An Evaluation of the Ability to Train Established Glaucoma Patients Who Have Difficulty in Drop Instillation

NCT ID: NCT01719809

Last Updated: 2017-04-12

Basic Information

• Recruitment Status: TERMINATED
• Total Enrollment: 18 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2012-10-31
• Study Completion Date: 2015-06-01

Brief Summary

This is a prospective, observational, single-center study. Patients with at least 3 months of experience using topical medications for glaucoma and who state that they administer their own eye drops will be recruited. Subjects will be videotaped instilling a sterile artificial eye drop, will be identified at the time of a regularly scheduled exam. If the patient can get a drop onto the eye and also not touch their lids or ocular surface with the eye drop bottle, the subject will be thanked but not enrolled. All other patients who agree to participate will be enrolled. Upon completion of videotaped instillation of an eye drop, each enrolled patient will be shown a video demonstrating an instillation technique and will be given an instructional handout highlighting a proper drop instillation technique. If necessary, an instillation technique will be demonstrated to them by an investigator or trained personnel.

A patient will be identified as properly instilling a drop if they satisfy the following criteia:

They are able to instill one (and only one) drop to the ocular surface or lower fornix without allowing the bottle touch the adnexa, eyelid, eye lashes or eye.

All patients routinely return between 3 and 6 months. At this regularly scheduled visit,the investigator or trained personnel would direct the patient to instill an eye drop into the study eye.Additionally, the short glaucoma self-efficacy questionnaire will be re-administered.

All of the video-recordings of participants' eye drop instillation techniques will be reviewed and assessed using a standard checklist. Their ability to administer an eye drop after training will be compared to baseline.

Conditions

Glaucoma; Ocular Hypertension

Study Design

• Observational Model Type: OTHER
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• Patients aged 18 years or older
• Patients currently using topical ocular antihypertensive medications at the time of enrollment in at least one eye, and who have been using these drops consistently for a period of at least three months prior to enrollment.
• Patients with primary open angle glaucoma, pigmentary glaucoma, exfoliation glaucoma, ocular hypertension, normal-tension glaucoma, neovascular glaucoma, uveitic glaucoma and chronic narrow angle glaucoma.
• Patients CAN be enrolled even if they have co-existing morbidities such as Parkinson's Disease or arthritis

Exclusion Criteria

• Patients who do not instill their own eye drops
• Patients who are not expected to still be using topical antihypertensive medications at the time of study follow-up
• Patients with no light perception vision
• Patients with a history of adverse reaction to artificial tears or any component of artificial tears
• Patients who have a typical follow-up period of greater than 6 months
• Patients who have not completed a Humphrey Visual Field C24-2 or C10-2 within 7 months of enrollment or study exit.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Robin, Alan L., M.D.

INDIV

Sponsor Role: lead

Responsible Party

Adam C. LePosa

Adam C. LePosa, O.D

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Adam C LePosa, OD

Role: PRINCIPAL_INVESTIGATOR

Alan L. Robin, MD, PA

Locations

Alan L. Robin, MD, PA

Baltimore, Maryland, United States

Countries

United States

Other Identifiers

ALR 0054

Identifier Type: -

Identifier Source: org_study_id