The Effect of Food Labelling and Satiety on Individuals Food Choice
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| ClinicalTrials.gov Identifier: NCT03537781 |
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Recruitment Status : Unknown
Verified September 2018 by Kim Wright, St Mary's University College.
Recruitment status was: Recruiting
First Posted : May 25, 2018
Last Update Posted : September 19, 2018
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Previous research has shown that nutritional knowledge is a key indicator in healthy eating choices, but real-life examinations of the associations between both nutritional knowledge and state of hunger and satiety on individuals' food choice of healthy vs unhealthy snacks is limited.
The present study aims to investigate whether the presence of nutritional information on food labels will affect participants' food choice when hungry and when satiated.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Food Preferences Hunger | Behavioral: Food labelling versus no food labelling | Not Applicable |
Previous research has shown that nutritional knowledge is a key indicator in healthy eating choices, but real-life examinations of the associations between both nutritional knowledge and state of hunger and satiety on individuals' food choice of healthy vs unhealthy snacks is limited.
As there is currently little research combining these facets, it would be interesting to investigate whether individuals who are provided with food labelling information would choose unhealthy snacks when hungry as than when satiated and whether this would differ for those who are not provided with food labelling information.
Based on this, the present study aims to investigate whether the presence of nutritional information in the form of food labels will affect participants' food choice when hungry and when satiated. The General Nutrition Knowledge Questionnaire will be used to assess participants baseline nutritional knowledge and will be used as a covariate in the research project.
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 112 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Intervention Model Description: | Participants will be randomly allocated to a food labelling or no food labelling condition. Participants in each condition will be tested when hungry and when satiated |
| Masking: | Single (Participant) |
| Primary Purpose: | Other |
| Official Title: | Nutritional Knowledge and the Effects of Hunger & Satiety on Snack Choice: a Randomised Controlled Trial |
| Actual Study Start Date : | June 12, 2018 |
| Estimated Primary Completion Date : | September 30, 2018 |
| Estimated Study Completion Date : | October 30, 2018 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Food label available, hungry state
foods will be displayed with food labels present and when participants had nothing to eat
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Behavioral: Food labelling versus no food labelling
Food labelling availability and satiety status |
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Experimental: food label available, satiated
foods will be displayed with food labels present and when participants had already eaten breaksfast
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Behavioral: Food labelling versus no food labelling
Food labelling availability and satiety status |
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Experimental: food label unavailable, hungry state
foods will be displayed without food labels present and when participants had nothing to eat
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Behavioral: Food labelling versus no food labelling
Food labelling availability and satiety status |
|
Experimental: food label unavailable, satiated
foods will be displayed without food labels present and when participants had already eaten breakfast
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Behavioral: Food labelling versus no food labelling
Food labelling availability and satiety status |
- food choice [ Time Frame: 2 days ]participants will have to choose one snack from a choice of six differing on their fat content
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years to 65 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria: Male and females aged 18-65 years old; in general good health; not known allergies and any medical conditions (e.g. heart disease, asthma)
Exclusion Criteria: Those who are currently following a weight loss diet; have food allergies and any medical conditions which might restrict their food intake
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03537781
| Contact: Kyriaki Myrissa, PhD | 020 8240 4000 ext 8247 | kyriaki.myrissa@stmarys.ac.uk |
| United Kingdom | |
| St Marys University | Recruiting |
| London, United Kingdom, TW1 4SX | |
| Principal Investigator: Freddy Brown, MSc | |
| Sub-Investigator: Jessica Hill, PhD | |
| Principal Investigator: | Conor Gissane, PhD | St. Mary's University |
| Responsible Party: | Kim Wright, Research administrator, St Mary's University College |
| ClinicalTrials.gov Identifier: | NCT03537781 |
| Other Study ID Numbers: |
SMU_SHAS_2018_01. |
| First Posted: | May 25, 2018 Key Record Dates |
| Last Update Posted: | September 19, 2018 |
| Last Verified: | September 2018 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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food choice, food labels |

