跳至主要内容
临床试验/ISRCTN70221670
ISRCTN70221670已完成3 期

Community-based Prevention of Diabetes (ComPoD): a randomised trial with a waiting list control group to evaluate the effectiveness and cost-effectiveness of a third sector led, community-based diabetes prevention programme

niversity of Exeter (UK)0 个研究点目标入组 314 人开始时间: 2014年9月5日最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
314

研究概览

简要总结

2019 results in https://www.ncbi.nlm.nih.gov/pubmed/31771589 (added 31/12/2019)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • As per existing programme eligibility criteria we will recruit people who:
  • 1. Are aged 18-74 years.
  • 2. Are considered on the basis of recent blood glucose tests to be at high risk for type 2 diabetes according to the criteria in the recent NICE diabetes prevention guidance (fasting plasma glucose level 6.1-
  • 6.9 mmol/L, or HBA1c 42-47 mmol/l recorded at any point within the last year). A check for progression to diabetes amongst trial participants will be made at baseline using point-of-testing HbA1c assessment equipment.
  • 3. Are resident in Exeter and Tiverton (postcodes EX1-6; EX 16) or Birmingham (postcodes B1-21).
  • 4. Have a BMI of at least 25 (23 for certain ethnic minority populations e.g. South Asians) and less than 45 kg/m2

排除标准

  • 1. We will exclude people who have a terminal illness or do not have the mental capacity to give informed consent and understand study procedures with assistance from the researcher, an interpreter or other representative as necessary (e.g., due to dementia, severe learning disability)
  • 2. Participants who have an HbA1c reading recorded at their baseline assessment indicating progression to Type 2 diabetes will also be excluded from the trial but will still be able to access the diabetes management component of the Living Well, Taking Control programme and will be referred accordingly
  • There are no other exclusion criteria as the programme providers cater for people with low literacy, needing translation services or with mental health problems, learning or physical disabilities, and will support consenting and collecting data from these groups.

研究者

发起方
niversity of Exeter (UK)

相似试验