Impact of a Satiating Diet in Obese Men With a Low Satiety Phenotype

Obesity Clinical Trial

Official title:

Clinical Evaluation to Improve Obesity Intervention Prescription: Functional Foods as a Potential Solution for Individuals With a Low Satiety Quotient Phenotype?

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03128697
• Other study ID #: MOP-68858
• Status: Completed
• Phase: N/A
• First received: April 13, 2017
• Last updated: April 25, 2017
• Start date: October 1, 2004
• Est. completion date: September 30, 2008

Study information

• Verified date: April 2017
• Source: Laval University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The global research project was organized as a clinical process starting with an evaluation aiming at the determination of a diagnosis pertaining to the degree of satiety signal capacity. It was extended by a phase of metabolic and behavioural characterization to better understand the clinical condition of the patients. The main part of the program was a weight loss intervention that was focused on high satiating foods. Finally, the process was completed by an evaluation allowing to determine the impact of the intervention on the metabolic and behavioural conditions of the patients.

Description:

Dietary restriction, being prescribed as low and very low calorie diets, has been largely used as a strategy of dietary management of obesity. Beyond the fact that these diets fully respect the first law of thermodynamics, they are also rather easy to supervise and they offer a guarantee of substantial weight loss to compliant patients. Dietary restriction strategies also carry important limitations which include their failure to take into account appetite sensations of the obese patient. This point is important since it dictates the extent to which the patient can tolerate his/her dietary regimen without hunger over time as well as its related body weight loss. In this regard, experimental and clinical data show that weight regain up to initial body weight and even more occurs over years after a diet-induced weight loss. Moreover, evidence also revealed that restraint behaviour is difficult to maintain over time and that a decrease in this behaviour is related to weight gain on a long term basis. The challenge thus becomes the search of a strategy that can promote a substantial spontaneous energy deficit without significantly altering hunger and satiety levels as well as their related well-being. Up to now, the only approach which emerges as having the potential to respect these two criteria is the design of functional foods, i.e. foods with sufficient satiety-promoting properties to compensate for the enhancing effect of body fat loss on appetite. The food specialists can rely on a catalogue of functional ingredients that can be used to prepare functional menus in order to improve the regulation of energy balance and body weight stability in individuals prone to obesity. As described above, this issue would be particularly relevant for obese individuals displaying a low satiety phenotype, i.e. individuals experiencing difficulty to match energy intake to expenditure in a context promoting excess food intake.

The objectives of this study were to characterize obese men displaying the low satiety phenotype (metabolic and behavioral characteristics) and to determine the impact of highly satiating foods on body weight loss, satiety feelings and compliance in this population.

EXPERIMENTAL DESIGN

Recruitment of subjects and satiety phenotype determination

Each patient referred by a physician was contacted by phone and a first screening interview was performed to validate the inclusion criteria. After recruitment, every subject was met to read and sign the letter of consent as well as to discuss every aspect of the program about which he might have some questions. We took advantage of this brief meeting to measure height, body weight and waist circumference to determine BMI and to estimate the level of abdominal fat.

This phase also included a 2-hour session of evaluation in order to determine satiety signal capacity (SQ). At the end of this session, each subject completed the Three-Factor Eating Questionnaire with the specific preoccupation to measure cognitive dietary restraint as an exclusion criterion. The information collected in this first phase of testing was used to subsequently classify subjects on the basis of their satiety signal capacity (low SQ vs normal/high SQ). Subjects not selected to participate in the next phase of the project received, in addition to their health report, a free dietary consultation focusing on the adoption of healthy behaviours. This first phase of testing allowed to rank order subjects on the basis of their score obtained with the satiety quotient. Seventy participants were selected to participate in the study

Initial metabolic and behavioural characterization (Time 0)

This phase of testing began by a standard medical examination performed by the physician of our research team several days before the main testing session. This permitted to identify potential illnesses influencing appetite control and to evaluate the general health condition of each subject. In order to evaluate the reproducibility over time of the satiety quotient determination and to ascertain the status of subjects determined at the initial evaluation, the standardized breakfast test meal was repeated. However, this test was performed in a session of longer duration that allowed to characterize metabolic and behavioural factors associated with a low/high satiety capacity. The measurements included in this phase of testing were used as baseline measurements for the next phase of this project.

Intervention study

The 70 participants were randomly assigned to either a weight loss program consisting of a highly satiating diet (n=35) (low to moderate in fat (30-35%), high in fibres (> 25g/day), high protein (20-25% of total energy intake) and including 45-50% energy as carbohydrate mainly provided by foods with low glycemic index and adequate to slightly increased vitamin and mineral intakes) which is expected to induce a spontaneous energy deficit or a diet supervision based on the guidelines concordant with the Canadian Food Guide (n=35) (10-15, 55-60 and 30% energy as protein, carbohydrate, and lipid, respectively). For statistical analysis, 4 subgroups have been created based on the SQ classification: 1) low SQ, high satiating diet 2) low SQ, conventional healthy diet, 3) normal/high SQ, high satiating diet, 4) normal/high SQ, conventional healthy diet. This experimental environment thus corresponded to a two by two factorial design in which the two independent variables are SQ and diet. Participants were encouraged to comply with the diets for a 16-week period even if a resistance to weight loss (i.e weight maintenance during one month) was observed during the protocol.

Final metabolic and behavioural characterization (Post-tests; week 16)

All the measurements performed at Time 0 were repeated immediately after the 16-week intervention period for each of the four subgroups of subjects.

POTENTIAL OUTCOME AND FUTURE PERSPECTIVES

The main conceptual outcomes of this were: 1) the characterization of factors implicated in different satiety signal capacities; 2) the investigation of the role of individual capacity of satiety signal in body weight loss and diet compliance, and 3) the determination of the impact of functional menus promoting satiety to compensate for the low spontaneous satiety level in some obese individuals. In addition, this project provided clinical and economical outcomes. Indeed, it represented the first study documenting the weight-reducing impact of a healthy diet based on foods whose functionality have been upgraded by food design. If this project confirms that such a diet can promote weight loss without restriction, but while rather being associated with well-being, this will be a major gain for clinical nutritionists who have up to now unsuccessfully try to counteract the obesity epidemic and who have to deal with consumers who primarily request palatable foods instead of a priori focusing on healthy food. From an economical standpoint, this program will be a reference source of validation for the industry seeking justifications and claims to promote healthy foods facilitating body weight control.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 70
• Est. completion date: September 30, 2008
• Est. primary completion date: September 30, 2008
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 30 Years to 50 Years

Eligibility

Inclusion Criteria:

• aged between 30 and 50 years

• obese (BMI between 30 and 40 kg/m2)

• overall good health

Exclusion Criteria:

• Participants taking medication which could influence appetite sensations (hormones, tranquillizers such as chlorpromazine and benzodiazepin, lithium carbonate for bipolar disorders, cyproheptadine, antihistaminic, serotonin antagonist, sulfonylurea and glucocorticoids)

• Type 2 diabetic patients treated with insulin

• Large body weight fluctuations (>4 kg over the last two months)

• High level of restraint behaviour (score > 10 as measured with the Three Factor Eating Questionnaire)

• Performing more than 3 x 30 minutes/week of physical activity.

Related Conditions & MeSH terms

• Appetite Disorders
• Feeding and Eating Disorders
• Obesity

Intervention

Behavioral:
• Satiating diet

• Control diet

Locations

Country	Name	City	State
Canada	Laval Hospital	Quebec
Canada	Laval University	Quebec

Sponsors (2)

Lead Sponsor	Collaborator
Laval University	Canadian Institutes of Health Research (CIHR)

Country where clinical trial is conducted

Canada, 

References & Publications (3)

Drapeau V, Blundell J, Gallant AR, Arguin H, Després JP, Lamarche B, Tremblay A. Behavioural and metabolic characterisation of the low satiety phenotype. Appetite. 2013 Nov;70:67-72. doi: 10.1016/j.appet.2013.05.022. Epub 2013 Jun 20. — View Citation

Filiatrault ML, Chaput JP, Drapeau V, Tremblay A. Eating behavior traits and sleep as determinants of weight loss in overweight and obese adults. Nutr Diabetes. 2014 Oct 20;4:e140. doi: 10.1038/nutd.2014.37. — View Citation

McNeil J, Drapeau V, Gallant AR, Tremblay A, Doucet E, Chaput JP. Short sleep duration is associated with a lower mean satiety quotient in overweight and obese men. Eur J Clin Nutr. 2013 Dec;67(12):1328-30. doi: 10.1038/ejcn.2013.204. Epub 2013 Oct 16. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change from baseline body weight at 16 weeks	Body weight (kg)	Pre (Week 0)- and post-intervention (after 16 weeks)
Primary	Change from baseline satiety responsiveness (satiety quotients) at 16 weeks	Measured by a standardized breakfast test meal using visual analogue scales for 4 appetite sensations (hunger, desire to eat, fullness and prospective food consumption) (mm/100kcal)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline BMI at 16 weeks	kg/m2	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline waist circumference at 16 weeks	cm	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline resting blood pressure at 16 weeks	mmHg	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline resting heart rate at 16 weeks	beat/min	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline resting energy expenditure at 16 weeks	kcal/day	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline fat mass at 16 weeks	kg	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline lean body mass at 16 weeks	kg	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline percent fat mass at 16 weeks	percent (%)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline spontaneous energy intake at 16 weeks	Measured following an ad-libitum buffet-type meal (kcal)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline daily energy intake at 16 weeks	Three-day dietary record (kcal/day)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline diet quality (macronutrient composition) at 16 weeks	Three-day dietary record (% carbohydrates, proteins and lipids)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline appetite sensations at 16 weeks (desire to eat, fullness, hunger and prospective food consumption)	Measured following an ad-libitum buffet-type meal (0-150 mm).	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline binge eating tendencies at 16 weeks	Binge Eating Scale (possible score between 0-46)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline distress-related body esteem at 16 weeks	Body Esteem Scale (possible score between 0-92)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline cognitive restraint at 16 weeks	Three Factor Eating Questionnaire (possible score between 0-21)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline flexible restraint at 16 weeks	Three Factor Eating Questionnaire (possible score between 0-7)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline rigid restraint at 16 weeks	Three Factor Eating Questionnaire (possible score between 0-7)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline disinhibition at 16 weeks	Three Factor Eating Questionnaire (possible score between 0-16)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline susceptibility for hunger at 16 weeks	Three Factor Eating Questionnaire (possible score between 0-14)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline depression symptoms at 16 weeks	Beck Depression Inventory (possible score between 0-63)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline anxiety symptoms at 16 weeks	State-Trait Anxiety Inventory (possible score between 20-80)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline level of stress at 16 weeks	Perceived Stress Scale (possible score between 0-40)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline sleeping quality at 16 weeks	Pittsburgh Sleep Quality (possible score between 0-21)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline fasting blood glucose at 16 weeks	mmol/L	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline fasting blood insulin at 16 weeks	mmol/L	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline fasting blood leptin at 16 weeks	ng/ml	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline fasting blood cortisol at 16 weeks	nmol/L	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline fasting blood total cholesterol at 16 weeks	mmol/L	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline fasting blood HDL-cholesterol at 16 weeks	mmol/L	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline fasting blood LDL-cholesterol at 16 weeks	mmol/L	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline fasting blood phospholipids at 16 weeks	mmol/L	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline fasting blood triglycerides at 16 weeks	mmol/L	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline fasting blood LDL-apolipoprotein at 16 weeks	mmol/L	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline fasting blood free T4 at 16 weeks	nmol/L	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline fasting blood total T3 at 16 weeks	nmol/L	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline awakening cortisol response at 16 weeks (T0)	Determined from salivary samples taken at the time of awakening (ug/dl)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline awakening cortisol response at 16 weeks (T15min)	Determined from salivary samples taken 15 minutes after the awakening (ug/dl)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline awakening cortisol response at 16 weeks (T30min)	Determined from salivary samples taken 30 minutes after the awakening (ug/dl)	Pre- and post-intervention (week 0 and 16)
Secondary	Change from baseline awakening cortisol response at 16 weeks (T60min)	Determined from salivary samples taken 60 minutes after the awakening (ug/dl)	Pre- and post-intervention (week 0 and 16)