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NCT06919536 · ClinicalTrials.gov registry record
Controlled Feeding With 24 Hour Recall
A clinical trial of Evaluate Accuracy 24 Dietary Recall, sponsored by Texas Tech University.
- Completed
- Registry status
- 75
- Enrollment target
- 1
- Study location
NCT06919536: Completed study of Evaluate Accuracy 24 Dietary Recall, sponsored by Texas Tech University.
NCT06919536 is a study of Evaluate Accuracy 24 Dietary Recall that has completed, run by Texas Tech University. The registered enrollment target is 75 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06919536, a study of Evaluate Accuracy 24 Dietary Recall, has completed, sponsored by Texas Tech University.
- COMPLETED
- Registry status
- 75 participants
- Enrollment target
- 1
- Study location
Study 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.
Primary Outcome
The primary outcome is the difference between the calories of weighed actual intake and the reported intake from the ASA\_24
Conditions Studied
Interventions
- OTHER No intervention (observational study)
Study Locations (1)
Texas
- Texas Tech University Nutrition and Metabolic Health Initiative - Lubbock
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 75 participants |
| Start Date | 2025-04-21 |
| Est. Completion | 2025-09-22 |
What the finished NCT06919536 record still lists
NCT06919536 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 75 participants, a relatively small participant target.
The record links to 1 condition, with Evaluate Accuracy 24 Dietary Recall appearing as the primary indexed condition, and to 1 intervention - of which No intervention (observational study) is the first listed.
NCT06919536 reports a single indexed study location in Texas.
Frequently Asked Questions
What is clinical trial NCT06919536 about?
NCT06919536 is a clinical study titled "Controlled Feeding With 24 Hour Recall". 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 un...
What is the current status of trial NCT06919536?
This trial is currently completed. The enrollment target is 75 participants. The study started on 2025-04-21. Estimated completion is 2025-09-22.
What conditions does trial NCT06919536 study?
This clinical trial studies the following conditions: Evaluate Accuracy 24 Dietary Recall.
What interventions are being tested in trial NCT06919536?
The interventions under investigation include: No intervention (observational study) (OTHER).
Who is sponsoring clinical trial NCT06919536?
This trial is sponsored by Texas Tech University, which has 69 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06919536 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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