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Efficacy of Movement Breaks in Real-World Settings

Efficacy of Movement Breaks in Real-World Settings

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05574426
Enrollment
77
Registered
2022-10-10
Start date
2022-10-01
Completion date
2023-12-05
Last updated
2025-03-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

Exercise Snack, Movement Break, Sedentary Time, Lifestyle Exercise, Physical Activity Breaks, VILPA

Brief summary

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.

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.

Interventions

BEHAVIORALMovement Breaks

Participants will be asked to perform 30-60 second movement breaks 3-4 times per day on at least 3 days per week.

Sponsors

Canadian Cancer Society (CCS)
CollaboratorOTHER
Canadian Institutes of Health Research (CIHR)
CollaboratorOTHER_GOV
McMaster University
CollaboratorOTHER
University of British Columbia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

Outcome assessors will not be aware of group allocation and statistics performed on data with group identity blinded.

Intervention model description

Participants will be randomized (1:1 allocation ratio) into Mobility or Cardiovascular movement break groups for 12-weeks. Both groups will perform 3-4 movement breaks on at least 3 days of the week.

Eligibility

Sex/Gender
ALL
Age
40 Years to 64 Years
Healthy volunteers
Yes

Inclusion criteria

1. Physically inactive (performing \<150 minutes of moderate-to-vigorous intensity aerobic exercise per week, assessed by pre-screening Get Active Questionnaire); 2. Body Mass Index: 18.5-30.0 kg/m2; 3. Not currently diagnosed with or being treated for cardiometabolic disease (e.g., coronary artery disease, diabetes); 4. Not a current smoker; 5. Cleared to engage in physical activity using the Get Active Questionnaire and, if applicable, consultation with a Qualified Exercise Professional; 6. Access to a computer, tablet or smartphone for intervention delivery and tracking

Exclusion criteria

1. Chronic health condition preventing participation in exercise; 2. Lack of access to internet connection

Design outcomes

Primary

MeasureTime frameDescription
Change From Baseline in Cardiorespiratory Fitness at 12 WeeksBaseline and Week 12Cardiorespiratory fitness will be assessed as the highest 30-s average from a laboratory-based graded VO2peak test on a cycle ergometer.

Secondary

MeasureTime frameDescription
Change From Baseline in Plasma GlucoseBaseline and 12 weeksA fasted venous blood sample will be obtained and glucose measured by biochemical assay.
Change From Baseline in Insulin ResistanceBaseline and 12 weeksA fasted venous blood sample will be obtained and insulin resistance estimated by homeostasis model assessment (HOMA) score
Change From Baseline in Inflammatory CytokinesBaseline and 12 weeksA fasted venous blood sample will be obtained and inflammatory cytokines measured by multiplex assay
Change From Baseline in Body MassBaseline and 12 weeksBody mass will be measured by weigh scale
Change From Baseline in Plasma InsulinBaseline and 12 weeksA fasted venous blood sample will be obtained and insulin measured by commercial assay.
Device-Measured Adherence to Movement BreaksWeek 2 and week 11Participants will wear accelerometers to assess adherence near the beginning and the end of the intervention.
Self-Reported Adherence to Movement BreaksOnce per week for 12 weeksParticipants will be sent weekly surveys asking them to recall the total number of movement breaks performed that week.
Movement Break Enjoyment Assessed by the Exercise Enjoyment Scale (EES)Immediately following each movement break for entire 12-week interventionThe EES is a validated, single-item 7-point scale to assess exercise enjoyment. Possible scores range from 1 (not at all) to 7 (extremely).
Rating of Perceived Exertion (RPE) Following Movement BreaksImmediately following each movement break for entire 12-week interventionA 10 point RPE scale will be used to assess perceived exertion ranging from 0 (rest) to 10 (maximal).
Change From Baseline in Waist CircumferenceBaseline and 12 weeksWaist circumference (in centimetres) will be measured using a measurement tape.

Countries

Canada

Participant flow

Recruitment details

Online recruitment primarily through use of third-party service.

Pre-assignment details

77 participants were included in the intention-to-treat analyses

Participants by arm

ArmCount
Cardiovascular Movement Breaks
Participants were instructed to perform 3-4 exercise snacks (30-60s bursts of exercise) on at least 3 days of the week. The exercises prescribed in this arm were designed to increase heart rate.
38
Mobility Movement Breaks
Participants were instructed to 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 were not designed to increase heart rate.
39
Total77

Baseline characteristics

CharacteristicTotalCardiovascular Movement BreaksMobility Movement Breaks
Age, Continuous54 Years
STANDARD_DEVIATION 6
54 Years
STANDARD_DEVIATION 6
53 Years
STANDARD_DEVIATION 7
Race and Ethnicity Not Collected0 Participants
Sex: Female, Male
Female
56 Participants27 Participants29 Participants
Sex: Female, Male
Male
21 Participants11 Participants10 Participants
VO2peak24.5 ml/kg/min
STANDARD_DEVIATION 4.4
24.4 ml/kg/min
STANDARD_DEVIATION 4.3
24.6 ml/kg/min
STANDARD_DEVIATION 4.5

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 380 / 39
other
Total, other adverse events
0 / 380 / 39
serious
Total, serious adverse events
0 / 380 / 39

Outcome results

Primary

Change From Baseline in Cardiorespiratory Fitness at 12 Weeks

Cardiorespiratory fitness will be assessed as the highest 30-s average from a laboratory-based graded VO2peak test on a cycle ergometer.

Time frame: Baseline and Week 12

Population: Intention-to-treat

ArmMeasureValue (MEAN)
Cardiovascular Movement BreaksChange From Baseline in Cardiorespiratory Fitness at 12 Weeks-0.6 ml/kg/min
Mobility Movement BreaksChange From Baseline in Cardiorespiratory Fitness at 12 Weeks-1.0 ml/kg/min
Secondary

Change From Baseline in Body Mass

Body mass will be measured by weigh scale

Time frame: Baseline and 12 weeks

Secondary

Change From Baseline in Inflammatory Cytokines

A fasted venous blood sample will be obtained and inflammatory cytokines measured by multiplex assay

Time frame: Baseline and 12 weeks

Secondary

Change From Baseline in Insulin Resistance

A fasted venous blood sample will be obtained and insulin resistance estimated by homeostasis model assessment (HOMA) score

Time frame: Baseline and 12 weeks

Secondary

Change From Baseline in Plasma Glucose

A fasted venous blood sample will be obtained and glucose measured by biochemical assay.

Time frame: Baseline and 12 weeks

Secondary

Change From Baseline in Plasma Insulin

A fasted venous blood sample will be obtained and insulin measured by commercial assay.

Time frame: Baseline and 12 weeks

Population: Intention-to-treat

ArmMeasureValue (MEAN)
Cardiovascular Movement BreaksChange From Baseline in Plasma Insulin-13 percent change
Mobility Movement BreaksChange From Baseline in Plasma Insulin-2 percent change
Secondary

Change From Baseline in Waist Circumference

Waist circumference (in centimetres) will be measured using a measurement tape.

Time frame: Baseline and 12 weeks

Secondary

Device-Measured Adherence to Movement Breaks

Participants will wear accelerometers to assess adherence near the beginning and the end of the intervention.

Time frame: Week 2 and week 11

Secondary

Movement Break Enjoyment Assessed by the Exercise Enjoyment Scale (EES)

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).

Time frame: Immediately following each movement break for entire 12-week intervention

Secondary

Rating of Perceived Exertion (RPE) Following Movement Breaks

A 10 point RPE scale will be used to assess perceived exertion ranging from 0 (rest) to 10 (maximal).

Time frame: Immediately following each movement break for entire 12-week intervention

Secondary

Self-Reported Adherence to Movement Breaks

Participants will be sent weekly surveys asking them to recall the total number of movement breaks performed that week.

Time frame: Once per week for 12 weeks

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026