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Lowering Caloric Density of the Diet (Lower CD)

The University of Tennessee, Knoxville logo

The University of Tennessee, Knoxville

Status

Active, not recruiting

Conditions

Feeding Behavior
Obesity

Treatments

Behavioral: Common components of intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT02674971
UTKIRB-15-02609

Details and patient eligibility

About

For weight loss to occur, energy intake needs to be reduced to incur an energy deficit. One dietary strategy that may facilitate reducing energy intake and enhancing weight loss is consuming a diet low in dietary energy density (ED). The ED of a given food, defined as the ratio of energy of the food to the weight of the food (kcal/g), is largely determined by water content, but is also affected by fat and fiber. Although the 2010 Dietary Guidelines encourage an eating pattern low in energy density (ED) to manage weight, it is currently not known what the best strategy is for reducing ED in the diet. Eating a greater number of foods low in ED or reducing the number of foods high in ED may reduce overall dietary ED. As ED is believed to reduce intake by allowing a greater weight of food relative to total energy consumed assisting with enhancing feelings of fullness, it is anticipated that either increasing consumption of low-ED foods in the diet alone or combining an increase in consumption of low-ED foods with a decrease in consumption of high-ED foods may be the best strategies for reducing overall dietary ED for weight loss.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

    1. age between 18 and 65 years and 2) a body mass index (BMI)7 between 27 and 45 kg/m2.

Exclusion criteria

  1. report a heart condition, chest pain during periods of activity or rest, or loss of consciousness on the Physical Activity Readiness Questionnaire (PAR-Q)8 (medical conditions that could limit exercise for safety reasons will be required to obtain written physician consent before participating in the investigation)
  2. report being unable to walk for 2 blocks (1/4 mile) without stopping
  3. are currently participating in a weight loss program and/or taking weight loss medication or lost > 5% of body weight during the past 6 months
  4. report major psychiatric diseases or organic brain syndromes
  5. have had bariatric surgery or are planning to have bariatric surgery within the next 4 months
  6. intend to move outside of the metropolitan area within the time frame of the investigation
  7. are pregnant, lactating, < 6 months post-partum, or plan to become pregnant during the investigation.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

INCREASE
Active Comparator group
Description:
This condition will be instructed to make food consumption decisions based solely upon the ED of a food. The goal of the ED condition will be to consume at least 10 foods ≤ 1.0 kcal/g (i.e., fruits and vegetables, broth based soups, non-fat yogurts, some legumes, egg substitutes, some white fish, etc.) per day.
Treatment:
Behavioral: Common components of intervention
COMBINATION
Active Comparator group
Description:
This condition will be identical to the INCREASE condition, except it will also have a goal regarding the number of high-ED foods to consume and substituting low-ED foods for high-ED foods. Thus, this condition will have ED goals to consume at least 10 foods ≤ 1.0 kcal/g (i.e., fruits and vegetables, broth based soups, non-fat yogurts, some legumes, egg substitutes, some white fish, etc.) and no more than 2 foods ≥ 3.0 kcal/g (i.e., crackers, chips, cookies, hard cheeses, hot dogs, salad dressings, etc.) per day. Foods with an ED \>1.0 kcal/g but \< 3.0 kcal/g will be unlimited; however, lower ED foods will be strongly encouraged. Furthermore, additions to beverages (i.e., sugar, cream) will count toward the \> 3.0 kcal/g goal if the additions meet that ED criteria.
Treatment:
Behavioral: Common components of intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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