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Clinical Trials/NCT06000813
NCT06000813
Active, not recruiting
Not Applicable

REACH-Es: Adapting a Digital Health Tool to Improve Diabetes Medication Adherence Among Latino Adults

Massachusetts General Hospital1 site in 1 country70 target enrollmentJune 18, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Type 2 Diabetes (Adult Onset)
Sponsor
Massachusetts General Hospital
Enrollment
70
Locations
1
Primary Endpoint
Diabetes Medication adherence
Status
Active, not recruiting
Last Updated
6 months ago

Overview

Brief Summary

Latino individuals, the fastest growing ethnic minority population in the United States, have a higher prevalence of type 2 diabetes and diabetes-related complications, and are more likely to report inconsistent use of diabetes medications than non-Hispanic White individuals. The proposed project will test an interactive text message-based tool tailored to address barriers to taking diabetes medications that are relevant to Latino adults. If found feasible, acceptable, and usable, this intervention could serve as a scalable tool to improve diabetes management and reduce diabetes-related complications among Latino adults in the United States.

Detailed Description

Latino adults have a disproportionate burden of type 2 diabetes and diabetes-related complications. Diabetes medication non-adherence is an important modifiable contributor to suboptimal glycemic management among Latino adults, who are nearly twice as likely to report non-adherence to diabetes medications as non-Hispanic White individuals. Besides language barriers, additional commonly reported barriers that contribute to non-adherence in this population include negative perceptions about insulin use and misunderstanding ongoing need for diabetes medications once HbA1c has improved. Mobile health (mHealth) technology can reduce medication adherence barriers and improve adherence behavior, but mHealth tools that address commonly reported barriers to diabetes medication adherence among Latino adults are lacking. One such mHealth platform is REACH (Rapid Encouragement/Education And Communications for Health), a text message-based tool that improved diabetes medication adherence and glycemic control among English-speaking adults with type 2 diabetes. This study will evaluate REACH-Español (hereafter "REACH-Es), an mHealth platform adapted from the original REACH intervention that will incorporate qualitative input from Latino adults with type 2 diabetes on barriers to diabetes medication adherence relevant to this population. Specifically, the investigators will conduct a pilot RCT (n=70) to assess feasibility, acceptability, and usability of REACH-Es, as well as intervention targets (diabetes medication adherence and barriers to adherence) comparing REACH-Es to enhanced treatment as usual; secondary outcomes are HbA1c and diabetes self- efficacy. The project will generate preliminary data for an R01 hybrid-effectiveness implementation trial of REACH-Es.

Registry
clinicaltrials.gov
Start Date
June 18, 2024
End Date
February 28, 2027
Last Updated
6 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jacqueline A. Seiglie, MD

Principal Investigator

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • Type 2 diabetes mellitus
  • Have current or prior (since 2018) HbA1c ≥8.0%
  • Take at least one diabetes medication
  • Receive care at MGH- affiliated primary care practices (≥2 visits in the past 3 years)
  • Identify as Latino and/or Hispanic
  • Speak and read in Spanish as preferred language
  • Willing and able to provide informed consent
  • Access to a mobile telephone with text messaging capability
  • Suboptimal diabetes medication adherence, assessed using the first 2 items in the Adherence to Refill and Medication Scale (ARMS-d) questionnaire combined: "How frequently do you forget or decide to not take your diabetes medications?" Participants who answer sometimes, almost always, and/or always will be considered eligible for the study.

Exclusion Criteria

  • Auditory limitations and/or inability to communicate orally
  • Inability to receive, read, or send a text message (assessed by a trained research assistant)

Outcomes

Primary Outcomes

Diabetes Medication adherence

Time Frame: Collected at 0, 3, and 6 months

Assessed using the 11-item Adherence to Refill and Medication Scale (ARMS-d) questionnaire scored on a 0-4 Likert scale (range 12-48).

Feasibility (recruitment rate)

Time Frame: Collected at 0 months

Number of eligible participants who enroll/ Number of eligible participants who are contacted and reached by phone

Feasibility (response rate to 2-way text messages)

Time Frame: Collected at 3 and 6 months

Number of 2-way text messages answered/ Number of 2-way text messages received

Acceptability

Time Frame: Collected at 3 and 6 months

Assessed quantitatively based on utility of REACH-Es on a 0-10 Likert scale and qualitatively through exit interviews.

Feasibility (retention rate)

Time Frame: Collected at 3 and 6 months

Number of participants enrolled in the study at follow-up/ Number of participants enrolled at the start of the study

Usability

Time Frame: Collected at 3 and 6 months

Assessed quantitatively by administering the 10-item Spanish version of the System Usability Scale (SUS) questionnaire, scored on a 0-5 Likert-type scale.

IMB barrier sum score

Time Frame: Collected at 0, 3, and 6 months

Calculated by rating each barrier item on a 0-10 scale (1=never to 10=a lot) and identifying each participant's 4 highest- scored barriers (range 4-40).

Secondary Outcomes

  • HbA1c(Collected at 0, 3, and 6 months)
  • Diabetes self-efficacy(Collected at 0, 3, and 6 months)

Study Sites (1)

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