Trial of a New Online Programme for Physical Activity and Healthy Eating.
Overweight/Obesity

About this trial
This is an interventional prevention trial for Overweight/Obesity focused on measuring Physical activity, Diet, Health Behavior
Eligibility Criteria
Inclusion Criteria:
- Able to give informed consent to participate in the study.
- Male or female and aged between 35-74 years.
- Defined as overweight or obese, i.e. BMI>25kg/m2.
- Able to travel to the university for assessment days.
Exclusion Criteria:
- Individuals who are not fluent in the English language, and who do not have access to and do not regularly use the internet and an email account.
- Individuals diagnosed with coronary heart disease, chronic kidney disease, type 2 diabetes, stroke, heart failure, severe hypertension (BP>180/110mmHg) and peripheral arterial disease.
- BMI>40kg/m2 (morbidly obese).
- Currently using weight loss drugs or other medication that can affect weight.
- Any reported recent (i.e. last 6 months) shift (>5%) in body mass or large change in habitual lifestyle.
- Individuals unable to change their physical activity (e.g. through disability).
- Current (pre-baseline) or recent (i.e. last 2 months) participation in another research trial or lifestyle supportive intervention or referral.
- Pregnant
Sites / Locations
- University of Bath
Arms of the Study
Arm 1
Arm 2
Experimental
Other
Website and pedometer Intervention
Control
Participants allocated to this group will be given a one-off set-up session in which a researcher will show them the intervention website, create a user profile for them and provide guidance on how to use the site to gain health information, set personal behavioural goals and record and monitor their behaviour in relation to their goals. The researcher will also provide the participant with a pedometer and instruct them how to use this and where they can record their daily steps on the website. For 6 weeks, participants will be asked to use the website and be sent weekly email reminders to do so and log their goal progress. After 6 weeks, no further emails will be sent but participants will still be able to access the website and use the pedometer if they wish.
Participants allocated to this group will be given a one-off session in which a researcher shows them publicly available web-based resources for health behaviour change (provided by the National Health Service (NHS)). Like those participants in the intervention group, they will be assessed again after 6 and 12 weeks. Participants in the control arm will be offered the intervention (access to the study website and a pedometer) after 12 weeks.