Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Cody Stansel
Objectives:
Primary Objective:
\- To deploy and evaluate virtual reality as an intervention for stress, pain, and negative affect
Secondary Objective:
\- To evaluate cyber sickness and patient satisfaction related to the virtual reality treatment
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
At or above the age of 18
English Speaking
Diagnosed with cancer
No previous history of seizures, losses of awareness, or other symptoms linked to an epileptic condition
Not sensitive to motion sickness
Not currently experiencing any contagious conditions, infections, or diseases (particularly of the eyes, skin, or scalp)
Does not use a device to regulate heart rate or rhythm (such as a pacemaker)
Not taking antiarrhythmic medications
Not actively receiving radiopharmaceutical therapy
Exclusion:
To ensure that there is sufficient time to complete the virtual reality treatment, patients who are scheduled for visits for periods of less than one hour will not be included in this study. Additionally, patients must consent to participating in the study on the day of the experience.
Patients who are asleep prior to consenting will not be asked to participate in the study
