The Effectiveness of a Virtual Reality-based Multisensory Intervention
ConditionGynecological Disease
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-75
SponsorWeifang Medical University
About this trial
This study explores the effectiveness of a virtual reality-based multisensory intervention for postoperative recovery in patients receiving gynecological surgery.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
None
Trial design
Design model
Parallel
Treatments tested in this trial
Virtual Reality intervention
Other interventionThe head-mounted virtual reality device is used to provide patients with relaxing videos of nature scenes accompanied by calming music and guided meditations.
Aromatherapy
Other interventionThe cotton ball soaked in lavender essential oil is placed near the patient's pillow.
Treatment groups
100 Participants
are divided into 3 treatment groupsGroup A: VR-Aromatherapy groupOther 2 interventions
Group B: Aromatherapy groupOther 1 intervention
Group C: VR groupOther 1 intervention
Trial outcomes
Primary outcomes
1
Pain response
The Visual Analog Scale (VAS) scale was used to assess the pain response of patients.
Time frame
The pain response of patients was assessed at 0.5 hour, 3 hour, 6 hour, 12 hour, 24 hour postoperatively, and immediately after intervention.2
Anxiety
The Beck Anxiety Inventory (BAI) scale was used to assess the anxiety of patients.
Time frame
The anxiety level of patients was assessed immediately after the intervention.3
Sleep quality
The Pittsburgh Sleep Quality Index (PSQI) scale was used to assess the postoperative sleep quality of patients.
Time frame
The sleep quality of patients was assessed at 24 hour postoperatively.Locations
Sponsors and contacts
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Source ClinicalTrials.gov
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