Repeated Sweet Breakfasts and Subsequent Sweet Food Preferences and Intakes
NCT ID: NCT03442829
Last Updated: 2020-09-23
Study Results
Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.
View full resultsBasic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
54 participants
INTERVENTIONAL
2018-02-23
2020-03-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Repeated Sweet Consumption and Subsequent Sweet Food Preferences and Intake
NCT03427658
Effect of Exercise With or Without Breakfast, on Metabolism, Appetite and Cognition
NCT01229345
The Feasibility of Early Time-Restricted Eating in a Student Population
NCT05750277
Provision of Small vs. Large Portion Sizes and Later Food Intake
NCT03241576
The Effect of Breakfast Size Prior to Morning Exercise on Cognition, Mood and Appetite in Habitually Active Women
NCT01711008
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
BASIC_SCIENCE
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Sweet food consumption
Sweet breakfasts. Participants are asked to consume a sweet breakfast every day for three weeks (excepting on three days when outcomes will be assessed (days 0, 7 and 21, day 21 reported). All foods will be provided.
Sweet food consumption
Sweet food consumption at breakfast
Non-sweet food consumption
Non-sweet breakfasts. Participants are asked to consume a non-sweet breakfast every day for three weeks (excepting on three days when outcomes will be assessed (days 0, 7 and 21, day 21 reported). All foods will be provided.
Non-sweet food consumption
Non-sweet food consumption at breakfast
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Sweet food consumption
Sweet food consumption at breakfast
Non-sweet food consumption
Non-sweet food consumption at breakfast
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* No known taste or appetite abnormalities
* Non-smoker
* Habitually eats breakfast
* Able to provide consent and complete all study measures
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Bristol
OTHER
Bournemouth University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Katherine Appleton, PhD
Role: PRINCIPAL_INVESTIGATOR
Bournemouth University, UK
Peter Rogers, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Bristol
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Bournemouth University
Bournemouth, US and Canada Only, United Kingdom
Countries
Review the countries where the study has at least one active or historical site.
Provided Documents
Download supplemental materials such as informed consent forms, study protocols, or participant manuals.
Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
KAPR2018
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.