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Pediatric ObesityLEGENDNCT06572345

Low EnerGy DiEt iN Adolescents With Obesity and Type 2 Diabetes: The LEGEND Study

A study testing Low-energy diet, Qualitive interview - LED participants and Qualitive interview - Participants declining LED in people with Pediatric Obesity and Type 2 Diabetes, run by Nottingham University Hospitals NHS Trust at 1 site in United Kingdom.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial 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. Read more about this study

Who is it for?
Ages 12 to 17 years
Conditions the study is for
Pediatric Obesity, Type 2 Diabetes
What is being tested?
Low-energy diet, Qualitive interview - LED participants and Qualitive interview - Participants declining LED
Could I receive a placebo?
No, everyone receives an active treatment
How many people
73 participants
Where
1 siteUnited Kingdom
Study dates
30 Jun 2025to 29 May 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 12 to 17 years
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • LED intervention
  • Diagnosis of T2DM (defined as an HbA1C ≥48mmol/mol, in the absence of features of type 1 or monogenic/syndromic diabetes).
  • Current HbA1C ≥48 (or ≥42 on antidiabetic medication) and ≤ 80 mmol/mol. To allow for the day-to-day variation in HbA1C and differences between point of care laboratory tests, -2 or +2 mmol/mol in the HbA1C result will be allowed in the current criteria if one of them is between or equal to 42-80mmol/mol.
  • Aged 12 to 17 years old.
  • BMI ≥981st centile (+2 SD) for age and sex (UK90 growth reference data).
  • Informed consent:
Show all 33Show fewer
  • Received from the young person (age 16-17) OR
  • Received from young person's parent/carer, with patient assent (age 12-15).
  • Willing to engage in and commit to low energy diet, FR and weight management phases including follow-up and attending study visits.
  • LED Intervention Interviews
  • The same interview inclusion criteria for LED intervention, with the following additional requirements:
  • Patients:
  • Informed consent:
  • Received from the young person (age 16-17) OR
  • Received from young person's parent/carer, with patient assent (age 12-15).
  • Willing to take part in a qualitative interview alongside a parent/carer.
  • Relative/Carer:
  • A relative/carer for a young person meeting the above LED participant eligibility criteria.
  • Informed consent from the relative/carer to participate in the interview.
  • Willing to take part in a qualitative interview alongside the young person.
  • Non-LED Qualitative Interview only participants
  • Diagnosis of T2DM (defined as an HbA1C ≥48mmol/mol, in the absence of features of type 1 or monogenic/syndromic diabetes).
  • Current HbA1C ≥48 (or ≥42 on antidiabetic medication) and ≤80 mmol/mol.
  • Aged 12 to 17 years old.
  • BMI ≥91st centile (+2 SD) for age and sex (UK90 growth reference data).
  • Informed consent:
  • Received from the young person (age 16-17) OR
  • Received from young person's parent/carer, with patient assent (age 12-15).
  • Willing to take part in a qualitative interview alongside a parent/carer only.
  • HCPs
  • Registered HCP.
  • Experience of delivering this trial to the adolescents.
  • Willing to take part in a qualitative interview about undertaking motivational interviewing training and conducting/delivering the LED intervention study.

Who cannot join

  • LED intervention
  • HbA1C greater than 82mmol/mol (to allow for the variation in HbA1c differences).
  • Presence of diabetes-related autoantibodies, as per local centre guidelines.
  • Confirmed mono-genetic cause of obesity (e.g. SIM1 mutation) or diabetes-associated syndrome such as Prader-Willi syndrome, Bardet-Biedl or Wolfram's syndrome.
  • Secondary diabetes (post bone marrow transplant/chemotherapy).
  • Significant psychiatric co-morbidity.
Show all 28Show fewer
  • Breastfeeding, pregnant or planning to conceive during the LED and FR phases (female participants will be advised on need for effective contraceptive methods during the 12-month study period, section 5.1.1.10).
  • Any other condition which, in the opinion of the study investigator, would make it inappropriate to undertake a period of LED. (All reasons for not approaching patients will be recorded and analysed anonymously. Cases can be discussed with the core study group if there is doubt).
  • Participation in another interventional trial within 6 months.
  • Informed consent and/or assent not received.
  • Pre-existing retinopathy.
  • Dietary avoidance (including, but not limited to, due to allergies, intolerances, religious reasons and lifestyle choices) to any ingredients in the meal replacement products, including lactose.
  • Previous scoliosis repair.
  • Non-LED Qualitative Interview only participants
  • HbA1C greater than 80mmol/mol.
  • Presence of diabetes-related autoantibodies, as per local centre guidelines.
  • Confirmed mono-genetic cause of obesity (e.g. SIM1 mutation) or diabetes-associated syndrome such as Prader-Willi syndrome, Bardet-Biedl or Wolfram's syndrome.
  • Secondary diabetes (post bone marrow transplant/chemotherapy).
  • Significant psychiatric co-morbidity.
  • Breastfeeding, pregnant or planning to conceive during the LED and FR phases (female participants will be advised on need for effective contraceptive methods during the 12-month study period, section 5.1.1.10).
  • Any other condition which, in the opinion of the study investigator, would either make it inappropriate to undertake a period of LED. (All reasons for not approaching patients will be recorded and analysed anonymously. Cases can be discussed with the core study group if there is doubt).
  • Participation in another interventional trial within 6 months.
  • Informed consent and/or assent not received.
  • Pre-existing retinopathy.
  • Dietary avoidance (including, but not limited to, due to allergies, intolerances, religious reasons and lifestyle choices) to any ingredients in the meal replacement products, including lactose.
  • Previous scoliosis repair.
  • HCPs
  • None.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Gemma Boam, PhD contact

gemma.boam@nhs.net

United Kingdom1 site, 1 recruiting
  • Nottingham University Hospital NHS Trust

    Nottingham, NG7 2UH

    Pooja Sachdev, MD, 0115 924 9924 ext. 82367, pooja.sachdev@nhs.net

    James Law, MD

    Recruiting

Other trials in United Kingdom

About this study

Official title: A Multicentre Open-Label, Feasibility Study of the Use of a Short-Term Low-Energy Diet in Adolescents With Obesity and Type-2 Diabetes Mellitus

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.

Read the 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.

Being tested
Low-energy diet, Qualitive interview - LED participants, Qualitive interview - Participants declining LED, Qualitive interview - Health Care Professionals (HCPs)
Keywords
Type 2 diabetes mellitus, Paediatric, Obesity, Low-energy diet, Adolescent, Remission
Medical subject headings
Pediatric Obesity, Diabetes Mellitus, Type 2, Obesity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Low-energy dietDietary supplement

    For the first 12 weeks during the LED, participants will have 4 meal replacement products each day. The following 12 weeks consists of a gradual reintroduction of food one meal at a time, in a structured stepwise progression, under the supervision of a dietitian. They will then undergo 28 weeks of weight maintenance to see if they are able to keep their weight stable.

  • Qualitive interview - LED participantsOther

    Semi-structured interviews with 10 of the LED participants and their relative/carer.

  • Qualitive interview - Participants declining LEDOther

    Semi-structured interviews with 10 participants who declined the LED, and their relative/carer.

  • Qualitive interview - Health Care Professionals (HCPs)Other

    Semi-structured interviews with 10 HCPs involved in delivery of the trial.

Study groups in NCT06572345
Study groupRoleWhat they receive
Low Energy Diet (LED)Experimental33 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.
Receives: Dietary Supplement: Low-energy diet; Other: Qualitive interview - LED participants; Other: Qualitive interview - Participants declining LED; Other: Qualitive interview - Health Care Professionals (HCPs)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Proportion of potential participants that can be recruited to an LED intervention

    Number of eligible participants identified compared to those consented, passed screening and started on LED intervention.

    Measured: 12 months

  2. Retention rate measured by by data availability for participant height.

    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)

    Measured: 12 months

  3. Retention rate measured by by data availability for participant weight.

    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)

    Measured: 12 months

  4. Retention rate measured by by data availability for participant HbA1C.

    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)

    Measured: 12 months

Secondary outcomes (44)
  1. Proportion of participants that adhere to the LED

    Defined by at least 5% weight loss at end of LED phase compared to baseline.

    Measured: 12 weeks

  2. Degree of weight loss achieved in those who adhere to the LED and if this is maintained at 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.

    Measured: 12 months

  3. 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).

    Percentage 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.

    Measured: 12 months

  4. 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).

    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.

    Measured: 12 months

  5. Adverse effects

    Collection of adverse events at every study visit.

    Measured: 12 months

  6. Is the study, including the intervention, investigations and assessments, deliverable consistently across different sites using the standardised study resources.

    Qualitative interviews with patients and carers (patient and carers interviewed together) who participate in the LED, and those who do not.

    Measured: 12 months

  7. Is the study, including the intervention, investigations and assessments, deliverable consistently across different sites using the standardised study resources.

    Qualitative interviews with healthcare professionals who are involved in delivering the study.

    Measured: 12 months

  8. Which biomarkers and pathways are upregulated and which are downregulated in young people with T2DM and what is the response to an LED intervention.

    Understanding the pattern of and metabolic changes in:

    • water soluble 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).

    Measured: 12 months

  9. Which biomarkers and pathways are upregulated and which are downregulated in young people with T2DM and what is the response to an LED intervention.

    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).

    Measured: 12 months

  10. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Changes in clinical markers, such as blood pressure, including both systolic and diastolic measurements (mmHg).

    Measured: 12 months

  11. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    HbA1C

    Measured: 12 months

  12. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Full Blood Count

    Measured: 12 months

  13. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Ferritin

    Measured: 12 months

  14. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    White Blood Cell Count

    Measured: 12 months

  15. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Platelet count

    Measured: 12 months

  16. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Urea and electrolytes

    Measured: 12 months

  17. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    alanine transaminase (ALT)

    Measured: 12 months

  18. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Aspartate Transferase (AST)

    Measured: 12 months

  19. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Gamma Glutamyl Transferase (GGT)

    Measured: 12 months

  20. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Albumin

    Measured: 12 months

  21. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Lipid Profile - Cholesterol, triglycerides, low density lipoprotein, high density lipoprotein (all mg/DL)

    Measured: 12 months

  22. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Bone profile - Parathyroid hormone (PTH)

    Measured: 12 months

  23. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Bone profile - Calcium and Phosphate (mmol)

    Measured: 12 months

  24. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Bone profile - Alkaline Phosphatase (ALP) (U/L)

    Measured: 12 months

  25. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Bone profile - Vitamins A and E (ummol/L)

    Measured: 12 months

  26. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Bone profile - Vitamin D (nmol/L)

    Measured: 12 months

  27. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Thyroid function tests - T3 and T4 (pmol/L)

    Measured: 12 months

  28. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Thyroid function tests - Thyroid Stimulating Hormone (TSH) (mU/L)

    Measured: 12 months

  29. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    luteinizing hormone (LH), follicle stimulating hormone (FSH) (u/L)

    Measured: 12 months

  30. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Testosterone, sex hormone binding globulin (nmol/L)

    Measured: 12 months

  31. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Oestradiol (pmol/L)

    Measured: 12 months

  32. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Changes in imaging markers such as liver fat on MRI

    Measured: 12 months

  33. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Changes in metabolic disease based on DXA scan

    Measured: 12 months

  34. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Changes in bone mineral density based on DXA scan

    Measured: 12 months

  35. What are the positive and potential negative effects of a period of LED on the biological wellbeing of adolescents.

    Changes in body composition based on DXA scan

    Measured: 12 months

  36. What are the positive and potential negative effects of a period of LED on the psychological wellbeing of adolescents.

    Change in eating disorder score or development of eating disorders and binge eating, assessed via the Eating Disorder Examination Questionnaire EDE-Q/EDE-A.

    Measured: 12 months

  37. What are the positive and potential negative effects of a period of LED on the psychological wellbeing of adolescents.

    Change in psychological outcomes via the Generalised Anxiety Disorder Assessment (GAD-7).

    Measured: 12 months

  38. What are the positive and potential negative effects of a period of LED on the psychological wellbeing of adolescents.

    Change in psychological outcomes via the Revised Children's Anxiety and Depression Scale (RCAS).

    Measured: 12 months

  39. What are the positive and potential negative effects of a period of LED on the social wellbeing of adolescents.

    Change in health-related quality of life via Child Health Utility instrument (CHU9D).

    Measured: 12 months

  40. What are the positive and potential negative effects of a period of LED on the social wellbeing of adolescents.

    Change in health-related quality of life via the paediatric quality of life inventory - PedsQL 3.2.

    Measured: 12 months

  41. What are the positive and potential negative effects of a period of LED on the social wellbeing of adolescents.

    Change in health-related quality of life via EQ-5D-Y, a standardised measure adapted for use with young people.

    Measured: 12 months

  42. What are the positive and potential negative effects of a period of LED on the behavioural wellbeing of adolescents.

    Change in activity via activity monitors.

    Measured: 12 months

  43. What are the positive and potential negative effects of a period of LED on the behavioural wellbeing of adolescents.

    Change in activity through self-report via Physical Activity Questionnaire (PAQ-A/PAQ-C).

    Measured: 12 months

  44. What are the positive and potential negative effects of a period of LED on the behavioural wellbeing of adolescents.

    Acceptability of the intervention from semi-structured interviews conducted with participants and their family/carer, simultaneously.

    Measured: 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Aug 2024
  2. Study start30 Jun 2025
  3. Primary completion29 May 2028 (estimated)
  4. Study completion29 May 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Model description
73 participants in total: * Thirty-three participants to trial the LED intervention * Ten participants from the LED intervention and their parents/carers for the interviews. * Ten dyads undertaking interviews only (1 adolescent and 1 parent/carer) who declined the intervention. * Ten healthcare practitioners (interviews only).
Masking
None (open label)
Enrolment
73 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06572345
Sponsor's protocol ID
22CS007
Other IDs
21/0006341, 317544
Acronym
LEGEND
Status last verified
Jul 2026
First submitted
7 Jun 2024
Last updated
9 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Low-energy diet, Qualitive interview - LED participants and Qualitive interview - Participants declining LED in people with Pediatric Obesity and Type 2 Diabetes, run by Nottingham University Hospitals NHS Trust at 1 site in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 33 inclusion and 28 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 9 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Pooja Sachdev, MD (0115 924 9924 ext. 82367, pooja.sachdev@nhs.net), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Proportion of potential participants that can be recruited to an LED intervention (time frame: 12 months). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Jul 2026.

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