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Completed

NCT Number: NCT03869658

Food Talk: A New App for Daily Food Monitoring

This project will pilot test a new app for self-monitoring food intake using natural spoken language (by voice recognition or text) to provide daily estimates of energy and nutrient intakes with a phone app.

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Human Nutrition Research Center on Aging

Boston, Massachusetts, 02111, United States

About this study

Self-recording food intake is recommended for weight management and healthy eating. However, current methods, including web platforms and apps, are often burdensome leading to short-term use by the consumer. The solution uses cutting-edge speech and language understanding technology to streamline the food logging process. With this technology, the user simply describes what they ate and the system automatically selects the appropriate items and quantities consumed from the USDA food database, which calculates the nutrition profile of the entry.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Generally healthy men and women 18-65 years if age
  • Currently participating in ongoing studies at the HNRCA
  • Willing and able to sign written informed consent prior to study entry
  • iPhone (iOS 11 or higher) user willing to download the COCO application and record food intake for 5 days

Exclusion criteria

  • Android or iPhone (iOs 10 or lower) user unable to download and use the COCO application
  • Holds a graduate degree in nutrition

Treatment and study plan

COCO application

Behavioral

All participants will complete a screening survey to determine their eligibility for the study, if eligible and willing to participate, he or she will sign an informed consent form. Once participants are enrolled in the study, a demographics questionnaire will be completed along with 5 days of food tracking on the COCO application. Between days 3 and 7, participants will complete two 24-hr diet recall, one a day, and a patient satisfaction questionnaire.

Primary outcomes

  1. Change in energy intake using food application COCO

    Time frame: Between days 3 and 7 of the study

    The primary outcome will be to assess whether food capture using the mobile application is comparable with conventional 24-hour dietary recall. This will be done by measuring the energy intake (mean of two days) in the two methods.

  2. Change in energy intake using 24 hour dietary recall

    Time frame: Between days 3 and 7 of the study

    The primary outcome will be to assess whether food capture using the mobile application is comparable with conventional 24-hour dietary recall. This will be done by measuring the energy intake (mean of two days) in the two methods.

Secondary outcomes

  1. Accuracy of food capture method using mobile application

    Time frame: Between days 3 and 7 of the study

    The secondary outcome will measure the energy and nutrient content reported by the mobile application over time. Measured energy intake in a subset of participants in another study that provides dietary intake data will be compared to food intake data using the mobile application.

Other outcomes

  1. Application feasibility

    Time frame: Betweens days 5 and 7

    Feasibility of the use of the application to record dietary intake will be measured through a patient satisfaction questionnaire.

Sponsors and collaborators

Lead sponsor

Tufts University

Other

Collaborators

  • Massachusetts Institute of Technology

Registry information

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Mar 11, 2019
Registry last updated
Sep 13, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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