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Clinical Trials/NCT03318367
NCT03318367
Terminated
N/A

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

Sidney Kimmel Cancer Center at Thomas Jefferson University0 sites23 target enrollmentAugust 6, 2014
ConditionsProstate

Overview

Phase
N/A
Intervention
Not specified
Conditions
Prostate
Sponsor
Sidney Kimmel Cancer Center at Thomas Jefferson University
Enrollment
23
Primary Endpoint
Standard deviation for difference in questionnaire response from pre-education to post-education
Status
Terminated
Last Updated
last year

Overview

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.

Registry
clinicaltrials.gov
Start Date
August 6, 2014
End Date
August 11, 2016
Last Updated
last year
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Eligibility Criteria

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

Outcomes

Primary Outcomes

Standard deviation for difference in questionnaire response from pre-education to post-education

Time Frame: Through study completion, an average of 2 years

A one-sided one-sample t-test will be used to analyze the average change score (pre - post) for each questionnaire.

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