ISRCTN21321635已完成未知
Increasing uptake of self-management education programmes for Type 2 Diabetes in multi-ethnic primary care settings: A feasibility study
niversity of Leicester0 个研究点目标入组 423 人开始时间: 2017年7月7日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 423
研究概览
简要总结
2020 results in https://pubmed.ncbi.nlm.nih.gov/32477589/ (added 02/06/2020)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Use either EMIS Web or TPP System One (required for data extraction)
- •2. Located within the participating CCGs
- •3. Able to refer patients with type 2 diabetes to a structured education programme.
- •4. Willing to sign a data sharing and remote data collection agreement with PRIMIS allowing the collection of one line per patient anonymised and, where patient consent is given, identifiable data as required for analysis.
- •Primary Care stakeholder eligibility criteria:
- •1. Employed by, or involved in the delivery of/or commissioning of any aspect of the Embedding Package at a participating practice/CCG
- •2. Willing and able to give informed consent (written or verbal)
- •Patient participant eligibility criteria:
- •1. Aged =18 years old
- •2. Coded in their primary care medical record as diagnosed with T2DM, before or during the study
- •3. Registered at a participating practice
排除标准
- •Practice exclusion criteria:
- •1. Does not use EMIS Web or TPP System One
- •2. Located outside of participating CCG
- •3. Unable to refer patients with type 2 diabetes to a structured education programme
- •4. Not willing to sign a data sharing and remote data collection agreement with PRIMIS
- •Primary care stakeholder exclusion criteria:
- •1. Not employed by or involved in the delivery or commissioning of any aspect of the Embedding Package at participating practice or CCG
- •2. Not willing or able to give informed consent
- •Patient participant exclusion criteria:
- •1. Aged under 18 years old
- •2. A record of a terminal illness
- •3. Life expectancy < 12 months
- •4. Coded in their primary care medical records as housebound or in residential care
- •5. A dissent code in their primary care medical records to sharing data as part of a research study
研究者
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