Skip to content

Virtual Reality-Based Transitional Care for ICU Survivors

Impact of a Virtual Reality-Based Transitional Care Program on Heart Rate Variability, Pain, Relocation Stress, and Unplanned ICU Readmission Among Adult ICU Survivors: A Randomized Controlled Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07482722
Acronym
VRICU
Enrollment
150
Registered
2026-03-19
Start date
2026-03-09
Completion date
2027-02-01
Last updated
2026-03-19

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

Conditions

Critical Illness, Intensive Care Units, Stress, Psychological

Keywords

Virtual Reality, ICU Survivors, Relocation Stress, Heart Rate Variability, Transitional Care, Unplanned ICU Readmission, Randomized Controlled Trial

Brief summary

This study aims to evaluate the effectiveness of a virtual reality (VR)-based transitional care program for adult survivors of intensive care unit (ICU) care. ICU survivors frequently experience relocation stress, anxiety, pain, and physiological instability after transfer from the ICU to general wards, which may increase the risk of unplanned ICU readmission. Participants will be randomly assigned to receive either standard transitional care or additional VR-based intervention sessions during their ICU stay. The VR intervention is designed to provide psychological support, environmental orientation, and stress reduction. Primary outcomes include short-term physiological indicators within 48 hours after ICU transfer. Secondary outcomes include pain, relocation stress, and unplanned ICU readmission within 7 days.

Detailed description

This is a single-center, randomized controlled trial designed to investigate the effects of a virtual reality (VR)-based transitional care intervention on physiological stability and psychological adaptation among adult ICU survivors. Critically ill patients often experience relocation stress syndrome following transfer from the ICU to general wards. This transition period is associated with increased anxiety, pain perception, autonomic imbalance, and a higher risk of unplanned ICU readmission. Eligible participants will be randomized using block randomization into the intervention or control group. The intervention group will receive three VR sessions during their ICU stay in addition to standard transitional care. The control group will receive standard care alone. The primary outcome is short-term physiological stability measured within 48 hours after ICU transfer. Secondary outcomes include heart rate variability parameters, pain intensity, relocation stress, and unplanned ICU readmission within 7 days. This study seeks to determine whether VR-assisted transitional care can enhance recovery, reduce stress-related responses, and improve patient outcomes following ICU discharge.

Interventions

BEHAVIORALVirtual Reality-Based Transitional Care

Participants assigned to this arm will receive three structured virtual reality (VR) sessions during their ICU stay in addition to standard transitional care. Each VR session is designed to provide environmental orientation, psychological support, and stress reduction through immersive audiovisual content. The intervention aims to improve short-term physiological stability and reduce relocation stress following ICU transfer.

Sponsors

Mackay Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Participants will be randomly assigned in a 1:1 ratio to either the VR intervention group or the standard care control group using block randomization.

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 20 years or older * Adult patients admitted to the intensive care unit (ICU) * Planned transfer from ICU to the general ward * Able to communicate and provide informed consent or have a legal representative provide consent

Exclusion criteria

* Severe cognitive impairment or delirium preventing participation * Severe visual or hearing impairment interfering with VR use * Hemodynamic instability requiring immediate life-saving intervention * Isolation precautions prohibiting device use * Participation in another interventional study that may affect outcomes

Design outcomes

Primary

MeasureTime frameDescription
Heart Rate Variability - RMSSDWithin 48 hours after transfer from the ICU to the general wardHeart rate variability measured using the Root Mean Square of Successive Differences (RMSSD) derived from electrocardiographic recordings.
Heart Rate Variability - High Frequency PowerWithin 48 hours after transfer from the ICU to the general wardHeart rate variability measured using high-frequency (HF) power derived from electrocardiographic recordings.

Secondary

MeasureTime frameDescription
Pain IntensityWithin 48 hours after ICU transferPain intensity will be assessed using the Defense and Veterans Pain Rating Scale (DVPRS), a numeric rating scale ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst possible pain.
Unplanned ICU ReadmissionWithin 7 days after ICU transferOccurrence of unplanned readmission to the ICU within 7 days after transfer to the general ward.
Relocation StressWithin 48 hours after ICU transferRelocation stress will be assessed using the Relocation Stress Syndrome Scale - Short Form (RSSS-SF). The scale consists of items rated on a Likert scale, with higher scores indicating greater relocation stress.

Countries

Taiwan

Contacts

CONTACTYu-Ling Yang, RN, NP
yihannurse@gmail.com+886-2-25433535
PRINCIPAL_INVESTIGATORTe-Yu Wu, PhD

MacKay Medical University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 20, 2026