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Feasibility Study Evaluating the Silva Module During the Anaesthesiology Consultation Before an Elective Surgery

Feasibility Study Evaluating the Silva Module During the Anaesthesiology Consultation Before an Elective Surgery

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04379882
Acronym
Silva
Enrollment
0
Registered
2020-05-08
Start date
2020-11-10
Completion date
2020-12-20
Last updated
2021-06-30

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

Conditions

Preoperative Anxiety

Brief summary

In this feasibility study, feasibility, acceptability and an initial clinical efficacy of the new module of Hypnosis and Virtual Reality (or Digital Sedation), Silva, will be evaluated. This feasibility study meets objectives of Oncomfort's design validation and design verification steps. Silva will be tested on a sample of 10 patients in the environment where the product is intended to be used, a hospital environment. If results do not fit with user needs, design will be adapted according to results and a new phase of design validation will be implemented. The Silva module is a Digital Sedation module designed for management of pain and anxiety in perioperative patients.

Detailed description

Subjects will be recruited during the anaesthesiology consultation preparing to an elective surgery. First, subject will be asked to self-assess anxiety and comfort. In order to evaluate anxiety, subject will use a 0-10 rating Visual Analogue Scale (VAS) where 0 = no anxiety at all, and 10= the worst imaginable anxiety. The same scale will be used to measure the level of comfort where 0 means no comfort at all and 10 very comfortable. Subject should be positioned laying on a reclining chair during the session. This session will last for 30 minutes. After the experiment, participants will be asked to rate anxiety, level of comfort, level of immersion and dissociation. Several questions will be asked to the patient to evaluate his/ her experience, the Silva module, and the sensations experienced. The study will be ended by an evaluation of adverse event (AE) and the evaluation of the caregivers.

Interventions

DEVICEDigital Sedation (Silva)

Use of Digital Sedation (virtual reality associated with psychological interventions) for preoperative anxiety management

Sponsors

Erasme University Hospital
CollaboratorOTHER
Oncomfort
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

• Subject more than 18 years old

Exclusion criteria

* Deaf subject * Blind * Non-proficiency in French (Module language) * Psychiatric disorder * Head or face wounds * Neurological disease * Chronic pain and/or chronic analgesics consumption * Medication affecting the autonomic nervous system * Dizziness

Design outcomes

Primary

MeasureTime frameDescription
Evaluate the acceptability and the patient's qualitative reported experience of SilvaDay 1 of the interventionquestionnaire

Secondary

MeasureTime frameDescription
Evaluate AnxietyDay 1 of the interventionquestionnaire VAS 0 (no anxiety)- 10 (max anxiety)
Evaluate ComfortDay 1 of the interventionquestionnaire VAS 0 (extreme discomfort)- 10 (extreme comfort)
Evaluation of agreeability of the Digital Sedation sessionDay 1 of the interventionquestionnaire VAS (0-10) 0: not agreeable, 10: extremely agreeable

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026