mDAS: mHealth for Diabetes Adherence Support

Sponsor
University of Illinois at Chicago (Other)
Overall Status
Completed
CT.gov ID
NCT02990299
Collaborator
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (NIH)
221
1
2
57.5
3.8

Study Details

Study Description

Brief Summary

The purpose of this research study is to determine the benefit and cost of including health coaches, clinical pharmacists and mobile health (mHealth) tools such as text messaging and videoconferencing in diabetes management support services for African-Americans and Latinos with uncontrolled Type 2 Diabetes.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: mHealth for Diabetes Adherence Support
N/A

Detailed Description

Many African-Americans and Latinos with diabetes do not achieve recommended diabetes goals placing them at high risk for complications. Team-based models of care can help in reaching goals of therapy. Additionally, mobile health (mHealth) technologies can further improve outcomes among those more difficult to reach. This study will evaluate the impact of a team-based, mHealth intervention designed to improve medication adherence, healthy eating, and physical activity behaviors. The investigators will compare this mHealth approach with usual care.

Clinical pharmacists and health coaches (HC) will deliver our proposed team-based intervention. mHealth delivery includes mobile phone text messaging, secure videoconferencing, and HC home visits. Pharmacists will focus on medication reconciliation and adherence. Health coaches will help identify psychosocial and environmental challenges to adherence in a culturally-sensitive manner. Together, they can assist in goal-setting, problem-solving, negotiation of competing priorities, and provide social support leveraging mHealth technologies.

Preliminary data from previous research by the research team supports the role of health coaches partnering with clinic- based pharmacists in improving diabetes outcomes in minorities. In the proposed mHealth intervention, patient- pharmacist videoconferencing will eliminate the need for in-person visits with a pharmacist, which is impractical for many low-income patients. In addition, pilot work suggests that text messaging is a preferable means of communication and may facilitate more frequent contact with patients.

This is a randomized, controlled trial to evaluate the effectiveness of an mHealth diabetes adherence support intervention delivered by clinical pharmacists and health coaches. The research team will randomize 220 patients through UI Health to either: (1) mHealth diabetes adherence support through clinical pharmacists and health coaches; or (2) usual care. After one year, patients completing the mHealth intervention will be monitored for an additional year while the usual care group receives the mHealth approach. Outcomes include medication adherence, hemoglobin A1c, blood pressure, and LDL-cholesterol levels. The specific aims include: (1) evaluate the effectiveness of an mHealth diabetes adherence support intervention delivered by clinical pharmacists and health coaches to African-American and Latino adults with uncontrolled type 2 diabetes; (2) evaluate the maintenance of improved diabetes behaviors as well as clinical outcomes one year after completing the intervention; (3) evaluate the cost and cost-effectiveness of mHealth diabetes adherence support compared to usual care; and (4) evaluate the reach, adoption, and implementation of mHealth diabetes adherence support based on the RE-AIM framework.

Study Design

Study Type:
Interventional
Actual Enrollment :
221 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
mHealth for Diabetes Adherence Support
Actual Study Start Date :
Mar 24, 2017
Actual Primary Completion Date :
Jan 7, 2022
Actual Study Completion Date :
Jan 7, 2022

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Usual Care

Participants will receive their usual care for the first year of their enrollment in the study. They will receive a referral to a diabetes educator and a clinical pharmacist, a one-page sheet of contact information for their healthcare providers, and paper-based, low-literacy diabetes information. After one year, they will crossover to the mDAS intervention arm for one year.

Experimental: mHealth for Diabetes Adherence Support

Participants will receive in-person support from a health coach and a clinical pharmacist with whom they will meet with regularly via videoconference. After one year, participants who have completed the mDAS intervention will be monitored for an additional year with usual care to evaluate maintenance.

Behavioral: mHealth for Diabetes Adherence Support
Participants will be paired with a health coach who will provide ongoing support and resources in medication and lifestyle adherence and diabetes self-management. The health coach will perform regular home visits, telephone support and tailored text-messages based on the participant's preferences and needs. They will help assess barriers to adherence and use motivational interviewing to help patients set goals and create action plans. They will also facilitate videoconferences with an assigned clinical pharmacist who will provide consultation on medication use, reconciliation and adherence, identify therapeutic goals and formulate an approved plan of care.
Other Names:
  • mDAS
  • Outcome Measures

    Primary Outcome Measures

    1. Hemoglobin A1c [24 months]

    Secondary Outcome Measures

    1. Self-reported medication adherence [24 months]

      A 3-item questionnaire will be administered to measure adherence to diabetes medications.

    2. Blood Pressure [24 months]

    3. LDL Cholesterol [24 months]

      LDL Cholesterol will be measured as part of a Full Lipid profile blood test.

    4. Diabetes Self-Management [24 months]

      Self-management will be measured by the revised 11-item Summary of Diabetes Self Care Activities questionnaire.

    5. Health related quality of life [24 months]

      General health-related quality of life will be measured by the EuroQOL 5D (EQ-5D).

    6. Diabetes related quality of life [24 months]

      Diabetes-related quality of life will be measured by the Diabetes Distress Screening Instrument (DDS4).

    7. Depression [24 months]

      Measured with the nine-item Patient Health Questionnaire (PHQ-9)

    8. Alcohol Misuse [24 months]

      Measured using the 3-item AUDIT-C questionnaire

    9. BMI [24 months]

      Height and weight will be taken at each time point to determine BMI

    10. Social Support [24 months]

      4-item questionnaire measuring satisfaction with support from friends, family and health care team

    11. Diabetes Self-efficacy [24 months]

      8 -item questionnaire measuring confidence in diabetes self-management skills

    Other Outcome Measures

    1. Healthcare utilization [24 months]

      This will include costs associated with hospital admissions, emergency room and outpatient visits and prescription medications.

    2. Program cost [24 months]

      This will include costs associated with the intervention including pharmacists and health coaches (training, salaries, implementation), educational materials, tablet computers and associated data service, text messaging and videoconferencing.

    3. Health Coach Satisfaction [1 year after health coach assignment]

      A survey administered to the patient for feedback on their assigned health coach.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    21 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Self-identified as Latino/Hispanic or African-American

    • Verbal fluency in English or Spanish

    • Latest A1c ≥ 8.0% (within 3 mo)

    • History of Type 2 Diabetes (> 1 year)

    • Between the ages of 21 and 75 years

    • Unlimited mobile phone/text messaging plan with ability to reply to text messages

    • Home environment capable of video conferencing with wireless signal

    • Receives primary care at UI Health clinical site for at least one year, with one visit during past year

    • Able and willing to provide informed consent (agree to data collection requirements, accept randomization, agree to home visitation with HC and pharmacist involvement, and participate for two years)

    Exclusion Criteria:
    • Unable to verbalize comprehension of study or impaired decision making

    • Family/household member already participating in same study

    • Currently receiving regular pharmacist support through Medication Therapy Management or equivalent

    • History of, or planned, gastric bypass or transplant surgery

    • History of bipolar or psychotic disorder

    • Other severe comorbidities that require complex, aggressive, or palliative treatment, e.g., stage 4 or greater renal disease, liver failure, cancer (other than nonmelanoma skin cancer), terminal illness

    • Investigator discretion for safety concerns

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Illinois Hospital and Health Sciences System Chicago Illinois United States 60612

    Sponsors and Collaborators

    • University of Illinois at Chicago
    • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

    Investigators

    • Principal Investigator: Ben S Gerber, MD, MPH, University of Illinois at Chicago
    • Principal Investigator: Lisa K Sharp, PhD, University of Illinois at Chicago

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ben Gerber, Professor of Medicine, University of Illinois at Chicago
    ClinicalTrials.gov Identifier:
    NCT02990299
    Other Study ID Numbers:
    • 2016-0380
    • 1R01DK108141
    First Posted:
    Dec 13, 2016
    Last Update Posted:
    Apr 25, 2022
    Last Verified:
    Apr 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Ben Gerber, Professor of Medicine, University of Illinois at Chicago
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 25, 2022