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Behavioral Intervention

Meditation for Improving Quality of Life in Glaucoma Patients

N/A
Waitlist Available
Research Sponsored by Lawson Health Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Patients aged 65-75
Patients diagnosed with mild glaucoma
Must not have
Having acutely unstable medical illnesses, including delirium or acute cerebrovascular or cardiovascular events within the last 6 months
Inability to provide valid informed consent
Timeline
Screening 3 weeks
Treatment Varies
Follow Up week 1, week 3, week 6, week 12
Awards & highlights
No Placebo-Only Group

Summary

This trial will test if online mindfulness meditation can help glaucoma patients by reducing eye pressure and improving their quality of life and mental health.

Who is the study for?
This trial is for individuals aged 65-75 with mild glaucoma, who can use a computer, sit comfortably for over half an hour, and have good hearing. They should be in overall good health without significant mental disorders or severe depression. Participants must understand English and provide informed consent.
What is being tested?
The study tests if online meditation can improve life quality and mental health in glaucoma patients. It compares the effects of meditation to usual care using questionnaires on health, depression, anxiety, and sleep at multiple points during the study.
What are the potential side effects?
Meditation is generally safe but may include temporary discomfort like restlessness or difficulty concentrating. Rarely it could trigger emotional distress especially if there are underlying mental health issues.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am between 65 and 75 years old.
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I have been diagnosed with mild glaucoma.
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I can use a computer by myself for online meditation sessions.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I have not had a stroke, heart attack, or severe illness in the last 6 months.
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I am unable to understand or sign the consent form.
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I have been diagnosed with severe depression.
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I have been diagnosed with a serious mental disorder like bipolar or schizophrenia.
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I cannot complete questionnaires due to irreversible vision loss.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~week 1, week 3, week 6, week 12
This trial's timeline: 3 weeks for screening, Varies for treatment, and week 1, week 3, week 6, week 12 for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
The 12-item short form survey
Secondary study objectives
Anxiety
Depression
Sleep quality

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Meditation to Remove Stress and Create A Proper System in MindExperimental Treatment1 Intervention
The study intervention will be administered to participants randomized to the intervention arm. The meditation intervention will be delivered virtually via the hospital-approved Microsoft Teams platform. Participants will be taught an evidence-based meditation technique which includes two online sessions (60 minutes/day) with a trained, experienced, and certified teacher of Prasanna Wellness, a non-profit service organization. Participants will learn how to respond to experiences that arise in meditation, will discuss what enhances or detracts from effective meditation, and review methods for meditating at home. The participants in the intervention arm will complete 60-minute follow-up sessions with the Prasanna Wellness staff which will include 33 minutes of guided meditation practice, and then a discussion of participants' experiences with meditation during the week, additional observations, and a review of relevant knowledge to support their home practice.
Group II: Usual CareActive Control1 Intervention
Participants will continue with their usual care.

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The primary goal of glaucoma treatments is to reduce intraocular pressure (IOP) to prevent optic nerve damage and subsequent vision loss. Common treatments include medications such as prostaglandin analogs, which increase the outflow of aqueous humor, and beta-blockers, which reduce aqueous humor production. Surgical options like trabeculectomy create new drainage pathways for fluid. Non-pharmacological interventions, such as mindfulness-based meditation, have shown promise in reducing IOP and improving quality of life by lowering stress and potentially influencing physiological processes that affect eye pressure. These mechanisms are crucial for glaucoma patients as they help preserve vision and enhance overall well-being.

Find a Location

Who is running the clinical trial?

Lawson Health Research InstituteLead Sponsor
680 Previous Clinical Trials
421,833 Total Patients Enrolled
6 Trials studying Glaucoma
508 Patients Enrolled for Glaucoma

Media Library

Art of Meditation (Behavioral Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT05697094 — N/A
Glaucoma Research Study Groups: Usual Care, Meditation to Remove Stress and Create A Proper System in Mind
Glaucoma Clinical Trial 2023: Art of Meditation Highlights & Side Effects. Trial Name: NCT05697094 — N/A
Art of Meditation (Behavioral Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05697094 — N/A
~8 spots leftby Dec 2024