Evaluation of Diabetes and WELLbeing Programme

  • STATUS
    Recruiting
  • participants needed
    800
  • sponsor
    Canterbury Christ Church University
Updated on 19 February 2024

Summary

This study evaluates the impact of 'DWELL' - a 12-week psycho-social education programme designed to help people with type 2 diabetes to better self-manage their condition. Up to 800 patients will participate in the programme, while a non-intervention group will receive routine care for their diabetes

Description

The DWELL (Diabetes and WELLbeing) 12-week programme has been designed to incorporate specific elements of diabetes education and is underpinned by motivational interviewing to ensure it is tailored to individuals. Each of the four elements of the programme - education, nutrition, physical activity and wellbeing - have been carefully selected based on previous research into diabetes education. The Canterbury Christ Church University (CCCU) DWELL Team are responsible for the evaluation of DWELL, which will explore whether the combination of the programme elements is effective in improving self-management. Additionally, a process evaluation and cost effectiveness analysis will be conducted alongside participant outcomes

The programme will be delivered at five sites (two in the UK, one in Belgium, one in France, one in the Netherlands). The CCCU DWELL research team will be responsible for quality assurance, management and analysis of data, sample size assessment and reporting of adverse events. Each delivery site is responsible for adhering to their own Standard Operating Procedures.

Details
Condition NIDDM, Diabetes Mellitus, Type 2 Diabetes Treated With Insulin
Age 18-100 years
Treatment DWELL (Diabetes and WELLbeing) Programme
Clinical Study IdentifierNCT04274660
SponsorCanterbury Christ Church University
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Clinical diagnosis of type 2 diabetes
Over the age of 18

Exclusion Criteria

Under the age of 18
Pregnant women
Individuals who do not have the mental capacity to participate
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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