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Glaucoma Related Quality of Life

Glaucoma Related Quality of Life

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07510087
Acronym
GR-QoL
Enrollment
5000
Registered
2026-04-03
Start date
2024-12-30
Completion date
2027-05-30
Last updated
2026-04-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glaucoma

Keywords

glaucoma, quality of life

Brief summary

Subjects with a diagnosis of glaucoma will be handed out different quality of life related questionnaires and their score will be evaluated at baseline and 3-6 months after treatment or surgery was initiated/performed.

Interventions

OTHERGQL-15

GQL-15 questionnaire

OTHERGlaucoma Symptom Scale

GSS questionnaire

OTHERNEI Vision Function Questionnaire

Vision function questionnaire

OSDI questionnaire

Sponsors

Marc Toeteberg-Harms
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Inclusion: * diagnosis of glaucoma (open- as well as closed-angle glaucoma, primary and secondary glaucomas) * 18 years of age or older with no upper limit * male and female subjects Exclusion: * absence of a diagnosis of glaucoma * less than 18 years of age

Design outcomes

Primary

MeasureTime frameDescription
Ocular Surface Disease Index (OSDI)At baseline and 3-6 months after glaucoma treatment (i.e. drops, SLT, or surgery) was initiated/performed.The OSDI© is assessed on a scale of 0 to 4, with higher scores representing greater disability. The index demonstrates sensitivity and specificity in distinguishing between normal subjects and patients with dry eye disease. The OSDI© is a valid and reliable instrument for measuring dry eye disease (normal, mild to moderate, and severe) and effect on vision-related function.
Glaucoma Symptom Scale (GSS)At baseline and 3-6 months after glaucoma treatment (i.e. drops, SLT, or surgery) was initiated/performed.The Glaucoma Symptom Scale (GSS; Lee et al., 1998) was developed as a brief symptom survey specific for persons with glaucoma. The GSS consists of a 10-item scale developed from a modified version of a symptom checklist that address ocular complaints, some of a nonvisual nature and some of a visual nature, common to patients with glaucoma. Items are scored from 0 to 100, where 100 represents the absence of symptoms and 0 represents severe, bothersome symptoms.
National Eye Institute Visual Function Questionaire (NEI VFQ)At baseline and 3-6 months after glaucoma treatment (i.e. drops, SLT, or surgery) was initiated/performed.Vision-specific instrument designed to measure vision-related quality of life (VRQoL) in adults, incorporating body, activity, and participation content according to the WHO ICF Framework in order to measure the effects of a variety of ocular conditions on daily functioning and QOL. It was originally designed as a 51-point questionnaire and is currently available in both self-administered and interview-based formats. The raw scores are converted to a 0-100 scale; after reverse scoring, a high score (100) indicates better vision-specific quality of life, while a low score (0) indicates poor function.
Glaucoma Quality of Life-15 (GQL-15)At baseline and 3-6 months after glaucoma treatment (i.e. drops, SLT, or surgery) was initiated/performed.The Glaucoma Quality of Life-15 (GQL-15) is a validated 15-item, self-report questionnaire used to measure visual disability and quality of life (QoL) in glaucoma patients. It covers four key areas-peripheral vision, central/near vision, glare/dark adaptation, and outdoor mobility-using a 5-point scale (1=no difficulty to 5=severe difficulty).

Countries

United States

Contacts

CONTACTMarc Toeteberg-Harms, MD
marc-toeteberg-harms@uiowa.edu+1 319 356 3938
CONTACTHelen Gomez Study Coordinator
helen-gomez@uiowa.edu+1 319 356 3938

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 7, 2026