Eyelid Movement Sensor Device- Blinking Characterizing

Sponsor
HaEmek Medical Center, Israel (Other)
Overall Status
Completed
CT.gov ID
NCT02309814
Collaborator
(none)
80
1
19

Study Details

Study Description

Brief Summary

The investigators have developed a simple to use device that facilitates the monitoring of the upper eyelids motion, acquires the eyelid vertical movement and enables analysis and graphic presentation of the results. the device system consists 3 components : glasses for the patient including magneto sensitive probes, hardware and dedicated software.

Our purpose is to characterize eyelid motion in normal population. The methods include measuring each patient 10 minutes during watching a short movie.

Condition or Disease Intervention/Treatment Phase
  • Device: eyelid motion sensor device (Hall-probe)
N/A

Detailed Description

Essentially, for Hall-probes monitor the magnetic field generated by a tiny magnets attached to the upper eyelid.

Study Design

Study Type:
Interventional
Actual Enrollment :
80 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Eyelid Movement Sensor Device- Blinking Characterizing
Study Start Date :
Jan 1, 2015
Actual Primary Completion Date :
Aug 1, 2016
Actual Study Completion Date :
Aug 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: eyelid motion sensor device

all volunteers will wear the monitor eyelid sensor device (including the tiny magnets on the upper eyelid). a 10 minutes movie will be screened on 40 inch television screen in a 3 meters distance.

Device: eyelid motion sensor device (Hall-probe)
all volunteers will wear the eyelid motion sensor device (Hall-probe) (including the tiny magnets on the upper eyelid). a 10 minutes movie will be screened on 40 inch television screen in a 3 meters distance

Outcome Measures

Primary Outcome Measures

  1. Demonstrate and describe measurable blinking character in normal population.(Hall-probes monitor the magnetic field generated by a tiny magnets attached to the upper eyelid) [10 minutes]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 67 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • healthy 18-67 year olds with no eye medical history
Exclusion Criteria:
  • pregnancy

  • head trauma history

  • using contact lens

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • HaEmek Medical Center, Israel

Investigators

  • Principal Investigator: daniel briscoe, haemek medical center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
daniel briscoe, Head of ophthalmology departement, HaEmek Medical Center, Israel
ClinicalTrials.gov Identifier:
NCT02309814
Other Study ID Numbers:
  • 0133-13-EMC
First Posted:
Dec 5, 2014
Last Update Posted:
Sep 8, 2016
Last Verified:
Sep 1, 2016
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 8, 2016