- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04940481
TROLLEY Study - TRansit Opportunities for HeaLth, Livability, Exercise and EquitY (TROLLEY)
October 2, 2024 updated by: Katie Crist, University of California, San Diego
The researchers are evaluating longitudinal changes in multiple health, economic, and environmental outcomes over a 3-year COVID recovery period and in the context of a new light rail transit (LRT) line, called the Mid-Coast Trolley, among 465 UC San Diego (UCSD) staff.
The primary aim is to evaluate change in objectively measured total and moderate to vigorous physical activity (MVPA), travel mode, and vehicle miles traveled (VMT).
Study Overview
Status
Active, not recruiting
Conditions
Study Type
Observational
Enrollment (Actual)
479
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
-
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California
-
La Jolla, California, United States, 92093
- UC San Diego
-
-
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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
We will study UCSD staff.
We will aim to recruit 50% from people of color, and 50% low income (<80% Area Median Income), 50% female, and 50% living within 1 mile of a transit stop that connects to the Mid-Coast Trolley.
Description
Inclusion Criteria:
- are 18 years of age or older;
- are a full or part-time employee at UC San Diego
- Prior to COVID-19, you used to commute to La Jolla at least 2 days per week;
- have lived in the neighborhood selected for the study for at least one year;
- are able to walk without human assistance;
- are comfortable reading and writing in English or Spanish;
- have a reliable phone where you can be reached;
- spend most of your time in San Diego County;
- don't plan on moving in the next year;
- are able to give informed consent and comply with the protocol;
- are willing to complete all assessments and wear all devices for 7 days at 3 different time points in the next 2 years.
Exclusion Criteria:
1) pregnant, 2) mental state that would preclude understanding the protocol, 3) medical condition that would affect physical activity, 4) taking part in another physical activity related research study, and 5) live or regularly travel outside of San Diego County.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Moderate to vigorous physical activity
Time Frame: 2 years
|
Minutes
|
2 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Active commute mode
Time Frame: 2 years
|
%
|
2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
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)
July 15, 2021
Primary Completion (Estimated)
June 14, 2025
Study Completion (Estimated)
June 14, 2025
Study Registration Dates
First Submitted
June 17, 2021
First Submitted That Met QC Criteria
June 17, 2021
First Posted (Actual)
June 25, 2021
Study Record Updates
Last Update Posted (Actual)
October 4, 2024
Last Update Submitted That Met QC Criteria
October 2, 2024
Last Verified
October 1, 2024
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 78646
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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