ExerciseMOVDNCT06372327
Move Often eVery Day 2.0
A study testing Daily Exercise Snacks in people with Exercise, run by Stanford University at 1 site in United States.
Trial summary
The purpose of this study is to assess a novel, widely-accessible intervention to both promote active breaks from work and improve cognitive and psychological performances at work in motivationally-accessible bouts. Read more about this study
- Who is it for?
- Ages 30 years and older, women onlyHealthy volunteers can take part
- Conditions the study is for
- Exercise
- What is being tested?
- Daily Exercise Snacks
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 40 participants
- Where
- 1 siteUnited States
- Study dates
- 31 Jul 2024to 1 Jul 2026
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 30 years and older
- Women only
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Participants must be 30 years of age or older.
- English speaking
- Sedentary job with 90% of the work day sitting
- Not currently taking regular activity breaks at work
Who cannot join
- Yes to any Physical Activity Readiness Questionnaire questions or any condition where increased activity is contraindicated
- Currently doing another worksite physical activity intervention
Trial locations and contacts
1 site in 1 country.
United States1 site
Stanford University School of Medicine
Stanford, California, 94305-7240
About this study
The purpose of this study is to assess a novel, widely-accessible intervention to both promote active breaks from work and improve cognitive and psychological performances at work in motivationally-accessible bouts. This will be done by interrupting prolonged sitting with 1-4 short (1-4 minutes), moderate-to-vigorous physical activity (MVPA) bouts with no equipment, and simple video-based instructions. The short bouts will be referred to as "exercise snacks." In this proposed exercise snacks intervention, investigators explicitly target a population with sedentary jobs due to the generalizability.
Read the detailed description
Participants will answer a short 5-10-minute survey to determine eligibility. Eligible candidates will be invited to attend a 30-minute self-directed orientation session to provide a description of the consent form, study objectives and time commitments, the purpose of randomization, and the importance of completing follow-up assessments regardless of outcome. After the orientation sessions, interested and eligible individuals will be sent the e-consent form.
After participants consent to the study, they will be invited to take the baseline survey, and get assistance with study account set-ups (Garmin, GroupMe). Researchers will handle account set ups. Participants will be asked to download both apps and sign into the apps with the study provided accounts. Many individuals may have GroupMe accounts and will be asked to make a profile for their buddy chat with whatever name they prefer (able to hide their real name if preferred). Baseline measures will last for 2 weeks. And then the 6-week intervention will begin.
All consented participants will receive a 6-week intervention. The study is a 2x2 factorial design with 4 different group. We will be assessing the length of snacktivities (1 minute versus 4 minutes) as well as frequency of snacktivities through the day (1 per day versus 4 per day). Therefore, participants will be randomized into 4 groups: One 1-minute snacktivity per day, four 1-minute snacktivities per day, one 4-minute snacktivity per day, or four 4-minute snacktivities per day.
The intervention will consist of the following empirically supported components shown to promote engagement, adherence, and behavior change:
- Self-monitoring of activity: Participants will be instructed to timestamp and track their snacktivities each day using their phone. Each participant will receive bracelets (1 or 4) that can used to track progress. For example, participants will be taught how they can move the bracelets from one arm to the other to act as a visual aid of how many snacktivities they have done each day.
- Nightly reporting: Participants will be sent nightly texts to track progress on snacktivities as well as productivity, alertness, and physical energy.
- Weekly progress reports and tailored feedback: Each week of completion the participant will get a report of their adherence to the protocol for that week and their goals for next week. Embedded in the progress report will be a link for an interactive action plan survey to plan next week's exercises; the action plan is personalized, and incorporates motivational interviewing and problem-solving strategies. Action planning has high acceptability and is identified as an effective behavioral technique that enhances self-monitoring.
- Relatable modeling: Social modeling theory supports the use of relatable models representing the learner in behavior change and motivation. Dr. Oppezzo's previous work showed high acceptability when the exercise video models were representative of a diverse -body, -ethnicity, and -aged population. Each snacktivity instructional video will feature diverse models performing the moves in work clothes.
- Barrier problem solving: At baseline, study team members will work with participants to identify a feasible, safe, and comfortably private workday location for performing the activity breaks.
- Peer support: participants will be assigned a peer buddy who will act as a health-buddy motivational coach. This person will be in a private group-chat with their designated buddy (another participant) and our study account. The study account will monitor conversation and give motivational prompts, when needed, to boost conversation amongst the 2 buddies.
During the maintenance phase (after the intervention phase and lasting 6 months), participants will take part in booster sessions. The first 2 booster sessions will be completed every month, and the following 2 booster sessions will be completed every 6 weeks, following a scaffolded design to ease participants off of the program.
During the follow-up, investigators will collect behavioral data only via zoom. At the end of the study, we will conduct semi-structured interviews on study experience.
- Conditions
- Exercise
- Being tested
- Daily Exercise Snacks
- Keywords
- Sedentary Behavior
- Medical subject headings
- Motor Activity, Sedentary Behavior
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Daily Exercise SnacksBehavioural
Participants will be encouraged to break up prolonged sitting at work with brief, high-intensity exercise snacks of varying length / total number depending on condition assignment.
| Study group | Role | What they receive |
|---|---|---|
| 1 x 1 minute Exercise Snack / Day | Experimental | Participants will be assigned a daily goal of 1, 1-minute exercise snack to break up prolonged sitting. Receives: Behavioral: Daily Exercise Snacks |
| 1 x 4 Exercise Snack / Day | Experimental | Participants will be assigned a daily goal of 1, 4-minute exercise snack to break up prolonged sitting. Receives: Behavioral: Daily Exercise Snacks |
| 4x1 Exercise Snacks / Day | Experimental | Participants will be assigned a daily goal of 4, 1-minute exercise snack to break up prolonged sitting. Receives: Behavioral: Daily Exercise Snacks |
| 4x4 Exercise Snacks/Day | Experimental | Participants will be assigned a daily goal of 4, 4-minute exercise snack to break up prolonged sitting. Receives: Behavioral: Daily Exercise Snacks |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of self-reported exercise snack breaks at work at week 7
For the post-test week after the 6 week intervention, participants will self-report the number of exercise snacks they do each day.
Measured: Collected 1 work week at week 7 (the week after the 6 week intervention)
Number of self-reported exercise snack breaks at work at week 18
For one week (at week 18) participants will self-report the number of exercise snacks they do each day.
Measured: collected 1 work week at week 18 (3 months after the intervention)
Number of self-reported exercise snack breaks at work at week 30 during follow-up
For one week (at week 30) participants will self-report the number of exercise snacks they do each day.
Measured: collected 1 work week at week 30 (6 months after the intervention)
Secondary outcomes (1)
Liking of exercise snacks
5-point likert scale From not at all to extremely of how much did you like doing exercise snacks
Measured: at week 7, post test, immediately after 6 weeks of treatment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Apr 2024
- Study start31 Jul 2024
- Primary completion1 Jul 2026 (estimated)
- Study completion1 Jul 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for ExerciseStudies of the same condition, open and under way.
- More trials run by Stanford UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Factorial
- Model description
- This will be a 2 (Exercise snack number) x 2 (Exercise snack length) factorial design.
- Masking
- None (open label)
- Enrolment
- 40 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Stanford University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Marily Ann Oppezzo, Stanford University
- Investigators
- Marily Oppezzo, PhD, Principal investigator, Stanford University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06372327
- Sponsor's protocol ID
- 73468
- Acronym
- MOVD
- Status last verified
- Oct 2024
- First submitted
- 13 Apr 2024
- Last updated
- 3 Aug 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 3 Aug 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Move Often eVery Day 2.0
- ClinicalTrials.gov ID
- NCT06372327
- Acronym / sponsor ID
- MOVD / 73468
- Conditions
- Exercise
- Keywords
- Sedentary Behavior
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 40 participants (estimated)
- Lead sponsor
- Stanford UniversityUniversity, hospital or other
- Study start
- 31 Jul 2024 (actual)
- Primary completion
- 1 Jul 2026 (estimated)
- Study completion
- 1 Jul 2026 (estimated)
- First posted
- 18 Apr 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to assess a novel, widely-accessible intervention to both promote active breaks from work and improve cognitive and psychological performances at work in motivationally-accessible bouts. This will be done by interrupting prolonged sitting with 1-4 short (1-4 minutes), moderate-to-vigorous physical activity (MVPA) bouts with no equipment, and simple video-based instructions. The short bouts will be referred to as "exercise snacks." In this proposed exercise snacks intervention, investigators explicitly target a population with sedentary jobs due to the generalizability.
Detailed description
Participants will answer a short 5-10-minute survey to determine eligibility. Eligible candidates will be invited to attend a 30-minute self-directed orientation session to provide a description of the consent form, study objectives and time commitments, the purpose of randomization, and the importance of completing follow-up assessments regardless of outcome. After the orientation sessions, interested and eligible individuals will be sent the e-consent form.
After participants consent to the study, they will be invited to take the baseline survey, and get assistance with study account set-ups (Garmin, GroupMe). Researchers will handle account set ups. Participants will be asked to download both apps and sign into the apps with the study provided accounts. Many individuals may have GroupMe accounts and will be asked to make a profile for their buddy chat with whatever name they prefer (able to hide their real name if preferred). Baseline measures will last for 2 weeks. And then the 6-week intervention will begin.
All consented participants will receive a 6-week intervention. The study is a 2x2 factorial design with 4 different group. We will be assessing the length of snacktivities (1 minute versus 4 minutes) as well as frequency of snacktivities through the day (1 per day versus 4 per day). Therefore, participants will be randomized into 4 groups: One 1-minute snacktivity per day, four 1-minute snacktivities per day, one 4-minute snacktivity per day, or four 4-minute snacktivities per day.
The intervention will consist of the following empirically supported components shown to promote engagement, adherence, and behavior change:
- Self-monitoring of activity: Participants will be instructed to timestamp and track their snacktivities each day using their phone. Each participant will receive bracelets (1 or 4) that can used to track progress. For example, participants will be taught how they can move the bracelets from one arm to the other to act as a visual aid of how many snacktivities they have done each day.
- Nightly reporting: Participants will be sent nightly texts to track progress on snacktivities as well as productivity, alertness, and physical energy.
- Weekly progress reports and tailored feedback: Each week of completion the participant will get a report of their adherence to the protocol for that week and their goals for next week. Embedded in the progress report will be a link for an interactive action plan survey to plan next week's exercises; the action plan is personalized, and incorporates motivational interviewing and problem-solving strategies. Action planning has high acceptability and is identified as an effective behavioral technique that enhances self-monitoring.
- Relatable modeling: Social modeling theory supports the use of relatable models representing the learner in behavior change and motivation. Dr. Oppezzo's previous work showed high acceptability when the exercise video models were representative of a diverse -body, -ethnicity, and -aged population. Each snacktivity instructional video will feature diverse models performing the moves in work clothes.
- Barrier problem solving: At baseline, study team members will work with participants to identify a feasible, safe, and comfortably private workday location for performing the activity breaks.
- Peer support: participants will be assigned a peer buddy who will act as a health-buddy motivational coach. This person will be in a private group-chat with their designated buddy (another participant) and our study account. The study account will monitor conversation and give motivational prompts, when needed, to boost conversation amongst the 2 buddies.
During the maintenance phase (after the intervention phase and lasting 6 months), participants will take part in booster sessions. The first 2 booster sessions will be completed every month, and the following 2 booster sessions will be completed every 6 weeks, following a scaffolded design to ease participants off of the program.
During the follow-up, investigators will collect behavioral data only via zoom. At the end of the study, we will conduct semi-structured interviews on study experience.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Factorial
- Masking
- None (open label)
- Number of arms
- 4
- Model description
- This will be a 2 (Exercise snack number) x 2 (Exercise snack length) factorial design.
| Arm | Type | Receives |
|---|---|---|
| 1 x 1 minute Exercise Snack / Day | Experimental | Behavioral: Daily Exercise SnacksParticipants will be assigned a daily goal of 1, 1-minute exercise snack to break up prolonged sitting. |
| 1 x 4 Exercise Snack / Day | Experimental | Behavioral: Daily Exercise SnacksParticipants will be assigned a daily goal of 1, 4-minute exercise snack to break up prolonged sitting. |
| 4x1 Exercise Snacks / Day | Experimental | Behavioral: Daily Exercise SnacksParticipants will be assigned a daily goal of 4, 1-minute exercise snack to break up prolonged sitting. |
| 4x4 Exercise Snacks/Day | Experimental | Behavioral: Daily Exercise SnacksParticipants will be assigned a daily goal of 4, 4-minute exercise snack to break up prolonged sitting. |
Who may qualify
- Ages
- 30 years and older
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Participants must be 30 years of age or older.
- English speaking
- Sedentary job with 90% of the work day sitting
- Not currently taking regular activity breaks at work
Key exclusion criteria (2 listed)
- Yes to any Physical Activity Readiness Questionnaire questions or any condition where increased activity is contraindicated
- Currently doing another worksite physical activity intervention
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Daily Exercise SnacksParticipants will be encouraged to break up prolonged sitting at work with brief, high-intensity exercise snacks of varying length / total number depending on condition assignment. | Behavioural | 1 x 1 minute Exercise Snack / Day, 1 x 4 Exercise Snack / Day, 4x1 Exercise Snacks / Day, 4x4 Exercise Snacks/Day |
Primary outcome
Number of self-reported exercise snack breaks at work at week 7
Time frame: Collected 1 work week at week 7 (the week after the 6 week intervention)
For the post-test week after the 6 week intervention, participants will self-report the number of exercise snacks they do each day.
Number of self-reported exercise snack breaks at work at week 18
Time frame: collected 1 work week at week 18 (3 months after the intervention)
For one week (at week 18) participants will self-report the number of exercise snacks they do each day.
Number of self-reported exercise snack breaks at work at week 30 during follow-up
Time frame: collected 1 work week at week 30 (6 months after the intervention)
For one week (at week 30) participants will self-report the number of exercise snacks they do each day.
1 secondary outcome
Liking of exercise snacks
Time frame: at week 7, post test, immediately after 6 weeks of treatment
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Aug 2025.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Marily Oppezzo, PhD principal investigator
Stanford University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Daily Exercise Snacks in people with Exercise, run by Stanford University at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 3 Aug 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of self-reported exercise snack breaks at work at week 7 (time frame: Collected 1 work week at week 7 (the week after the 6 week intervention)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Aug 2025.