Phase
Condition
High Cholesterol (Hyperlipidemia)
Metabolic Syndrome
Obesity
Treatment
Healthy, balanced Diet B
Behavioural support intervention
Healthy, balanced Diet A
Clinical Study ID
Ages 18-65 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Staff at University College London Hospitals (UCLH)
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 3months)
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 eachintervention and reporting adherence).
Females of childbearing potential and males agree to use an effective method ofcontraception from the time consent is signed until the end of the interventionperiod and final follow-up assessment. Effective methods of contraception acceptablefor this trial are outlined in Appendix 2.
Females of childbearing potential must be on highly effective contraception and havea negative pregnancy test within 7 days of being randomised. NOTE: Participants areconsidered not of childbearing potential if they have undergone a hysterectomy,bilateral tubal ligation, or bilateral oophorectomy) or they are postmenopausal.
Exclusion
Exclusion Criteria:
Contraindication for dietary intervention
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 tothe intervention diet
Dietary restrictions (e.g. vegan or vegetarian) which limit the ability to adhere tothe interventions
BMI >40 kg/m2 or basal metabolic rate ≥2300/kcal/day (to ensure intervention dietsare 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.
Study Design
Study Description
Connect with a study center
UCL
London, WC1E 6JF
United KingdomSite Not Available
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