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Clinical Trials/NCT03022266
NCT03022266CompletedNot Applicable

A Behavioral Economics-Based Telehealth Intervention to Improve Post-MI Medication Adherence

Wellth Inc.1 site in 1 country130 target enrollmentStarted: February 1, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
130
Locations
1
Primary Endpoint
Medication Adherence

Study Overview

Brief Summary

The proposed study is a pilot randomized clinical trial (RCT). Participants in the intervention arm will participate in a 90-day adherence promotion program based on the theory of behavioral economics and administered through the Wellth mobile phone application. Subjects will be provided a CleverCap® Lite BLE C035 smart pill bottle (electronic monitoring (EM), device) containing a 90-day supply of aspirin (90 pills) and those in the intervention arm will be offered $150 for app-based medication check-ins, which consist of uploading daily photos of pills at the time of administration through the Wellth app. Subjects will have $2 deducted from total rewards for each day that a medication check-in is missed. Subjects in the control arm will receive usual care and be monitored with the same EM device types used in the intervention arm.

Detailed Description

Medication adherence is a quantifiable parameter detailing when and how consistently doses are taken. Elements of medication adherence include: 1) the proportion of prescribed drug taken or %PDT (primary outcome); 2) the proportion of days with the correct number of doses taken; 3) the proportion of doses taken on time, in relation to a prescription-defined time interval between successive doses; 4) the distribution of inter-dose intervals; 5) the number of drug holidays; and 6) the longest interval between two doses [Vrijens et al. British journal of clinical pharmacology. 2012;73(5):691-705]. Medication adherence will be assessed in all participants using EM technology manufactured by CleverCaps®. Electronic Monitoring (EM) is more sensitive, reliable and valid than other measurement techniques such as pill counts, self-reports, or clinical judgment [Vrijens et al. Expert review of clinical pharmacology. 2014;7(5):633-644]. In this study the investigators will monitor a single drug, aspirin, in MI patients prescribed aspirin on hospital discharge.

In addition to measurement of medication adherence using an EM device, the investigators will measure adherence using the Wellth cell phone app in the intervention arm. Participants in the intervention arm will also be asked to track their medication-taking habits by uploading photos of their medications at the appropriate dosage times using the Wellth app.

Readmissions will be measured using the EMR and by interview to capture events outside the Penn system. Events will be classified according to timing (e.g. 30-day readmission) and cause (e.g. cardiac, all-cause). This study is not designed to detect a statistically significant difference in readmissions.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Investigator)

Eligibility Criteria

Ages
21 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Over 21 years of age
  • •Admitted to one of the University of Pennsylvania hospitals for acute myocardial infarction (ICD-10 codes I21.xx) or unstable angina (ICD 10 codes I20.xxx)
  • •Prescribed once-per-day aspirin at discharge
  • •The patient administers his or her own medications
  • •Own a smartphone with a sufficient data plan or home Wi-Fi to enable app use and avoid overage charges
  • •Able to speak and understand English

Exclusion Criteria

  • •Diagnosis of MI following non-cardiac admission
  • •Discharge to any facility other than the patient's home
  • •Cognitive impairment that limits ability to understand and complete questionnaires
  • •Inability to operate a mobile phone and the Wellth app
  • •Physician-estimated life expectancy less than 6 months

Arms & Interventions

Usual Care Control Arm

No Intervention

Participants in the usual care control arm will receive the usual education about medications provided by hospital staff. Medication adherence will be measured via a CleverCap(R) electronic monitoring pillbox.

Intervention Arm

Experimental

Participants receiving the Financial Incentive and Mobile Phone App will be given an smartphone app offering pill reminders and $50/month financial incentives for three months to upload photos of medication each day for 90 days. Medication adherence will be measured via a CleverCap(R) electronic monitoring pillbox.

Intervention: Financial Incentive and Mobile Phone App (Behavioral)

Outcomes

Primary Outcomes

Medication Adherence

Time Frame: 90 Days

Better medication adherence at 90 days as Percentage of Doses Taken (%PDT) using CleverCap(R) electronic monitoring devices

Secondary Outcomes

  • 30-Day All-cause Readmissions(30 Days)
  • 90-Day All-cause Readmissions(90 Days)
  • Self-reported self-care(90 Days)
  • Medication adherence assessed using patient smartphone photos(90 Days)

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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