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The Influence of Factors on Accuracy of Reported Dietary Intake

The University of Tennessee, Knoxville logo

The University of Tennessee, Knoxville

Status

Completed

Conditions

Dietary Restraint
Dietary Assessment
24-hour Dietary Recall
Social Desirability

Treatments

Other: Lunch meal with 24 hour dietary recall

Study type

Interventional

Funder types

Other

Identifiers

NCT00939016
University of TN IRB 7701 B

Details and patient eligibility

About

The purpose of this study is to evaluate the influence of dietary restraint, social desirability, and food type on the accuracy of dietary intake reported during a 24-hour recall.

Full description

The purpose of this study is to investigate the influence of the interaction among dietary restraint, social desirability, and food type ("healthy" vs. "unhealthy") on the accuracy of reporting consumption of a laboratory meal during a 24-hour dietary recall. The automated multiple-pass method (AMPM) of 24-hour dietary recall is considered the gold standard of dietary assessment however the potential for error and biases is widely acknowledged with a tendency towards underreporting. Underreporting has been linked to many factors including two individual characteristics, dietary restraint and social desirability. Both dietary restraint and social desirability have been extensively studied however the influence of their interaction on reported dietary intake is not fully understood. In addition, a relationship to the types of foods (healthy vs. unhealthy) has also been found. For this study, 40 normal-weight female participants will be recruited at The University of Tennessee using flyers inviting volunteers. Participants will be categorized by dietary restraint, high or low, and social desirability, high or low, based on questions during the initial screening. In a laboratory setting participants will consume a meal of pre-weighed foods, including both "healthy" and "unhealthy" foods. The following day, an AMPM 24-hr dietary recall will be conducted with the participant over the telephone. Accuracy of the reported dietary intake of the laboratory meal will be determined by the equation [(reported intake - measured intake)]/measured intake] x100 for amount (weight or volume) and energy (kilocalories) with comparisons between groups and within food types using mixed factorial analysis of variance.

Enrollment

40 patients

Sex

Female

Ages

18 to 25 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Normal weight status (BMI 18.5-24.9)
  • Willing to sample study foods

Exclusion criteria

  • Individuals majoring in Nutrition or Exercise Science
  • Smokers
  • Individuals taking medication for ADHD
  • Individuals who are pregnant
  • Individuals with allergies to food in study

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

Single Blind

40 participants in 4 patient groups

High SD/ Low DR
Active Comparator group
Description:
This group contains females that exhibit characteristics of high social desirability and low dietary restraint.
Treatment:
Other: Lunch meal with 24 hour dietary recall
High SD/ High Dr
Active Comparator group
Description:
This group contains females that exhibit characteristics of high social desirability and high dietary restraint.
Treatment:
Other: Lunch meal with 24 hour dietary recall
Low SD/ High DR
Active Comparator group
Description:
This group contains females that exhibit characteristics of low social desirability and high dietary restraint.
Treatment:
Other: Lunch meal with 24 hour dietary recall
Low SD/ Low DR
Active Comparator group
Description:
This group contains females that exhibit characteristics of low social desirability and low dietary restraint.
Treatment:
Other: Lunch meal with 24 hour dietary recall

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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