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Therapeutic application of virtual reality in a pulmonary clinic

Therapeutic application of virtual reality in a pulmonary clinic - TAVIREL-Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00035436
Enrollment
50
Registered
2024-11-27
Start date
2024-10-25
Completion date
Unknown
Last updated
2025-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

The study investigates the influence of VR applications in the treatment of various lung diseases.

Interventions

Group 1: VR application on patients on various wards at the Thoraxklinik Heidelberg. After each application on the respective wards, the participants and the hospital staff who carried out the VR appl

Sponsors

Thoraxklinik Heidelberg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion criteria for patients -Age = 18 years -Sufficient cognitive ability to understand the meaning and purpose of the study - Sufficient decision-making capacity - Ability to give informed consent Inclusion criteria for clinical staff -Age = 18 years -Employed by the Thoraxklinik Heidelberg -Trained in the use of the VR glasses -Informed about the study

Exclusion criteria

Exclusion criteria: Patient exclusion criteria - Treating or caring hospital staff consider the patient is not suitable for the study - not in full possession of his/her mental faculties - Not able to consent to the study - Migraine - Taking opioids (only in the intensive care unit) - Epilepsy - Severe mental illness - Dementia, Parkinson's disease - Delirium - Known motion sickness - Post-operative nausea and vomiting (PONV)

Design outcomes

Primary

MeasureTime frame
-Patient interest in using a VR application - Tolerance of the VR application by the patients - Feasibility of implementing a VR application in the opinion of the staff

Secondary

MeasureTime frame
The secondary objective criteria depend on the clinical setting in which the VR application takes place. They include the following: - Influence of a relaxing VR application on the current state of mind (measured with the ASTS without the anger item, which was constructed from the “Profile of Mood States”) - Influence on the subjectively perceived pain (measured with the Numerical Rating Scale (NRS, pain scale)) - Influence on the subjectively perceived quality of pain (assessed using the multidimensional Bried Pain Inventory (BPI-SF)) - Influence on heart rate, respiratory rate, blood pressure, oxygen saturation (read on the monitor) - Frequency and extension of the time interval for spontaneous breathing (weaning station)

Countries

Germany

Contacts

Public ContactClaudia Bauer-Kemeny

Thoraxklinik Heidelberg

claudia.bauer@med.uni-heidelberg.de+49 6221 396 7888

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026