NCT00760240

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Sep 2008

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2008

Completed
24 days until next milestone

First Submitted

Initial submission to the registry

September 25, 2008

Completed
1 day until next milestone

First Posted

Study publicly available on registry

September 26, 2008

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2009

Completed
Last Updated

April 26, 2010

Status Verified

April 1, 2010

Enrollment Period

1 year

First QC Date

September 25, 2008

Last Update Submit

April 23, 2010

Conditions

Keywords

complianceeyedrop instillationHow patients with low vision due to glaucoma or retinal pathology instill eyedrops into their own eyes.

Outcome Measures

Primary Outcomes (1)

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

    2 minutes

Study Arms (2)

Glaucoma patients

This is a group of patients with restricted visual fields or ETDRS visual acuity of 20/60 or worse

Retina patients

A group of patients with retinal pathology(ARMD, CME, diabetic retinopathy) contributing to their decreased vision.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients reporting for appointments at outpatients referral practices shared by 2 glaucoma and 3 retina specialists

You may qualify if:

  • ETDRS visual acuity 20/60 or worse

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Glaucoma Specialists/Retina Care Center

Baltimore, Maryland, 21209, United States

Location

MeSH Terms

Conditions

GlaucomaPatient Compliance

Condition Hierarchy (Ancestors)

Ocular HypertensionEye DiseasesPatient Acceptance of Health CareTreatment Adherence and ComplianceHealth BehaviorBehavior

Study Design

Study Type
observational
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER

Study Record Dates

First Submitted

September 25, 2008

First Posted

September 26, 2008

Study Start

September 1, 2008

Primary Completion

September 1, 2009

Study Completion

September 1, 2009

Last Updated

April 26, 2010

Record last verified: 2010-04

Locations