Skip to main content
Clinical Trials/NCT00760240
NCT00760240CompletedNot Applicable

Objective Evaluation of the Ability of Patients With Decreased Vision or Restricted Visual Fields to Properly Instill Eye Drops

Mid-Atlantic Glaucoma Experts1 site in 1 country200 target enrollmentStarted: September 2008Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
200
Locations
1
Primary Endpoint
Successful instillation of a single eyedrop onto the surface of the eye

Study Overview

Brief Summary

The investigators are interested in seeing how people with low vision (decreased visual acuity or restricted visual fields) instill eye drops into their own eyes. The investigators hypothesis is that this population will have more difficulty with self-instillation of drops than a better-seeing population. The investigators aim to explore whatever factors may be involved in preventing this population from getting prescribed eyedrops into their eyes, whether it is more related to visual field or visual acuity.

Detailed Description

This is a study that involves a questionnaire that a study participant fills out, detailing their experience with eyedrops (if any), followed by a video recording of them instilling artificial tears into their worse-seeing eye, with their dominant hand. Patients must have visual acuity worse than 20/60 in at least one eye, and/or have a recent visual field that demonstrated Hodapp criteria for Moderate or Severe visual field damage. This is an observational study of how patients with low vision due to either glaucoma or retinal disease instill eyedrops. Each video will be "graded" by the principal investigator for "success" at instilling eyedrops, and patients will be stratified by their visual acuity or visual field, and whether they have a primary diagnosis of glaucoma or retinal disease.

Study Design

Study Type
Observational
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • ETDRS visual acuity 20/60 or worse

Exclusion Criteria

  • Unwilling to participate
  • Light perception vision
  • No light perception vision

Outcomes

Primary Outcomes

Successful instillation of a single eyedrop onto the surface of the eye

Time Frame: 2 minutes

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Mid-Atlantic Glaucoma Experts
Sponsor Class
Other

Study Sites (1)

Loading locations...

Similar Trials

Ability of Patients With Low Vision to... | Clinical Trial