ClinicalTrials.gg
CompletedNCT03477305Updated Jan 19, 2023

BerryCare: A Community Engagement Program

An interventional study of Blackberry Consumption in Cardiovascular Risk Factor, sponsored by Dawn Brewer. Completed at 5 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-01-19.

Sponsored by Dawn Brewer · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 1 year 2 months after the study started (first participant enrolled Jan 2017, registered Mar 2018).
Phase
Not applicable
Study type
Interventional
Enrollment
38
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

BerryCare teaches people about the health benefits of blackberries, how to harvest and maintain blackberry bushes and then assesses changes in knowledge and behaviors associated with blackberries and physical measurements.

Read the detailed description

BerryCare seeks to teach community members how to grow thornless, erect blackberry brambles and to healthily consume fresh blackberries using Plate It Up Kentucky Proud recipes. Horticulture, nutrition, and extension experts are working together to design a blackberry-growing program that engages citizens and their community in each step of the process, from planting to harvesting berries. The lessons will be delivered by experts in their respective field, with accompanying extension publications and supplemental materials provided for replication of the curriculum in other counties.

02

Conditions studied

  • Cardiovascular Risk Factor

Keywords

  • older adults
  • community gardening
  • cooperative extension
03

In context

Lead sponsor

Dawn Brewer is the lead sponsor of 6 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 18 years of age or older

Exclusion criteria

Exclusion Criteria:

  • Physically incapacitated
  • Mentally incapacitated
05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
38 participants (actual)

Study arms

  • Experimental
    BerryCare Participants

    Subjects will be recruited to participate in a community gardening program where they will learn the benefits of both physical active gardening and consuming homegrown foods through blackberry consumption.

    Behavioral: Blackberry Consumption

Interventions

  • BehavioralBlackberry Consumption

    Measures of biomedical and behavioral changes resulting from the consumption of blackberries.

06

What researchers measure

Primary outcomes

  1. Change in consumption of blackberries

    Blackberry consumption will be measured in participants during pre screening and throughout the course of the study.

    Time frame: Baseline, 6 months, 12 months, 18 months

Secondary outcomes

  1. Change in blood pressure

    The effect of blackberry consumption on blood pressure will be assessed at baseline and throughout the study.

    Time frame: Baseline, 6 months, 12 months, 18 months

  2. Change in total cholesterol

    The effect of blackberry consumption on total cholesterol will be assessed at baseline and throughout the study.

    Time frame: Baseline, 6 months, 12 months, 18 months

  3. Change in HDL cholesterol

    The effect of blackberry consumption on HDL cholesterol will be assessed at baseline and throughout the study.

    Time frame: Baseline, 6 months, 12 months, 18 months

  4. Change in LDL cholesterol

    The effect of blackberry consumption on LDL cholesterol will be assessed at baseline and throughout the study.

    Time frame: Baseline, 6 months, 12 months, 18 months

  5. Change in A1c

    The effect of blackberry consumption on A1c will be assessed at baseline and throughout the study.

    Time frame: Baseline, 6 months, 12 months, 18 months

  6. Change in carotenoids

    The effect of blackberry consumption on carotenoid status will be assessed at baseline and throughout the study.

    Time frame: Baseline, 6 months, 12 months, 18 months

  7. Change in weight

    The effect of blackberry consumption on weight will be assessed at baseline and throughout the study.

    Time frame: Baseline, 6 months, 12 months, 18 months

  8. Change in waist circumference

    The effect of blackberry consumption on waist circumference will be assessed at baseline and throughout the study.

    Time frame: Baseline, 6 months, 12 months, 18 months

  9. Change in knowledge

    The effect of blackberry consumption on knowledge of phytonutrients and recommended servings of fruits and vegetables will be assessed at baseline and throughout the study.

    Time frame: Baseline, 6 months, 12 months, 18 months

  10. Change in self-reported fruit and vegetable intake

    The effect of blackberry consumption on self-reported fruit and vegetable intake will be assessed at baseline and throughout the study.

    Time frame: Baseline, 6 months, 12 months, 18 months

  11. Change in group cohesion

    The effect of blackberry consumption on group cohesion will be assessed at baseline and throughout the study.

    Time frame: Baseline, 6 months, 12 months, 18 months

  12. Change in physical function

    The effect of blackberry consumption on physical function will be assessed at baseline and throughout the study.

    Time frame: Baseline, 6 months, 12 months, 18 months

07

Study locations

5 sites
  • Red Bird Mission
    Beverly, Kentucky 40913, United States
  • Harlan County Extension Office
    Harlan, Kentucky 40831, United States
  • University of Kentucky
    Lexington, Kentucky 40506, United States
  • Jessamine County Senior Citizens Center
    Nicholasville, Kentucky 40356, United States
  • Cowan Community Center
    Whitesburg, Kentucky 41858, United States
08

References and documents

Individual participant data

Plan to share: No — No plan to share data.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 19, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03477305
Lead sponsor
Dawn Brewer
Responsible party
Dawn Brewer (Assistant Professor, University of Kentucky) — Sponsor-investigator
First posted
Mar 26, 2018
Start date
Jan 18, 2017
Primary completion
Sep 26, 2018
Completion
Sep 26, 2018
Last update
Jan 19, 2023

Study contacts

Dawn Brewer, PhD
principal investigator · University of Kentucky

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2023. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion