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Harvard tests cooking classes as a prescription for obesity

NCT ID NCT05628649

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing This study
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether a year-long program that teaches cooking, nutrition, mindfulness, and exercise can help adults with obesity improve their health. 320 participants will attend weekly classes for 16 weeks, then monthly boosters. Researchers will measure changes in eating habits, lab values, and weight. The goal is to see if this approach is practical and effective when added to regular doctor care.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Teaching Kitchen Collaborative Curriculum (behavioral program: cooking, nutrition, mindfulness, exercise, health coaching)
What this could lead to
If it works, this could offer a practical, non-drug way for doctors to help patients with obesity improve eating habits, activity, and weight.
What could go wrong
This is an early feasibility study, not a large-scale effectiveness trial. Results may not apply to everyone, and long-term weight loss is hard to sustain.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 320 people

The number the study aims to enrol. It can still change while the study runs.

Started

Sep 2023

Expected to finish

Dec 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

25 to 70 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Capacity for consent * Adults living independently * English literate * Aged 25-70 (to capture adults living independently) * Diagnosis of class I or II obesity (BMI 30-39.9 kg/m2) * Abnormality in one of the following metabolic markers (fasting plasma concentrations of glucose, insulin, ALT/AST and lipids including cholesterol, triglycerides, LDL, or HDL) * Available and willing to commit to the 18 month study including: 16 consecutive weekly classes; 8 once a month classes; along with assessments at 0, 4, 12, and 18 months. * Participants must be able to commit to both in person and virtually participation * Access to two devices, one device with a camera (smartphone, tablet, computer) * Reliable internet connect in their home * Capable of operating device independently * Minimal operational cooking appliances; specifically cooktop and oven at home. Biometric and Anthropometric Markers: * Fasting glucose - minimum: 100 mg/dL; maximum: 125 mg/dL * Hemoglobin A1C - minimum: 5.7% maximum: 6.4% * Triglycerides - minimum: 150 mg/dL; maximum: 500 mg/dL * LDL - minimum: 130 mg/dL; maximum: 190 mg/dL * HDL - minimum: men \< 40 mg/dL; women \< 50 mg/dL * LDL/HDL ratio - minimum: men \> 3.0; women \> 2.5 * Blood Pressure - minimum: systolic 130 mmHg and diastolic \<80 mmHg; maximum: uncontrolled HTN per PCP * Waist Circumference - minimum: men \> 94 cm; women \> 80 cm * ALT - minimum: men \> 55 unit/L; women \> 30 unit/L; maximum: 4x limit Exclusion Criteria: * Anaphylactic reaction to food allergens * Relocating out of area in the next 18 months * Taking obesity or diabetes medication (with the exception of metformin) as assessed by the study medical director * Current or past diagnosis of Type 1 or 2 diabetes (excluding past gestational diabetes) * History of severe obesity (BMI\>=40kg/m2) * History of bariatric surgery * Current or planned (during study period) participation in a formal longitudinal culinary or weight management program at the time of recruitment (ie-any smart phone apps, a virtual classes, or in person classes or coaching) * Psychiatric hospitalization in the past 12 months * History of significant mental health diagnoses or recent life-threatening illnesses (including unstable cardiovascular disease) * Alcohol or substance abuse within the past 12 months * Diet / exercise contraindications to program participation * Other medical, psychiatric, or behavioral limitations that in the judgment of the principal investigator or study site PI's may interfere with study participation or the ability to follow the intervention protocols determined by each site's PI * Prisoners, pregnant women, and women planning to become pregnant over the next 18 months * Unable or unwilling to give informed consent or communicate per protocol with local study staff * Unwilling or unable to participate in all study-related activities

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Dartmouth Health

    Lebanon, New Hampshire, 03766, United States

  • Harvard Coordinating Site

    Boston, Massachusetts, 02115, United States

  • UTHealth Houston

    Houston, Texas, 77030, United States

  • University of California Irvine

    Irvine, California, 92697, United States

  • University of California Los Angelos

    Los Angeles, California, 90095, United States

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