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临床试验/NCT06000813
NCT06000813已完成不适用

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

Massachusetts General Hospital1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2024年6月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
70
试验地点
1
主要终点
Diabetes Medication adherence

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •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.

排除标准

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

研究组 & 干预措施

Enhanced treatment as usual (ETAU)

Active Comparator

Participants will maintain care as usual (medication treatment and physician monitoring) in addition to a welcome SMS following enrollment, a SMS each time an HbA1c is collected with a link to a secure website that displays the result, and bi-monthly information on diabetes self-care education.

干预措施: ETAU (Behavioral)

REACH-Es

Experimental

Participants in the REACH-Es arm will receive REACH-Es short message service (SMS), as follows: 1) Daily SMS (information related to diet, exercise, self-monitoring of blood glucose, their specific diabetes medication(s), and top 4 medication adherence barriers); 2) Daily two-way SMS (diabetes medication adherence question); 3) Weekly one-way SMS (participants receive weekly feedback on Sunday regarding how many of the last 7 days they took their medicine); 4) A SMS each time an HbA1c is collected with a link to a secure website that displays the result.

干预措施: REACH-Es (Behavioral)

结局指标

主要结局

Diabetes Medication adherence

时间窗: 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)

时间窗: 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)

时间窗: Collected at 3 and 6 months

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

Acceptability

时间窗: 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)

时间窗: 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

时间窗: 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

时间窗: 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).

次要结局

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

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jacqueline A. Seiglie, MD

Principal Investigator

Massachusetts General Hospital

研究点 (1)

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