Impact of Meditation on Reducing Stress in Glaucoma Patients: An Electronic Feasibility Study
2 other identifiers
interventional
158
0 countries
N/A
Brief Summary
Glaucoma is a chronic disease that causes loss of vision and potentially blindness as a result of optic nerve damage, often due to increased intraocular pressure. Glaucoma is currently the leading cause of irreversible blindness worldwide.1 In 2020, 4.1 million and 3.6 million adults over the age of 50 suffered from mild to severe glaucoma-induced visual impairment and blindness, respectively.1 However, these figures are likely underestimated since glaucoma can remain asymptomatic until later stages in disease progression.2 The relaxation response evoked by mind-body interventions, such as breathing exercises and meditation, is known to reduce stress and improve quality of life (QOL). In a recent study, mindfulness-based meditation was found to reduce intraocular pressure and improve QOL in patients with glaucoma.3 A feasibility study will be conducted using a mixed-method design to assess the feasibility of the online delivery of meditation for potentially enhancing the QOL and reducing stress in glaucoma patients. Upon recruitment, participants will undergo blocked randomization to either the intervention arm or usual care arm. Participants in each arm will complete online questionnaires at baseline and weeks 1, 3, 6, and 12 to collect data on health-related quality of life (HRQOL), perceived stress, and behaviour using REDCap. REDCap is an online data collection and survey tool hosted by the Office of Research Services of Lawson Research Institute. Our study can help to assess the feasibility of conducting a study on breathing exercises followed by meditation to assess its effects in a sample of patients with glaucoma.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Nov 2026
Typical duration for not_applicable
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
First Submitted
Initial submission to the registry
August 14, 2026
CompletedFirst Posted
Study publicly available on registry
August 18, 2026
CompletedStudy Start
First participant enrolled
November 1, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2028
Study Completion
Last participant's last visit for all outcomes
December 1, 2028
August 18, 2026
August 1, 2026
2 years
August 14, 2026
August 14, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Incidence of Quality of Life as measured by GQOL- 15 in Glaucoma Patients
HRQoL will be assessed using Glaucoma Quality of Life-15 (GQL-15). GQL-15 is a disease-specific, validated, self-administered questionnaire designed to measure HRQoL in patients with glaucoma. The questionnaire comprises of 15 items on daily functioning across 5 factors: central and near vision (2 items), peripheral vision (6 items), glare and dark adaptation (6 items), and outdoor mobility (1 item). Patients rate these questions on a 5-point Likert scale of difficulty ranging from "1 = no difficulty" to "5 = severe difficulty".
Data will be collected at baseline and post-intervention at Week 1, 3, 6, and 12.
Secondary Outcomes (2)
Incidence of Stress as Measured by PSS-10 in Glaucoma Patients
Data will be collected at baseline and post-intervention at Week 1, 3, 6, and 12.
Incidence of Behavior as measured by Consideration of Future Consequences - 14 (CFC-14) in Glaucoma Patients
Data will be collected at baseline and post-intervention at Week 1, 3, 6, and 12.
Study Arms (2)
Meditation + Usual Care
OTHERUsual Care
NO INTERVENTIONInterventions
Meditation is a guided technique that helps to reduce stress, therefore inducing physiological and mental relaxation whilst the eyes are shut.
Eligibility Criteria
You may qualify if:
- Diagnosed with glaucoma or suspected to have glaucoma.
- Aged 65 and above.
- Able to provide valid informed consent to participate in the research study.
- Able to read and understand English.
- No significant self-reported or physician-diagnosed mental health disorder.
- Independent access to a computer to participate in virtual sessions.
- Able to sit comfortably for 30 minutes without any major pain or discomfort, can hear well enough to follow verbal instructions when the eyes are closed, and be in good general physical health.
- Willing to practice meditation at home for \~15 minutes per day.
You may not qualify if:
- Inability to provide valid informed consent.
- Significant communication barriers or lack of English proficiency that prevents participants from completing the questionnaires.
- Self-reported substance abuse or dependence within the past 3 months.
- Having acutely unstable medical illnesses, including delirium or acute cerebrovascular or cardiovascular events within the last 6 months.
- Having irreversible vision loss that prevents one from completing the questionnaires.
- Participation in a study involving similar techniques.
- Established meditation practice, defined as engaging in any formal meditation (e.g., mindfulness, mantra, breath-focused) more than twice per week within the past 3 months.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 14, 2026
First Posted
August 18, 2026
Study Start (Estimated)
November 1, 2026
Primary Completion (Estimated)
November 1, 2028
Study Completion (Estimated)
December 1, 2028
Last Updated
August 18, 2026
Record last verified: 2026-08