AI-Powered Micro-Breaks at Work

October 1, 2025 updated by: West University of Timisoara

"Smart Breaks" During Working Hours: Feasibility of an AI-Based Application to Enhance Well-Being Through Active Micro-Breaks Among Office Workers

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.

Study Overview

Status

Completed

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

Interventional

Enrollment (Actual)

16

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

    • Timiș County
      • Timișoara, Timiș County, Romania, 300223
        • West University of Timișoara

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

Accepts Healthy Volunteers

Yes

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

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: 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.

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.
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.
Post-intervention (1 week)
Treatment adherence
Time Frame: Post-intervention only (1 week)
Dropout rate and frequency of app usage.
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.
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
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.
Baseline only
Sociodemographic information
Time Frame: Baseline only
Age, gender, background, educational level, average monthly income, work experience, etc.
Baseline only

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

April 7, 2025

Primary Completion (Actual)

June 27, 2025

Study Completion (Actual)

July 16, 2025

Study Registration Dates

First Submitted

September 9, 2025

First Submitted That Met QC Criteria

October 1, 2025

First Posted (Estimated)

October 7, 2025

Study Record Updates

Last Update Posted (Estimated)

October 7, 2025

Last Update Submitted That Met QC Criteria

October 1, 2025

Last Verified

October 1, 2025

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)?

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

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.

Clinical Trials on Musculoskeletal Discomfort

Clinical Trials on Mobi

Subscribe