MedPath

Adherence to Medical Treatments for Telemedicine Patients

Not Applicable
Terminated
Conditions
Medication Adherence
Stroke
Interventions
Device: MedRem application
Registration Number
NCT04180475
Lead Sponsor
University of Virginia
Brief Summary

This study will test the feasibility of MedRem, a novel medication reminder and tracking system on wearable wrist devices, specifically with the Apple Watch 4. The study team will load the MedRem app onto two Apple Watch 4s for use during the study. As the device is placed on the wrist, it is free from the limitations of smartphones. However, one of the major challenges in developing interactive systems for wrist devices is their form factor. The touch screens available on these devices are tiny and much smaller compared to smart phones and tablet computers. MedRem enables user interactions by incorporating speech recognition and text-to-speech features along with clever interface design. The tiny display of the device is used for minimal inputs and outputs, while a user can retrieve and provide more information from/to the system through voice commands. Personalized models are built and updated over time to reduce errors in recognizing users' voice commands, and thus better user experience is provided.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
5
Inclusion Criteria
  • Phase 1 (Controls)

    • 18 - 75 years old
    • Good general health (self-reported), with no history of cerebral vascular accident (CVA)
    • English-speaking
    • Willingness and ability to comply with scheduled visits and study procedures

Phase 2 (Stroke Patients)

  • 18 - 75 years old
  • English-speaking
  • Willingness and ability to comply with scheduled visits and study procedures
  • Have requirements for home- based therapy regimens (i.e. physical/occupational therapy)
  • Require medications for secondary stroke prevention (e.g. antithrombotic therapy to prevent ischemic stroke, stroke risk factor management with blood pressure, diabetes, cholesterol medications).
  • Have a Modified Rankin Scale for Neurologic Disability (MDS) of 2 - 4
Exclusion Criteria
  • Phase 1 (Controls)

    • Pregnant women, fetuses, neonates, children, prisoners, cognitively impaired, non-English speaking subjects
    • Prohibitive cognitive impairments or language deficits
    • Does not have wireless internet connection at home

Phase 2 (Stroke Patients)

  • Pregnant women, fetuses, neonates, children, prisoners, cognitively impaired, non-English speaking subjects
  • Have a Modified Rankin Scale for Neurologic Disability (MDS) of 0-1 or 5
  • Prohibitive cognitive impairments or language deficits
  • Significant weakness, dystonia, or spasticity that will prevent proper use and response to the Apple Watch device
  • Live in nursing home or rehabilitation facility
  • Does not have wireless internet connection at home

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
MedRem applicationMedRem applicationMedRem smartwatch application
Primary Outcome Measures
NameTimeMethod
Use of MedRem System30 days

Assess the patients' adherence to medications and exercise. Adherence will be measured by patient responses to questions prompted by the MedRem System.

Assessment of Survey30 days

Acceptance and usability will be measured by the Intervention Patient MedRem Usability Survey. Steps were taken and distance covered data will also be collected from the Apple Watch.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Virginia

🇺🇸

Charlottesville, Virginia, United States

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