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

Primary Purpose

Overweight/Obesity

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Website and pedometer intervention
Control
Sponsored by
University of Bath
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Overweight/Obesity focused on measuring Physical activity, Diet, Health Behavior

Eligibility Criteria

35 Years - 74 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Arm Type

Experimental

Other

Arm Label

Website and pedometer Intervention

Control

Arm Description

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.

Outcomes

Primary Outcome Measures

Change in mean daily physical activity level (PAL)
Mean daily physical activity level (PAL) will be assessed using accelerometers (BodyMedia, worn on the upper arm), worn for a continuous 7-day period, being removed during this time only for water-based activities such as showering or swimming. The accelerometers gather minute by minute total energy expenditure (TEE) data, which will be used to calculate PAL (PAL = TEE/BMR, where BMR = basal metabolic rate, to be calculated using the Schofield equation).
Change in mean daily energy intake (EI)
Mean daily energy intake (EI) will be assessed using 3-day weighed food diaries, incorporating 2 week days and 1 weekend day .

Secondary Outcome Measures

Fasting plasma glucose concentration
Comparison of glucose concentration in the blood plasma at rest across all three measurement points.
Fasting plasma insulin concentration
Comparison of insulin concentration in the blood plasma at rest across all three measurement points.
Fasting triglyceride concentration
Comparison of triglyceride concentration in the blood serum at rest across all three measurement points.
Fasting total cholesterol concentration
Comparison of total concentration in the blood serum at rest across all three measurement points.
Fasting LDL cholesterol concentration
Comparison of LDL concentration in the blood serum at rest across all three measurement points.
Fasting HDL cholesterol concentration
Comparison of HDL concentration in the blood serum at rest across all three measurement points.
C-reactive protein (CRP) concentration
Comparison of CRP concentration in the blood serum at rest across all three measurement points.
Body mass index (BMI)
Comparison of BMI (defined as mass in kg divided by height in metres squared) across all three measurement points.
Waist circumference
Comparison of waist circumference (in centimetres) across all three measurement points.
Blood pressure
Comparison of blood pressure (systolic/diastolic mmHG) across all three measurement points.
Quality of diet
Diet quality will be assessed based on the proportion of fibre, free sugars and refined carbohydrates, and saturated fats in the diet. The intervention aims to promote an increase in fibre intake and decrease in free sugar, refined carbohydrate and saturated fat intake. Data will be collected using 3-day weighed food diaries, incorporating 2 week days and 1 weekend day.
Motivation for physical activity
Motivation will be assessed using the Behavioural Regulation for Exercise Questionnaire 3 (BREQ 3: Markland & Tobin, 2004; Wilson, Rodgers, Loitz & Scime, 2006) adapted for physical activity.
Motivation for healthy eating
Motivation will be assessed using the Behavioural Regulation for Exercise Questionnaire 3 (BREQ 3: Markland & Tobin, 2004; Wilson, Rodgers, Loitz & Scime, 2006) adapted for diet.
Self-efficacy for physical activity and healthy eating
Self-efficacy will be measured using the Barriers Self-Efficacy Scale for Exercise (BARSE; McAuley, 1992) adapted for physical activity.
Self-efficacy for healthy eating
Self-efficacy will be measured using the self-efficacy scale for eating a healthy diet developed by Pawlak and Colby (2009).

Full Information

First Posted
January 19, 2017
Last Updated
March 15, 2019
Sponsor
University of Bath
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1. Study Identification

Unique Protocol Identification Number
NCT03032731
Brief Title
Trial of a New Online Programme for Physical Activity and Healthy Eating.
Official Title
Trial of a Self-directed Behaviour Change Intervention for Physical Activity and Healthy Eating.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
January 16, 2017 (Actual)
Primary Completion Date
September 12, 2017 (Actual)
Study Completion Date
September 12, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Bath

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Many healthy lifestyle interventions have been developed to help people change their activity and diet, lose weight and thus reduce their risk of developing type 2 diabetes (T2DM) and cardiovascular disorders (CVD). However, these interventions often fail to engage their target audience, which undermines their effectiveness in changing behaviour and health outcomes. The purpose of this study is to investigate the effectiveness of a self-directed, website-based intervention to promote physical activity and healthy dietary behaviours. The intervention frames health information from a novel perspective, which our previous work has indicated can help to promote interest in the health information and improve attitudes, self-efficacy and motivation towards physical activity and healthy dietary behaviours. The intervention comprises a website of information resources and personal recording areas to set goals and monitor activity and diet, weekly emails and pedometers. In this trial we aim to see whether the intervention has any impact on people's physical activity and diet, as well as their risk of developing CVD and T2DM. The intervention will be compared with a control condition in which participants will be shown standard resources available on NHS websites. Overweight/obese (BMI 25 - 39.5) males and females aged 35-74 years will be recruited from the community. The active intervention will last 6 weeks (during this period participants will receive weekly emails from the research team) and there will be a 6-week follow-up phase (in which participants will still have access to the website but contact from the research team). Activity, diet, disease risk markers and psychological antecedents of behaviour will be assessed at baseline, post-intervention (6-weeks) and post follow-up (12- weeks).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overweight/Obesity
Keywords
Physical activity, Diet, Health Behavior

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
Open label
Allocation
Randomized
Enrollment
59 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Website and pedometer Intervention
Arm Type
Experimental
Arm Description
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.
Arm Title
Control
Arm Type
Other
Arm Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Website and pedometer intervention
Intervention Description
Self-directed, website-based intervention delivered with a pedometer to promote understanding of health and health behaviour change.
Intervention Type
Other
Intervention Name(s)
Control
Intervention Description
Standard, publicly available NHS resources for healthy lifestyles.
Primary Outcome Measure Information:
Title
Change in mean daily physical activity level (PAL)
Description
Mean daily physical activity level (PAL) will be assessed using accelerometers (BodyMedia, worn on the upper arm), worn for a continuous 7-day period, being removed during this time only for water-based activities such as showering or swimming. The accelerometers gather minute by minute total energy expenditure (TEE) data, which will be used to calculate PAL (PAL = TEE/BMR, where BMR = basal metabolic rate, to be calculated using the Schofield equation).
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Title
Change in mean daily energy intake (EI)
Description
Mean daily energy intake (EI) will be assessed using 3-day weighed food diaries, incorporating 2 week days and 1 weekend day .
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Secondary Outcome Measure Information:
Title
Fasting plasma glucose concentration
Description
Comparison of glucose concentration in the blood plasma at rest across all three measurement points.
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Title
Fasting plasma insulin concentration
Description
Comparison of insulin concentration in the blood plasma at rest across all three measurement points.
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Title
Fasting triglyceride concentration
Description
Comparison of triglyceride concentration in the blood serum at rest across all three measurement points.
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Title
Fasting total cholesterol concentration
Description
Comparison of total concentration in the blood serum at rest across all three measurement points.
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Title
Fasting LDL cholesterol concentration
Description
Comparison of LDL concentration in the blood serum at rest across all three measurement points.
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Title
Fasting HDL cholesterol concentration
Description
Comparison of HDL concentration in the blood serum at rest across all three measurement points.
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Title
C-reactive protein (CRP) concentration
Description
Comparison of CRP concentration in the blood serum at rest across all three measurement points.
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Title
Body mass index (BMI)
Description
Comparison of BMI (defined as mass in kg divided by height in metres squared) across all three measurement points.
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Title
Waist circumference
Description
Comparison of waist circumference (in centimetres) across all three measurement points.
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Title
Blood pressure
Description
Comparison of blood pressure (systolic/diastolic mmHG) across all three measurement points.
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Title
Quality of diet
Description
Diet quality will be assessed based on the proportion of fibre, free sugars and refined carbohydrates, and saturated fats in the diet. The intervention aims to promote an increase in fibre intake and decrease in free sugar, refined carbohydrate and saturated fat intake. Data will be collected using 3-day weighed food diaries, incorporating 2 week days and 1 weekend day.
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Title
Motivation for physical activity
Description
Motivation will be assessed using the Behavioural Regulation for Exercise Questionnaire 3 (BREQ 3: Markland & Tobin, 2004; Wilson, Rodgers, Loitz & Scime, 2006) adapted for physical activity.
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Title
Motivation for healthy eating
Description
Motivation will be assessed using the Behavioural Regulation for Exercise Questionnaire 3 (BREQ 3: Markland & Tobin, 2004; Wilson, Rodgers, Loitz & Scime, 2006) adapted for diet.
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Title
Self-efficacy for physical activity and healthy eating
Description
Self-efficacy will be measured using the Barriers Self-Efficacy Scale for Exercise (BARSE; McAuley, 1992) adapted for physical activity.
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period
Title
Self-efficacy for healthy eating
Description
Self-efficacy will be measured using the self-efficacy scale for eating a healthy diet developed by Pawlak and Colby (2009).
Time Frame
Baseline, 6 weeks and 12 weeks after starting the intervention/control period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
74 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dylan Thompson, PhD
Organizational Affiliation
University of Bath
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Bath
City
Bath
ZIP/Postal Code
BA2 7AY
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31654276
Citation
Grey EB, Thompson D, Gillison FB. Effects of a Web-Based, Evolutionary Mismatch-Framed Intervention Targeting Physical Activity and Diet: a Randomised Controlled Trial. Int J Behav Med. 2019 Dec;26(6):645-657. doi: 10.1007/s12529-019-09821-3. Erratum In: Int J Behav Med. 2023 Apr;30(2):305.
Results Reference
derived

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

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