Can cooking classes cut heart risk? new study tests community approach
NCT ID NCT04305431
First seen Jun 27, 2026 · Last updated Sep 17, 2026 · Updated 10 times
Summary
This study explores whether a community-based cooking program can help African-American adults at risk for heart disease cook and eat healthier. About 43 participants from Washington, D.C. will take surveys, attend cooking classes led by a chef, and track their eating habits. The goal is to see if the program is practical and well-received, not to test a medical treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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43 people
The number who actually took part.
- Started
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Feb 2021
- Expected to finish
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Aug 2028
An estimate. End dates often move.
- Lead sponsor
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A government research agency
The lead sponsor is the US National Institutes of Health.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 99 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
* FIRST PHASE: A sample of AA adults (n= 20) living in Wards 7 or 8 of Washington, D.C. will be recruited for this phase. INCLUSION CRITERIA: English-speaking Self-identified AA adults (defined as age greater than or equal to 18) Live in Wards 7 or 8 in Washington, D.C. At least one self-reported risk factor for CV disease known by participant or told to participant by a clinician within the last 12 months. Specific risk factors are: * overweight or obese (self-reported height and weight compute to BMI if needed greater than or equal to 25) * elevated waist to hip ratio * elevated cholesterol * clinical hypertension or prehypertension * prediabetes * elevated fasting glucose level on laboratory report * current smoker or prior (within the past 12 months) smoker. EXCLUSION CRITERIA: Under the age of 18 Do not live in Wards 7 or 8 in Washington, D.C. No risk factors for CVD Or adults not of AA descent (self-identified) Non-English speaking SECOND PHASE: A sample of AA adults (n= 35) living in Wards 7 or 8 of Washington, D.C. will be recruited for this phase. INCLUSION CRITERIA: English-speaking Self-identified AA adults (defined as age greater than or equal to 18) Who live in Wards 7 or 8 in Washington, D.C. At least one self-reported risk factor for CV disease known by participant or told to participant by a clinician within the last 12 months. Specific risk factors are: * overweight or obese (self-reported height and weight compute to BMI if needed \>= 25) * elevated waist to hip ratio * elevated cholesterol * clinical hypertension or prehypertension * prediabetes * elevated fasting glucose level on laboratory report * current smoker or prior (within the past 12 months) smoker. Not pregnant at the time of screening and enrollment.\* Willing to not attend or enroll in another cooking/culinary education program or class during participation in this study Not enrolled currently or in the prior 12 months (at time of recruitment) in another ongoing cooking/culinary education program or class EXCLUSION CRITERIA: AAs who are not age greater than or equal to 18 AA Adults not living in Wards 7 or 8 in Washington, D.C. AA Adults living in the same household as another participant AA adults without at least one risk factor for CVD Or adults not of AA descent Non-English speaking Those enrolled currently or in the prior 12 months at time of recruitment in another ongoing cooking/culinary education program Those not willing to not attend or enroll in another cooking/culinary education program or class during participation in this study \* If individuals become pregnant during their participation, they can continue to participate if they want to. The pregnant participant will not undergo DEXA scanning procedure.
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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
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National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
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Other studies related to the condition(s) this trial covers.
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