Effect of Virtual Reality Intervention on Stress Levels of Surgical Nurses

Sponsor
Trakya University (Other)
Overall Status
Completed
CT.gov ID
NCT06022783
Collaborator
(none)
30
2
2
6.3
15
2.4

Study Details

Study Description

Brief Summary

The aim this crossover designed study is to examine the effect of watching a relaxing video with using virtual reality glasses (VR-G) during the break period of a working shift on the stress levels of surgical nurses.

Nurses will be asked to watch a relaxing video with using VR-G for 20 minutes at their break time (the first procedure).

After one-week wash-out period, researchers will compare second procedure (no video watch with VR-G) to see if there is any difference on the stress levels of the nurses.

Condition or Disease Intervention/Treatment Phase
  • Other: Virtual reality intervention
N/A

Detailed Description

Allocation of the nurses to the procedure groups (with VR-G and no VR-G procedures) is done with using Random Allocation Software program.

Among the with VR-G procedure:

The nurses were asked to watch a relaxing video with using VR-G for 20 minutes at their break time. The researcher visited the nurses at the beginning of the working shift and asked the nurse stress scale items to them in the nursing room, scheduled a break period with them individually and visited them again at the scheduled time. Then, the researcher prepared the video and googles, asked nurses to sit on the chair in the nursing room at the surgical unit, helped them to wear the VR-G and let them alone to watch the video for 20 minutes.

At the end of their working shift, the researcher visited them and asked the scale items once again.

Among the no VR-G procedure:

The nurses did not watch any video and copleted their routine working shift and break times. The researcher visited the nurses at the beginning and at the end of their working shift and asked the nurse stress scale items to them in the nursing room.

Study Design

Study Type:
Interventional
Actual Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
crossover designed randomized controlled studycrossover designed randomized controlled study
Masking:
Single (Outcomes Assessor)
Masking Description:
The data analysed by a independent researcher from the data collection and coding procedures.
Primary Purpose:
Prevention
Official Title:
The Effectiveness of Virtual Reality Intervention on Stress Levels of Surgical Nurses: A Crossover Designed Study
Actual Study Start Date :
Jan 24, 2023
Actual Primary Completion Date :
Jul 24, 2023
Actual Study Completion Date :
Aug 4, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: with VR-G

The nurses in this procedure were asked to watch a relaxing video with using VR-G for 20 minutes at their break time.

Other: Virtual reality intervention
Watching a relaxing video with using VR-G for 20 minutes

No Intervention: no VR-G

The nurses in this procedure did not watch any video and completed their routine working shift and break times.

Outcome Measures

Primary Outcome Measures

  1. Stress level [At the beginning and end of nurses daily working shift through study completion, an average of six months.]

    will be evaluated with using the "Nurse Stress Scale (NSS)" which is developed by Gray-Toft and Anderson and, translated and validated in Turkish by Mert, Sayilan and Baydemir. This scale consists of seven subcategories and 34 positive items rated using a 4-point Likert scoring system "1-never", "2-sometimes", 3-often," "4-very often". The total scale score, which reflects the frequency of the stress experienced by nurses, ranges from 34 to 136 points. A higher score indicates more frequent stress, while a lower score indicates less stress for the same situations.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • working in a surgical unit for at least one year

  • able to use virtual reality glasses

  • volunteering to participate in this study

Exclusion Criteria:
  • having a visual and/or audial problems

  • leaving surgical unit for any reason

Contacts and Locations

Locations

Site City State Country Postal Code
1 Seher Ünver Edirne Turkey 22030
2 Trakya University Edirne Turkey 22030

Sponsors and Collaborators

  • Trakya University

Investigators

  • Principal Investigator: Seher Ünver, Trakya University
  • Principal Investigator: Seda C Yeniğün, Akdeniz University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Seher Ünver, Associate Professor, Trakya University
ClinicalTrials.gov Identifier:
NCT06022783
Other Study ID Numbers:
  • 2023-KAEK-655
First Posted:
Sep 5, 2023
Last Update Posted:
Sep 5, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Seher Ünver, Associate Professor, Trakya University

Study Results

No Results Posted as of Sep 5, 2023