Awakening to the Taste of Food Among Restrained Women
Flaveur
1 other identifier
interventional
50
1 country
1
Brief Summary
Energy-restricted diets often require dieting rules, which forced the dieter to eat according to cognitive norms, which increase his vulnerability to external food cues. Allowing the recognition of internal hunger and satiety cues by using conscious food tasting could be helpful among restrained eaters to facilitate an internalized regulation of food intake. The objectives of the proposed study are to investigate among restrained women whether conscious food tasting can influence 1) attitudes and behaviors associated with food and eating; 2) reliance on hunger and satiety signals; and 3) development of taste and olfactory memory. Females (n=50) will be randomly assigned to: 1) experimental group (conscious food tasting intervention) (n=24), or 2) control group (n=26). The conscious food tasting intervention will be conducted by a registered dietitian into groups of ten to twelve women during six weekly 2-hour workshops. Women in the control group will not receive any intervention. Measurements will be taken at baseline, at the end of the intervention period, and at 12-week post-intervention. Restraint Scale, Three-Factor Eating Questionnaire, Mindful Eating Questionnaire, Intuitive Eating Scale, Body-Esteem Scale and Rosenberg Self-Esteem Scale will measure attitudes and behaviors associated with food and eating as well as some aspects related to psychological functioning. The Intuitive Eating Scale and a snack-meal taste rating task (visual analogue scales) will assess internal hunger/satiety cues. Vocabulary used to describe the foods will be recorded from the snack-meal taste rating task and use to assess taste and olfactory memory. Sensory capabilities will be assessed by odour detection and identification test, and a taste detection test. The proposed study will provide a better understanding of the effects of conscious food tasting on eating attitudes and behaviors, which is relevant to dietetic practice as it could help to promote sustainable healthy eating habits.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2011
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2011
CompletedFirst Submitted
Initial submission to the registry
February 13, 2012
CompletedFirst Posted
Study publicly available on registry
February 20, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2012
CompletedApril 25, 2013
April 1, 2013
1.2 years
February 13, 2012
April 24, 2013
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Attitudes and behaviors associated with food and eating
To evaluate the effects of conscious food tasting on attitudes and behaviors associated with food and eating. This measure is made through a questionnaire.
Up to 3 months
Secondary Outcomes (2)
Physical signals for hunger and satiety
Up to 3 months
Development of taste and olfactory memory
Up to 3 months
Study Arms (2)
Conscious food tasting intervention
EXPERIMENTALInstead of focusing on dieting rules to restrict food intake, paying attention to sensory stimulation allow the recognition of internal cues of hunger and satiety which can be helpful to facilitate a more internalized regulation of food intake among restrained eaters. In the experimental group, the conscious food tasting intervention will be conducted by a registered dietitian into small groups of ten to twelve women during six weekly 2-hour workshops. Workshops will be taking place in a well-ventilated room to insure that there are no extraneous odours or noises that may hamper the activities involving senses.
Control
NO INTERVENTIONInterventions
Six weekly 2-hour workshops
Eligibility Criteria
You may qualify if:
- females aged 25 to 60 year-old
- stable weight (± 2.5 kg) for at least 2 months
- restrained eaters (scores of 15 or higher at the Restraint Scale)
You may not qualify if:
- food allergies
- taking medication (e.g., corticosteroids, tricyclic antidepressants, atypical antipsychotics)
- chronic health problems (e.g., eating disorders, type 1 and type 2 diabetes, hyperthyroidism)
- pregnant or lactating
- smoker
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Laval Universitylead
- Canadian Foundation for Dietetic Research (CFDR)collaborator
Study Sites (1)
Institute of Nutraceuticals and Functionnal Foods (INAF)
Québec, Quebec, G1V 0A6, Canada
MeSH Terms
Conditions
Study Officials
- PRINCIPAL INVESTIGATOR
Véronique Provencher, Ph.D.
Laval University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
February 13, 2012
First Posted
February 20, 2012
Study Start
January 1, 2011
Primary Completion
April 1, 2012
Study Completion
December 1, 2012
Last Updated
April 25, 2013
Record last verified: 2013-04