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Healthcare WorkersNCT06926257

Effects of VR-based Respiratory Training on Motor Reaction Time and Correctness, Stress Levels, Attention, Motor Skills, Postural Stability and Sleep Quality in Shift Healthcare Workers

A study testing Experimental group (B) - breathing training using VR and Experimental group (C) - breathing training using relaxation music in people with Healthcare Workers and Stress Level, run by Poznan University of Physical Education at 1 site in Poland.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This study investigates the effects of virtual reality (VR)-based respiratory training on various physiological and cognitive functions in shift-working healthcare professionals, including paramedics and nurses. Read more about this study

Who is it for?
Ages 23 to 45 yearsHealthy volunteers can take part
What is being tested?
Experimental group (B) - breathing training using VR and Experimental group (C) - breathing training using relaxation music
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 sitePoland
Study dates
7 Apr 2025to 30 Dec 2025
Phase
Interventional
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 23 to 45 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

The study will be conducted in a group of paramedics and nurses of both sexes, aged 23-45. It is expected that 60 people will be examined. The study will include hospital emergency department employees, working shifts, with a minimum of two years of work experience. Those who receive a doctor's consent to participate in the study and give informed consent will be admitted to the study.

Trial locations and contacts

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

Łucja Rząsa, MSc contact

+48790885122

rzasa@awf.poznan.pl

Poland1 site
  • Poznań University of Physical Education

    Poznan, 61871

    Marzena Szerment, 61 835 50 00, szerment@awf.poznan.pl

Other trials in Poland

About this study

This study investigates the effects of virtual reality (VR)-based respiratory training on various physiological and cognitive functions in shift-working healthcare professionals, including paramedics and nurses. The research will evaluate how VR-guided breathing exercises influence: stress levels, motor reaction time and accuracy, attention and cognitive performance, motor skills and postural stability, sleep quality

Participants will be divided into three groups:

Read more

VR-based respiratory training group - performing guided breathing exercises in a VR environment.

Music-based relaxation group - listening to relaxing music without structured breathing instructions.

Control group - no intervention.

The findings will help determine whether VR-based respiratory training is an effective method for improving stress resilience, cognitive function, and physical performance in shift-working healthcare professionals.

Being tested
Experimental group (B) - breathing training using VR, Experimental group (C) - breathing training using relaxation music
Medical subject headings
Emergencies, Sleep Disorders, Circadian Rhythm

What participants receive

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

  • Experimental group (B) - breathing training using VROther

    The Flowborne VR - Biofeedback Breathing Meditation game is an interactive training environment that guides the participant through a series of breathing exercises. The app adjusts the difficulty level and pace of the workout in real time based on the participant's physiological parameters, such as breathing rhythm.

    Types of exercises in the game:

    1. diaphragmatic breathing - the participant takes slow, controlled breaths, inhaling into the diaphragm and exhaling at a set pace. The game visualizes breathing through animations of water waves and background color changes.
    2. rhythmic breathing - the participant sts his breathing rhythm to the changing visual and audio stimuli, allowing for synchronous breathing control.
    3. Controlled exhalation lengthening - the participant learns the technique of slow exhalation of air to improve relaxation and reduce tension.
  • Experimental group (C) - breathing training using relaxation musicOther

    • Diaphragmatic breathing - the conscious engagement of the diaphragm in the inhalation process.
    • Controlled exhalation lengthening - a technique to lengthen the exhalation phase.
    • Rhythmic breathing - synchronizing breathing with a set pace to improve breath control.

    Structure of each session:

    1. introductory phase (3 minutes)
    • Participants assume a comfortable sitting or lying position.
    • Brief instruction on proper breathing.
    1. training phase (15 minutes).
    • Participants listen to relaxation music while focusing on the breathing techniques they learned before the session.
    • Breathing techniques used include those learned during the training: diaphragmatic breathing, controlled expiration lengthening, rhythmic breathing. 3 Relaxation phase (2 minutes)
    • Gradual exit from the training session, focusing attention on the sensations of the body and mind.
Study groups in NCT06926257
Study groupRoleWhat they receive
Control group (A) - no interventionNo interventionAll participants will first be measured before and after their first night's duty to determine the baseline level of the accepted variables. Subsequently, the subjects will be informed not to use any additional forms of relaxation, and after four weeks, the study participants will undergo a final measurement.
Experimental group (B) - breathing training using VRExperimentalBreathing training in the experimental group will be carried out under controlled conditions, in a quiet room, using VR goggles and the Flowborne VR - Biofeedback Breathing Meditation application. The goal of the program is to learn conscious breathing and reduce stress levels through an immersive virtual reality environment. * A total of 8 sessions over 4 weeks. * 2 trainings per week (after the end of night duty). * Each session lasts 20 minutes.
Receives: Other: Experimental group (C) - breathing training using relaxation music
Experimental group (C) - breathing training using relaxation musicExperimentalBreathing training will be based on traditional relaxation methods using relaxation music. This program will be conducted under controlled conditions in a quiet room, without the use of VR technology. * A total of 8 sessions over 4 weeks. * 2 trainings per week (after the end of night duty). * Each session lasts 20 minutes.
Receives: Other: Experimental group (B) - breathing training using VR

What is being measured

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

  1. Attention and reaction time

    he MOXO Test is a computer-based diagnostic tool used to assess attention and impulse control. Participants respond to various visual and auditory stimuli appearing on the screen, where they must quickly and accurately recognize those that require a response while ignoring others designed to distract them. The test lasts approximately 15-18 minutes and evaluates four key indicators: reaction time, impulsivity, hyperactivity, and inattention. This allows for a detailed analysis of the participant's cognitive abilities and identification of potential attention deficits.

    Measured: At the beginning of the study and after 4 weeks of breathing exercises.

  2. Postural stability

    The assessment will be conducted using a standard, low, stable posturographic platform. The first measurement will be taken in an upright posture with an attempt to lean the body as far forward and backward as possible while maintaining stability. The second measurement involves standing on one leg.

    Measured: At the beginning of the study and after 4 weeks of breathing exercises.

  3. Sleep quality

    The impact of the intervention on participants' sleep quality, particularly in the context of shift work, will be assessed using the Polish version of the Pittsburgh Sleep Quality Index (PSQI). This measurement will be conducted twice: before the first night shift and before the last night shift (Mollayeva et al., 2016).

    Measured: At the beginning of the study and after 4 weeks of breathing exercises.

  4. Stress level and mood

    Stress levels will be assessed using the PSS-10 Perceived Stress Scale (Cohen S., Kamarck T., Mermelstein R., 1983), adapted to Polish (Juczyński Z., Ogińska-Bulik N., 2009), which evaluates the intensity of stress related to one's life situation over the past month (Matuszczak-Świgoń et al., 2023). Additionally, the PANAS (Positive and Negative Affect Schedule) questionnaire will be used to measure participants' positive and negative affect, assessing the intensity of their emotions before and after the intervention (Piotr Brzozowski, 2019). Subjective mood and the intensity of its changes will also be evaluated using a 0-10 scale before each measurement.

    Measured: At the beginning of the study and after 4 weeks of breathing exercises.

  5. Fine motor skills precision

    Fine motor skills precision will be assessed using the WorkAbility Rate of Manipulation Test (WRMT). This test is a tool for evaluating manual skills in a work-related context. It consists of a task requiring participants to transfer discs from one place to another, measuring precision, speed, and dexterity. WRMT is used in the assessment of manual task performance abilities in various industries, including vocational rehabilitation and work capacity evaluation (Wang et al., 2018).

    Measured: At the beginning of the study and after 4 weeks of breathing exercises.

Timeline

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

  1. First posted13 Apr 2025
  2. Study start7 Apr 2025 (estimated)
  3. Primary completion30 Oct 2025 (estimated)
  4. Study completion30 Dec 2025 (estimated)

Resources

More details

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

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06926257
Sponsor's protocol ID
165/25
Status last verified
Apr 2025
First submitted
7 Apr 2025
Last updated
13 Apr 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: The decision on data sharing has not been finalized. The availability of individual participant data (IPD) and supporting documents will be assessed after the study is completed. If data sharing is approved, details regarding access, format, and conditions will be provided in future updates.

Questions about this trial

What is this clinical trial studying?

A study testing Experimental group (B) - breathing training using VR and Experimental group (C) - breathing training using relaxation music in people with Healthcare Workers and Stress Level, run by Poznan University of Physical Education at 1 site in Poland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

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: opening soon, as of the sponsor's last update on 13 Apr 2025. 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 Poland. 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 Łucja Rząsa, MSc (+48790885122, rzasa@awf.poznan.pl), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Attention and reaction time (time frame: At the beginning of the study and after 4 weeks of breathing exercises.). 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 13 Apr 2025.

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