Factors Influencing Patient Satisfaction in a Glaucoma Population
FIPSS
1 other identifier
observational
250
1 country
1
Brief Summary
- 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.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.To assess the correlations between demographic factors, vision related quality of life, eye disease, and treatments with patient satisfaction survey responses.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2015
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2015
CompletedFirst Submitted
Initial submission to the registry
August 6, 2015
CompletedFirst Posted
Study publicly available on registry
December 11, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2016
CompletedNovember 10, 2016
November 1, 2016
8 months
August 6, 2015
November 8, 2016
Conditions
Keywords
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
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
- Wills Eyelead
Study Sites (1)
Wills Eye Hospital
Philadelphia, Pennsylvania, 19107, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jonathan Myers, MD
Wills Eye Hospital
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