NCT02628327

Brief Summary

  1. 1.To administer a questionnaire to patients seen by Wills Eye Glaucoma Department physicians at Wills Eye Hospital assessing satisfaction with their office visit, vision related quality of life, and related issues.
  2. 2.To collect and de-identify information from each participant's medical chart related to their care including information pertaining to demographics, disease severity, and prior and current treatment
  3. 3.To assess the correlations between demographic factors, vision related quality of life, eye disease, and treatments with patient satisfaction survey responses.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
250

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2015

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

June 1, 2015

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

August 6, 2015

Completed
4 months until next milestone

First Posted

Study publicly available on registry

December 11, 2015

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2016

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2016

Completed
Last Updated

November 10, 2016

Status Verified

November 1, 2016

Enrollment Period

8 months

First QC Date

August 6, 2015

Last Update Submit

November 8, 2016

Conditions

Keywords

glaucoma carequality of lifepatient satisfaction

Outcome Measures

Primary Outcomes (1)

  • Quality of Life assessment

    Correlate demographic factors to vision related quality of life, eye disease and treatment

    6 months

Study Arms (1)

Glaucoma subjects

Survey given to all glaucoma subjects agreening to study.

Eligibility Criteria

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

Glaucoma or glaucoma suspect

You may qualify if:

  • Age \> 18 years; patients who have a scheduled appointment at with a glaucoma specialist at Wills Eye Hospital; diagnosis of glaucoma or glaucoma suspect

You may not qualify if:

  • Children under the age of 18; inability to give informed consent; patients who are physically and/or mentally incapable of filling out a paper survey; patients who are not literate in English.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Wills Eye Hospital

Philadelphia, Pennsylvania, 19107, United States

Location

MeSH Terms

Conditions

GlaucomaPatient Satisfaction

Condition Hierarchy (Ancestors)

Ocular HypertensionEye DiseasesTreatment Adherence and ComplianceHealth BehaviorBehavior

Study Officials

  • Jonathan Myers, MD

    Wills Eye Hospital

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principle Investigator

Study Record Dates

First Submitted

August 6, 2015

First Posted

December 11, 2015

Study Start

June 1, 2015

Primary Completion

February 1, 2016

Study Completion

June 1, 2016

Last Updated

November 10, 2016

Record last verified: 2016-11

Data Sharing

IPD Sharing
Will share

A manuscript has been submitted to the Journal of Medical Quality

Locations