Anxiety Clinical Trial
— VRAP-GOfficial title:
The Effect of Virtual Reality on Anxiety and Pain in Patients Undergoing Gynecological Surgery; a Randomised Controlled Trial
Verified date | August 2022 |
Source | Zuyderland Medisch Centrum |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Rationale: Lack of postoperative acute pain management is associated with increased morbidity, longer recovery time, more opioid use and subsequently increased health care costs. There is increasing evidence virtual reality (VR) is effective in the reduction of acute pain. Alternative methods to reduce postoperative pain and multimodal analgesia are necessary for acute postoperative pain management and to reduce opioid use and their adverse effects. Objective: The aim of this study is to explore the effect of VR on pain in the immediate postoperative period after elective gynecological surgery. Secondary objectives are evaluating pre-and postoperative anxiety, pain catastrophizing, analgesic use, length of hospital stay between both groups and to explore tolerability, feasibility and satisfaction of VR use. Study design: The study concerns a non-blinded, single centre, randomised controlled trial. Study population: Eligible women fulfill the inclusion criteria and receive elective gynecological surgery in the Zuyderland Medical Centre location Heerlen. Intervention: The study population will be randomly divided into the intervention group (VR-group) or the standard care- group. The intervention group can choose for an immersive guided relaxation VR experience or an interactive VR experience during the pre- and postoperative period additional to the usual standard care. The participants randomised to the standard care- group will receive only the usual standard care pre-and postoperative. Main study parameters: The primary outcome is postoperative pain measured on a numeric rating scale (NRS). A total of 30 patients have to be included in each group. This means that a total of 60 women will have to be included in the study. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: The study population experiences a small medical risk when participating to this study. They can experience side-effects of VR for example dizziness or nausea and in rare cases epileptic insults. Participants of the study have to fill in a questionnaire before randomization and pre-and postoperative score of pain and anxiety on a zero to ten score scale.
Status | Completed |
Enrollment | 60 |
Est. completion date | July 9, 2022 |
Est. primary completion date | July 8, 2022 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Written and orally given informed consent - 18 years and older - Native Dutch speaker - Indication for elective gynecological surgery under spinal anesthesia - No contra-indication to anesthesia: Exclusion Criteria: - Chronic pain patients; defined as 'persistent or recurrent pain lasting longer than 3 months' . The pain is not due to the gynecological problem. - Chronical use of pain medication (opioids) - History of prior opioid use defined as use within 8 to 90 days prior to the surgical procedure - Alcohol or drug abuse - Known car sickness - Epileptic insults in previous history - Psychotically seizures in previous history - Claustrophobic - Blindness - History of mental illness |
Country | Name | City | State |
---|---|---|---|
Netherlands | Zuyderland Medical Centre | Heerlen |
Lead Sponsor | Collaborator |
---|---|
Zuyderland Medisch Centrum |
Netherlands,
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* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | NRS pain | reduction in postoperative pain score (NRS, numeric rating scale). Scaling from 0-10, where 0 means no pain and 10 means the worst imaginable pain | immediately after surgery | |
Secondary | STAI (State-Trait Anxiety Inventory) questionnaire (6 questions) | Pre-operative anxiety. The score ranges from 20 to 90 and the higher the score the more anxiety the person experiences | baseline | |
Secondary | Pain Catastrophizing Scale questionnaire | Pain catastrophizing. The subscales of the PCS can be calculated separately or overall with a maximum total score of 52. The higher the score, the more catastrophizing thoughts are present. | baseline | |
Secondary | NRS anxiety | Difference in anxiety scores pre-and post VR intervention. Scaling on a scale form 0 to 10, where 0 means no anxiety and 10 means the worst imaginable anxiety | baseline and immediately after surgery | |
Secondary | Analgesic use | daily use of paracetamol, NSAIDs, opioids | Within 24-48hours after surgery | |
Secondary | Length of hospital stay | Length of hospital stay | within 24-48hours after surgery | |
Secondary | VR Questionnaire | Tolerability, feasibility and satisfaction of VR use | within 24hours after surgery | |
Secondary | NRS pain preoperative | Preoperative pain score (NRS). Scaling from 0-10, where 0 means no pain and 10 means the worst imaginable pain | baseline |
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