- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05002985
Tanglewood Trail Walking Program in Rural Kentucky 2020
October 6, 2021 updated by: Dawn Brewer
Tanglewood Trail Walking Program to Increase Phytonutrient Intake and Physical Activity in a Rural Kentucky Town
The Tanglewood Trail Walking Program is a well established community health initiative that encourages community members to walk approximately 1 mile to the Whitesburg Farmers Market each Saturday.
The study aims to determine if walking to the market with a community health coach results in healthier options being selected at the market when compared to the driving group.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
In the summer of 2017, community members of Whitesburg, KY were recruited to join the Tanglewood Trail Walking Program to the Whitesburg farmers market.
Each Saturday, participants reported whether or not they walked the 1 mile trail to the farmers market and they reported which fruits and vegetables they purchased.
Participants completed questionnaires about fruit and vegetable consumption and physical activity.
Participants also provided physical and biological measurements.
The ClinicalTrials.gov
record for the original trial in 2017 is NCT03495648.
Study Type
Interventional
Enrollment (Actual)
49
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Kentucky
-
Lexington, Kentucky, United States, 40506
- University of Kentucky
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- ability to walk 1 kilometer
Exclusion Criteria:
- pregnant
- institutionalized adults
- impaired consent ability
- prisoners
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
EXPERIMENTAL: Walking Group
Subjects will participate in a walking group led by a community organizer as a means to get to a local farmer's market.
|
Subjects will walk 1 kilometer from a pre-determined point to a local farmer's market.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Self-reported Fruit Intake
Time Frame: 3 months
|
Subjects' self-reported fruit intake will be measured to determine if walking combined with a voucher for fruits and vegetables changes participant self-reported fruit intake.
|
3 months
|
Self-reported Vegetable Intake
Time Frame: 3 months
|
Subjects' self-reported vegetable intake will be measured to determine if walking combined with a voucher for fruits and vegetables changes participant self-reported vegetable intake.
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Hours of Walking Per Week
Time Frame: 3 months
|
Subjects will self-report the number of hours spent walking per week.
|
3 months
|
Understanding of Plant-based Phytonutrients
Time Frame: 3 months
|
Participants will be asked a question demonstrating their understanding of the importance of ingesting plant-based nutrients.
Possible answers are yes, no, or not sure.
Data will be presented as the number of participants in each group that understood the importance of plant-based nutrients.
|
3 months
|
Belief in the Benefit of Plant-based Nutrients
Time Frame: 3 months
|
Participants will be asked a question demonstrating their appreciation of plant-based nutrients.
Possible answers are yes, no, or not sure.
Data will be presented as the number of participants in each group that understood the importance of plant-based nutrients.
|
3 months
|
Belief in the Preventative Effects of Plant-Based Nutrients
Time Frame: 3 months
|
Participants will be asked a question demonstrating their beliefs of plant-based nutrients.
Possible answers are yes, no, or not sure.
Data will be presented as the number of participants in each group that understood the importance of plant-based nutrients.
|
3 months
|
Belief in the Role of Healthy Diet in Protecting Health From Pollutants
Time Frame: 3 months
|
Participants will be asked a question demonstrating their beliefs that a healthy diet might protect health from environmental pollutants.
Possible answers are yes, no, or not sure.
Data will be presented as the number of participants in each group that understood the importance of a healthy diet
|
3 months
|
Knowledge of Which Foods Contain Phytonutrients
Time Frame: 3 months
|
Participants will be asked a question about which foods contain phytonutrients.
Possible answers are meat, dairy, plant foods, all foods, or don't know.
Data will be presented as the number of participants in each group that correctly identified plant foods.
|
3 months
|
Knowledge of Environmental Pollutants
Time Frame: 3 months
|
Participants will be asked to identify environmental pollutants from a list.
Possible answers are polychlorinated biphenyls (PCBs), mercury, nitrites, all of those, none of those, or don't know.
Data will be presented as the number of participants in each group that correctly identified all of those.
|
3 months
|
Hours of Vigorous Exercise Per Week
Time Frame: 3 months
|
Subjects will self-report the number of hours spent in vigorous exercise per week.
|
3 months
|
Hours of Moderate Exercise Per Week
Time Frame: 3 months
|
Subjects will self-report the number of hours spent in moderate exercise per week.
|
3 months
|
Hours of Sitting Per Week
Time Frame: 3 months
|
Subjects will self-report the number of hours spent sitting per day.
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
May 17, 2020
Primary Completion (ACTUAL)
September 14, 2020
Study Completion (ACTUAL)
September 14, 2020
Study Registration Dates
First Submitted
August 10, 2021
First Submitted That Met QC Criteria
August 10, 2021
First Posted (ACTUAL)
August 12, 2021
Study Record Updates
Last Update Posted (ACTUAL)
November 5, 2021
Last Update Submitted That Met QC Criteria
October 6, 2021
Last Verified
October 1, 2021
More Information
Terms related to this study
Other Study ID Numbers
- 17-0283-P2H 2020
- P42ES007380 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
No current plan to share data.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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