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Virtual Reality Education Module in Reducing Anxiety and Increasing Knowledge in Patients With Prostate Cancer Undergoing Radiation Therapy

A Pilot Study to Determine if the Use of a Virtual Reality Education Module Reduces Anxiety and Increases Comprehension in Patients Receiving Radiation Therapy

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03318367
Enrollment
23
Registered
2017-10-23
Start date
2014-08-06
Completion date
2016-08-11
Last updated
2025-05-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate

Brief summary

This pilot clinical trial studies a virtual reality education module in reducing anxiety and increasing knowledge in patients with prostate cancer undergoing radiation therapy. A virtual reality education module may be useful in helping patients understand what they can expect to happen during their radiation treatments and help reduce stress relating to the radiation treatments.

Detailed description

PRIMARY OBJECTIVES: I. To determine if a virtual reality education module for prostate cancer patients is effective in increasing patient comprehension and decreasing patient anxiety related to radiation treatments. SECONDARY OBJECTIVES: I. This pilot study could have implications for a broader patient base undergoing radiation therapy.

Interventions

OTHEREducational Intervention

Complete virtual reality education module

Sponsors

Sidney Kimmel Cancer Center at Thomas Jefferson University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
MALE
Healthy volunteers
No

Inclusion criteria

* English speaking males capable of giving informed consent * Must be able to read English language * Receiving pre-treatment cone beam and volumetric modulated arc therapy (VMAT) for prostate cancer on the A or B treatment machines at the Bodine Center * Must be able to walk two city blocks * Must not have any auditory or visual deficits

Exclusion criteria

* If inclusion criteria are not met * Previous radiation therapy treatment * Employment in radiation oncology

Design outcomes

Primary

MeasureTime frameDescription
Standard deviation for difference in questionnaire response from pre-education to post-educationThrough study completion, an average of 2 yearsA one-sided one-sample t-test will be used to analyze the average change score (pre - post) for each questionnaire.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026