Obesity Nutritional, Metabolic, Endocrine Obesity
Conditions
Interventions
Participants are randomised into three groups.
Those randomised to the HWP group will initially spend approximately 90 minutes in total with a nutritional therapist and a personal tra
Sponsors
University of Bath (UK)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Apparently healthy males and females 2. Aged 18-50 years 3. BMI>30 kg·m-2
Exclusion criteria
Exclusion criteria: 1. Having been on a diet during the past 6 months 2. Classification as highly physically active on the International Physical Activity Questionnaire (IPAQ) 3. Uncontrolled blood pressure >140/90 mm Hg 4. Total blood cholesterol >6.21 mM 5. Fasted blood glucose >6.1 mM
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Body mass measured via Seca clinical grade weighing scale at the following timepoints: week -2 (pre screening), week 0 (baseline data collection), week 12 (post-intervention data collection), month 6 (6 months post-intervention), month 12 (12 months post-intervention) Updated 07/01/2019: Measured at week -2 (pre screening), week 0 (baseline data collection), week 12 (post-intervention data collection) only. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Blood glucose 2. Insulin 3. HbA1C 4. Lipids These analytes will measured from whole blood sample and will be processed within a Nuffield Health Clinical Pathology Laboratory. Time points for whole blood analysis will be: week 0 (baseline data collection), week 12 (post-intervention data collection) | — |
Countries
United Kingdom
Contacts
Public ContactBenjamin Kelly
Outcome results
None listed