Overweight Clinical Trial
— HAWLSOfficial title:
A Comparison of A Hypocaloric Diet Plus One Hass Avocado Per Day Versus An Equally Hypocaloric Diet for Weight Loss, Satiety, Changes in Body Composition, and Risk Factors for Chronic Disease (HAWLS)
| Verified date | December 2019 |
| Source | University of California, Los Angeles |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
This study will compare two energy reduced diets; one diet will include one Haas avocado/day while the other diet will follow the usual American dietary pattern. All subjects will receive a dietary plan that reduces their usual intake by 500kcal/day with the same percentage of fat, protein and carbohydrates. The results from this study may help to explain if eating one Haas avocado/day can achieve at least equivalent weight loss when compared to the usual American diet.
| Status | Completed |
| Enrollment | 60 |
| Est. completion date | December 20, 2017 |
| Est. primary completion date | December 20, 2017 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 20 Years to 60 Years |
| Eligibility |
Inclusion Criteria: Male or female between the ages of 20-60 years of age. - Body Mass Index (BMI) 27.0 -35.0 kg/m2. - Not currently taking a prescription medication for weight loss (e.g. orlistat (Xenical®), sibutramine (Meridia®) or phentermine etc.) If subject is willing to discontinue prescription medication(s) immediately and willing to refrain from taking medication(s) for duration of study, he/she may be enrolled after a four-week washout period. - Not currently taking any over-the-counter weight loss supplement(s) or appetite suppressants (including OTC stimulants). If subject is willing to discontinue supplement(s) immediately and willing to refrain from taking supplement(s) for duration of study, he/she may be enrolled after a two-week washout period. - Not currently enrolled in any commercial weight loss program (e.g. Jenny Craig, Weight Watchers), internet based weight-management program, self-help group (e.g. TOPS, Overeaters Anonymous) or participating in any food preparation/delivery program (eg Nutrisystems). If subject is willing to discontinue program immediately and willing to refrain from program for duration of study, he/she may be included after a two-week washout period. - Willing to keep and turn in a daily log/compliance book as required by study protocol. - Willingness and ability to make all scheduled appointments. - Willing to follow dietary recommendations required by study protocol. - Willingness to complete Dual X-Ray Absorptiometry (DXA) procedure. - Willingness to periodically have small blood samples drawn as indicated in the protocol. Exclusion Criteria: More than a 5 pound weight gain or weight loss within the 3 months prior to enrollment in the study. - History of thyroid disease, but not taking medication or medication dosage changed one or more times over last 6 months. History of thyroid disease and on a stable dose of prescription medication for 6 months or longer is acceptable. - Diagnosed with Type I or Type II diabetes. History of major surgery within three months of enrollment. - History of heart problems (e.g. angina, bypass surgery, MI, etc.) within three months prior to enrollment. - Presence of implanted cardiac defibrillator or pacemaker. - Uncontrolled hypertension/high blood pressure. - History of a surgical procedure for weight loss at any time (e.g. gastroplasty, gastric by-pass, gastrectomy or partial gastrectomy). - Gastrointestinal disorders including chronic malabsorptive conditions, peptic ulcer disease, Crohn's disease, chronic diarrhea or active gallbladder disease. - History of inflammatory bowel disease. - Following a diet that requires the elimination of FODMAPS• - Following a specific diet that restricts specific food groups (eg. Paleo) or with extreme macronutrient ratios (carbohydrates, fats and proteins). • History of fatty liver. - History or presence of cancer. Persons with successfully resected basal cell carcinoma of the skin may be enrolled if treatment completed more than 6 months prior to enrollment. - History of clinically diagnosed eating disorders including anorexia nervosa, bulimia nervosa or binge eating disorder. - Women who are pregnant, lactating or trying to become pregnant. - Currently taking any prescription medication for less than 3 months. - Currently taking any prescriptions drugs that may impact weight regulation - Currently consuming >14 alcoholic drinks (1 drink = 12 fl oz beer, 4 fl oz wine or 1.5 fl oz liquor) per week and/or unwilling to limit intake to less than 3 drinks per week during study participation. - Known allergy to avocados. - History of alcohol dependency. - Participation in another clinical trial within 30 days prior to enrollment. - Currently smoking cigarettes. - Any clinically significant food allergy. - Currently consuming an average of >1 avocado per week. |
| Country | Name | City | State |
|---|---|---|---|
| United States | UCLA Center for Human Nutrition | Los Angeles | California |
| Lead Sponsor | Collaborator |
|---|---|
| University of California, Los Angeles | Hass Avocado Board |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change in weight loss after consumption of 1 Haas Avocado per day with a hypocaloric diet | Individuals will be randomly assigned to a hypocaloric (500 Cal deficit) meal plans with or without one Hass avocado a day for 12 weeks. | Baseline to 12 weeks | |
| Secondary | Change in gut microbiome | Individuals will be randomly assigned to a hypocaloric (500 Cal deficit) meal plans with or without one Hass avocado a day for 12 weeks. | Baseline to 12 weeks |
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