Skip to content

Effect of Glaucoma Educators on Adherence to Prescribed Therapeutic Regimens in Glaucoma Patients

Effect of Glaucoma Educators on Adherence to Prescribed Therapeutic Regimens in Glaucoma Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00454922
Enrollment
44
Registered
2007-04-02
Start date
2007-10-31
Completion date
2012-01-31
Last updated
2012-12-06

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

Conditions

Glaucoma

Keywords

glaucoma, patient educator

Brief summary

Glaucoma is a leading cause of blindness worldwide. Non-adherence to glaucoma medication, which may result in loss of vision, is known to be prevalent. Available information regarding adherence to prescribed medical therapy suggests that some apparent treatment failures may actually be due to non-adherence. The investigators' specific aim is to conduct a study that will examine the effect of a glaucoma educator intervention on adherence to topical glaucoma therapy. The investigators' hypothesis is that patient education and counseling delivered by a trained glaucoma educator, through both planned visits and telephone contacts, will increase adherence to topical glaucoma therapy.

Interventions

BEHAVIORALstandard of care

no intervention

OTHEReducation

meet with trained glaucoma educator 6 times over life of study

Sponsors

University of Colorado, Denver
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Diagnosis of primary or secondary open angle glaucoma. * Currently on monotherapy drop treatment for glaucoma. * Age \> 18 years. * Patient has presented for care at the Rocky Mountain Lions Eye Institute Glaucoma Center.

Exclusion criteria

* Inability to independently administer eye drops due to physical disability as reported by the patient. * Cognitive impairment that would interfere with the ability to self-administer medications as evidenced by a TICS score \< 16. * Patients who demonstrate \> 80% adherence to glaucoma treatment during the 30 day run-in period. * It is anticipated that the patient will require glaucoma surgery within the next six months.

Design outcomes

Primary

MeasureTime frame
primary outcome is adherence.6 months

Secondary

MeasureTime frame
differences between patients randomized to standard of care and education intervention.6 months
differences between dropouts and non-dropouts.6 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026