The Transform Type 2 Diabetes Study (Transform)
Type2diabetes
About this trial
This is an interventional treatment trial for Type2diabetes focused on measuring Type 2 Diabetes, dietary intervention, digital, diverse population, low carbohydrate, low energy, intermittent fasting
Eligibility Criteria
Inclusion Criteria: Registered with one of the Nexus Group GP Practices Willing to give consent for participation including collection of clinical outcomes Diagnosis of type 2 diabetes Minimum age of 18 years Maximum age of 70 years Minimum BMI of 27kg/m² (adjusted to 25kg/m² in people of South Asian or Chinese origin) Upper weight limit of 180kg (due to upper weight limit of BodyTrace scales) HbA1c eligibility: If on diabetes medication, HbA1c ≥ 43 mmol/mol If on diet alone, HbA1c ≥ 48 mmol/mol HbA1c <108mml/mol Ability to speak, read and receive care in English Access to internet and email address Exclusion Criteria: Currently taking insulin Pregnant or planning to be pregnant in the next 6 months Current breastfeeding Significant physical comorbidities: Active cancer, receiving treatment Myocardial infarction or stroke in last 6 months Severe heart failure defined as equivalent to the New York heart Association grade 3 or 4 (NYHA) eGFR <30 mls/min/1.73m2 Active liver disease (except non-alcoholic fatty liver disease (NAFLD),Severe angina, cardiac arrhythmia including atrial fibrillation or prolonged QT syndrome Active substance use disorder Active eating disorder Porphyria On current weight management programme / had or awaiting bariatric surgery (unless willing to come off waiting list) Health professional assessment that the person is unable to understand or meet the demands of the programme and/or monitoring requirements Taking monoamine-oxidase inhibitor medication Taking warfarin Taking varenicline (smoking cessation medication) Have attended for monitoring and diabetes review when this was last offered, including retinal screening, and commit to continue attending reviews, even if remission is achieved Active/investigation for gastric or duodenal ulcers
Sites / Locations
- Oviva UK ltd
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
One-to-one
Group
All participants are offered a choice of three dietary approaches.
All participants are offered a choice of three dietary approaches.