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Controlled Feeding With 24 Hour Recall

Controlled Feeding With 24 Hour Recall

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06919536
Enrollment
75
Registered
2025-04-09
Start date
2025-04-21
Completion date
2025-09-22
Last updated
2025-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Evaluate Accuracy 24 Dietary Recall

Keywords

24 hour dietary recall, self report dietary intake, food frequency questionnaire, underreporting dietary intake, overreporting dietary intake, validity of 24 hour dietary recall, nutrition self report accuracy

Brief summary

This study examines how accurately adults report their food intake using a common self-report method called the 24-hour dietary recall. While this method is widely used in nutrition research, it often leads to underreporting, especially among individuals with overweight or obesity. However, it is unclear if specific foods are more likely to be misreported. To address this, participants will be served a controlled meal containing both simple foods (e.g., fruit snacks, saltine crackers, cookies, and a coke soft drink) and mixed dishes (e.g., chicken salad, macaroni and cheese with peas). Each food item will be precisely weighed before and after consumption. The following day, participants will complete an online 24-hour recall, and the process will be repeated one week later. The study will compare reported intake to actual intake to assess accuracy and determine whether underreporting is more common for mixed dishes. It will also explore whether reporting accuracy is influenced by body weight, gender, or race. Findings from this research may improve the understanding of self-report limitations and support the development of more accurate dietary assessment tools.

Detailed description

This prospective observational cohort study with repeated measures investigates the accuracy of self-reported dietary intake using the 24-hour dietary recall method, specifically the Automated Self-Administered 24-hour Dietary Assessment Tool (ASA-24). Research has consistently shown that individuals underreport energy intake using self-report tools, particularly those with overweight or obesity. However, there is limited understanding of which types of foods are most prone to misreporting and whether such tendencies are consistent across time or demographic groups. To address these gaps, this study uses a controlled feeding protocol in which participants consume a standardized lunch consisting of two mixed dishes (chicken salad and macaroni and cheese with peas) and single-item foods (e.g., fruit snacks, saltine crackers, cookies, and a coke soft drink). All foods are weighed precisely before and after consumption to the nearest 0.01g. The following day, participants complete an online 24-hour dietary recall using ASA-24. This process is repeated one week later to assess reproducibility of reporting patterns. The primary outcome is the portion-size reporting difference between actual and reported intake for each food item. Secondary outcomes include whether mixed dishes are more inaccurately reported than discrete foods, and whether underreporting is consistent across both sessions. Additional analyses will evaluate whether underreporting varies by BMI category, gender, or race. Participants (N=65) are adults aged 18-65 recruited from the Texas Tech University community using flyers, email announcements, and word of mouth. Inclusion criteria include availability to attend lunch visits and complete online recalls. Exclusion criteria include food allergies or aversions to the test meal.

Interventions

OTHERNo intervention (observational study)

There is no intervention, this is a observational study,

Sponsors

Texas Tech University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Able to attend the test site for a meal at least two times.

Exclusion criteria

* Any aversions to the test meal (including allergies)

Design outcomes

Primary

MeasureTime frameDescription
Per-item Portion-Size Difference (Weighed - 24-hour recall)From enrollment to 2 weeks (1 measurement with a ASA-24 the next day, and another identical measurement with recall the next day)The primary outcome is the difference between the calories of weighed actual intake and the reported intake from the ASA\_24

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026