Virtual Reality-Based Breathing Exercise Before Angiography in Children

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age9-18
SponsorGazi University

About this trial

hildren undergoing angiography frequently experience anxiety before the procedure, which may negatively affect physiological parameters and procedural cooperation. Although pharmacological approaches are commonly used to reduce anxiety, they may be associated with adverse effects and are not always necessary. Virtual reality (VR)-based guided breathing exercises offer a non-pharmacological approach that combines immersive distraction with breathing techniques to promote relaxation.

This randomized controlled trial aims to evaluate the effect of a VR-based guided breathing exercise administered before angiography on anxiety and physiological parameters in children aged 9-18 years. A total of 60 participants will be randomly assigned to either a VR-based guided breathing exercise group or a standard care group. Anxiety and physiological parameters, including heart rate, blood pressure, respiratory rate, oxygen saturation, and body temperature, will be assessed before and after the intervention. The findings of this study may provide evidence for the use of VR-based guided breathing exercises as a safe and effective nursing intervention to reduce pre-procedural anxiety in pediatric patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Virtual Reality-Based Guided Breathing Exercise

    Behavioral

    A single 5-7-minute virtual reality-based guided breathing exercise delivered before angiography. Participants will wear a virtual reality headset displaying immersive natural scenery while following standardized breathing instructions designed to promote relaxation and reduce pre-procedural anxiety.

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: experimentalExperimental treatment 1 intervention
Group B: standart careNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

State Anxiety

State anxiety will be assessed using the State Anxiety Inventory for Children. Higher scores indicate greater levels of state anxiety. Assessments will be performed immediately before and immediately after the interventio

Time frame
Immediately before the intervention and immediately after the intervention (approximately 10 minutes).

Secondary outcomes

1

Heart Rate

Heart rate will be measured in beats per minute using the standard clinical monitoring device. Measurements will be obtained immediately before and immediately after the intervention.

Time frame
Immediately before and immediately after the intervention, approximately 10 minutes apart.
2

Blood Pressure

Systolic and diastolic blood pressure will be measured in millimeters of mercury using a calibrated clinical blood pressure monitor. Measurements will be obtained immediately before and immediately after the intervention

Time frame
Immediately before and immediately after the intervention, approximately 10 minutes apart.
3

Respiratory Rate

Respiratory rate will be measured as breaths per minute immediately before and immediately after the intervention.

Time frame
Immediately before and immediately after the intervention, approximately 10 minutes apart.
4

Peripheral Oxygen Saturation

Peripheral oxygen saturation will be measured as a percentage using pulse oximetry immediately before and immediately after the intervention.

Time frame
Immediately before and immediately after the intervention, approximately 10 minutes apart.

Other outcomes

Sponsors and contacts

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