Testing a New Diabetes Adaptive Weight management Network (NewDAWN): A protocol for a randomised controlled trial

1788 people diagnosed with T2D in the last six years, who are willing to try to lose weight to achieve remission, will be recruited via GP practices and randomised to the NewDAWN service or PtR. Outcomes (weight, height, HbA1c, medications, BP, CVD risk score, PAID, EQ-5D, healthcare resource use) will be assessed at baseline and 12 months, with diabetes remission at 12 months as the primary outcome. An internal pilot assessment will follow 150 participants for 16 weeks to determine whether to progress using pre-specified criteria based on fidelity of programme delivery, adherence to the programme and change in weight. The decision will be reviewed by an external programme steering committee who will also advise on any other considerations they deem material to the likely successful completion of the full trial. A process evaluation will assess fidelity of delivery and collect both staff and participant feedback on the NewDAWN service to improve the effectiveness of implementation. The costs of NewDAWN and lifetime cost-effectiveness of the service will also be determined. ISRCTN Registration: 11090437.

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Publication Details

Journal
Contemporary Clinical Trials
Published
2025-08-25
DOI
https://doi.org/10.1016/j.cct.2025.108050
Primary Topic
Diet and metabolism studies
Type
article
Field-Weighted Citation Impact
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article

Testing a New Diabetes Adaptive Weight management Network (NewDAWN): A protocol for a randomised controlled trial

Elizabeth Morris, Paul Aveyard, Nicola Guess, Sarah Wane et al.
Contemporary Clinical Trials
Diet and metabolism studies
article

Testing a New Diabetes Adaptive Weight management Network (NewDAWN): A protocol for a randomised controlled trial

Elizabeth Morris, Paul Aveyard, Nicola Guess, Sarah Wane, Alan Brennan, Charlotte Albury, Ly‐Mee Yu, Susan Ann Jebb, Caroline Mitchell, Carolyn Newbert, Ushma Galal, Jack B. Joyce, Penny R. Breeze
article en

Abstract

1788 people diagnosed with T2D in the last six years, who are willing to try to lose weight to achieve remission, will be recruited via GP practices and randomised to the NewDAWN service or PtR. Outcomes (weight, height, HbA1c, medications, BP, CVD risk score, PAID, EQ-5D, healthcare resource use) will be assessed at baseline and 12 months, with diabetes remission at 12 months as the primary outcome. An internal pilot assessment will follow 150 participants for 16 weeks to determine whether to progress using pre-specified criteria based on fidelity of programme delivery, adherence to the programme and change in weight. The decision will be reviewed by an external programme steering committee who will also advise on any other considerations they deem material to the likely successful completion of the full trial. A process evaluation will assess fidelity of delivery and collect both staff and participant feedback on the NewDAWN service to improve the effectiveness of implementation. The costs of NewDAWN and lifetime cost-effectiveness of the service will also be determined. ISRCTN Registration: 11090437.

Contemporary Clinical TrialsVol. 157
University of Oxford (GB)
Openalex Percentile: Top 71%
Diet and metabolism studies
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