- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06909097
Better Breaks: Strength Breaks vs Walk Breaks for Sedentary Behavior Breaks
March 27, 2025 updated by: Marily Ann Oppezzo, Stanford University
MOV'D Strength Snacks vs Walk Breaks Study: Health Performance Gains Across Domains
This study investigates the benefits of two different types of 2 minute activity breaks during sedentary workdays for people who sit for long periods of time in sedentary jobs.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
For this study, participants are randomly assigned to one of two physical activity breaks and for 8 weeks are to do 4 per day and track their daily breaks and productivity.
There are many measurements including: in-person strength assessments at baseline, 1 month, and 2 months; daily tracking of breaks; pre and post oral glucose tolerance tests; pre and post 10-day diet tracking; pre and post 10-day Continuous Glucose Monitoring with a Dexcom; genome with saliva at pre; and -omics at pre and post.
Study Type
Interventional
Enrollment (Estimated)
40
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
-
-
California
-
Palo Alto, California, United States, 94304
- Recruiting
- Stanford Prevention Research Center
-
Contact:
- Marily Oppezzo, PhD, MS, RDN, DipACLM
- Phone Number: xxx-xxx-xxxx
- Email: betterbreaks@stanford.edu
-
Contact:
- Jessie Moore, MS
- Phone Number: xxx-xxx-xxxx
- Email: moveofteneveryday@stanford.edu
-
Contact:
- Marily Oppezzo, PhD, MS, RDN, DipACLM
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
-
Identify inclusion criteria.
- Sedentary occupation (e.g., clerical work, data entry, call center, receptionists)
- Full time employment remote or on-site
- Able to safely perform bodyweight squats and lunges
- Over 30 years old
- Not currently doing a strength training program
- Not currently taking planned activity breaks at work
- Has a smart phone with a camera and unlimited text plans
- Interested in participating
- Fluent in English
- Not currently on insulin or any glucose lowering medication
Exclusion Criteria:
- Yes to any of the physical activity readiness criteria questionnaire (e.g. cardiac symptoms with increasing heart rate, dizziness upon performing exercise)
- Participating in another research study on diet, weight loss, or any physical activity.
- If their doctor has ever said to not strength train
- Having insulin dependence
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: Strength Snacks
Participants will do 4 strength snacks throughout each work day, 2 of them post-prandial if possible.
|
Participants will take 2 minute physical movement breaks throughout a sedentary work day.
|
|
Active Comparator: Walk Snacks
Participants will take 4 x2 minute walk breaks throughout the sedentary workday, two of them post-prandial if possible.
|
Participants will take 2 minute physical movement breaks throughout a sedentary work day.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in average area under the curve for glucose from a 10 day continuous glucose monitors
Time Frame: from baseline to post (8 weeks)
|
Change from pre to post in average area under the curve for glucose from a 10 day continuous glucose monitors
|
from baseline to post (8 weeks)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in strength from pre to post
Time Frame: from baseline to 8 weeks
|
As many reps as possible of squats wearing a weighted vest with 20% of their bodyweight
|
from baseline to 8 weeks
|
|
Change in endurance from pre to post
Time Frame: from baseline to 8 weeks
|
As long as possible in as low as possible wall sit (matching pre and post joint angles for participant)
|
from baseline to 8 weeks
|
|
Change in one legged strength from pre to post
Time Frame: from baseline to 8 weeks
|
As many reps as possible standing up from a seated position on one leg and sitting back down
|
from baseline to 8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 5, 2024
Primary Completion (Estimated)
December 1, 2025
Study Completion (Estimated)
March 1, 2026
Study Registration Dates
First Submitted
March 27, 2025
First Submitted That Met QC Criteria
March 27, 2025
First Posted (Actual)
April 3, 2025
Study Record Updates
Last Update Posted (Actual)
April 3, 2025
Last Update Submitted That Met QC Criteria
March 27, 2025
Last Verified
September 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 73022
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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