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The Transform Type 2 Diabetes Study (Transform)

Primary Purpose

Type2diabetes

Status
Active
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Total diet replacement
Low-carbohydrate diet
Intermittent fasting 5:2
Sponsored by
Oviva UK Ltd
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Experimental

Arm Label

One-to-one

Group

Arm Description

All participants are offered a choice of three dietary approaches.

All participants are offered a choice of three dietary approaches.

Outcomes

Primary Outcome Measures

Intervention primary outcome- Change in Hba1c (mmol/l)
Evaluating improvement in Hba1c (mmol/l) upon dietary intervention

Secondary Outcome Measures

Intervention secondary outcome- weight
Change in weight (kg) and BMI (kg/m2)
Intervention secondary outcomes- lipids
Change in lipid markers (mmol/l) total cholesterol, LDL cholesterol, HDL cholesterol, triglycerides)
Intervention secondary outcomes- blood pressure
Change in blood pressure (systolic and diastolic) by British and Irish Hypertension Society validated monitors
Intervention secondary outcomes- NHS resource use including medication cost
The project will explore changes in primary and secondary care resource use and medication use at 12 and 24 months, and associated costs, by treatment arm for participating patients relative to the five years before enrolment. The net financial impact of the intervention will be analysed by combining the estimated costs of the intervention with the estimated changes in routine resource use before and after the intervention.
Intervention secondary outcomes- change in quality of life
Patient reported outcome measures (PROMs) including change in quality of life (EQ5D) and ability to self-manage diabetes
Intervention secondary outcomes- diabetes remission
Diabetes remission defined as 2 HbA1c readings < 48mmol/mol without diabetes medications at least 6 months apart

Full Information

First Posted
November 15, 2022
Last Updated
December 5, 2022
Sponsor
Oviva UK Ltd
Collaborators
Guy's and St Thomas' NHS Foundation Trust
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1. Study Identification

Unique Protocol Identification Number
NCT05648903
Brief Title
The Transform Type 2 Diabetes Study
Acronym
Transform
Official Title
The Transform Diabetes Study: A Mixed-methods Exploratory Study to Evaluate the Acceptability and Potential Clinical Impact of a Choice of Dietary Interventions Delivered Through a Digital Group or 1-to-1 Care to Support Weight Loss and Improve Glycaemic Control in Adults With Type 2 Diabetes Within an Ethnically Diverse Population
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 7, 2022 (Actual)
Primary Completion Date
July 30, 2024 (Anticipated)
Study Completion Date
July 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Oviva UK Ltd
Collaborators
Guy's and St Thomas' NHS Foundation Trust

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this mixed-methods, 12-month interventional study is to understand the effectiveness and acceptability of dietary interventions in type 2 diabetes mellitus (T2DM) in an ethnically diverse population. Three dietary interventions will be offered (total diet replacement, intermittent fasting and a low-carbohydrate diet) and two modes of remote care delivery will be used (group and one-to-one).
Detailed Description
To date, there is little evidence focusing on preferences, motivating factors, and engagement in adults with type 2 diabetes when following dietary interventions to improve glycaemic control, nor on patient responses to remote group and one-to-one programs. In particular, this evidence is not available in populations with high levels of deprivation and that are culturally and ethnically diverse in which diabetes is most prevalent. The 120 participants will be recruited from GP practices in the Southwark area. Practices will be split into two comparable groups based on the demographic and clinical data of eligible patients. Participants from one group of practices will be offered a one-to-one lifestyle coaching program. Patients from the other group of practices will be offered a group lifestyle coaching program. The aim is to recruit 60 patients for each arm. All participants will be offered a choice of three dietary approaches: total diet replacement (TDR), intermittent fasting 5:2 approach and a low-carbohydrate diet. Interventions will be led by Diabetes Specialist Dietitians (DSD) and all participants will have access to supporting learning materials. All care will be delivered remotely. Participants will receive intensive support in the first 16 weeks and follow-up support for a further 36 weeks. Participants on the one-to-one pathway will access their support via the Oviva app, telephone or video calls. Participants allocated to the group intervention will access their support through video group sessions hosted by their DSD, and will be offered the opportunity to use a secure group chat for patients, between sessions. The evaluation will use a mixed methods approach, combining qualitative and quantitative analysis. Surveys, interviews, written material, and quantitative data will be used. This will allow for establishing learnings regarding patient choice, preference, experience, motivation, and engagement. Gaining insight into these perceptions can support our understanding as to how to best support engagement, understand the suitability of dietary interventions for different patients, and improve the quality and delivery of lifestyle interventions to support patients with type 2 diabetes in the future.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type2diabetes
Keywords
Type 2 Diabetes, dietary intervention, digital, diverse population, low carbohydrate, low energy, intermittent fasting

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Two modes of remote care delivery are used (one-to one and group).
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
One-to-one
Arm Type
Experimental
Arm Description
All participants are offered a choice of three dietary approaches.
Arm Title
Group
Arm Type
Experimental
Arm Description
All participants are offered a choice of three dietary approaches.
Intervention Type
Other
Intervention Name(s)
Total diet replacement
Other Intervention Name(s)
TDR
Intervention Description
The TDR intervention involves a low-calorie, nutritionally complete diet for 12 weeks consuming four meal replacement products exclusively per day, followed by a 4-week food-based reintroduction period; and then weight loss maintenance support monthly to 12 months. The TDR products will be provided to participants free of charge. If a patient gains more than 2kg in the maintenance phase, they have the option to follow a TDR for an additional 4 weeks but participants would have to self-fund these products.
Intervention Type
Other
Intervention Name(s)
Low-carbohydrate diet
Intervention Description
Participants who choose this intervention will be supported to undertake a low-carbohydrate diet. During the first 12 weeks of the programme patients will be supported to consume below 100g carbohydrate per day, whilst being encouraged to increase protein, choose predominantly unsaturated fats alongside a high intake of non-starchy vegetables and low-carbohydrate fruits. After 12 weeks patients will be able to increase their carbohydrate intake up to 130g per day. If a patient gains more than 2kg in the maintenance phase, they have the option to follow a 100g carbohydrate for an additional 4 weeks.
Intervention Type
Other
Intervention Name(s)
Intermittent fasting 5:2
Other Intervention Name(s)
5:2
Intervention Description
Participants will have the option to follow a 5:2 dietary approach whereby calories are significantly reduced on two days of the week to 500 calories per day for women and 600 calories per day for men. The placement of the "fasting" days can vary each week, but there must be two "fasting" days in each seven-day period. After 12 weeks, patients will have the option of continuing with the 5:2 approach for further weight loss or adopting a 6:1 approach whereby patients would only fast on 1 day in each seven-day cycle for weight maintenance. If a patient gains more than 2kg in the maintenance phase, they have the option to follow a 5:2 approach for an additional 4 weeks.
Primary Outcome Measure Information:
Title
Intervention primary outcome- Change in Hba1c (mmol/l)
Description
Evaluating improvement in Hba1c (mmol/l) upon dietary intervention
Time Frame
at 6, 12 & 24 months
Secondary Outcome Measure Information:
Title
Intervention secondary outcome- weight
Description
Change in weight (kg) and BMI (kg/m2)
Time Frame
at 6, 12 & 24 months
Title
Intervention secondary outcomes- lipids
Description
Change in lipid markers (mmol/l) total cholesterol, LDL cholesterol, HDL cholesterol, triglycerides)
Time Frame
12 & 24 months
Title
Intervention secondary outcomes- blood pressure
Description
Change in blood pressure (systolic and diastolic) by British and Irish Hypertension Society validated monitors
Time Frame
12 & 24 months
Title
Intervention secondary outcomes- NHS resource use including medication cost
Description
The project will explore changes in primary and secondary care resource use and medication use at 12 and 24 months, and associated costs, by treatment arm for participating patients relative to the five years before enrolment. The net financial impact of the intervention will be analysed by combining the estimated costs of the intervention with the estimated changes in routine resource use before and after the intervention.
Time Frame
12 & 24 months
Title
Intervention secondary outcomes- change in quality of life
Description
Patient reported outcome measures (PROMs) including change in quality of life (EQ5D) and ability to self-manage diabetes
Time Frame
baseline & 12 months
Title
Intervention secondary outcomes- diabetes remission
Description
Diabetes remission defined as 2 HbA1c readings < 48mmol/mol without diabetes medications at least 6 months apart
Time Frame
12 & 24 months
Other Pre-specified Outcome Measures:
Title
Other study outcomes- Patient questionnaires on acceptability, motivations and preferences
Description
The project aims to explore the acceptability of three different dietary regimes and the choices patients make. It will explore differences between the 1 to 1 and group delivery approaches in terms of enrolment, retention, patient experience and patient outcomes. The online surveys shared with participants throughout the study will cover overall impressions of the intervention, which aspects of the service were most helpful, responses to the diets challenges experienced and whether and how these were overcome, and the effect on knowledge of diabetes and the ability to manage the condition.
Time Frame
4 & 12 months
Title
Other study outcomes- engagement with the programme
Description
Gaining insight into patient engagement and motivation in relation to the programme can support our understanding as to how to best support engagement and improve the quality and delivery of lifestyle interventions to support patients with type 2 diabetes in the future. Patient engagement will be assessed through attendance, app usage and patient outcomes.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lucy Jones
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oviva UK ltd
City
London
ZIP/Postal Code
SE1 9RS
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No

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The Transform Type 2 Diabetes Study

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