Comparing people with type 2 diabetes who initiate insulin in the community to standard care (people initiating insulin in hospital) in hospital length of stay, HbA1c and Diabetes Treatment Satisfaction.
试验速览
- 阶段
- 未知
- 状态
- 终止
- 发起方
- 入组人数
- 105
研究概览
简要总结
Aims: To trial the functionality and effectiveness of Transition Diabetes Team (TDT), comprising: a credentialled diabetes educator (CDE) and diabetes specialist in commencing or changing insulin in the home versus in the hospital. Results: • 103 hospital inpatients commenced on newly-established injectable diabetes therapies were randomised to receive TDT (n=55), or standard care (n=48). • There was no difference in rates of hospital readmission or emergency department presentations between groups, with one presentation in each group. • There was a significant improvement in diabetes treatment satisfaction in the TDT group. • There was no difference in HbA1c or LOS between groups. What does this study add to what we know: • This study demonstrates that the use of the TDT is safe and acceptable to patients being discharged on injectable diabetes therapies. • Inpatients with T2DM who initiate injectable therapy while in hospital find absorbing diabetes education challenging, despite supportive ward staff. • TDT participants felt having education provided at home after discharge is convenient, more comfortable, and having time to learn. • Health providers felt an educator and endocrinologist working together was convenient, and the professional support positive.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Educational / counselling / training
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit(—)
- 性别
- All
入选标准
- •a. Adults greater than 18 years of age
- •b. Type 2 diabetes patients needing insulin post discharge
- •c. Admitted into Austin Health
- •d. Diabetes management can be improved by adding or changing insulin or other injectable therapy to management.
排除标准
- •Those who do not fit the inclusion criteria, and patients who are unable to give informed consent
