Embedding diabetes educatio

Not Applicable

Completed

• Conditions: Specialty: Diabetes, Primary sub-specialty: Type 2; Diabetes mellitus; UKCRC code/ Disease: Metabolic and Endocrine/ Diabetes mellitus; Nutritional, Metabolic, Endocrine

• Registration Number: ISRCTN21321635
• Lead Sponsor: niversity of Leicester

Brief Summary

2020 results in https://pubmed.ncbi.nlm.nih.gov/32477589/ (added 02/06/2020)

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-07-07
• Study Completion: 2018-01-31
• Last Update Posted: 15 June 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 423

Inclusion Criteria

Practice
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

Exclusion Criteria

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

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The feasibility and suitability of the components of the Embedding Package within the participating practice and wider host organisations as assessed using ethnographic methods throughout the duration of this feasibility study.