The Beneficial Effects of Healthy Snacks on Appetite Control, Satiety, and Reward-driven Eating Behavior in Young People

This study has been completed.
Sponsor:
Collaborator:
Solae, LLC
Information provided by (Responsible Party):
Heather Leidy, University of Missouri-Columbia
ClinicalTrials.gov Identifier:
NCT01781286
First received: January 9, 2013
Last updated: October 21, 2014
Last verified: October 2014
  Purpose

The purpose of this study is to examine the effects of normal vs. protein-rich afternoon snacks on appetite control, satiety, and reward-driven eating (particularly in the evening) in young people. Indices of attention and mood will also be assessed.

Study hypotheses include the following:

  1. The consumption of a high-protein, soy-rich afternoon snack will lead to significant improvements in appetite control and satiety, reductions in food motivation and reward, and will delay the drive to eat in normal to overweight young people.
  2. The consumption of a high-protein, soy-rich afternoon snack will lead to reduced unhealthy, evening snacking, particularly on foods high in fat and/or sugar, in normal to overweight young people.
  3. The daily consumption of a high-protein, soy-rich afternoon snack will lead to significant improvements in afternoon alertness, concentration, fatigue, and well-being in normal to overweight young people.

Condition Intervention
Obesity
Behavioral: High Protein
Behavioral: Low Protein

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Double Blind (Subject, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: The Beneficial Effects of Protein-rich, Afternoon Snacks on Appetite Control, Satiety, and Reward-driven Eating Behavior in Young People

Resource links provided by NLM:


Further study details as provided by University of Missouri-Columbia:

Primary Outcome Measures:
  • Time to Dinner Request [ Time Frame: +30 min ] [ Designated as safety issue: No ]
    The participants will be asked whether they would like to request a dinner buffet throughout the 5 h post-snack period. When the response is "Yes, I want to eat right now", the time from snack consumption will be recorded.


Secondary Outcome Measures:
  • Functional Magnetic Resonance Imaging (fMRI) for Assessing Brain Activation [ Time Frame: -30 min, +30 min ] [ Designated as safety issue: No ]
    Brain activation responses will be assessed before and after the snack during each testing day. During the fMRI brain scan procedure, the participants will be placed in a supine position. A structural scan will be performed to identify anatomical structures. During the fMRI phase, the participants will view a set of photographs. The fMRI paradigm incorporates stimuli from 3 categories of pictures including food, nonfood (animals), and blurred baseline images. The pictures from each category will be presented in blocks of images (10 photographs (of the same type of stimuli) per block). The scan involves 3 repetitions of each block of stimulus-producing images (i.e., food, animal), alternated with blocks of randomized blurred images. The functional scan lasts 7 min and is performed in duplicate. Scanning will be performed at the MU-Brain Imaging Center on a 3 Tesla Siemens Trio scanner (Siemens Medical Solutions, Erlangen, Germany).

  • Appetite,Satiety, and Cravings Questionnaires [ Time Frame: -30 min, 0 min, + 30 min, +60 min, +90 min, +120 min, +150 min, +180 min, +210 min, +240 min, +270 min, +300 min ] [ Designated as safety issue: No ]

    Computerized questionnaires, assessing perceived sensations of appetite and satiety will be completed throughout the testing days. The questionnaires contain visual analog scales incorporating a 100 mm horizontal line rating scale for each response. The questions are worded as "how strong is your feeling of" with anchors of "not all" to "extremely." The following questions will be incorporated:

    1. How strong is your feeling of hunger?
    2. How strong is your feeling of being full?
    3. How strong is your desire to eat?
    4. How much food could you consume right now?
    5. How strong is your feeling of thirst?
    6. How strong is your craving for something sweet?
    7. How strong is your craving for something salty?
    8. Host strong is your craving for something savory?

    The Adaptive Visual Analog Scale Software (Neurobehavioral Research Laboratory and Clinic; San Antonio, TX) was used for these assessments.


  • Snack Palatability and Perception Questionnaires [ Time Frame: -30 min, 0 min, + 30 min, +60 min, +90 min, +120 min, +150 min, +180 min, +210 min, +240 min, +270 min, +300 min ] [ Designated as safety issue: No ]

    Computerized questionnaires, assessing snack palatability and perceptions of the snack will be completed during screening and after the first and last bite of each snack during the acclimation and testing days. The questionnaires contain visual analog scales incorporating a 100 mm horizontal line rating scale for each response. The questions are worded as "how strong is your feeling of" with anchors of "not all" to "extremely." The questions assess snack appearance, smell, flavor, texure (feel), liking.

    The Adaptive Visual Analog Scale Software (Neurobehavioral Research Laboratory and Clinic; San Antonio, TX) was used for these assessments.


  • Attention & Memory Questionnaires [ Time Frame: -30 min, + 60 min ] [ Designated as safety issue: No ]
    Cognitive function will be assessed immediately before and 60 min post-snack using the lap-top based Cantab® computerized assessment system. This program consisted of a core battery of tests grouped into 3 main categories including 1) Visual Memory; 2) Working Memory; 3) Executive Function; 4) Attention/Alertness; and 5) Planning. This program has been used in our previous breakfast studies with success.

  • Mood-state Questionnaires [ Time Frame: -30 min, +60 min ] [ Designated as safety issue: No ]
    Indices of mood state will be assessed immediately before and 60 min post-snack using the on-line, Profile of Mood States, 2nd Edition (POMS2). This program consisted of a core battery of tests with the following sub-categories 1) Tension; 2) Depression; 3) Anger; 4) Vigor; 5) Fatigue; 6) Confusion; and 7) Friendliness.

  • Energy Intake [ Time Frame: +300 min, 24 h ] [ Designated as safety issue: No ]

    Post-snack energy intake will be assessed through ad libitum dinner and snacking assessments. The ad libitum dinner will contain approximately 2,000 kcal and will consist of a chicken, rice, and stir-fry meal, chips, chocolate mints, ice tea, and water. The dinner meal will be consumed in the testing facility. The participants will be instructed to eat as much as or as little as they choose over a 30 min period. All contents will be weighed before the dinner and any remains will be re-weighed afterwards to determine the type and quantity of foods consumed.

    The ad libitum evening snacks will contain 3,000 kcal and will include common snack foods. After the testing day is complete, the participants will take the snack packout home and consume any of the foods he/she chooses until going to bed. All contents will be weighed before the packout and any remains will be re-weighed afterwards to determine the type and quantity of foods consumed.



Enrollment: 37
Study Start Date: January 2013
Study Completion Date: January 2014
Primary Completion Date: October 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: High Protein
Higher Protein Soy-based Snacks
Behavioral: High Protein
250 kcal; 40% Protein; 40% Carbohydrate; 20% Fat
Active Comparator: Low Protein
Typical, Low Protein Snacks
Behavioral: Low Protein
5% Protein; 50% Carbohydrates; 45% Fat
No Intervention: No Snack
No Snack

Detailed Description:

Forty adolescents will participate in the following randomized crossover-design study. Prior to the start of the study, the participants will be asked to document their habitual breakfast, lunch, and afternoon snack times. The snack patterns and associated testing days will be scheduled so that each participant consumes the afternoon snack (or refrains from snacking) 3 hours after lunch; however, the time of day when this occurs is based on the participant's previous, habitual snack time. Once this is determined, each participant will randomly acclimate to the following snack pattern for 3 consecutive days: 1) Higher Protein Soy-based Snacks (250 kcal; 40% Protein; 40% Carbohydrates; 20% Fat); 2) Typical, Low Protein Snacks (5% Protein; 50% Carbohydrates; 45% Fat); and 3) No Snack.

On day 4, the participants will consume a standard breakfast, at home, and lunch, at school, and will come in to our facility 1 hour prior to their habitual snack time. The participants will be placed in a window-less, comfortable room, void of all time cues. They will be informed that they will remain in this room for the next 6 hours. The participants will begin the testing day by completing baseline questionnaires assessing appetite, satiety, mood, and cognitive function. A brain scan will be completed using functional magnetic resonance imaging (fMRI) to identify brain activation patterns in response to food stimuli. Following the fMRI scan, the respective snack will be given to the participants; they will have 15 minutes to eat the snack. A second fMRI scan will then be performed. The participants will continue to complete the previous questionnaires until they voluntarily choose to eat. At this time, the volunteers will be presented with an 'all you can eat' snack buffet. They will be permitted to eat as much or as little as they would like to eat over the next 3-hour period. The participants will remain in the facility until the full 8-hour testing day is completed, regardless of when they requested to eat. Following the 6 hours, the participants will be permitted to leave the facility.

  Eligibility

Ages Eligible for Study:   13 Years to 19 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Age range 13-19 years
  • Normal to overweight (BMI: 50-85th percentile for BMI for age or BMI: 18-29.9 kg/m2)
  • No metabolic, psychological, or neurological diseases/conditions
  • Not currently or previously on a weight loss or other special diet (in the past 6 months)
  • Not clinically diagnosed with an eating disorder
  • Habitually eat (i.e., at least 5 times/week) breakfast between 7:00-9:00 am, lunch between 11:00 am-1:00 pm, an afternoon snack between 2:00-4:00 pm, and dinner
  • No food allergies or intolerances to soy products
  • Rates the overall liking of the study snack foods higher than "Neither Like nor Dislike" on the screening palatability questionnaire
  • Right handed

Exclusion Criteria:

  • Age 12 years or younger, or 20 years or older
  • Underweight or Obese (below 50th or above 85th percentile for BMI for age, or BMI below 18 or above 29.9 kg/m2)
  • Any metabolic, psychological, or neurological diseases/conditions
  • Currently or previously on a weight loss or other special diet (in the past 6 months)
  • Clinically diagnosed with an eating disorder
  • Does not habitually eat (i.e., at least 5 times/week) breakfast between 7:00-9:00 am, lunch between 11:00 am-1:00 pm, an afternoon snack between 2:00-4:00 pm, and dinner
  • Food allergies or intolerances to soy products
  • Does not rate the overall liking of the study snack foods higher than "Neither Like nor Dislike" on the screening palatability questionnaire
  • Not right handed
  Contacts and Locations
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01781286

Locations
United States, Missouri
University of Missouri-Columbia
Columbia, Missouri, United States, 65211
Sponsors and Collaborators
University of Missouri-Columbia
Solae, LLC
Investigators
Principal Investigator: Heather J Leidy, PhD University of Missouri-Columbia
  More Information

No publications provided

Responsible Party: Heather Leidy, Tenure-track Assistant Professor, Heather J Leidy, PhD, University of Missouri-Columbia
ClinicalTrials.gov Identifier: NCT01781286     History of Changes
Other Study ID Numbers: 00039414
Study First Received: January 9, 2013
Last Updated: October 21, 2014
Health Authority: United States: Institutional Review Board

Keywords provided by University of Missouri-Columbia:
Obesity
Snacking
Appetite
Protein
Soy
Reward driven eating
Satiety

Additional relevant MeSH terms:
Obesity
Body Weight
Nutrition Disorders
Overnutrition
Overweight
Signs and Symptoms

ClinicalTrials.gov processed this record on October 23, 2014