A Study Comparing the Health Effects of Two Diets Following UK Dietary Guidance in People Living With Overweight or Obesity
NCT ID: NCT05627570
Last Updated: 2025-06-24
Study Results
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Basic Information
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COMPLETED
NA
55 participants
INTERVENTIONAL
2023-03-01
2025-06-04
Brief Summary
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1. The investigators will study if the benefit from eating a healthy, balanced diet depends on the types of food processing in the diet. The investigators will do this by providing participants with two diets that follow the Eatwell Guide (referred to in this study as Diet A and Diet B to avoid unblinding), but containing foods with different types of food processing, for 8 weeks each. The investigators will collect data on blood pressure, body composition, physical activity and fitness, questions regarding quality of life, mental health and wellbeing, and blood samples at the start of each diet and at 4 and 8 weeks into each diet.
2. The investigators will then study whether participants are able to switch from their usual unhealthy diet to a healthy, balanced diet, and the benefits of doing so. The investigators will do this by providing participants with 6 months of personal support. The investigators will also look at what helps participants to maintain a healthy diet, and what makes it difficult. The investigators will also support participants to be more physically active.
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Detailed Description
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However, there are other parts of the diet that are not covered in the Eatwell Guide that may also be important for health. For example, research suggests that different types of food processing might influence health, but these types of food processing are not included within the recommendations.
It is unknown if the benefits of following the healthy diet advice in the Eatwell Guide depend on the types of food processing in the diet. It is important to find out if these types of food processing matter, in order to give people the best advice possible. It also means that the government and other health organisations may need to change the regulations around the food that people eat.
To answer this, the investigators will compare the effects of two healthy, balanced diets following the advice in the UK Eatwell Guide, but each based on a different type of food processing (referred to in this study as Diet A and Diet B to avoid unblinding). Participants will receive the first diet for 8 weeks, return to their normal diet for 4 weeks, and then receive the second diet for a further 8 weeks. Participants will have 6 months of support to help improve their diet and be more physically active. Participants will work with a behavioural scientist to create a personal plan to eat a healthier diet and be more physically active, using behaviour change techniques based on capability, opportunity, motivation - behaviour (COM-B) theory of behaviour change. This support will last for 6 months, with ongoing monthly telephone/video calls with the research team. The results from this study will be used to help inform UK dietary guidance and food policy.
There are two parts to this study:
1. The investigators will study if the benefit from eating a healthy, balanced diet depends on the types of food processing in the diet. The investigators will do this by providing participants with two diets (Diet A and Diet B) that follow the Eatwell Guide, but containing foods with different types of processing, for 8 weeks each.
2. The investigators will then study whether participants are able to switch from their usual unhealthy diet to a healthy, balanced diet, and the benefits of doing so. The investigators will do this by providing participants with 6 months of personal support. The investigators will also look at what helps participants to maintain a healthy diet, and what makes it difficult. The investigators will also support participants to be more physically active.
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
SINGLE
Study Groups
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Diet A then Diet B, followed by a 6-month behavioural support programme
8-weeks of Diet A then 8-weeks of Diet B, then 6 months of goal-based behavioural support for consuming a healthy, balanced diet, increasing physical activity and reducing sedentary behaviour.
Healthy, balanced Diet A
Healthy, balanced diet following Eatwell Guide recommendations
Healthy, balanced Diet B
Healthy, balanced diet following Eatwell Guide recommendations
Behavioural support intervention
Participants will work with a behavioural scientist to create a personal plan to eat a healthier diet and be more physically active. This support will last for 6 months, with ongoing monthly telephone/video calls with the research team.
Diet B then Diet A, followed by a 6-month behavioural support programme
8-weeks of Diet B then 8-weeks of Diet A, then 6 months of goal-based behavioural support for consuming a healthy, balanced diet, increasing physical activity and reducing sedentary behaviour.
Healthy, balanced Diet A
Healthy, balanced diet following Eatwell Guide recommendations
Healthy, balanced Diet B
Healthy, balanced diet following Eatwell Guide recommendations
Behavioural support intervention
Participants will work with a behavioural scientist to create a personal plan to eat a healthier diet and be more physically active. This support will last for 6 months, with ongoing monthly telephone/video calls with the research team.
Interventions
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Healthy, balanced Diet A
Healthy, balanced diet following Eatwell Guide recommendations
Healthy, balanced Diet B
Healthy, balanced diet following Eatwell Guide recommendations
Behavioural support intervention
Participants will work with a behavioural scientist to create a personal plan to eat a healthier diet and be more physically active. This support will last for 6 months, with ongoing monthly telephone/video calls with the research team.
Eligibility Criteria
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Inclusion Criteria
* Adults aged between \[18 and 65\] years old.
* BMI ≥25 kg/m2 (living with overweight or obesity)
* Weight stable for the past 3 months (≤5 % variation in body weight over preceding 3 months)
* Have a habitual dietary intake high in unhealthy food
* Able to read and write in English.
* Medically safe to participate in a dietary intervention programme.
* Willing and able to give written informed consent.
* Able to attend the relevant in person and online sessions.
* Able to comply with the study protocol (including dietary recommendations for each intervention and reporting adherence).
* Females of childbearing potential and males agree to use an effective method of contraception from the time consent is signed until the end of the intervention period and final follow-up assessment. Effective methods of contraception acceptable for this trial are outlined in Appendix 2.
* Females of childbearing potential must be on highly effective contraception and have a negative pregnancy test within 7 days of being randomised. NOTE: Participants are considered not of childbearing potential if they have undergone a hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or they are postmenopausal.
Exclusion Criteria
* Participation in another clinical intervention trial
* Concomitant usage of medications that cause weight gain or weight loss
* Cardiometabolic comorbidities (e.g. diabetes, on insulin)
* Coeliac disease
* Inflammatory bowel disease
* A diagnosed eating disorder
* Planning a weight management programme in the next 3 months
* Any diagnosed food allergy, or other allergies which limit the ability to adhere to the intervention diet
* Dietary restrictions (e.g. vegan or vegetarian) which limit the ability to adhere to the interventions
* BMI \>40 kg/m2 or basal metabolic rate ≥2300/kcal/day (to ensure intervention diets are at least 300kcal/day greater than maintenance energy needs).
* Females who are pregnant, breast-feeding, or intends to become pregnant.
* A history of drug or alcohol abuse
* Any other factor making the participant unsuitable in the view of investigator.
18 Years
65 Years
ALL
Yes
Sponsors
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University College London Hospitals
OTHER
University College, London
OTHER
Responsible Party
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Principal Investigators
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Rachel L Batterham, Professor
Role: PRINCIPAL_INVESTIGATOR
UCL, UCL Hospitals
Locations
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UCL
London, , United Kingdom
Countries
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References
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Heuchan GN, Buck C, Conway R, Dicken S, Brown AC, Jassil FC, Makaronidis J, Van Tulleken C, Gandini Wheeler-Kingshott CA, Batterham R, Fisher A. Development, content and planned evaluation of a behavioural support intervention to reduce ultraprocessed food intake and increase physical activity in UK healthcare workers: UPDATE trial stage 2 study protocol. BMJ Open. 2025 Oct 29;15(10):e107435. doi: 10.1136/bmjopen-2025-107435.
Dicken SJ, Jassil FC, Brown A, Kalis M, Stanley C, Ranson C, Ruwona T, Qamar S, Buck C, Mallik R, Hamid N, Bird JM, Brown A, Norton B, Gandini Wheeler-Kingshott CAM, Hamer M, van Tulleken C, Hall KD, Fisher A, Makaronidis J, Batterham RL. Ultraprocessed or minimally processed diets following healthy dietary guidelines on weight and cardiometabolic health: a randomized, crossover trial. Nat Med. 2025 Aug 4. doi: 10.1038/s41591-025-03842-0. Online ahead of print.
Dicken S, Makaronidis J, van Tulleken C, Jassil FC, Hall K, Brown AC, Gandini Wheeler-Kingshott CAM, Fisher A, Batterham R. UPDATE trial: investigating the effects of ultra-processed versus minimally processed diets following UK dietary guidance on health outcomes: a protocol for an 8-week community-based cross-over randomised controlled trial in people with overweight or obesity, followed by a 6-month behavioural intervention. BMJ Open. 2024 Mar 11;14(3):e079027. doi: 10.1136/bmjopen-2023-079027.
Other Identifiers
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151582
Identifier Type: -
Identifier Source: org_study_id
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