AI-Powered Micro-Breaks at Work (NCT07209553) | Clinical Trial Compass
CompletedNot Applicable
AI-Powered Micro-Breaks at Work
Romania16 participantsStarted 2025-04-07
Plain-language summary
This study evaluates the feasibility of an online intervention based on artificial intelligence-the Movebite app integrated into the Slack platform-aimed at promoting engagement in micro-breaks involving physical activity, with the goal of enhancing workplace well-being and reducing musculoskeletal discomfort among remote workers.
Who can participate
Age range
18 Years – 60 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Employees between the ages of 18-60 years' old
* Full-time working entirely from home (home office)
* Have a PC or laptop and basic digital competencies
* Proficient in English language
Exclusion Criteria:
* Other work arrangements such as shift-work, part-time work
* Unable to access the internet/computer/install Slack app (Yes/No questions)
* No proficiency for English
* Not working mainly from a desk (e.g., fieldwork)
* Current health issues (current pregnancy, any neurological, vascular, or acute musculoskeletal condition or any disease or symptom)
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial used an AI-powered system to prompt micro-breaks at work to address musculoskeletal discomfort — since the study is now completed, has any published data come out showing whether those scheduled breaks actually reduced pain or discomfort in participants?
2The trial measured things like vigor, focus, and positive affect alongside physical comfort — does my specific type of musculoskeletal discomfort fit the kind of work-related issues this intervention was designed for, or would a more targeted physical therapy approach make more sense for me?
3Since this was a non-drug, non-surgical study with no assigned phase, do you think the findings could be something I could try to apply in my own daily routine right now, or is it too early to draw practical conclusions from the results?
4The trial tracked treatment adherence as a key outcome — given what you know about my schedule and work situation, do you think I'd realistically be able to stick to a structured micro-break program, and does that affect whether this kind of approach is worth pursuing?
5Are there any standard ergonomic or occupational health interventions already recommended by clinical guidelines that I should try first, before looking at approaches like this that are still being studied?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Satisfaction with the intervention
Timeframe: Post-intervention (1 week).
2
System usability
Timeframe: Post-intervention (1 week)
3
Treatment adherence
Timeframe: Post-intervention only (1 week)
4
Vigor
Timeframe: Change from baseline to post-test (1 week; 5 workdays)
5
Focus
Timeframe: Change from baseline to post-test (1 week; 5 workdays).
6
Physical (dis)comfort
Timeframe: Change from baseline to post-test (1 week; 5 workdays)
7
Positive and negative affect
Timeframe: Change from baseline to post-test (1 week; 5 workdays)