- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07209553
- Original Trial
AI-Powered Micro-Breaks at Work
"Smart Breaks" During Working Hours: Feasibility of an AI-Based Application to Enhance Well-Being Through Active Micro-Breaks Among Office Workers
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Remote and hybrid work have intensified sedentary behavior, increasing the risk of professional burnout and negatively affecting employee health. This study investigates the feasibility and accessibility of the Movebite app, an AI-based tool integrated into Slack, designed to encourage active micro-breaks. Through a one-arm, pre-test post-test design, we evaluate the feasibility and usability of the AI-based virtual coach and its relevance for well-being of employees working from home.
This research contributes to the development and promotion of empirically grounded solutions in the field of occupational health psychology, testing an innovative technological approach to reduce the negative impact of sedentary work.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Timiș County
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Timișoara, Timiș County, Romania, 300223
- West University of Timișoara
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
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)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Device Feasibility
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
The intervention involved using the Mobi AI coach to set up and engage in active micro-breaks over five consecutive working days.
|
Mobi is a conversational AI coach that serves as an occupational health coach for employees.
Through coaching conversations, Mobi gets to know each employee and help them set micro-goals to work towards their overall health goal/objective.
Mobi suggests small, personalized activities for the micro-breaks that align with these goals.
To ensure ease of use it is integrated into Slack and MS Teams.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Satisfaction with the intervention
Time Frame: Post-intervention (1 week).
|
Seven additional items are open-ended and will be analyzed qualitatively.
These items allow participants to elaborate on what aspects of the program they found most or least valuable, describe their experience with communication tools within the intervention, and offer suggestions for improvement.
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Post-intervention (1 week).
|
|
System usability
Time Frame: Post-intervention (1 week)
|
We will use a 10 item questionnaire (Bangor et al., 2009) designed to measure participants' satisfaction with Mobi, the AI health coach.
The total score of System Usability Scale is 0 and the highest one is 100.
A higher score means a better outcome.
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Post-intervention (1 week)
|
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Treatment adherence
Time Frame: Post-intervention only (1 week)
|
Dropout rate and frequency of app usage.
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Post-intervention only (1 week)
|
|
Vigor
Time Frame: Change from baseline to post-test (1 week; 5 workdays)
|
Vigor refers to a positive affective state experienced at work.
It will be assessed using five items from the Physical Strength subscale of the instrument developed by Shirom (2003).
A higher score means a better outcome (i.e., increased employee vigor).
|
Change from baseline to post-test (1 week; 5 workdays)
|
|
Focus
Time Frame: Change from baseline to post-test (1 week; 5 workdays).
|
Focus refers to an employee's capacity to maintain attention and mental clarity while working.
It will be assessed using five items from the Cognitive Liveliness subscale of the instrument developed by Shirom (2003).
A higher score indicates a better outcome (i.e., increased cognitive focus at work).
|
Change from baseline to post-test (1 week; 5 workdays).
|
|
Physical (dis)comfort
Time Frame: Change from baseline to post-test (1 week; 5 workdays)
|
Physical discomfort (musculoskeletal pain) will be measured using a single-item instrument based on the Visual Analog Scale (VAS) (Häfeli & Elfering, 2006).
The VAS is a widely used and validated method for assessing subjective physical symptoms such as pain intensity.
Participants will indicate their level of discomfort by marking a point along a continuum, reflecting their experience over the past week.
Higher scores indicate greater musculoskeletal discomfort.
|
Change from baseline to post-test (1 week; 5 workdays)
|
|
Positive and negative affect
Time Frame: Change from baseline to post-test (1 week; 5 workdays)
|
Affect will be measured using the Positive Affect subscale from the Positive and Negative Affect Schedule (PANAS; Watson, Clark, & Tellegen, 1988).
This scale assesses the extent to which individuals have experienced a range of positive emotions (e.g., enthusiastic, inspired, alert) over the past week.
Participants rate each item on a 5-point scale, from "Very slightly or not at all" to "Extremely."
Higher scores reflect a higher level of positive emotional experience.
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Change from baseline to post-test (1 week; 5 workdays)
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Physical activity during work
Time Frame: Baseline only
|
What employees currently do to stay active during working hours (i.e., stretching, short walks, taking the stairs, using a standing desk, scheduled workout sessions during work, other)
|
Baseline only
|
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Before and/or after-work physical activities
Time Frame: Baseline only
|
To assess participants' engagement in physical activity outside working hours, we included two binary (Yes/No) items referring to typical weekly behaviors.
The first item evaluates whether participants engage in light movement after work hours (e.g., walking, stretching), while the second item assesses participation in regular, scheduled workout sessions either before or after the workday.
These items aim to provide a brief overview of participants' physical activity routines that may contribute to their overall well-being and complement the effects of the intervention.
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Baseline only
|
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Sociodemographic information
Time Frame: Baseline only
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Age, gender, background, educational level, average monthly income, work experience, etc.
|
Baseline only
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Watson D, Clark LA, Tellegen A. Development and validation of brief measures of positive and negative affect: the PANAS scales. J Pers Soc Psychol. 1988 Jun;54(6):1063-70. doi: 10.1037//0022-3514.54.6.1063.
- Haefeli M, Elfering A. Pain assessment. Eur Spine J. 2006 Jan;15 Suppl 1(Suppl 1):S17-24. doi: 10.1007/s00586-005-1044-x. Epub 2005 Dec 1.
- Bangor, A., Miller, J. & Kortum, P. (2009). Determining what individual SUS scores mean: Adding an adjective rating scale. Journal of Usability Studies, 4(3), 114-123. Retrieved from http://uxpajournal.org/determining-what-individual-sus-scores-mean-adding-an-adjective-rating-scale/
- Shirom, A. (2003). Feeling vigorous at work? The construct of vigor and the study of positive affect in organizations. In Emotional and physiological processes and positive intervention strategies (pp. 135-164). Emerald Group Publishing Limited.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimated)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- SmartBreaks
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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