跳至主要内容
临床试验/NCT07491471
NCT07491471撤回不适用

Improving Outcomes in Pediatric Diabetes: Building the Evidence Base to Inform Effective Diabetes Technology Interventions

Stanford University0 个研究点开始时间: 2025年8月15日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
主要终点
Interviews with you on your feedback on the intervention

研究概览

简要总结

Youth with public insurance underutilize diabetes care, particularly diabetes technology which is associated with improvement in diabetes-specific outcomes. Thus, we urgently need studies to understand and increase diabetes technology utilization. This proposed research will (1) address the gap in knowledge of barriers and promoters in youth working with clinicians to identify and address factors associated with diabetes technology uptake and utilization.

详细描述

As diabetes technologies have become more innovative and effective in the management of pediatric type 1 diabetes (T1D), research and usage has not engaged all youth living with T1D . Studies have consistently demonstrated lower rates of diabetes technology use in some youth. Although diabetes technology has the potential to improve in pediatric T1D outcomes. This proposal aims to build an evidence base for data-driven interventions designed to increase uptake and utilization of diabetes innovations by addressing barriers and supporting promoters of diabetes technology use. Focusing on clinicians, the overall objective of this proposal is to test a brief pilot intervention to increase provider recommendation of diabetes technology.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
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

入选标准

  • age 18+ years, providers who care for youth with T1D for at least 50% of their clinical efforts, practicing in the United States, care for youth with public insurance, health care role of physicians, advanced practice providers, or certified diabetes care & education specialists, and understand and willingness to follow study protocol.

排除标准

  • significant cognitive impairment or medical or psychiatric condition that would interfere with participation in the study or lack of access to a smartphone or Wi-Fi via computer.

结局指标

主要结局

Interviews with you on your feedback on the intervention

时间窗: Within 4 weeks upon intervention completion

The investigators will ask clincians questions in a 30-minute interview at the end of the four-week intervention. The investigators will evaluate feedback on ways the intervention could be more effective and what changes can be made to the intervention so that it is most effective. The investigators will ask clinicians if you they likely to change diabetes management after completing the intervention.

Survey questions on your feedback on the intervention

时间窗: Within 4 weeks upon intervention completion

The investigators will ask clincians questions in a feedback survey at the end of the four-week intervention. These questions will be developed by the investigators and will ask ways the intervention could be more effective and what changes can be made to the intervention so that it is most effective. Example questions of what the investigators plan to ask in the survey include: - Was the study explained appropriately? - Was it logistically easy to participate in the study? How could it have improved? - What parts of the intervention were most helpful? - What parts could be cut? - What parts need to be added? - Are there certain types of people who are likely to do better with this intervention?

Tracking people who complete the study

时间窗: Through study completion, an average of one year

The investigators will also keep track of who enrolled in the study and track how many people completed the intervention.

次要结局

  • Changes in diabetes technology usage(Within 4 weeks upon intervention completion)

研究者

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

Ananta Addala

Assistant Professor

Stanford University

相似试验

Clinican BEAD-T1D: Building the Evidence to Address... | 临床试验