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diEtitiaNs Helping pAtieNts CarE for Diabetes (ENHANCED) (ENHANCED)

2019年5月30日 更新者:Minneapolis Heart Institute Foundation

This study aims to randomly assign individuals with type 2 diabetes into the ENHANCED randomized control trial. The study is being conducted by the Minneapolis Heart Institute Foundation (MHIF) and will have two study sites 1) Hutchinson Health and 2) New Ulm Medical Center. The study is primarily funded through the Academy of Nutrition and Dietetics (AND).

The study will examine the impact of a registered dietitian-led, primary care integrated, telemedicine program on diabetes care measures (the 'D5') over one year as compared to usual care. The D5 goals include: blood pressure <140/90 mmHg, taking a statin as appropriate, A1c <8%, not using tobacco and taking an aspirin as appropriate.

研究概览

地位

完全的

条件

详细说明

Individuals will be invited to attend a baseline visit where they will have lab work done, anthropometrics (height, weight, waist circumference) and complete a lifestyle assessment. They will formally consent to participation by signing a study consent form. The same measures will be collected after completion of the one year study.

Study participants will receive two sessions of free lab work, a diabetes education book, and brief coaching with a registered dietitian/certified diabetes educator. In addition, those randomized to the phone coaching will have access to a registered dietitian/certified diabetes educator on a monthly basis for one year of personalized health coaching for free. The intent of this coaching is to help individuals achieve diabetes "optimal" care or meeting all 5 Diabetes Care measures (blood glucose, blood pressure, tobacco use, statin and aspirin use).

This program is designed to complement usual clinic-based primary care, with coaches documenting lab, biometrics and medication adjustments in the EHR, along with documenting phone encounters and communicating directly with patients' PCPs as needed. Documentation in the EHR uses an order created specifically for the study indicating the patient's research status.

Lab work required as part of this research study at baseline and 12 months is covered by the study. Any lab work and/or medication co-pays or fees outside of the baseline and 12 month study visits are the responsibility of the patient and/or their insurance

研究类型

介入性

注册 (实际的)

118

阶段

  • 不适用

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

40年 至 75年 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Diagnosis of Type 2 Diabetes
  2. Individuals who are not meeting 3 or more D5 goals,
  3. Have had a visit with a provider within the last 2 years

Exclusion Criteria:

  1. Type 1 Diabetes
  2. Chronic kidney disease (GFR <30)
  3. HIV
  4. Institutional residence
  5. Major cognitive or language barrier (as determined by program enrollment staff)
  6. Other active end-stage disease (e.g., late stage cancer or pulmonary disease)
  7. Actively receiving cancer treatment
  8. Pregnant

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Intervention
Individuals assigned to the intervention group will have supplemental care provided by a registered dietitian/certified diabetes educator which includes counseling on lifestyle to improve diabetes and overall health. Additionally, individuals in this group may be started on medications (or adjustments to current medications) for blood pressure, cholesterol or blood glucose to meet diabetes care goals
Focus on nutrition, activity and appropriate medication use and adherence
无干预:Standard of Care
Individuals will be followed by their Primary Care Provider as standard of care and per usual clinical need

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
A1c (Laboratory Assessment)
大体时间:1 year
The count of participants represents the number of individuals meeting A1c less than 8% at follow up
1 year

其他结果措施

结果测量
措施说明
大体时间
Blood Pressure (Calibrated Cuff Measurement- Average of 3 Readings)
大体时间:1 year
The count of participants represents the number of individuals meeting blood pressure less than 140/90 at follow up
1 year
Tobacco Use (Self-reported Questionnaire)
大体时间:1 year
The count of participants represents those not using tobacco at follow up
1 year
Statin Use (as Noted in EMR)
大体时间:1 year
The count of participants represents those taking a statin as indicated at follow up
1 year
Aspirin Use (as Noted in EMR)
大体时间:1 year
The count of participants represents taking aspirin as indicated at follow up
1 year

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2016年4月1日

初级完成 (实际的)

2017年12月13日

研究完成 (实际的)

2018年11月13日

研究注册日期

首次提交

2016年11月15日

首先提交符合 QC 标准的

2016年11月30日

首次发布 (估计)

2016年12月2日

研究记录更新

最后更新发布 (实际的)

2019年7月29日

上次提交的符合 QC 标准的更新

2019年5月30日

最后验证

2019年5月1日

更多信息

与本研究相关的术语

其他研究编号

  • ENHANCED

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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