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NCT Number: NCT07510087

Glaucoma Related Quality of Life

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

GQL-15

Other

GQL-15 questionnaire

Glaucoma Symptom Scale

Other

GSS questionnaire

NEI Vision Function Questionnaire

Other

Vision function questionnaire

Ocular Surface Disease Index

Other

OSDI questionnaire

Primary outcomes

  1. Ocular Surface Disease Index (OSDI)

    Time frame: 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.

  2. Glaucoma Symptom Scale (GSS)

    Time frame: 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.

  3. National Eye Institute Visual Function Questionaire (NEI VFQ)

    Time frame: 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.

  4. Glaucoma Quality of Life-15 (GQL-15)

    Time frame: 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).

Study contacts

Contact information is provided by the study sponsor or research team.

Helen Gomez Study Coordinator

CONTACT

[email protected]

+1 319 356 3938

Marc Toeteberg-Harms, MD

CONTACT

[email protected]

+1 319 356 3938

Sponsors and collaborators

Lead sponsor

Marc Toeteberg-Harms

Other

Registry information

Acronym: GR-QoL

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Apr 3, 2026
Registry last updated
Apr 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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