CClinicalTrials.gg
CompletedNCT05281978Updated Aug 28, 2023

One Step at a Time: An Intervention to Reduce Sedentary Behavior Among Working Adults

An interventional study of Decrease Sedentary Time + Increase MVPA group and Increase MVPA group in Sedentary Behavior, Exercise and Middle Age, sponsored by University of Illinois at Urbana-Champaign. Completed at 1 site in United States. Open to participants aged 45 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-08-28.

Sponsored by University of Illinois at Urbana-Champaign · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
88
Allocation
Randomized
Ages
45 Years to 65 Years
Sex
All
01

Study summary

The proposed study will test the preliminary efficacy of a novel 12-week social cognitive theory-based intervention that will target reducing daily sitting time and increasing exercise participation among middle-aged working adults. This is a population highly susceptible to excessive sedentary time and low levels of exercise engagement. This two-arm randomized controlled trial (RCT) will examine the preliminary efficacy of decreasing sedentary time in addition to increasing moderate-vigorous intensity physical activity (MVPA) engagement, compared to a group which only receives MVPA promotion.

02

Conditions studied

  • Sedentary Behavior
  • Exercise
  • Middle Age
  • Adult
03

In context

Lead sponsor

University of Illinois at Urbana-Champaign is the lead sponsor of 188 studies on the registry; 29 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
45 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • 45-65 years of age by study start date
  • Hold full-time employment (≥ 30 hours/week) at one or more jobs
  • Hold a sedentary-based job (which also allows for ability to freely move about during the workday)
  • Low active (engage in ≤2 days of 30+ minutes of structured moderate-vigorous intensity exercise/week)
  • Physician's consent to participate in aerobic testing and/or the exercise program (if needed based on Physical Activity Readiness Questionnaire responses)
  • Ambulatory
  • Absence of health conditions that may be made worse by exercise
  • Ability to complete all testing assessments in-person
  • Access to a laptop/desktop/phone with Zoom web-conferencing software
  • Fluent in English

Exclusion criteria

Exclusion Criteria:

  • Under 45 or over 65 years of age
  • Not holding full-time employment (work \< 30 hours/week at one or more jobs)
  • Hold a job(s) which is classified as light, medium, heavy, or very heavy work
  • Hold a sedentary-based job which does not allow for free movement throughout the workday (i.e., bus driver)
  • High active (engage in > 2 days or 30+ minutes of structured moderate-vigorous intensity exercise/week)
  • Non-consent of physician
  • Non-ambulatory (i.e., use of walkers, wheelchair, cane, etc.)
  • Presence of health conditions that may be made worse by exercise.
  • Unable to complete assessments in-person
  • No access to laptop/desktop/phone with Zoom software
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
88 participants (actual)

Study arms

  • Experimental
    Decrease Sedentary Time + Increase MVPA

    Participants in this group will receive a 12-week, social cognitive theory-based intervention targetting reduction of daily sedentary time. This information will be delivered to them in the form of Zoom workshops, a program workbook, personalized step count goals, and a private social media page. The aim of this component will be to have participants displace their daily sedentary time with light-intensity physical activity, such as casual walking. The second component of this intervention will be increasing participants' weekly MVPA engagement. Participants will participate in 1 live, virtual aerobics-based exercise class per week and complete 2 additional sessions on their own time. Participants will build up to exercising 150 minutes/week (the federal physical activity recommendations).

    Behavioral: Decrease Sedentary Time + Increase MVPA group

  • Active comparator
    Increase MVPA only

    Participants in this group will only receive the MVPA-promoting component (which will be the same delivery as the intervention group). Participants in this arm will participate in 1 live, virtual aerobics-based exercise class per week (held separately from the intervention group) and will complete 2 additional exercise classes on their own time. Participants will build up to exercising 150 minutes/week (the federal physical activity recommendations).

    Behavioral: Increase MVPA group

Interventions

  • BehavioralDecrease Sedentary Time + Increase MVPA group

    12 week home-based exercise program to promote engagement of 150 min/week of moderate-vigorous intensity exercise; personalized step count goals to increase daily volume of physical activity and displacement of sedentary time

  • BehavioralIncrease MVPA group

    12 week home-based exercise program to promote engagement of 150 min/week of moderate-vigorous intensity exercise

06

What researchers measure

Primary outcomes

  1. Changes in average daily step counts

    Participants will wear a hip-based pedometer for 7 days at baseline and 12 weeks

    Time frame: Baseline,12 weeks

  2. Changes in average daily sedentary time

    Participants will wear a hip-based accelerometer for 7 days at baseline and 12 weeks to measure their daily time spent sedentary.

    Time frame: Baseline,12 weeks

  3. Changes in average daily light-intensity physical activity

    Participants will wear a hip-based accelerometer for 7 days at baseline and 12 weeks to measure their daily time spent engaged in light-intensity physical activity.

    Time frame: Baseline,12 weeks

  4. Changes in average daily moderate-vigorous intensity physical activity

    Participants will wear a hip-based accelerometer for 7 days at baseline and 12 weeks to measure their daily time spent engaged in moderate-vigorous intensity physical activity.

    Time frame: Baseline, 12 weeks

07

Study locations

1 site
  • Univeristy of Illinois Urbana-Champaign
    Urbana, Illinois 61801, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 28, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05281978
Lead sponsor
University of Illinois at Urbana-Champaign
Responsible party
Sponsor
First posted
Mar 16, 2022
Start date
Apr 25, 2022
Primary completion
Aug 1, 2023
Completion
Aug 1, 2023
Last update
Aug 28, 2023

Study contacts

Neha P Gothe, MA, PhD
principal investigator · University of Illinois at Urbana-Champaign

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2023. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion