The Support Educate Empower (SEE) Program

  • STATUS
    Recruiting
  • End date
    Feb 15, 2024
  • participants needed
    230
  • sponsor
    University of Michigan
Updated on 15 May 2021

Summary

This study will test whether the Support, Educate, Empower (SEE) personalized Glaucoma Coaching Program improves eye drop medication adherence among glaucoma patients compared to enhanced standard care in a randomized controlled clinical trial. As a secondary outcome, the study will test whether glaucoma related distress decreases among SEE program participants compared to the control group.

The study hypothesis is that glaucoma patients with poor adherence who receive motivational-interviewing based counseling and personalized education from a trained non-physician glaucoma coach through the SEE Program will improve their medication adherence compared to glaucoma patients standard care enhanced by additional educational handouts.

Details
Condition Ocular Hypertension, Ocular Hypertension, Glaucoma, Glaucoma
Treatment Enhanced standard care, Personalized Glaucoma Coaching
Clinical Study IdentifierNCT04735653
SponsorUniversity of Michigan
Last Modified on15 May 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Taking greater or equal to 1 ocular hypotensive medication with a diagnosis of any kind of glaucoma, suspected glaucoma or ocular hypertension
Did not opt-out from recruitment letter

Exclusion Criteria

Do not speak English
Have a diagnosed serious mental illness (for example, Schizophrenia)
Diagnosed cognitive impairment
Do not instill their own eye drops
Had laser or incisional glaucoma surgery within three months of enrollment or scheduled during the six-month study period
Unable to attend all study visits
Active ocular infection or uveitis
Clear my responses

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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