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The Ready-to-Eat Meals for Cardiovascular Health Study

The Ready-to-EAt Meals for Cardiovascular Health (REACH) Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05472454
Acronym
REACH
Enrollment
20
Registered
2022-07-25
Start date
2022-10-07
Completion date
2023-05-01
Last updated
2026-06-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blood Pressure, Cardiovascular Diseases, Diet, Hypertension

Keywords

DASH, Dietary Approaches to Stop Hypertension, Meals, High Blood Pressure, Hypertension

Brief summary

The proposed project explores the acceptability and health benefits of ready-to-eat (RTE) meals based on the Dietary Approaches to Stop Hypertension (DASH) eating plan. The researchers have developed 14 recipes following the DASH eating plan, which is recommended for the prevention of cardiovascular disease (CVD). The prepackaged meals will be processed using Washington State University (WSU) microwave technologies to ensure food safety. In this pilot study, a sample of 30 participants will be recruited by to study the impact of the DASH meals on blood pressure. All meals will be provided to participants, who will consume the meals daily over a period of 4 weeks. Daily and weekly monitoring of participants (blood pressure and weight) will allow us to gain a scientific understanding on the preventive power of healthy diets in lowering blood pressure and reducing CVD risk.

Interventions

OTHERReady-to-eat meals

Participant group to consume ready-to-eat meals in accordance with the DASH diet for a period of 4 weeks.

Sponsors

Washington State University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Pre-post design

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Male or female * 18 years old or older * BMI 18.5-40.0 kg/m2 * Daily access to working internet, microwave, refrigerator, and freezer * English fluency

Exclusion criteria

* Regular use of drugs that affect BP, including weight loss medications * Diagnosed hypertension OR systolic BP \>130 and/or diastolic BP \>80 * Diagnosis of any hypotensive disorders OR systolic BP \<100 and/or diastolic BP\<65 * Dietary restrictions, including allergy/intolerances * Presence or history of diabetes * Previous cardiac event, congestive heart failure, or angina * Weight loss or gain\>15lb in previous 3 months * Following a diet to increase or decrease body weight * Cancer diagnosis or treatment in past 2 years * ≥14 alcoholic drinks/week for men; ≥ 7 alcoholic drinks/week for women * Use of nicotine, marijuana, or illicit drugs * Pregnancy, planned pregnancy, or breastfeeding * Inability to comprehend the nature of the study or instructions * No access to the internet * Planning to leave the Spokane area during the study * Not fluent in the English language

Design outcomes

Primary

MeasureTime frameDescription
Blood pressurethrough study completion, measured weekly for 5 weeksTo determine dietary patterns on blood pressure using an omron blood pressure monitor.

Secondary

MeasureTime frameDescription
Body weight (kg)through study completion, measured weekly for 5 weeksTo determine dietary patterns on body weight (kg) using a Angel USA 400 Pound Physician Digital Scale.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORPablo Monsivais, PhD, MPH

Washington State University

PRINCIPAL_INVESTIGATORMartine M Perrigue, PhD, RDN

Washington State University

PRINCIPAL_INVESTIGATORCatherine Jarrett, PhD, RDN

Washington State University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 4, 2026