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Feasibility of a virtual reality intervention targeting distress and anxiety symptoms in patients with primary brain tumors: Interim analysis of a phase 2 clinical trial

  1. Author:
    King, Amanda L
    Roche, Kayla N
    Leeper, Heather E
    Vera, Elizabeth
    Mendoza, Tito
    Mentges, Kelly
    Acquaye-Mallory, Alvina A
    Adegbesan, Kendra A
    Boris, Lisa
    Burton, Eric
    Choi, Anna
    Grajkowska, Ewa
    Kunst, Tricia
    Levine, Jason
    Lollo, Nicole
    Miller, Hope
    Panzer, Marissa
    Penas-Prado, Marta
    Pillai, Valentina
    Polskin, Lily
    Reyes, Jennifer
    Sahebjam, Solmaz
    Stockdill, Macy L
    Theeler, Brett J
    Wu, Jing
    Gilbert, Mark R
    Armstrong, Terri S
  2. Author Address

    Neuro-Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, USA. amanda.king2@nih.gov., Office of Patient-Centered Outcomes Research, National Cancer Institute, National Institutes of Health, 9030 Old Georgetown Road, Bethesda, MD, 20892, USA. amanda.king2@nih.gov., Frederick National Laboratory for Cancer Research, Leidos Biomedical Research, Inc., Frederick, USA., Center for Cancer Research Office of Information Technology, National Cancer Institute, National Institutes of Health, Bethesda, USA., Uniformed Services University of the Health Sciences, Bethesda, USA.,
    1. Year: 2023
    2. Date: Mar 08
    3. Epub Date: 2023 03 08
  1. Journal: Journal of Neuro-oncology
    1. Pages: 1-9
  2. Type of Article: Article
  1. Abstract:

    Cancer patients experience distress and anxiety when undergoing imaging studies to monitor disease status, yet these symptoms are not always appropriately identified or well-managed. This interim analysis of a phase 2 clinical trial explored feasibility and acceptability of a virtual reality relaxation (VR) intervention for primary brain tumor (PBT) patients at the time of clinical evaluation. English speaking, adult PBT patients with previous reports of distress and upcoming neuroimaging were recruited between March of 2021 and March 2022. A brief VR session was done within 2 weeks prior to neuroimaging with patient-reported outcomes (PROs) collected before and immediately post-intervention. Self-directed VR use over the next 1 month was encouraged with additional PROs assessments at 1 and 4 weeks. Feasibility metrics included enrollment, eligibility, attrition, and device-related adverse effects with satisfaction measured with qualitative phone interviews. Fifty-five patients were approached via email, 40 (73%) responded and 20 (50%) enrolled (9 declines, 11 screen fails). 65% of participants were less than or equal to 50 years, 50% were male, 90% were White/non-Hispanic, 85% had good KPS (greater than or equal to 90), and most were on active treatment. All patients completed the VR intervention, PROs questionnaires, weekly check-ins, and qualitative interview. Most (90%) reported frequent VR use and high satisfaction and only 7 mild AEs were recorded (headache, dizziness, nausea, neck pain). This interim analysis supports feasibility and acceptability of a novel VR intervention to target psychological symptoms for PBT patients. Trial enrollment will continue to assess for intervention efficacy. NCT04301089 registered on 3/9/2020. © 2023. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply.

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External Sources

  1. DOI: 10.1007/s11060-023-04271-0
  2. PMID: 36884201
  3. PMCID: PMC9993385
  4. PII : 10.1007/s11060-023-04271-0

Library Notes

  1. Fiscal Year: FY2022-2023
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