A combined diabetes and continuous glucose monitoring education program for adults with type 2 diabetes

Nanna Lind , Merete Bechmann Christensen , Kirsten Nørgaard
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引用次数: 0

Abstract

Objective

The lack of descriptions for education programs in studies evaluating the efficacy of continuous glucose monitoring (CGM) compared to blood glucose monitoring (BGM) for individuals with T2DM makes it difficult to compare results across trials. This study aimed to develop and evaluate a new education program for adults with insulin-treated T2DM and HbA1c ≥58 mmol/mol (7.5 %) initiating CGM.

Methods

A 3-h education program was created to provide information on diabetes self-management and CGM or BGM based on international guidelines and a pre-evaluation based on user needs assessment. Questionnaires were used to post-evaluate participant-rated benefits from the program.

Results

Seven individuals attended a user needs assessment of the program and 96 participated in the final education program (61.5 % men, mean age 61 (59.5;63) years, mean diabetes duration 18.2 (16.9;19.5) years, and median HbA1c 69 (63–78)mmol/mol (8.5 (7.9–9.3)%). Benefit from this program was rated good/very good by 95.5 % with no statistically significant difference between glucose monitoring groups.

Conclusions

This study presents a new well-received education program for T2DM for both the CGM and BGM group.

Innovation

The description of the development process and the education provided for both glucose monitoring groups may be useful for CGM initiation in clinics and trials.

针对成人 2 型糖尿病患者的糖尿病和持续葡萄糖监测联合教育计划
目的在评估连续血糖监测(CGM)与血糖监测(BGM)对 T2DM 患者疗效的研究中,缺乏对教育计划的描述,因此很难比较不同试验的结果。本研究旨在为接受胰岛素治疗且 HbA1c ≥58 mmol/mol (7.5 %) 的 T2DM 成年人开发和评估一项新的教育计划,帮助他们开始使用 CGM。结果7人参加了该计划的用户需求评估,96人参加了最终的教育计划(61.5%为男性,平均年龄61 (59.5;63)岁,平均糖尿病病程18.2 (16.9;19.5)年,HbA1c中位数69 (63-78)mmol/mol (8.5 (7.9-9.3)%)。95.5%的受访者对该项目给予了 "好"/"非常好 "的评价,血糖监测组之间的差异无统计学意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
PEC innovation
PEC innovation Medicine and Dentistry (General)
CiteScore
0.80
自引率
0.00%
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审稿时长
147 days
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