bpMedManage: Digital Technology to Support Adherence to Hypertension Medications

Last updated: January 30, 2025
Sponsor: University of Arizona
Overall Status: Active - Recruiting

Phase

N/A

Condition

Aging

Dementia

Alzheimer's Disease

Treatment

bpMedManage

MedManage

Clinical Study ID

NCT06307574
STUDY00002804
  • Ages > 60
  • All Genders

Study Summary

The purpose of the bpMedManage study is to rigorously test the efficacy of a smartphone technology to help improve high blood pressure medication adherence among older adults with mild cognitive impairment (MCI) in a 16-week randomized controlled trial. A total of 100 older adults will be recruited. There will be two treatment arms, bpMedManage-S and bpMedManage-P with 50 participants in each arm. Participants randomized into the bpMEDManage-S intervention arm will use a smartphone application with medication reminders plus receive education with standardized information on hypertension and antihypertensive medications on the education portal. Participants in the bpMedManage-P group will use a smartphone to receive education with standardized information on hypertension and antihypertensive medications on an education portal. Both groups will complete baseline assessments followed by 4 weeks of medication adherence monitoring. At the end of the adherence monitoring period, participants will be randomized into one of the two treatment arms. Immediate outcomes on primary and secondary measures will be assessed 4 weeks after beginning of the intervention. Follow-up outcomes will be assessed 12 weeks after the beginning of the intervention.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Age 60+

  2. Community-dwelling older adults

  3. Self-reported fluent in English

  4. Adequate self-reported visual and hearing ability

  5. Self-reported memory, thinking, or concentration challenges

  6. Self-manage at least one prescribed antihypertensive medication

  7. Have and use a smartphone

  8. No self-reported history of major depression or other mental health diagnoses

  9. No self-reported diagnosis of dementia or other neurological disorder such asstroke, TBI, and Parkinson's disease

  10. TICS-M score between 27-37 and Montreal Cognitive Assessment (MoCA) score between 20-26

  11. Willing to participate in the study for at least 4 months

Exclusion

Exclusion Criteria:

  1. Diagnosis of dementia

  2. Lives in assisted living facility or skilled nursing facility

Study Design

Total Participants: 100
Treatment Group(s): 2
Primary Treatment: bpMedManage
Phase:
Study Start date:
February 29, 2024
Estimated Completion Date:
December 31, 2025

Connect with a study center

  • University of Arizona

    Tucson, Arizona 85721
    United States

    Active - Recruiting

  • University of Illinois, Urbana-Champaign

    Champaign, Illinois 61820
    United States

    Active - Recruiting

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