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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02434237
Other study ID # EK 04 2005
Secondary ID
Status Completed
Phase N/A
First received October 13, 2014
Last updated May 4, 2015
Start date March 2005
Est. completion date March 2015

Study information

Verified date April 2015
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational

Clinical Trial Summary

Task-oriented repetitive movement can improve movement performance in patients with neurological or orthopedic lesions. The application of robotics can serve to assist, enhance, evaluate, and document neurological and orthopedic rehabilitation of movements. Arm therapy is used in neurological rehabilitation for patients with paralyzed upper extremities due to lesions of the central or peripheral nervous system, e.g. after stroke or spinal cord injury. The goal of the therapy is to recover motor function, improve movement coordination, learn new motion strategies ("trick movements"), and/or prevent secondary complications such as muscle atrophy, osteoporosis, and spasticity.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date March 2015
Est. primary completion date March 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

Patients with neurological disability of the upper limb with qualification for arm training, e.g. after stroke and spinal cord injury

Exclusion Criteria:

- limitations of the join mobility

- osteoporosis

- cardiovascular disease

- injury of the upper limb

- decubitus

- psychic diseases (like schizophrenia, dementia, depression)

- Body weight > 120kg

- pacemaker.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Robot-aided Arm Therapy, Brain Injury, Motor Relearning Programme, Activities of Daily Living

Locations

Country Name City State
Switzerland University of Zurich, Swiss Federal Institute of Technology Zurich

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary The acceptanece of the arm rehabilitation robot therapy and the influence to the motivation through the visual feedback. A measure lasts approx. 90 minutes. Every participant once. Yes