitted: April 8, 2014
First Posted: April 21, 2014
Last Update Posted: October 25, 2017
Last Verified: October 2017

Keywords provided by University of Zurich:
upper limb
lower limb
monitoring
assessment
sensor

Additional relevant MeSH terms:
Stroke
Cerebrovascular Disorders
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Vascular Diseases
Cardiovascular Diseases