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Benefits of Using Virtual Reality Preoperatively in Managing Anxiety During Outpatient Foot Bone Surgery

Benefits of Using Virtual Reality Preoperatively in Managing Anxiety During Outpatient Foot Bone Surgery

Status
Terminated
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07639320
Acronym
Parcours RV
Enrollment
19
Registered
2026-06-10
Start date
2023-12-20
Completion date
2026-04-14
Last updated
2026-07-16

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

Conditions

Foot Surgery, Virtual Reality

Brief summary

Forefoot bone surgeries, such as surgical correction of hallux valgus, are routine orthopedic procedures. Outpatient surgery is offered in the vast majority of cases with regional anesthesia. Even though it is a simple and quick surgical procedure, it affects the patient's body image, who will worry about the outcome. Furthermore, because the anesthesia is regional, the patient can hear the surgical procedures being performed, which generates anxiety. Finally, the lack of information about the preoperative process, from arrival at the hospital and then in the ward to the operating room, can generate additional anxiety for the patient. One way to reduce anxiety related to surgery could be the use of virtual reality (VR) techniques. VR uses technologies that simulate a user's physical presence in an environment artificially generated by software. VR has already been used in studies to distract patients from pain and stress. During surgery, wearing a VR headset can reduce anxiety and stress related to the procedure. However, there are currently few studies investigating the use of VR to reduce preoperative anxiety and postoperative pain. This research is based on the hypothesis that visualizing the perioperative journey via a VR headset, some time before the procedure, would reduce preoperative anxiety and postoperative pain. The main objective is to evaluate the effect of using virtual reality on preoperative anxiety, through the visualization of a virtual perioperative journey by patients before surgery.

Interventions

OTHERVirtual reality

Watching a movie in virtual reality

OTHERQuestionnaires

satisfaction questionnaire Amsterdam Preoperative Anxiety and Information Scale Score MSP-9

Sponsors

GCS Ramsay Santé pour l'Enseignement et la Recherche
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

* Patient aged 18 years or older at the time of study enrollment * Patient hospitalized for scheduled outpatient forefoot bone surgery with regional anesthesia * Patient capable and willing to follow the protocol procedures as directed by the investigator * Patient with a compatible smartphone * Patient with a personal email address * Patient affiliated with or covered by a social security plan * Patient who has given their free, informed, and explicit written consent

Exclusion criteria

* Patient with a contraindication to regional anesthesia * Emergency patient * Epileptic patient * Patient with significant visual impairment or uncorrected strabismus * Patient with a cognitive barrier (dementia, major psychiatric disorders, etc.) * Patient taking medication for stress or anxiety (benzodiazepines, anxiolytics, antidepressants, etc.) or analgesics chronically * Patient with agoraphobia * Patient with a history of motion sickness, vertigo, or vestibular neuritis * Patient who does not understand or speak French * Pregnant, breastfeeding, or parturient patient * Protected patient: adult under guardianship, curatorship, or other legal protection, deprived of liberty by judicial or administrative decision.

Design outcomes

Primary

MeasureTime frameDescription
Score of the self-questionnaire "Amsterdam Preoperative Anxiety and Information Scale" (APAIS)17 monthsa questionnaire with 6 items and each item has a score between 1 and 5.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 17, 2026