- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03010163
Taxi STEP (Social Networks, Technology, and Exercise Through Pedometers)
July 1, 2025 updated by: Memorial Sloan Kettering Cancer Center
This study is divided into four groups.
Group 1 includes Health Fairs implemented at NYC taxi garage bases and airport taxi holding lots and pedometers.
Group 2 includes Health Fairs, pedometers and text messaging to facilitate walking and living a healthier lifestyle.
Group 3 includes Health Fairs, pedometers and social network support.
Group 4 includes Health Fairs, pedometers, text messaging and social network support.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
290
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
-
-
New York
-
New York, New York, United States, 10065
- Memorial Sloan Kettering Cancer Center
-
-
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
21 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Male
- Over 21 years of age
- Planning on remaining in NYC for at least 7 months
- Licensed taxi driver for at least three months
- Speaks English, Bengali, Hindi, Spanish or French
- Currently owns a cell phone, uses text messaging services and is willing to accept text messages for this study
Exclusion Criteria:
- Part-time driver (fewer than 5 shifts/week, totaling less than 35 hours per week)
History of any CVD or any other medical conditions (e.g. severe osteoarthritis) that will prevent him from walking
- Please note: All inclusion/exclusion criteria are based upon self reported information captured during study screening procedures.
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: Prevention
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Health Fair + Pedometer
Participants will get free weight, height, waist, and blood pressure testing at health fairs stationed at NYC taxi garage bases and airport taxi holding lots.
Health fair staff will follow up with participants who need to see a doctor due to a high blood pressure reading or other unusual result that needs a physician follow-up.
All participants will be given a pedometer with instructions on how to use it to track their daily step counts.
Participants will be randomized by envelope provided by Memorial Sloan Kettering's Department of Epidemiology and Biostatistics during an in person meeting after the completion of the 1 month run-in or by phone in case we are unable to meet them in person.
|
Testing includes weight, height, waist and blood pressure testing.
In the event that the participants are unable to meet in person for health measurements, the staff will accept self-reported measurements over the phone.
The Fitbit One/Alta/Inspire wireless tracking pedometers measures steps taken, calories burned, distance traveled and sleep pattern.
The Fitbit Alta/Inspire also sends reminders to move, which are notifications that remind the wearer to walk at least 250 steps each hour.
If the wearer has not walked 250 steps within the hour, the device will vibrate and send an on-screen reminder 10 minutes before the hour.
The reminders to move will be turned off during baseline and will be turned on at randomization for all participants.
|
|
Experimental: Health Fair, Pedometer + Text Messaging
In addition to the health fair services with general follow-up, and giving each driver a pedometer with instructions on how to use the devise to track daily step counts, all participants in this group will receive daily healthy living advice and encouraging messages about walking through text messages sent by study staff to participants' cellular phone.
Participants will be randomized by envelope provided by Memorial Sloan Kettering's Department of Epidemiology and Biostatistics during an in person meeting after the completion of the 1 month run-in or by phone in case we are unable to meet them in person.
|
Testing includes weight, height, waist and blood pressure testing.
In the event that the participants are unable to meet in person for health measurements, the staff will accept self-reported measurements over the phone.
The Fitbit One/Alta/Inspire wireless tracking pedometers measures steps taken, calories burned, distance traveled and sleep pattern.
The Fitbit Alta/Inspire also sends reminders to move, which are notifications that remind the wearer to walk at least 250 steps each hour.
If the wearer has not walked 250 steps within the hour, the device will vibrate and send an on-screen reminder 10 minutes before the hour.
The reminders to move will be turned off during baseline and will be turned on at randomization for all participants.
Daily healthy living advice and encouraging messages about walking through text messages
|
|
Experimental: Health Fair, Pedometer, Social Network Support
Each participant in this group will receive the health fair services with general follow-up along with a pedometer with instructions on how to use the device to track daily step counts.
Additionally, participants in this group will be asked to provide the names of family or friends who will form a social support network team.
This team will provide encouragement and remind participants to maintain a healthy lifestyle and increase daily walking activities.
Participants will be given a social network guide to train their family and/or friends on how to best motivate the participants .
Participants will be randomized by envelope provided by Memorial Sloan Kettering's Department of Epidemiology and Biostatistics during an in person meeting after the completion of the 1 month run-in or by phone in case we are unable to meet them in person.
|
Testing includes weight, height, waist and blood pressure testing.
In the event that the participants are unable to meet in person for health measurements, the staff will accept self-reported measurements over the phone.
The Fitbit One/Alta/Inspire wireless tracking pedometers measures steps taken, calories burned, distance traveled and sleep pattern.
The Fitbit Alta/Inspire also sends reminders to move, which are notifications that remind the wearer to walk at least 250 steps each hour.
If the wearer has not walked 250 steps within the hour, the device will vibrate and send an on-screen reminder 10 minutes before the hour.
The reminders to move will be turned off during baseline and will be turned on at randomization for all participants.
Family or friends will provide encouragement and remind participants to maintain in a healthy lifestyle and increase daily walking activities
|
|
Experimental: Health Fair, Pedometer, Text Msg, Social Network Support
Participants in this group will receive the health fair service with general follow-up, along with a pedometer with instructions on how to use the device to track daily step counts.
Participants will also receive daily healthy living advice through encouraging text messages about walking through text messages sent by our staff to participants' cellular phones.
Participants will also be asked to provide the names of family or friends who will form a social support network team.
This team will provide encouragement and remind participants to maintain a healthy lifestyle and increase daily walking activities.
Participants will be given tools to train their family and/or friends on how to best motivate the drivers.
Participants will be randomized by envelope provided by Memorial Sloan Kettering's Department of Epidemiology and Biostatistics during an in person meeting after the completion of the 1 month run-in or by phone in case we are unable to meet them in person.
|
Testing includes weight, height, waist and blood pressure testing.
In the event that the participants are unable to meet in person for health measurements, the staff will accept self-reported measurements over the phone.
The Fitbit One/Alta/Inspire wireless tracking pedometers measures steps taken, calories burned, distance traveled and sleep pattern.
The Fitbit Alta/Inspire also sends reminders to move, which are notifications that remind the wearer to walk at least 250 steps each hour.
If the wearer has not walked 250 steps within the hour, the device will vibrate and send an on-screen reminder 10 minutes before the hour.
The reminders to move will be turned off during baseline and will be turned on at randomization for all participants.
Daily healthy living advice and encouraging messages about walking through text messages
Family or friends will provide encouragement and remind participants to maintain in a healthy lifestyle and increase daily walking activities
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Increase average daily step counts
Time Frame: 6 months post randomization
|
Increase average step counts per day
|
6 months post randomization
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Francesca Gany, MD, MS, Memorial Sloan Kettering Cancer Center
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
December 1, 2016
Primary Completion (Estimated)
June 1, 2026
Study Completion (Estimated)
June 1, 2026
Study Registration Dates
First Submitted
January 3, 2017
First Submitted That Met QC Criteria
January 3, 2017
First Posted (Estimated)
January 4, 2017
Study Record Updates
Last Update Posted (Actual)
July 2, 2025
Last Update Submitted That Met QC Criteria
July 1, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 16-1659
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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