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AdapTive Personalized Dietitian coacHing, Messaging and pRoduce prescrIption to improVE Healthy Dietary Behaviors

THRIVE: AdapTive Personalized Dietitian coacHing, Messaging and pRoduce prescrIption to improVE Healthy Dietary Behaviors

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06257550
Acronym
THRIVE
Enrollment
80
Registered
2024-02-14
Start date
2024-06-10
Completion date
2025-10-31
Last updated
2025-11-05

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

Conditions

Hypertension

Brief summary

THRIVE intervention is a 2-arm randomized pilot trial testing the feasibility and preliminary efficacy of producing prescriptions, tailored dietitian counseling with adaptive messages, and linkages to social resources among 80 Black adults with hypertension.

Detailed description

Nearly 55% of Black adults have hypertension and uncontrolled blood pressure. Dietary Approaches to Stop Hypertension (DASH) promotes a dietary pattern rich in fruits and vegetables (fruits and vegetables), low-fat dairy, lean meats with reduced saturated fat, and sweets, which is effective in lowering blood pressure. The proposed THRIVE intervention will enroll 80 Black adults with hypertension living in Healthy Food Priority Areas (HFPAs) in a 2-arm randomized pilot study. One group will receive Produce prescriptions, personalized dietitian coaching, and adaptive bi-directional messaging; the other group will receive standard produce bags. Both groups will be linked to needed social services. The investigators will assess changes in overall DASH adherence, acceptability, and feasibility at 3- and 6-months post-randomization. The investigators will: 1) Develop and beta test THRIVE among Black adults with hypertension living in HFPAs; 2) Test feasibility and preliminary efficacy of THRIVE at 6 & 12 weeks; 3) Determine short-term sustainability of THRIVE at 6 months.

Interventions

THRIVE Intervention includes: 1. Weekly Pulse Surveys 2. Adaptive culturally tailored messages 3. Personalized Dietitian Coaching 4. Produce Prescription FARMacy Mobile Market 5. Linkages to Social Services

BEHAVIORALActive Comparator

The Active Comparator arm will receive standard produce bags through our food is medicine partner, and will receive the linkages to needed social and health resources intervention components.

Sponsors

American Heart Association
CollaboratorOTHER
Johns Hopkins University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

Outcomes assessors and data analysts will be masked to treatment allocation.

Eligibility

Sex/Gender
ALL
Age
18 Years to 79 Years
Healthy volunteers
Yes

Inclusion criteria

1. 18 years or older 2. Self-identify as Black/African American 3. Have diagnosed hypertension stages 1 (130-139/80-89 mm Hg) OR 2 (\>140/90 mm Hg), determined via self-report and/or Electronic Medical Records (EMR) 4. Live in census tracts identified by Montgomery County Department of Planning as HFPA: 1. Healthy Food Availability Index score is low (0-9.5), 2. Median household income ≤185% of Federal Poverty Level 3. \>30% households have no vehicle, Distance to supermarket \>1/4 mile. 5. Participants must have refrigeration, food appliances (microwave, stove), 6. Cell phone to receive messages

Exclusion criteria

1. Age \<18 years 2. Type 1 or Type 2 Diabetes defined as a hemoglobin A1c ≥6.5% or diabetes treatment 3. Diagnosis of end-stage renal disease (ESRD) 4. Condition which interferes with outcome measurement (e.g., dialysis) 5. Serious medical condition which either limits life expectancy or requires active management (e.g. cancer) 6. Significant food allergies, preferences, intolerances, or dietary requirements that would interfere with diet adherence 7. Patients with cognitive impairment or other condition preventing their participation in the intervention 8. Current participation in a care management program related to health conditions (e.g., weight reduction, smoking cessation) 9. Current participation in another clinical trial that could interfere with the study protocol 10. Those planning to move out of the geographic area in 12 months 11. Unwillingness to provide informed consent 12. Other conditions or situations at the discretion of the Investigative team

Design outcomes

Primary

MeasureTime frameDescription
DASH Adherence as assessed by the Automated Self-Administered 24-hour Dietary Assessment Tool (ASA24)0, 12 weeks and 24 weeksAdherence will be assessed by the Automated Self-Administered 24-hour Dietary Assessment Tool (ASA24). The scores range from 0 to 100, with higher scores reflecting greater adherence.

Secondary

MeasureTime frameDescription
Cost of the intervention0, 12 weeks, 24 weeksIntervention cost/person will be estimated based on the cost of the intervention
Participant Accrual0, 12 weeks and 24 weeksReferrals, participation rates, and recruitment yields.
Number of referrals to health and social need resources0, 12 weeks and 24 weeksSocial needs as assessed by the number of participants connected to health services and services for social needs.
Systolic Blood pressure0, 12 and 24 weeksBlood pressure measured in millimeters of mercury (mmHg)
Recruitment rate0, 12 weeks, 24 weeksRecruitment yield per time
Hemoglobin A1c0, 12 and 24 weeksHemoglobin A1c (percent)
Height in inches0, 12 and 24 weeksHeight will be measured
Weight in pounds0, 12 weeks and 24 weeksWeight will be measured
Diastolic Blood pressure0, 12 and 24 weeksBlood pressure measured in millimeters of mercury (mmHg)

Countries

United States

Outcome results

None listed

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