ClinicalTrials.Veeva

Menu

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

Washington State University logo

Washington State University

Status

Completed

Conditions

Hypertension
Cardiovascular Diseases
Diet
Blood Pressure

Treatments

Other: Ready-to-eat meals

Study type

Interventional

Funder types

Other

Identifiers

NCT05472454
19288-001

Details and patient eligibility

About

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.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Ready-to-eat meals
Other group
Description:
Pre-Post
Treatment:
Other: Ready-to-eat meals

Trial contacts and locations

1

Loading...

Central trial contact

Martine Perrigue, PhD, RDN, CD; Anna Gisselman, MS

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems