Low EnerGy DiEt in Adolescents with Obesity and Type 2 Diabetes: the LEGEND Study
- Conditions
- Type 2 DiabetesPediatric Obesity
- Interventions
- Dietary Supplement: Low-energy dietOther: Qualitive interview - LED participantsOther: Qualitive interview - Participants declining LEDOther: Qualitive interview - Health Care Professionals (HCPs)
- Registration Number
- NCT06572345
- Lead Sponsor
- Nottingham University Hospitals NHS Trust
- Brief Summary
This is a multicentre, single-arm, feasibility study in adolescents with T2DM and obesity to investigate the recruitment and retention rates to a study using Low Energy Diets(LED). It will also provide estimates of weight loss needed to bring about remission to inform a larger randomised study. In addition a subgroup of participants and their parents/carers undertaking a period of LED will be interviewed to understand the participants experience of taking part. Two further groups will also be interviewed: participants and their parents/carers who have declined to take part in the LED to understand their motivations and barriers and healthcare practitioners who have participated in conducting the trial to understand their experience of the study.
- Detailed Description
LED intervention
The three-stage intervention, will be delivered by the local study dietitian and doctor. Participants will typically undergo a 12-week intensive LED intervention followed by a 12-week Food Re-introduction (FR) phase and then a Weight Maintenance (WM) phase. The aim is for participants to lose 15kg (or 15% of starting body weight if\<80kg at baseline) and achieve remission defined as an HbA1C \<48 mmol/mol three months apart.
The LED phase consists of a total meal replacement (TMR) diet for 12 weeks which contains 800-1000cal/day (with LED diets typically containing 800-1200kcal/day), and has been previously shown to be safe in young people. Available products include shakes, soups and bars from providers such as Cambridge 1:1, Lighter Life and Optifast. TMR products will be supplied and distributed by the study team at no cost to the participant. The experience of other investigators suggests that having prepared shakes and bars reduces the anxiety associated with meal choices and preparation. If participants are not able to adhere to only four meal replacement products a day, a low-energy meal option for up to one meal a day (instead of a TMR product and using low-calorie recipes provided as part of the study) may be suggested and discussed by the research team.
Following the initial LED phase, participants will enter the FR phase, typically over the next 12 weeks. This consists of a gradual reintroduction of food one meal at a time, in a structured stepwise progression and under the supervision of a dietitian. A recipe book of 400-500 kcal recipes has been developed for this purpose.
If the target weight is achieved before 12 weeks, the FR phase may be brought forward.
If the HbA1C has fallen to below the pre-diabetes range (less than 42 mmol/mol) on point of care testing, but the target weight has not been achieved, FR phase may still be initiated at 12 weeks. If the target weight is not achieved by 12 weeks and the HbA1C remains 48 mmol/mol or above, the LED phase could be extended to a maximum of a total of 20 weeks duration, in discussion with the participant and the parents/carers, as appropriate.
If, during FR, the participant gains 2kg or more, there is flexibility to regress a step along the FR pathway, at the discretion of the local team and in discussion with the participant and their family, mirroring the successful pragmatic approach of the DiRECT study. For instance, a participant who has introduced their first meal and gains 2kg, may go back to full LED; someone who has gained weight after moving from two to three meals a day may go back to two meals. A participant who gains 2kg or more in the WM phase, may similarly go back one step to two meals a day. Locally, our experience using the LED showed the importance of a flexible approach, with some young people finding benefit from a short break (e.g. for a family celebration) or a preference to start during school holidays.
Current standard practice is to measure weight at each clinic with height and HbA1C checked once every 3 months. In addition to these routine measurements, data on participants' weight, height, HbA1C and adherence will be collected by the local diabetes team at each face-to-face visit and entered directly into the study data collection forms by either a study healthcare professional (HCP) or research nurse, as well as recorded in the participants medical record.
During the LED and FR phases, participants will have two-weekly clinical contact with face-to-face contact at least every four weeks which will include repeat anthropometry (including weight and blood pressure). Biochemistry will be repeated.
During the maintenance phase, contacts will aim to be every four weeks with no more than six weeks between contacts.
Participants' data will be collected by the local diabetes team or research nurses at each visit and recorded in the participants medical record. Data will be entered into the study approved electronic case-report form (CRF) system by the local diabetes or research teams.
Study questionnaires will be undertaken at baseline, during LED, during FR and in the follow-up period using an approved electronic CRF system by either the participant or research nurse. Physical activity assessment, MRI scans and dual x-ray anthropometry (DXA) scans will be undertaken at baseline, during the transition between phases and at the end of the study period. Physical activity level will be assessed by using activity trackers, six-minute walking test and a physical activity questionnaire. MRI scans will measure internal adipose deposits and DXA will measure fat and lean mass, bone mineral density and bone mineral content. Blood samples will be taken and analysed in local laboratories of units participating in the study. Results of tests undertaken locally will be entered on participants' CRF by the local research team.
Additional Interviews
Semi-structured interviews will be undertaken by a chartered clinical psychologist with a subset of the young people who took part in the LED intervention to understand the adolescents experience of taking part in the study midway through the study and at the end.
Semi-structured interviews will also be undertaken by a chartered clinical psychologist with 10 young people and/or their family who opted not to take part in the LED study to help understand barriers to participation and how these can be minimised.
Qualitative interviews will also be conducted with at least 10 healthcare professionals from different sites involved in the study to garner feedback and experience as well as the HCPs impression of the experience of the study for the participants and their families.
It is suggested that the proposed number of interview participants will be sufficient to meet the research aims. However, data saturation (whereby no new information is reported) will guide the recruitment process. In each case, purposefully constructed interview guides will be formulated to enhance the rigour of the data generated. All interviews will be conducted remotely with Hilton Health Consultancy via an approved platform. All interviews will be recorded and transcribed and analysed by Hilton Health Consultancy.
This feedback will be instrumental in informing and shaping any subsequent randomised control trial.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 73
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Low Energy Diet (LED) Qualitive interview - Participants declining LED 33 participants will undergo a 12 week low energy diet (LED), followed by a 12 week food reintroduction phase and 24 week weight maintenance phase. 10 participant across all sites from this intervention will be asked to complete a qualitative interview at 2 time points throughout the study, alongside their parent/carer, to understand their thoughts around the intervention, their experience taking part in the study and suggestions for improvement. Additionally, further interviews will be undertaken with participants and their relatives/carers who declined to take part in the LED portion of the study to understand the reasons why/barriers to them taking part in the intervention. Furthermore, 10 health care professionals (HCPs) from different sites involved in the study will be invited to take part in interviews to garner feedback and experience as well as their impression of the experience of the study for the participants and their families. Low Energy Diet (LED) Qualitive interview - Health Care Professionals (HCPs) 33 participants will undergo a 12 week low energy diet (LED), followed by a 12 week food reintroduction phase and 24 week weight maintenance phase. 10 participant across all sites from this intervention will be asked to complete a qualitative interview at 2 time points throughout the study, alongside their parent/carer, to understand their thoughts around the intervention, their experience taking part in the study and suggestions for improvement. Additionally, further interviews will be undertaken with participants and their relatives/carers who declined to take part in the LED portion of the study to understand the reasons why/barriers to them taking part in the intervention. Furthermore, 10 health care professionals (HCPs) from different sites involved in the study will be invited to take part in interviews to garner feedback and experience as well as their impression of the experience of the study for the participants and their families. Low Energy Diet (LED) Low-energy diet 33 participants will undergo a 12 week low energy diet (LED), followed by a 12 week food reintroduction phase and 24 week weight maintenance phase. 10 participant across all sites from this intervention will be asked to complete a qualitative interview at 2 time points throughout the study, alongside their parent/carer, to understand their thoughts around the intervention, their experience taking part in the study and suggestions for improvement. Additionally, further interviews will be undertaken with participants and their relatives/carers who declined to take part in the LED portion of the study to understand the reasons why/barriers to them taking part in the intervention. Furthermore, 10 health care professionals (HCPs) from different sites involved in the study will be invited to take part in interviews to garner feedback and experience as well as their impression of the experience of the study for the participants and their families. Low Energy Diet (LED) Qualitive interview - LED participants 33 participants will undergo a 12 week low energy diet (LED), followed by a 12 week food reintroduction phase and 24 week weight maintenance phase. 10 participant across all sites from this intervention will be asked to complete a qualitative interview at 2 time points throughout the study, alongside their parent/carer, to understand their thoughts around the intervention, their experience taking part in the study and suggestions for improvement. Additionally, further interviews will be undertaken with participants and their relatives/carers who declined to take part in the LED portion of the study to understand the reasons why/barriers to them taking part in the intervention. Furthermore, 10 health care professionals (HCPs) from different sites involved in the study will be invited to take part in interviews to garner feedback and experience as well as their impression of the experience of the study for the participants and their families.
- Primary Outcome Measures
Name Time Method Retention rate measured by by data availability for participant HbA1C. 12 months HbA1C obtained for the participant at:
1. End of LED phase (12 weeks)
2. End of FR phase (24 weeks)
3. End of maintenance phase (12 months)Proportion of potential participants that can be recruited to an LED intervention 12 months Number of eligible participants identified compared to those consented, passed screening and started on LED intervention.
Retention rate measured by by data availability for participant height. 12 months Height obtained for the participant at:
1. End of LED phase (12 weeks)
2. End of FR phase (24 weeks)
3. End of maintenance phase (12 months)Retention rate measured by by data availability for participant weight. 12 months Weight obtained for the participant at:
1. End of LED phase (12 weeks)
2. End of FR phase (24 weeks)
3. End of maintenance phase (12 months)
- Secondary Outcome Measures
Name Time Method Proportion of participants that adhere to the LED 12 weeks Defined by at least 5% weight loss at end of LED phase compared to baseline.
Degree of weight loss achieved in those who adhere to the LED and if this is maintained at 12-months. 12 months Weight as measured at end of LED phase (12 weeks), compared against weight as measured at baseline.
Weight as measured at end of FR phase (24 weeks), compared against weight as measured at baseline.
Weight as measured at end of maintenance (12 months) compared against weight at baseline.
Weight as measured at end of FR compared against weight at the end of LED phase.
Weight as measured at end of maintenance (12 months) compared against weight at the end of LED phase.Do those who adhere to the LED achieve remission? To determine the standard deviation of the proportion of participants that achieve remission (to estimate the sample size for a definitive randomised trial). 12 months Absolute weight loss in those who achieve remission of T2DM defined as an HbA1C \<48 mmol/mol on two occasions at least 3 months apart, in the absence of anti-diabetes medication. This will help to determine the standard deviation of the proportion of participants that achieve remission, to enable an estimation of sample size for a future, definitive, randomised control trial.
Adverse effects 12 months Collection of adverse events at every study visit.
Is the study, including the intervention, investigations and assessments, deliverable consistently across different sites using the standardised study resources. 12 months Qualitative interviews with healthcare professionals who are involved in delivering the study.
Which biomarkers and pathways are upregulated and which are downregulated in young people with T2DM and what is the response to an LED intervention. 12 months Understanding the pattern of and metabolic changes in:
• lipid metabolites before (at baseline) and after following a LED (at end of LED - 12 weeks, end of FR -24 weeks and end of WM - 12 months).What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents. 12 months Changes in body composition based on DXA scan
What are the positive and potential negative effects of a period of LED on the psychological wellbeing of adolescents. 12 months Change in psychological outcomes via the Revised Children's Anxiety and Depression Scale (RCAS).
What are the positive and potential negative effects of a period of LED on the social wellbeing of adolescents. 12 months Change in health-related quality of life via EQ-5D-Y, a standardised measure adapted for use with young people.
What are the positive and potential negative effects of a period of LED on the behavioural wellbeing of adolescents. 12 months Acceptability of the intervention from semi-structured interviews conducted with participants and their family/carer, simultaneously.
Trial Locations
- Locations (1)
Nottingham University Hospital NHS Trust
🇬🇧Nottingham, United Kingdom