Effect of biophilic VR video intervention on reducing the stress of night shift nurses

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200059542

Enrollment

Unknown

Registered

2022-05-04

Start date

2022-05-15

Completion date

Unknown

Last updated

2024-03-11

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

Conditions

sleep deprivation

Interventions

Group A1:Watch VR video first, and be on duty one week later

Group A2:Regular duty first, watch VR video one week later

Eligibility

Sex/Gender

All

Age

25 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Subjects working in hospitals; 2. Subjects aged 25-45 years; 3. The patients they manage are Class I or II patients according to the standards of the American Society of Anesthesiologists (ASA); 4. Need to work 2 to 4 hours per operation.

Exclusion criteria

Exclusion criteria: 1. Participants who refuse to sign the informed consent form; 2. Participants with severe cardiopulmonary disease; 3. Participants who have experienced physical discomfort (such as seizures), or vertigo dazzlers when they put on a VR headset.

Design outcomes

Primary

Measure	Time frame
Pychological Vigilance Test;	—

Secondary

Measure	Time frame
Cyber-Physical-Social Systems;Multidimensional Fatigue Scale;Heart rate;Blood pressure;Incidence of chest tightness, headache, palpitations;Satisfaction of nurse;	—

Countries

China

Contacts

Public ContactZhu Binbin

The Affiliated Hospital of Medical School of Ningbo University

pingchi1983@126.com+86 15957485723

Outcome results

None listed

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