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The Effect of a Multi-component Weight Management Program on Appetite, Food Preference and Body Weight

The Effect of a Multi-component Weight Management Program on Appetite, Food Preference and Body Weight

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02012426
Acronym
SWSS
Enrollment
96
Registered
2013-12-16
Start date
2014-01-31
Completion date
2016-05-31
Last updated
2017-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Overweight, Obesity, Sedentary Lifestlye

Brief summary

The aim of the current study is to demonstrate that a commercial weight management diet (i.e. low energy density) influences satiation, hunger and satiety and leads to lower energy intake during ad-libitum meals and over a full day. We further seek to demonstrate the sustainability of this effect following 12- week weight loss on the weight management program. * We hypothesise that formulated (low energy) meals will lead to decreased hunger, greater fullness and reduced desire to eat compared to standard meals. * We hypothesise that the commercial weight management program will lead to greater weight loss compared to control program. * We hypothesise that formulated meals (high consumer acceptance) will improve hedonic control over eating (lower wanting for high fat food) * We hypothesise that the commercial weight management program will improve hedonic control over eating (reduced experience food cravings)

Interventions

Sponsors

University of Leeds
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* BMI of 28 - 45 kg/m2 * Reporting an interest in weight loss, not actively participating in a commercial weight loss program, * Not increased physical activity levels in the past 2-4 weeks * Able to eat most everyday foods and fruits and vegetables * Written informed consent to be given

Exclusion criteria

* Significant health problems that could cause confounding effects between intervention and control. * Taking any medication or supplements known to affect appetite or weight within the past month and/or during the study * Pregnant, planning to become pregnant or breastfeeding * History of anaphylaxis to food * Known food allergies or food intolerance * Smokers and those who have recently ceased smoking * Participants receiving systemic or local treatment likely to interfere with evaluation of the study parameters * Those who have previously taken part in a commercial weight loss program in the last 6 months? . * Participants who work in appetite or feeding related areas * Participants unable to consume foods used in the study * Participants who have had bariatric surgery * Participants with a history of eating disorder * Presence of untreated hypothyroidism * Inability to fully comply with intervention or study procedures * Insufficient English language skills to complete study questionnaires

Design outcomes

Primary

MeasureTime frameDescription
Food preferenceWeek 0 and week 14Measured changes in food preference and liking and wanting profiles for food (HF\<LF) following consumption of formulated test meal in comparison to equi-energetic control
Test Meal Energy IntakeWeek 0 and week 12Measured reductions in ad-libitum energy intake following consumption of formulated test meal in comparison to control.
24h Energy IntakeWeek 0 and week 12Measured reduction in total within-day energy intake following consumption of formulated meals in comparison to control
Appetite sensationsWeek 0 and week 14Measured reduction in hunger and increase in satiety quotient following consumption of formulated test meal in comparison to equi-energetic control

Secondary

MeasureTime frameDescription
Body WeightWeekly from week 0 to week 12Measured change in weight and energy balance parameters over a 12 week period following participation in commercial weight management program compared to control group.

Other

MeasureTime frameDescription
Food diaryWeek 0 and week 12Intervention adherence and compensation through 1) food diary analysis.
AccelerometerWeek 0 and week 12Intervention adherence and compensation through accelerometer analysis.
InterviewWeek 12Detailed feedback on participant experience of commercial weight management program through qualitative interview and marketing survey.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 6, 2026