- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05574426
Efficacy of Movement Breaks in Real-World Settings
March 4, 2025 updated by: Jonathan Little, University of British Columbia
The purpose of this study is to determine the efficacy of performing "exercise snacks" (short movement breaks throughout the day) on various measures of cardiometabolic health.
Study Overview
Detailed Description
After being informed about the study and potential risks, all eligible participants who have provided consent will undergo a baseline visit to assess pre-intervention basic anthropometrics, cardiorespiratory fitness, and provide a blood sample.
Participants will then be randomized in a 1:1 ratio to one of two groups: 1) Mobility movement breaks (stretching or range of motion exercises); or 2) Cardiovascular movement breaks (designed to raise heart rate).
Both groups will be encouraged to perform 3-4 daily movement breaks on at least 3 days of the week with support from an online platform and app that provides video instructions and reminders to complete the movement breaks.
After 12 weeks, participants will be asked to return to the lab for the same testing performed at baseline.
Study Type
Interventional
Enrollment (Actual)
77
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
-
-
British Columbia
-
Kelowna, British Columbia, Canada, V1V 1V7
- University of British Columbia
-
-
Ontario
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Hamilton, Ontario, Canada
- McMaster University
-
-
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
40 years to 64 years (Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Physically inactive (performing <150 minutes of moderate-to-vigorous intensity aerobic exercise per week, assessed by pre-screening Get Active Questionnaire);
- Body Mass Index: 18.5-30.0 kg/m2;
- Not currently diagnosed with or being treated for cardiometabolic disease (e.g., coronary artery disease, diabetes);
- Not a current smoker;
- Cleared to engage in physical activity using the Get Active Questionnaire and, if applicable, consultation with a Qualified Exercise Professional;
- Access to a computer, tablet or smartphone for intervention delivery and tracking
Exclusion Criteria:
- Chronic health condition preventing participation in exercise;
- Lack of access to internet connection
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: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Cardiovascular Movement Breaks
Participants will perform 3-4 exercise snacks (30-60s bursts of exercise) on at least 3 days of the week.
The exercises prescribed in this arm will be designed to increase heart rate.
|
Participants will be asked to perform 30-60 second movement breaks 3-4 times per day on at least 3 days per week.
Other Names:
|
|
Active Comparator: Mobility Movement Breaks
Participants will perform 3-4 mobility snacks (30-60s of mobility exercises or stretching) on at least 3 days of the week.
The exercises prescribed in this arm are not designed to increase heart rate.
|
Participants will be asked to perform 30-60 second movement breaks 3-4 times per day on at least 3 days per week.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change From Baseline in Cardiorespiratory Fitness at 12 Weeks
Time Frame: Baseline and Week 12
|
Cardiorespiratory fitness will be assessed as the highest 30-s average from a laboratory-based graded VO2peak test on a cycle ergometer.
|
Baseline and Week 12
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Device-Measured Adherence to Movement Breaks
Time Frame: Week 2 and week 11
|
Participants will wear accelerometers to assess adherence near the beginning and the end of the intervention.
|
Week 2 and week 11
|
|
Self-Reported Adherence to Movement Breaks
Time Frame: Once per week for 12 weeks
|
Participants will be sent weekly surveys asking them to recall the total number of movement breaks performed that week.
|
Once per week for 12 weeks
|
|
Change From Baseline in Plasma Insulin
Time Frame: Baseline and 12 weeks
|
A fasted venous blood sample will be obtained and insulin measured by commercial assay.
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Baseline and 12 weeks
|
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Change From Baseline in Plasma Glucose
Time Frame: Baseline and 12 weeks
|
A fasted venous blood sample will be obtained and glucose measured by biochemical assay.
|
Baseline and 12 weeks
|
|
Change From Baseline in Insulin Resistance
Time Frame: Baseline and 12 weeks
|
A fasted venous blood sample will be obtained and insulin resistance estimated by homeostasis model assessment (HOMA) score
|
Baseline and 12 weeks
|
|
Change From Baseline in Inflammatory Cytokines
Time Frame: Baseline and 12 weeks
|
A fasted venous blood sample will be obtained and inflammatory cytokines measured by multiplex assay
|
Baseline and 12 weeks
|
|
Change From Baseline in Body Mass
Time Frame: Baseline and 12 weeks
|
Body mass will be measured by weigh scale
|
Baseline and 12 weeks
|
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Change From Baseline in Waist Circumference
Time Frame: Baseline and 12 weeks
|
Waist circumference (in centimetres) will be measured using a measurement tape.
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Baseline and 12 weeks
|
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Movement Break Enjoyment Assessed by the Exercise Enjoyment Scale (EES)
Time Frame: Immediately following each movement break for entire 12-week intervention
|
The EES is a validated, single-item 7-point scale to assess exercise enjoyment.
Possible scores range from 1 (not at all) to 7 (extremely).
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Immediately following each movement break for entire 12-week intervention
|
|
Rating of Perceived Exertion (RPE) Following Movement Breaks
Time Frame: Immediately following each movement break for entire 12-week intervention
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A 10 point RPE scale will be used to assess perceived exertion ranging from 0 (rest) to 10 (maximal).
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Immediately following each movement break for entire 12-week intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Jonathan Little, University of British Columbia
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 (Actual)
October 1, 2022
Primary Completion (Actual)
December 5, 2023
Study Completion (Actual)
December 5, 2023
Study Registration Dates
First Submitted
October 6, 2022
First Submitted That Met QC Criteria
October 6, 2022
First Posted (Actual)
October 10, 2022
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 4, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- H21-03417
- 707246 (Other Grant/Funding Number: Canadian Cancer Society)
- POC-181042 (Other Grant/Funding Number: Canadian Institutes of Health Research)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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