A Randomized, Controlled, Cross-over Study of the Effect of Snacks on Appetite Control
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Healthy Canadians
- Sponsor
- St. Boniface Hospital
- Enrollment
- 46
- Locations
- 1
- Primary Endpoint
- Total Area Under the Curve (AUC) for Hunger, Fullness, Desire to Eat and Prospective Consumption Using Visual Analog Scales (VAS)
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
This clinical trial is being conducted to study whether eating certain snacks will reduce your desire to eat and for a longer period of time compared to other snacks. The investigators are testing 2 different snacks. Study #1 will involve eating 2 different seed-like snacks or water. Study #2 will involve eating pita bread with jam, bread with jam or water. The test snack is higher in protein and/or fibre compared to the reference product.
Detailed Description
Healthy adults will be recruited to participate in a randomized, controlled, crossover study to investigate whether or not eating snacks made with buckwheat would increase satiety and reduce their energy intake when compared to a comparable snack. Water was included as a non-caloric control. The study consisted of 3 visits and participants would receive a different treatment at each visit. Visits were scheduled at least 7 days apart. Visual analog scales will be used to assess appetite related sensations at 7 time points, fasting, 30 minutes after consuming the snack and then at 30 minute intervals for 180 minutes. Participants will be provided with a lunch and the amount of food consumed will be weighed. I addition, participants will be asked to maintain a food record for the remainder of the day.
Investigators
Dr. Heather Blewett
Principal Investigator
St. Boniface Hospital
Eligibility Criteria
Inclusion Criteria
- •Body mass index 18-30kg/m2
- •males and non-pregnant or non-lactating females
Exclusion Criteria
- •Diagnosis of disease by a medical doctor that requires medical treatment during the study period.
- •Daily tobacco use.
- •Physical Activity Level \>1.
- •Eat meals at irregular or unusual times.
- •Food allergy, aversion or unwillingness to eat study foods.
- •Use of any prescription or non-prescription drug, herbal or nutritional supplement known to affect appetite.
- •Presence of a gastrointestinal disorder.
- •Score \>65% on any 1 of the 3 categories of the Three Factor Eating Questionnaire-R18.
Outcomes
Primary Outcomes
Total Area Under the Curve (AUC) for Hunger, Fullness, Desire to Eat and Prospective Consumption Using Visual Analog Scales (VAS)
Time Frame: VAS administered pre-snack and then every 30 minutes after the first bite up to 180 minutes for a total of 7 time points.
Appetite assessment was measured using a VAS questionnaire administered pre-snack and every 30 minutes post snack up to 180 minutes, for a total of 7 time points. The questionnaire included 4 questions (1) How hungry are you? (2) How full are you? (3) How strong is your desire to eat? (4) How much do you think you want to eat right now? Each question was followed by a 10 cm line anchored at the left and right ends by the opposing statements "not at all" and "extremely" for questions 1 and 2, "very weak " and "very strong" for question 3, and "nothing at all" and "a very large amount" for question 4. Participants provided their response to each question by marking a perpendicular line on the 10-cm line to indicate their answer. Scores were determined by measuring the distance in centimeters from the left anchor to the perpendicular line drawn by the participant. VAS scores over time were graphed and AUC was calculated using the trapezoid method.
Secondary Outcomes
- Number of Calories Consumed Post-snack Until Bedtime(time between snack consumption and bedtime (12 hours))