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Occupational StressNCT07126444

Effects of an Exercise Snack Intervention on Employee Health and Work Performance

An observational study of Occupational Stress, run by Kaohsiung Medical University Chung-Ho Memorial Hospital at 1 site in Taiwan.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

To create brief exercise videos addressing physical discomfort, fitness goals, and movement skills. To design personalized exercise menus to enhance staff adherence. To apply the "exercise snacking" model with multiple short daily sessions and evaluate its effects on health, work performance, and exercise behavior. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Occupational Stress
How many people
130 participants
Where
1 siteTaiwan
Study dates
2 Sep 2025to 31 Dec 2027
Phase
Observational
Are there results?
Not yet: the study is under way

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 Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Study population: This study will recruit full-time faculty and staff from a university and its affiliated hospital. The participants are generally healthy adults who may experience varying levels of musculoskeletal discomfort or reduced physical fitness due to prolonged sedentary or standing work conditions. Individuals are expected to be capable of independent physical activity and willing to engage in brief, self-directed exercise sessions integrated into their daily routine.

Who may be able to join

  • Currently employed at Kaohsiung Medical University or Kaohsiung Medical University Hospital.
  • Willing to participate in a 12-week exercise intervention, complete related questionnaires, and undergo physical performance assessments.

Who cannot join

  • Pregnant individuals, due to safety concerns related to exercise intensity and physical assessments.
  • Individuals with a diagnosed neurological disorder (e.g., stroke, Parkinson's disease).
  • Individuals experiencing severe pain in the upper or lower limb joints that interferes with their ability to complete the assessments.
  • Individuals assigned to high-intensity exercise who have unstable cardiac conditions (e.g., angina, myocardial infarction, heart failure).

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Taiwan1 site, 1 recruiting
  • Kaohsiung Medical University

    Kaohsiung City, 807

    Liaw Lih-Jiun CS515, 886-073121101#2663, lijili@kmu.edu.tw

    Recruiting

Other trials in Taiwan

About this study

Official title: Effects of an Exercise Snack Intervention on Employee Health and Work Performance: A Study at Kaohsiung Medical University

To create brief exercise videos addressing physical discomfort, fitness goals, and movement skills.

To design personalized exercise menus to enhance staff adherence.

To apply the "exercise snacking" model with multiple short daily sessions and evaluate its effects on health, work performance, and exercise behavior.

Read the detailed description
  1. To develop brief exercise videos targeting different areas of physical discomfort (e.g., neck and shoulders, lower back, lower limbs), specific fitness goals (e.g., localized muscle stretching, targeted muscle strengthening, cardiorespiratory endurance, balance training), high-intensity interval training (HIIT), or the acquisition of specific movement skills (e.g., core stability, pelvic floor muscle contraction, and multi-directional pelvic mobility).
  2. To design personalized exercise "menus" based on individual needs identified through a preliminary assessment, with the goal of improving adherence to voluntary exercise routines among staff.
  3. To apply the concept of "exercise snacking" by implementing a daily routine of 3 to 8 brief exercise sessions, and to evaluate changes in staff members' physiological health, work performance, and exercise behavior after a 12-week intervention.
Medical subject headings
Occupational Stress

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07126444
Study groupRoleWhat they receive
EmployeeEmployees of Kaohsiung Medical University, including faculty and administrative staff. Participants are adults (≥20 years) currently working full-time or part-time at the university. This group is selected because prolonged sedentary work and job-related demands are associated with musculoskeletal discomfort, stress, and reduced physical activity. They represent the target population for evaluating the feasibility and effectiveness of brief workplace exercise interventions ("exercise snacks").

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Physical fitness test

    Measured: 30 minutes

  2. Work Ability Index

    Measured: 5 minutes

  3. Copenhagen Burnout Inventory

    Measured: 5 minutes

  4. Perceived Stress Scale-14

    Measured: 5 minutes

  5. Exercise adherence

    Measured: 1 minutes/per day

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Aug 2025
  2. Study start2 Sep 2025
  3. Primary completion31 Dec 2027 (estimated)
  4. Study completion31 Dec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Cross-sectional
Enrolment
130 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07126444
Sponsor's protocol ID
KMUHIRB-F(I)-20250189
Other IDs
113825017999UC003-6
Status last verified
Aug 2026
First submitted
11 Aug 2025
Last updated
10 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Occupational Stress, run by Kaohsiung Medical University Chung-Ho Memorial Hospital at 1 site in Taiwan.

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 2 inclusion and 4 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: looking for participants now, as of the sponsor's last update on 10 Aug 2026. 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 Taiwan. 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?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Lih-Jiun Liaw (Taiwan: 886+73121101, lijili@kmu.edu.tw), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Physical fitness test (time frame: 30 minutes). The study lists 5 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 10 Aug 2026.

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