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MD.2 Medication Dispenser Medication Adherence Study

Medication Dispenser: MD2: Improving Health Outcomes

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00560001
Enrollment
600
Registered
2007-11-19
Start date
2006-01-31
Completion date
2008-05-31
Last updated
2009-10-08

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

Conditions

Frail Elderly, Medication Errors

Keywords

frail elderly, medication errors, patient compliance & attitudes, guideline adherence

Brief summary

The objective of this study is to quantify the benefits of using the MD.2 on health outcomes.

Detailed description

A sizeable portion of admissions to hospital and even nursing homes can be avoided if individuals with medication management problems were provided assistive devices to assist with their medications. The MD.2 medication dispenser and monitoring system was developed by Interactive Medical Developments LC and may offer increased support to the elderly with fewer human resources and a substantially reduced cost to the public health system. A rigorous evaluation of this technology has not been conducted. The objective of this Phase III clinical trial (Phase II of this STTR Fast Track Application) is to quantify the benefits of using the MD.2 on health outcomes. The specific aims are to: (1) Quantify healthcare utilization including hospitalizations and emergency room visits for MD.2 clients compared to control clients, (2) Determine the length of time in case management for MD.2 clients compared to control clients, (3) Measure changes in caregiver burden between those with the MD.2 and those with usual medication routines and (4) Determine if cognitive and functional characteristics influence compliance rates among the MD.2 clients and control clients. This study will be conducted in all counties in four of the Area Agencies on Aging in Iowa (who participated in the Phase I study), with the Veteran's Administration(VA)in Iowa, and with Area Agencies on Aging in Illinois. One hundred and fifty clients will be randomized to receive the MD.2 and 150 clients will be randomized to the control group. Primary caregivers for these 300 subjects will also be recruited. Nurses employed by Interactive Medical Developments LC will collect all data. From homecare charts/claims, age, sex, residence, living status, social support, activities of daily living, instrumental activities of daily living, cognition, medical conditions and medication lists will be obtained. Enrolled subjects will also complete an interviewer-administered survey of the Geriatric Depression Scale, SF-12 Health Status Inventory, self-reported medication compliance and recent hospitalizations and emergency room visits. Caregivers will complete the Caregiver Burden Interview. Poisson regression and Cox proportional hazards models will be the primary statistical approaches.

Interventions

BEHAVIORALMD.2 Medication Dispenser

For those subjects receiving an MD.2 Medication Dispenser, the machine organizes medications and provides verbal and auditory explicit reminders for individuals to take their medications. At the scheduled time, the patient gets a series of reminders. The patient is then expected to push a single button to dispense a pre-filled medication cup. An automatic record is kept of the subject's medication adherence. Interviewer-administered surveys of the Geriatric Depression Scale, SF-12 Health Status Inventory, self-reported medication compliance and recent hospitalizations and emergency room visits will be given. Caregivers will complete the Caregiver Burden Interview.

Sponsors

University of Iowa
CollaboratorOTHER
Department of Health and Human Services
CollaboratorFED
National Institutes of Health (NIH)
CollaboratorNIH
Interactive Medical Developments
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

A client must: * Be coming up for regular review in Case or Medication Management * Require medication management services * Have two or more doses of medication per day * Have someone to fill MD.2 * Be in independent living (may be assisted living with NO medication management services) * Be expected to live through follow-up period of six months * Have an active phone line that can be utilized by the MD.2 system.

Exclusion criteria

A client cannot have/or be the following: * Have someone available to administer medications for every dose * Have someone in household who is likely to interfere with MD.2 * Blind AND deaf * Eligible for hospice * An MD.2 currently

Design outcomes

Primary

MeasureTime frame
The rate of hospitalizations and emergency room visits will be compared between the MD.2 and control clientsper month (30 client days) over 6 consecutive months

Secondary

MeasureTime frame
Compare the length of time in case management for MD.2 clients to control clients.Over 6 consecutive months.
Measure changes in caregiver stressors and burden between those with the MD.2 and those with their usual medication routine.Over 6 consecutive months
Determine if cognitive and functional characteristics influence compliance rates among the frail elderly using the MD.2.Over 6 consecutive months

Countries

United States

Contacts

Primary ContactKaren Farris, Ph.D.
karen-farris@uiowa.edu319-384-4516
Backup ContactJulie Lang, M.S.; M.B.A
julie-lang@uiowa.edu319-384-2815

Outcome results

None listed

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