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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03061357
Other study ID # 505314
Secondary ID
Status Completed
Phase N/A
First received February 9, 2017
Last updated February 17, 2017
Start date August 6, 2015
Est. completion date December 31, 2016

Study information

Verified date February 2017
Source Texas Tech University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This project was to examine the effects of incorporating modern wearable technology into the credit-based Physical Activity Instructional Program for promoting habitual levels of physical activity among college students.


Description:

This project was a cluster randomized trial examining the effects of utilizing a wearable activity tracker in a credit-based Physical Activity Instructional Program on promoting habitual levels of physical activity (PA) in college students.

The project was conducted in a large public university located in the mid-south region of the US. The university offers more than one hundred 1-credit hour PAIPs per academic semester. Considering the pilot nature of the study, the target PAIPs was limited to those meeting the following inclusion criteria: 1) PAIP with a size of 30 students that generally show an approximately equal gender distribution; and 2) PAIP that delivers the principles and practice of individually tailored habitual activity plans. The investigators randomly selected 14 eligible PAIPs and assigned them into intervention (k=7) and control (k=7) groups. The outcome measures of interests were the changes in objectively and subjectively measured physical activity over an academic semester.


Recruitment information / eligibility

Status Completed
Enrollment 187
Est. completion date December 31, 2016
Est. primary completion date July 31, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- healthy college students who were enrolled in 1-credit physical activity instruction programs.

Exclusion Criteria:

- did not wish to participate;

- have currently used their own wearable activity tracker;

- indicated any major physical, psychiatric, or cardiovascular-related problems diagnosed by a physician.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Activity tracker
Misfit Flash (Misfit Wearables Co., Burlingame, CA) activity tracker

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Texas Tech University

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline in objectively measured physical activity to 15 weeks Physical activity was objectively measured using an ActiGraph Actitrainer (ActiGraph LLC, Pensacola, FL, USA) accelerometer. baseline and 15 weeks
Secondary Change from baseline in subjectively measured physical activity Physical activity was subjectively measured using International Physical Activity Questionnaire. baseline and 15 weeks
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