Virtual Reality for Psychological Symptoms in Cancer Patients
This study is testing a Virtual Reality (VR) Intervention to help cancer patients manage psychological symptoms like anxiety and depression during treatment. The VR Intervention involves a single 20-30 minute session where you'll experience calming virtual environments, such as nature scenes or guided meditations. Researchers want to see if this VR experience is easy to use and helpful for patients. You might be able to join if you are 18-90 years old, have a history of cancer, and are currently receiving inpatient chemotherapy, bone marrow transplant (BMT), CAR-T therapy, or outpatient chemotherapy. The study aims to enroll 24 participants.
- Study design
- This is an interventional study with a planned enrollment of 24 participants. It is not specified if it is randomized or blinded.
- What's involved
- You would complete questionnaires before and after a single 20-30 minute Virtual Reality (VR) Intervention session.
- Compensation
- Not stated in the trial record.
- Follow-up
- Feasibility and acceptability are measured at baseline, which is when the VR intervention is successfully completed and administered.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Virtual Reality Intervention to Improve Psychological Symptom Burden for Cancer Patients Undergoing Treatment
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Juan C. Cardenas Rosales, MD · PRINCIPAL_INVESTIGATOR · Mayo Clinic
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Successfully complete the virtual reality (VR) intervention (Feasibility)Baseline
Feasibility of VR will be assessed by the proportion of participants who successfully complete the intervention.
- Absence of major issues during administration (Feasibility)Baseline
Feasibility of VR will be evaluated by the absence of (low/no recorded incidence of) major technical or usability issues during administration
- AcceptabilityBaseline
Will be assessed via the Post-Study Exit Interview Questionnaire, a questionnaire developed specifically for this study. It consists of 17 questions. Eight questions relate to the VR experience (e.g., comfort of headset, control of actions in VR environment, understandability of instructions, technical issues). Five questions relate to symptoms (e.g., dizziness, nausea, headache) or discomfort experienced during and immediately following VR use. The remaining questions relate to helpfulness of intervention, improvement suggestions, other feedback, and interest in learning more about services and resources. Results will be analyzed descriptively.