A Clinical Trial to Evaluate the Efficacy of a Healthy Meal Plan in Improving Health Biomarkers and Promoting Healthy Weight Management.
1 other identifier
interventional
100
1 country
1
Brief Summary
This is a 16-week, two-arm, hybrid, randomized controlled clinical trial designed to evaluate the effect of the Green Chef Calorie Smart \& Brain Health meal plans on health biomarkers and perceived well-being. The study aims to measure improvements in blood lipids, body composition, weight, and blood pressure, as well as subjective health indicators through surveys.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 19, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2025
CompletedFirst Submitted
Initial submission to the registry
August 21, 2025
CompletedFirst Posted
Study publicly available on registry
August 26, 2025
CompletedAugust 26, 2025
August 1, 2025
7 months
August 21, 2025
August 21, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Change in Blood Lipid Biomarkers (LDL, HDL, Triglycerides)
Blood lipid levels (LDL, HDL, triglycerides) will be measured at baseline and week 16 via fasting blood draws to evaluate the effect of the Green Chef meal plan on cardiovascular health.
Baseline to Week 16
Change in Weight and Body Composition
Body weight and composition will be measured using a Withings smart scale at baseline, week 8, and week 16 to assess changes related to the dietary intervention.
Baseline, Week 8, Week 16
Change in Blood Pressure
Systolic and diastolic blood pressure will be measured using a Withings smart blood pressure cuff at baseline, week 8, and week 16 to assess impact of the meal plan on cardiovascular function.
Baseline, Week 8, Week 16
Secondary Outcomes (1)
Change in Self-Reported Health Perceptions
Baseline, Week 4, Week 8, Week 12, Week 16
Study Arms (2)
Intervention Group
EXPERIMENTALParticipants in the intervention group will receive Green Chef meals for lunch and dinner, along with guidelines for preparing healthy breakfasts. Participants will follow this diet for 16 weeks.
Control Group
NO INTERVENTIONParticipants in the control group will continue their usual eating habits with no dietary changes for 16 weeks.
Interventions
Participants will receive Green Chef meals for lunch and dinner, delivered weekly for 16 weeks. Meals include organic produce, responsibly sourced protein, and nutritionist-approved recipes. Participants will also receive guidelines for preparing healthy breakfasts and will use smart devices to record biomarker data.
Eligibility Criteria
You may qualify if:
- Males and females aged 25 years or older.
- Participants who struggle with healthy weight management and have a desire to lose weight.
- Participants who eat takeout or at restaurants at least four times per week.
- Participants not currently using a meal kit.
- Participants who are willing to cook meals twice daily for the 16-week study period.
- Participants who are willing to cook and consume meals as instructed, fill out regular questionnaires, take regular weight and blood pressure measurements, and attend blood tests at Quest for Baseline and Endline assessments for the 16-week study period.
- Participants must not have introduced any new prescription medications, supplements, or herbal remedies targeting weight management within the past three months.
- Participants must be willing to discontinue any prescription medications, supplements, or herbal remedies that target weight management for the duration of the trial.
- Participants must agree to not introduce any new prescription medications, vitamins, minerals, nutraceuticals, or herbal supplements for the duration of the trial.
- Participants must consider themselves in good general health and not have any chronic health conditions that could impact their participation in the study.
- Participants must reside in the United States.
You may not qualify if:
- Individuals who have undergone surgeries or invasive treatments in the last six months or have any planned for the duration of the trial.
- Individuals who have undergone weight loss surgery.
- Individuals who have experienced dramatic weight changes (gain or loss) within the past three months.
- Individuals who consider themselves to be chronic dieters or "always on a diet" (e.g., those who have been dieting or restricting calories for a prolonged period of time or who tend to jump from one diet to the next regularly).
- Individuals with a known history of severe digestive disorders, including but not limited to acid reflux, Irritable Bowel Syndrome (IBS), Inflammatory Bowel Disease (IBD), ulcerative colitis (UC), Crohn's disease, or gastrointestinal tract surgeries.
- Individuals with a known history of any chronic illness such as hypertension, diabetes, or cancer.
- Individuals with any known allergies or hypersensitivities to foods.
- Individuals with a history of disordered eating behaviors or an eating disorder.
- Individuals who regularly take laxatives, or antacids.
- Individuals who regularly take anticoagulants (also referred to as blood thinners).
- Individuals with chronic health conditions, including oncological or psychiatric disorders, that could impact participation.
- Individuals with known serious allergic reactions requiring the use of an Epi-Pen.
- Individuals who are currently pregnant, trying to conceive, or breastfeeding.
- Individuals currently participating or planning to participate in another research study within the next 16 weeks.
- Individuals with a history of substance abuse.
- +2 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Green Chef Corporationlead
- Citruslabscollaborator
Study Sites (1)
Citruslabs
Las Vegas, Nevada, 89118, United States
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 21, 2025
First Posted
August 26, 2025
Study Start
November 19, 2024
Primary Completion
June 30, 2025
Study Completion
June 30, 2025
Last Updated
August 26, 2025
Record last verified: 2025-08