Health TrialsbyHealthPanel

Harvest Share Clinical Outcomes

ConditionDiet Habit
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNYU Langone Health

About this trial

This pilot study aims to assess the feasibility and acceptability of collecting clinical outcomes amongst Building Access to Food through System and Solidarity (BASIS) participants (s22-00299). BASIS aims to implement a whole-of-community intervention in Brooklyn for improving diet and the social and build environments for English-, Chinese-, and Spanish-speaking communities. BASIS is a single-site program that is being evaluated over a period of 4 years. Each year, culturally appropriate produce will be provided weekly in the form of community-supported agriculture for 20 weeks to community members in Sunset Park, Brooklyn and surrounding neighborhoods. Specifically, we aim to collect cholesterol, blood pressure (BP), and dietary inflammation measures to evaluate impacts of BASIS on clinical outcomes.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Adult age 18 years and over

Participates in the Harvest Share CSA program

Speaks English, Chinese, or Spanish

Willing and able to provide consent

Disqualifiers

None

Trial design

Design model

Single group

Treatments tested in this trial

  • Community Supported Agriculture (CSA)

    Behavioral

    Community-supported agriculture (CSA) involves a community of individuals who support a farm and in return receive distributions of the farm's produce throughout the growing season.

Treatment groups

75 Participants
are divided into 1 treatment group
Group A: HS CSA ParticipantsExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Cholesterol

Assessed using standardized point-of-care cholesterol measurement procedures.

Time frame
Baseline, Post-Visit (approx. Week 18), Follow-Up Visit (approx. Week 40)
2

Blood pressure (BP)

Assessed using standardized point-of-care community BP measurement procedures.

Time frame
Baseline, Post-Visit (approx. Week 18), Follow-Up Visit (approx. Week 40)
3

Dietary Inflammation

Assessed with 24-hour dietary recalls.

Time frame
Baseline, Follow-Up Visit (approx. Week 40)

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

NYU Langone Health

Lead sponsor

National Institute on Minority Health and Health Disparities (NIMHD)

Collaborator

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: