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Clinical Trials/NCT03601650
NCT03601650
Completed
Not Applicable

The Effect of Mindful Eating on Calorie Intake and Diet Over a 3-day Period Among Healthy Weight Women.

City, University of London1 site in 1 country99 target enrollmentJanuary 21, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Diet Modification
Sponsor
City, University of London
Enrollment
99
Locations
1
Primary Endpoint
Calorie intake
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The study will examine the effect of focussing on the sensory properties of food whilst eating. It will look at effects on calorie intake and diet over a 3-day period among women of a healthy weight. Participants asked to focus on the sensory properties of their food will be compared with a second group of participants who will be asked to eat their food without distractions and a third group who will not be provided with any strategy.

Detailed Description

The research will be conducted as a between subject design over a period of three days (Tuesday-Thursday). Upon arrival at the laboratory (on a Monday), participants will be provided with more information about the study and will complete a demographics questionnaire. A smartphone app will be downloaded onto the participant's phone and the participant will be provided with login details to access the food diary Intake24. Participants will be asked to complete the food diary every night over a period of three days. The diary will ask participants to record what they consumed for breakfast, lunch, dinner, as well as snack on a daily basis. All participants will receive a reminder notification on their phone each evening during the 3-day period to complete the Intake 24 food diary. They will also be asked to rate how well they think they remembered the food they had eaten that day. During the 3-day period, some participants will also be asked to open reminders in sealed envelopes at particular times of the day. The app will additionally include a recording that participants will be able to listen to at their own convenience, as many times as they wish. The content of the reminders and recording will differ between participants depending on the condition they are allocated to. There will be three conditions: intervention, no distraction control, and no strategy control. In the intervention condition, participants will open reminders related to focusing on the sensory properties of their food while eating their meals. These participants will also have access to a recording that will encourage them to focus on the sensory properties of the food (e.g. its smell, look, texture). Participants in the no distraction control condition will open reminders related to eating their meals with no distractions. The recording provided to participants in this condition will encourage them to consume their meals with no surrounding distractions (e.g. to avoid watching television or listening to the radio). During the study, the number of times the recording is played as well as the date and time it is played will be recorded. In the intervention and no distraction control group, at the end of each of the three days participants will also be asked to rate the extent to which they adhered to the strategy they were provided with. In the no strategy control condition, participants will not receive any reminders to open or have access to a recording. After the three days (i.e. on a Friday), participants will return to the laboratory. They will be asked to complete a questionnaire regarding the usability of the mobile app and the online food diary. Via this questionnaire, they will also be asked about whether they thought taking part in the study influenced their eating behaviour and the amount of pleasure they got from their food during the three-day period. Additionally they will complete a questionnaire measuring sensitivity to reward. At this session participants will be asked if they are happy to have their weight and height measured. If they are, the researcher will measure their weight and height.

Registry
clinicaltrials.gov
Start Date
January 21, 2017
End Date
February 1, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Katy Tapper

Dr Katy Tapper

City, University of London

Eligibility Criteria

Inclusion Criteria

  • Fluent English speaker
  • BMI of 20 to 25 based on reported weight and height
  • Access to data or wifi during the evenings

Exclusion Criteria

  • Dieting to lose weight
  • Taking medication that may affect appetite
  • Current or previous diagnosis of an eating disorder
  • Completion of related studies

Outcomes

Primary Outcomes

Calorie intake

Time Frame: Three days during intervention delivery

Total calorie intake over three days

Secondary Outcomes

  • Fruit and vegetable intake(Three days during intervention delivery)
  • Intake of non milk extrinsic sugars(Three days during intervention delivery)
  • Intake of saturated fat(Three days during intervention delivery)
  • Intake of fibre(Three days during intervention delivery)

Study Sites (1)

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