FOOD PRESCRIPTION APP

NCT ID: NCT05562180

Last Updated: 2024-07-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Clinical Phase

PHASE2/PHASE3

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-04-08

Study Completion Date

2025-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study will develop and test and app that will create meal plans to improve diet quality and support weight loss. This app will allow participants to customize their meal plans and substitute recipes for nutritionally equivalent options that they find more appealing, thus potentially increasing adherence.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

We are specifically planning app to create meal plans that are affordable, meet the recommended dietary allowances (RDAs) and adhere to sustainability guidelines to reduce the food-related carbon footprint. The app will enable participants to customize their weekly meal plans. We hypothesize that having the ability to customize the weekly menus through a FoodRx app will improve outcomes, as the lack of customization appeared to be a barrier for some families to improve their diet quality and achieve weight loss goals. (eg, some families did not like tofu or oatmeal, and would have preferred a substitute). We will be able to test the impact of the Food Rx app by comparing participants who use it to our control group that does not currently have access to the standard menus/grocery delivery or FoodRx app.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Diet, Healthy

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Intervention arm

These participants will use the app to customize their weekly meal plan and grocery delivery

Group Type EXPERIMENTAL

Customized meal plan and grocery delivery

Intervention Type BEHAVIORAL

Participants will use an app to customize their meal plans

comparison

These participants will not receive a weekly meal plan and will not get grocery delivery

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Customized meal plan and grocery delivery

Participants will use an app to customize their meal plans

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

Already enrolled in FoodRx study \>18 years BMI\>27 and wants to lose weight -

Exclusion Criteria

Not enrolled in Food Rx

\-
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Kaiser Permanente

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Deborah A Cohen

Research Scientist

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Kaiser Permanente

Pasadena, California, United States

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

United States

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Kelly Lopez, MPH

Role: CONTACT

(626) 564-7752

Deborah A Cohen, MD, MPH

Role: CONTACT

626 564 7705

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Deborah A Cohen, MD, MPH

Role: primary

626-564-7705

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

3P50MD017344-02S1

Identifier Type: NIH

Identifier Source: org_study_id

View Link

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Food Insecurity, Social Determinants of Health
NCT06784310 ACTIVE_NOT_RECRUITING NA
RHWP Prescription Produce Plan
NCT04995237 COMPLETED NA
PortionSize Study 2 Free-Living Evaluation
NCT05166226 ACTIVE_NOT_RECRUITING
Attentive Eating for Weight Loss
NCT03602001 COMPLETED NA
Food as Medicine for Families
NCT06160973 COMPLETED NA
Medifast 5 & 1 Plan
NCT01211301 COMPLETED NA