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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03194828
Other study ID # 17-05074-XP
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date May 8, 2017
Est. completion date July 15, 2018

Study information

Verified date May 2017
Source University of Tennessee
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will evaluate the effectiveness of real-time data collected on patients taking topical medication to treat glaucoma. Patients will be randomized to two groups, the first of which will only use the study device to take their medication, while the second will use the study device and receive on-demand reminder messages, when necessary.


Description:

Adherence to topical medications to treat glaucoma remains sub optimal; however, our understanding of this behavior remains limited due to biased measures of medication use. The Kali Drop device is a potential improvement in our ability to capture medication use in patients using dropper bottles by precisely capturing the amount dispensed in real-time. Moreover, such technology creates data that can be leveraged into driving behavior change using connected mobile technology in order to improve adherence and, ultimately, health outcomes. While evidence suggests that reminders may improve adherence to glaucoma medications, the power of doing so using real-time data has yet to be explored. This study will compare simple monitoring of patients to those who are being monitored and who receive reminder messages when the system determines one is necessary due to a missed dose.


Recruitment information / eligibility

Status Terminated
Enrollment 5
Est. completion date July 15, 2018
Est. primary completion date July 15, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years of age and older

- Glaucoma diagnosis

- Prescription for a prostaglandin indicated for glaucoma

- Nonadherent (MPR<80%) in the last 3 months according to pharmacy records

- Owns and operates a mobile phone and willing to receive periodic reminder messages

Exclusion Criteria:

- Existing chronic eye condition in addition to glaucoma

- Scheduled for eye surgery in the next 90 days

- Prescription for a medication that will not fit in the device

- Non-English speaking

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Medication reminder
Using the real-time data capture of the electronic device, an automated voice call or text message will be sent to active arm participants only when a missed dose is determined
Medication monitoring only
Patients will use an electronic medication monitoring device to record their actual medication use

Locations

Country Name City State
United States Barney's Pharmacy Augusta Georgia
United States Barney's Pharmacy Augusta Georgia
United States Hutton Pharmacy Blackwell Oklahoma
United States Creative Care Pharmacy Edmond Oklahoma
United States Barney's Pharmacy Grovetown Georgia
United States Barney's Pharmacy Louisville Georgia
United States Mustang Drug Mustang Oklahoma
United States University of Tennessee College of Pharmacy Nashville Tennessee

Sponsors (6)

Lead Sponsor Collaborator
University of Tennessee Barney's Pharmacy, Creative Care Pharmacy, Hutton Pharmacy, Kali Care, Mustang Drug

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Adherence Changes and differences in adherence to glaucoma medication between groups From study baseline through the 3 months of the intervention
Primary Adherence follow-up Changes and differences in adherence to glaucoma medication between groups after the intervention From study endpoint through the subsequent 3 months
Secondary Medication self-efficacy using the 10-item Glaucoma Medication Adherence Self-Efficacy Scale Differences in self-reported medication-related self-efficacy between groups Change from baseline over the 3-month intervention
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