Impact of Almond Supplementation on Body Composition in Overweight/Obese Minority Adults
| Status: | Active, not recruiting |
|---|---|
| Conditions: | Obesity Weight Loss, Obesity Weight Loss, Endocrine, Gastrointestinal |
| Therapuetic Areas: | Endocrinology, Gastroenterology |
| Healthy: | No |
| Age Range: | 30 - 65 |
| Updated: | 7/19/2018 |
| Start Date: | October 2014 |
| End Date: | December 31, 2018 |
Impact of Almond Supplementation, Relative to a Low-fat, High Carbohydrate Control, on Body Composition in Overweight and Obese Black and Hispanic Adults
The purpose of this study is to determine whether introducing almonds into the diet of
overweight and obese Blacks and Hispanics improves body composition, decreases liver fat, and
lowers cardiovascular disease profile.
overweight and obese Blacks and Hispanics improves body composition, decreases liver fat, and
lowers cardiovascular disease profile.
The study is a randomized, controlled study aimed at testing whether almonds, consumed within
a free-living, self-selected diet, improve body composition and liver fat, relative to a
low-fat/high-carbohydrate cereal bar (LF-HC) in overweight and obese Blacks and Hispanics. A
secondary aim is to determine whether almond consumption will lead to an overall lower CVD
risk profile.
Participants will be randomized to consume approximately 17.5% of their estimated energy
requirements from almonds daily (2-3 oz) or a high-carbohydrate cereal bar (2 g of fat or
less per 100 kcal) providing an equivalent amount of calories. Prescribed energy requirements
will be determined for each participant individually using the Mifflin St Jeor Equation
equation with an activity factor of 1.3. Participants will be asked to consume half of their
food supplement as a mid-afternoon snack and the rest at a meal of their choice.
At the baseline visit, participants will be given a 2-week supply of their allocated food
supplement and will obtain additional supplies at bi-weekly visits for the first 8 weeks.
After the week 8 visit, participants will be given monthly rations of their food supplement,
either almonds or LF-HC cereal bar, and will be asked to come to research center every 4
weeks to obtain their next supply. At those visits, body weight and blood pressure will be
measured and participants will turn in weekly dietary diaries, reporting their supplement
intake. Participants will also receive one random phone call every 4 weeks to provide a 24-h
recall. This recall will be used as an index of dietary quality but also as a compliance
check with dietary supplements. In addition, 3-day food records will be collected prior to
the start of the study and during the final week to assess any dietary changes due to the
intervention. A food frequency questionnaire will also be administered at screening and
endpoint of the study. This food-frequency questionnaire will target nut consumption.
At the end of the study, intention to continue eating almonds or a low-fat diet will be
assessed using questions adapted from de Bruijn et al. Participants in the almond group will
be asked the following questions: (1) "I intend to include almonds in my diet" (+2 = yes,
definitely; -2 = no, definitely); (2) "How certain are you that you will include almonds in
your diet?" (+2 = very certain; -2 = very uncertain); (3) "Including almonds in my diet is"
(instrumental attitude: +3 = healthy; -3 = unhealthy; affective attitude: +3 = pleasant; -3 =
unpleasant); (4) "I find including almonds in my diet" (perceived behavioral control: +3 =
easy; -3 = difficult). Corresponding questions for the control group will replace "include
almonds" with "reduce the amount of fat". Participants will be called 4 weeks later to obtain
information on their actual almond and fat intakes by questionnaire and 24-h recall.
a free-living, self-selected diet, improve body composition and liver fat, relative to a
low-fat/high-carbohydrate cereal bar (LF-HC) in overweight and obese Blacks and Hispanics. A
secondary aim is to determine whether almond consumption will lead to an overall lower CVD
risk profile.
Participants will be randomized to consume approximately 17.5% of their estimated energy
requirements from almonds daily (2-3 oz) or a high-carbohydrate cereal bar (2 g of fat or
less per 100 kcal) providing an equivalent amount of calories. Prescribed energy requirements
will be determined for each participant individually using the Mifflin St Jeor Equation
equation with an activity factor of 1.3. Participants will be asked to consume half of their
food supplement as a mid-afternoon snack and the rest at a meal of their choice.
At the baseline visit, participants will be given a 2-week supply of their allocated food
supplement and will obtain additional supplies at bi-weekly visits for the first 8 weeks.
After the week 8 visit, participants will be given monthly rations of their food supplement,
either almonds or LF-HC cereal bar, and will be asked to come to research center every 4
weeks to obtain their next supply. At those visits, body weight and blood pressure will be
measured and participants will turn in weekly dietary diaries, reporting their supplement
intake. Participants will also receive one random phone call every 4 weeks to provide a 24-h
recall. This recall will be used as an index of dietary quality but also as a compliance
check with dietary supplements. In addition, 3-day food records will be collected prior to
the start of the study and during the final week to assess any dietary changes due to the
intervention. A food frequency questionnaire will also be administered at screening and
endpoint of the study. This food-frequency questionnaire will target nut consumption.
At the end of the study, intention to continue eating almonds or a low-fat diet will be
assessed using questions adapted from de Bruijn et al. Participants in the almond group will
be asked the following questions: (1) "I intend to include almonds in my diet" (+2 = yes,
definitely; -2 = no, definitely); (2) "How certain are you that you will include almonds in
your diet?" (+2 = very certain; -2 = very uncertain); (3) "Including almonds in my diet is"
(instrumental attitude: +3 = healthy; -3 = unhealthy; affective attitude: +3 = pleasant; -3 =
unpleasant); (4) "I find including almonds in my diet" (perceived behavioral control: +3 =
easy; -3 = difficult). Corresponding questions for the control group will replace "include
almonds" with "reduce the amount of fat". Participants will be called 4 weeks later to obtain
information on their actual almond and fat intakes by questionnaire and 24-h recall.
Inclusion Criteria:
- Black and/or Hispanic
- Body Mass Index (BMI) 25-35 kg/m^2
- Weight stable (+/- 2.5 kg) for at least 3 months prior to screening
- Body weight less than 300 pounds
- Adherence to an acceptable form of contraception (for women)
- If taking medicine, dose must have been stable before study; must remain on same
medication and dose throughout study.
Exclusion Criteria:
- Diabetes
- Uncontrolled hypertension (high blood pressure)
- Cardiovascular disease
- Weight loss attempted in past 3 months
- Eating disorder
- Stroke, seizure disorder, or significant neurological disease
- Unstable of uncontrolled medical illness including active malignancies within past 5
years
- Untreated or unstable hypothyroidism
- Hyperthyroidism
- Diagnosis of psychoses, bipolar disorder, major depression, severe personality
disorder; history of suicidal tendencies
- Alcohol or substance abuse in the past 6 months
- Pregnant, planning pregnancy in the next 6 months, or breast-feeding
- Participating or planning to participate in a commercial diet or behavior modification
program (ex: Weight Watchers)
- Allergy or sensitivity to wheat/grain products or nuts
- Gastrointestinal disorder.
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