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Completed

NCT Number: NCT02609438

An Intervention to Reduce Sitting Time at Work: Effects on Metabolic Health and Inactivity

The purpose of this study is to determine whether varying the frequency and length of activity breaks during the workday will differentially impact sedentary behavior and health outcomes. Participants will be randomly assigned to take short, frequent breaks (i.e., 1 minute every half hour) or longer, planned breaks (i.e., two 15-minute walks) from sitting during the workday. They will be instructed to follow the assigned protocols for an 8-week intervention and the effects of their participation on sedentary behavior and a variety of health outcomes will be assessed. The investigators anticipate participants in both intervention arms will demonstrate significant reductions in daily sitting time, bit do not have an a priori hypothesis regarding the relative effectiveness of each approach.

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Key information

Age range

25 year–50 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

About this study

The purpose of this study is to determine whether varying the frequency and length of activity breaks during the workday will differentially impact sedentary behavior and health outcomes. Women aged 25-50 who work full-time in sedentary jobs and participate in less than 60 minutes of overall physical activity per week will be recruited. At the beginning of the study participants will visit the laboratory to complete baseline health assessments and meet with a research assistant to outline their plan for reducing sitting time at work. At this time they will be randomly assigned to one of two groups: 1) Group A will be asked to take two 15-minute walks during each workday, or 2) Group B will be asked to stand up and move around for 1-2 minutes every half hour throughout the workday. The total duration of this program will be eight weeks. During this time participants will be asked to keep a brief daily log of their activity breaks during the workday. At the end of the 8-week program participants will return to the laboratory to repeat the health assessments.

ASSESSMENTS:

All participants will complete the following tests and procedures:

  • Metabolic blood panel. Blood will be drawn from a quick finger stick to assess total cholesterol, triglycerides, LDL, HDL, and fasting glucose.
  • DEXA scan. Participants will lie down on a body scanner for about 10 minutes to assess body composition.
  • Body measurements. A trained research assistant will measure height, weight, and waist circumference.
  • Blood pressure. A trained research assistant will measure blood pressure using an automated blood pressure cuff.

In addition, participants will complete the following assessments outside of the laboratory:

  • Questionnaires: Participants will be asked to complete a series of questionnaires. This should take 15-20 minutes.
  • Accelerometer: Participants will be asked to wear a motion sensor for a total of 21 days (three 7-day periods). This small apparatus is worn around the waist during the day. Participants will complete a log indicating when they were wearing the accelerometer each day.
  • Food diary: Participants will be asked to record their food intake for a total of 9 days (three 3-day periods).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Work at least 35 hours per week
  • Spend at least 80% of working hours sitting (self-reported)
  • Engage in less than 60 minutes per week of leisure-time exercise (self-reported)
  • Not pregnant or planning to become pregnant in the next 3 months
  • Not currently trying to change weight
  • Speak English
  • Able to attend assessments
  • Willing to wear accelerometer
  • No anticipated significant conflicts during 8-week intervention

Exclusion criteria

  • Male
  • Working less than 35 hours per week
  • Spend >25% of working hours standing or active
  • Engage in more than 60 minutes per week of leisure-time exercise
  • Pregnant
  • Actively dieting or attempting to change weight

Treatment and study plan

Short breaks

Behavioral

Following baseline testing, participants will attend a 30-minute individual orientation session, during which they will complete a planning worksheet with a research assistant. They will identify specific strategies they will use to accomplish the pre-specified goal (i.e., to take a 1-minute active break every 30 minutes during the workday). They will also identify potential barriers they will face and devise strategies for overcoming them. The intervention will officially start the Monday after the orientation session and will last for 8 weeks. Participants will receive a weekly email containing tips related to reducing sitting time at work. All participants will complete daily activity logs indicating the time and duration of all breaks from sitting across the 8-week intervention.

Other names: Up4Health - short breaks

Long breaks

Behavioral

Following baseline testing, participants will attend a 30-minute individual orientation session, during which they will complete a planning worksheet with a research assistant. They will identify specific strategies they will use to accomplish the pre-specified goal (i.e., to take two 15-minute activity breaks during each workday). They will also identify potential barriers they will face and devise strategies for overcoming them. The intervention will officially start the Monday after the orientation session and will last for 8 weeks. Participants will receive a weekly email containing tips related to reducing sitting time at work. All participants will complete daily activity logs indicating the time and duration of all breaks from sitting across the 8-week intervention.

Other names: Up4Health - long breaks

Primary outcomes

  1. Change in sedentary behavior during the workday

    Time frame: Baseline - week 8

    Measured by GT3X accelerometer

Secondary outcomes

  1. Change in weight

    Time frame: Baseline - week 9

  2. Change in blood pressure

    Time frame: Baseline - week 9

  3. Change in resting heart rate

    Time frame: Baseline - week 9

  4. Change in total cholesterol, HDL cholesterol, LDL cholesterol

    Time frame: Baseline - week 9

  5. Change in triglycerides

    Time frame: Baseline - week 9

  6. Change in fasting blood glucose

    Time frame: Baseline - week 9

  7. Change in waist circumference

    Time frame: Baseline - week 9

  8. Change in body composition

    Time frame: Baseline - week 9

    DEXA or bioelectrical impedance

  9. Change in energy, tiredness, tension, and calmness

    Time frame: Baseline - week 8

    Activation-Deactivation Checklist

  10. Change in fatigue severity, interference, and duration

    Time frame: Baseline - week 8

    Fatigue Symptom Inventory

  11. Change in mood

    Time frame: Baseline - week 8

    Positive and Negative Affect Scale

  12. Change in overall self-reported physical activity

    Time frame: Baseline - week 8

    International Physical Activity Questionnaire

  13. Change in overall objectively measured physical activity

    Time frame: Baseline - week 8

    Measured by GT3X accelerometer

  14. Change in diet quantity

    Time frame: Baseline - week 8

    Measured by 3-day food diary

  15. Change in diet quality

    Time frame: Baseline - week 8

    Dietary Screener Questionnaire

  16. Adherence to assigned protocols

    Time frame: up to 8 weeks

    Measured by activity logs

Sponsors and collaborators

Lead sponsor

Kansas State University

Other

Registry information

Official study title

The Effects of Short, Frequent Breaks in Sitting Versus Longer, Planned Breaks in Sitting on Sedentary Behavior and Metabolic Health Among Inactive Females Working Sedentary Jobs

Acronym: Up4Health

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Nov 20, 2015
Registry last updated
Nov 20, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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