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CompletedNCT02659709GlaucomaAppUpdated Aug 5, 2019Results posted

Interest in Electronic Applications for Patients With Glaucoma

An observational study in Glaucoma, sponsored by Wills Eye. Completed at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-08-05.

Sponsored by Wills Eye · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
50
Ages
18 Years and older
Sex
All
01

Study summary

To evaluation interest in use of smartphone- and tablet-based application (app) for participants with glaucoma, ocular hypertension, those at risk and their caregivers.

Read the detailed description

This study is designed to determine the amount of interest in an educational application (app) on social media for glaucoma patients and their caregivers.

The purpose of this App is to enhance understanding of glaucoma by using short video tutorials. The App will include glaucoma eye drop medication reminders, a short video tutorial which aims to improve understanding of how visual field testing should be performed, how to administer eye drops and a feature that will enable participants to store and organize testing results using a mobile device.

02

Conditions studied

  • Glaucoma

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Keywords

  • Glaucoma
  • Smartphone
  • Tablet
  • Application
  • Eye Drops
03

In context

Glaucoma

1,818 studies on the registry are indexed under Glaucoma; 231 are open to participants now.

This study's enrollment of 50 is below the median of 103 across 454 observational studies indexed under Glaucoma.

Browse Glaucoma studies →

Lead sponsor

Wills Eye is the lead sponsor of 74 studies on the registry; 3 are open to participants now.

Of its 12 completed or terminated interventional studies of FDA-regulated products, 10 (83%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Glaucoma patients or care givers

Inclusion criteria

  • Anyone affected by glaucoma
  • Family and friends of someone with glaucoma

Exclusion criteria

Exclusion Criteria:

  • unable to complete survey
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
50 participants (actual)
Patient registry
No

Groups and cohorts

  • Glaucoma Patients and Caregivers

    Glaucoma patients and caregivers will complete a 20 item questionnaire providing demographic information, glaucoma eye drop compliance, interest in medication reminders, availability to smartphone, tablet and social media technology and interest in using a glaucoma application on social media.

    Device: Interest in medical education through social media

Interventions

  • DeviceInterest in medical education through social media

    Measuring interest in social media technology designed to educate glaucoma patients about disease, testing, and treatments with reminders for taking medications.

    Also known as: Glaucoma App Interest

06

What researchers measure

Primary outcomes

  1. Patients Owning Smartphone/Tablet Technology

    Responses collected from participants about owning access to social media via smartphone or tablet technology obtained by completing a 20 item questionnaire.

    Time frame: 1 hour

  2. Patients Having Access to Social Media Via Smartphone or Tablet in the Home

    Responses collected from participants about their personal access, through other members in the home, to social media via smartphone or tablet technology obtained by completing a 20 item questionnaire.

    Time frame: 1 hour

Secondary outcomes

  1. Glaucoma Medication Compliance

    Responses collected from participants about compliance to using their glaucoma drops as prescribed obtained by completing a 20 item questionnaire.

    Time frame: 1 hour

  2. Use of Medication Reminder

    Responses collected from participants about use of medication reminders for their glaucoma drops obtained by completing a 20 item questionnaire.

    Time frame: 1 hour

07

Results

Posted Aug 5, 2019
Limitations and caveats
Participants were recruited from single urban eye care hospital. Results did not distinguish between glaucoma patients and caregivers. Participation did not include testing of the application.

Participant flow

Glaucoma patients and Caregivers were recruited from the Glaucoma Service at Wills Eye Hospital, Philadelphia, PA, USA.

Participant flow — Overall Study
MilestoneGlaucoma Patients and Caregivers
Started50
Completed50
Not completed0

Outcome measures

PrimaryPatients Owning Smartphone/Tablet Technology

Responses collected from participants about owning access to social media via smartphone or tablet technology obtained by completing a 20 item questionnaire.

Time frame:
1 hour
Reported as:
Count of participants · Participants
Patients Owning Smartphone/Tablet Technology
ParticipantsGlaucoma Smartphone Application
Patients Owning Smartphone/Tablet Technology34
PrimaryPatients Having Access to Social Media Via Smartphone or Tablet in the Home

Responses collected from participants about their personal access, through other members in the home, to social media via smartphone or tablet technology obtained by completing a 20 item questionnaire.

Time frame:
1 hour
Reported as:
Count of participants · Participants
Patients Having Access to Social Media Via Smartphone or Tablet in the Home
ParticipantsGlaucoma Smartphone Application
Patients Having Access to Social Media Via Smartphone or Tablet in the Home39
SecondaryGlaucoma Medication Compliance

Responses collected from participants about compliance to using their glaucoma drops as prescribed obtained by completing a 20 item questionnaire.

Time frame:
1 hour
Reported as:
Count of participants · Participants
Glaucoma Medication Compliance
ParticipantsGlaucoma Smartphone Application
Glaucoma Medication Compliance25
SecondaryUse of Medication Reminder

Responses collected from participants about use of medication reminders for their glaucoma drops obtained by completing a 20 item questionnaire.

Time frame:
1 hour
Reported as:
Count of participants · Participants
Use of Medication Reminder
ParticipantsGlaucoma Smartphone Application
Use of Medication Reminder28

Adverse events

Collected over 1 hour. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Glaucoma Smartphone Application0/50 (0%)0/50 (0%)0/50 (0%)

Baseline characteristics

Fifty participants agreed to answer questions in the survey.

Age, Categorical
Age, Categorical(Participants)Glaucoma Patients and Caregivers
<=18 years1
Between 18 and 65 years32
>=65 years17
Sex: Female, Male
Sex: Female, Male(Participants)Glaucoma Patients and Caregivers
Female32
Male18
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Glaucoma Patients and Caregivers
American Indian or Alaska Native0
Asian2
Native Hawaiian or Other Pacific Islander0
Black or African American9
White33
More than one race3
Unknown or Not Reported3
Region of Enrollment
Region of Enrollment(participants)Glaucoma Patients and Caregivers
United States50
08

Study locations

1 site
  • Wills Eye Hospital
    Philadelphia, Pennsylvania 19107, United States
09

References and documents

Publications

  • Waisbourd M, Dhami H, Zhou C, Hsieh M, Abichandani P, Pro MJ, Moster MR, Katz LJ, Hark LA, Myers JS. The Wills Eye Glaucoma App: Interest of Patients and Their Caregivers in a Smartphone-based and Tablet-based Glaucoma Application. J Glaucoma. 2016 Sep;25(9):e787-91. doi: 10.1097/IJG.0000000000000504. PubMed 27552513 ↗

Individual participant data

Plan to share: No

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 5, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT02659709
Lead sponsor
Wills Eye
Responsible party
Jonathon Myers (Principal Investigator, Wills Eye) — Principal investigator
First posted
Jan 20, 2016
Start date
Jun 2015
Primary completion
Oct 2016
Completion
Oct 2016
Results posted
Aug 5, 2019
Last update
Aug 5, 2019

Study contacts

Jonathan S Myers, MD
principal investigator · Wills Eye Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2019. You cannot join it, but the record below documents what was studied.

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