SBIR/STTR Research Award

Automated Call Center Intervention on Medication Adherence (ACCIOM)

Award identifier 2de2e218a5701981275bfd79562369e4d4afa733f164b983a3d3249c8df6e74bAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$298,091

Program and phase

SBIR · Phase I

Award year

2008

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
HEALTHHONORS
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
PHS2007-2
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): Medication non-adherence is a widespread problem with serious ramifications at every point in the human life cycle. Most of this burden is borne by adults 55 and older. Nationwide statistics make it clear that non- adhe rence presents a formidable problem for efforts to promote active lifestyles and increase health expectancy. Annually, non-adherence is responsible for 10 percent of hospitalizations, 125,000 deaths, and 100 B in healthcare costs. Most prior attempts to i mprove adherence have proven costly, labor-intensive, and overall minimally effective. The problem has been particularly refractory for chronic asymptomatic conditions such as hypercholesterolemia. The solution to be studied in this SBIR was develo ped by two physician-scientists who have first-hand familiarity with non-adherence. They have developed a low-cost, consumer- and pharmacist-tested, telemedicine intervention that empowers patients to practice better adherence. This informatics-powered int ervention has demonstrated usability in multiple Focus Groups, a randomized crossover pilot study, and most recently a commercial trial at a local pharmacy. In the controlled pilot study, medication adherence rose 33 percent relative to controls (p lt 0.00 01). We now propose a randomized controlled trial of the intervention for a common and important application: statin use in adults 55 years and older with asymptomatic hypercholesterolemia. The main hypothesis to be tested is that the proprietary i ntervention can be used to boost and sustain medication adherence for senior adults with chronic asymptomatic illnesses. The study will randomize 100 subjects who already use atorvastatin to receive the intervention versus control (standard of care) and fo llow them over 8 months. Outcome measures will be daily adherence rates as measured by Medication Event Monitoring System (MEMS) caps, monthly refill rates, persistency, over-medication error rates, and serum lipid profiles. Specific aims are to: (1) measu re the effect of the intervention on atorvastatin adherence and persistency; and (2) assess the ability of the intervention to collect data on medication adherence, with MEMS caps as a reference. We anticipate that the intervention will (1) boost adherence and persistency; (2) reduce over-medication errors; and (3) provide an automated medication adherence database for patient care and public health surveys. Based on iterative Focus Groups, consumer tests, materials trials, and pharmacist-directed d evelopment, we expect the intervention to be clinically effective, economical, easy-to-use, and widely accessible to patients. If the results support these predictions, the system can be scaled up rapidly to benefit the American population. A detailed busi ness plan is in place to market the system to health care payers and pharmaceutical companies. The company has partnered with a nationwide pharmaceutical distributor to distribute medications in specially labeled bottles, and with various health-oriented m erchants to fulfill rewards.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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