Skip to main content
Clinical Trials/NCT02544867
NCT02544867
Completed
Not Applicable

Optimizing Sedentary Behavior Interventions to Affect Acute Physiological

University of California, San Diego1 site in 1 country30 target enrollmentSeptember 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Sedentary Behavior
Sponsor
University of California, San Diego
Enrollment
30
Locations
1
Primary Endpoint
Acceptability and feasibility
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

An emerging body of epidemiological evidence suggests that various forms of sedentary behavior, including TV viewing, occupational sitting, and total daily sitting, may be associated with all-cause and cardiovascular mortality, overweight and obesity, type 2 diabetes, depression and psychological well-being. Importantly, many of these associations were independent of participation in moderate to vigorous intensity physical activity. We propose a pilot study to assess the feasibility, acceptability and preliminary efficacy of two interventions targeting sedentary behavior. Since it is currently unknown what component of sedentary behavior exposure presents the greatest risk to health, we propose separate interventions to reduce overall sedentary time and to promote breaks in sedentary time.

Detailed Description

Primary aim: To determine the acceptability and feasibility of selected personal, social and environmental strategies to reduce overall sitting time and increase the number of times participants stand up in a day. Secondary aim: To assess whether existing and new measurement approaches can detect specific changes in sedentary behavior. Exploratory aim: To establish whether specified intervention strategies were efficacious in reducing sedentary behavior and whether intervention effects were specific to the targeted sedentary behavior construct (e.g. decreased overall sitting time or increased number of breaks in sitting).

Registry
clinicaltrials.gov
Start Date
September 2013
End Date
March 2014
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jacqueline Kerr

Associate Professor

University of California, San Diego

Eligibility Criteria

Inclusion Criteria

  • Males or females 50 -70 years of age
  • Able to attend 4 measurement visits with study staff in 3 consecutive weeks
  • Spend at least 8 hours per day sitting
  • Willing and able to wear study device for 21 days
  • Able to read and write in English
  • Able to provide written informed consent

Exclusion Criteria

  • Do not sit for at least 8 hours per day
  • Unable to attend 4 visits
  • Diagnosis of serious chronic condition that would limit the ability to stand

Outcomes

Primary Outcomes

Acceptability and feasibility

Time Frame: 3 weeks

To determine the acceptability and feasibility of selected personal, social and environmental strategies to reduce overall sitting time and increase the number of times participants stand up in a day

Secondary Outcomes

  • Measurement(3 weeks)
  • Sedentary behavior(3 weeks)

Study Sites (1)

Loading locations...

Similar Trials