CODY Testing 1

Purpose

We are testing a Virtual Reality – or VR -- program for using and experiencing home modifications. Virtual Reality is a three-dimensional computer simulation of an environment that you see in a headset. We call this VR program “CODY.”

The purpose of this research is to assess how useful CODY is in assisting and enhancing the ability of adults to experience and choose appropriate home modifications for themselves.

Procedures

  • You will be asked to participate in VR (virtual reality) testing
  • Research staff will be there to help you with technical equipment, instructions and monitor your safety and comfort
  • Once you have completed testing you will be asked to answer a few surveys about your demographic information and about your perceptions of the usability of and satisfaction with the system and of perceived anxiety.

Eligibility 

  • Patients with a mild-to-moderate diagnosis of PD, evaluated using the Unified Parkinson’s Disease Rating Scale (UPDRS) and the Modified Hoehn and Yahr stages I-III, by a fellowship trained neurologist, arriving at the diagnosis by applying strict UK Brain Bank criteria
  • Disease duration is less than 5 years
  • With phone area code of 352; 904
  • Currently on their medications

Additional eligibility criteria apply. Please contact Sherry Ahrentzen for additional information about the study:

Age

65 and over

Gender

Male
Female

Monetary compensation

Yes

Can be done from home

No

Keywords

Parkinson disease, Parkinson's disease, Parkinson's disease - resources, Neurology

Principal Investigator

Sherry Ahrentzen, PhD

Department

Neurology

Contact Information

ahrentzen@ufl.edu

(352) 273-1229


Be an Informed Participant

Before deciding to participate in a research study, take time to learn about clinical research, how it's conducted and your rights as a research participant. Following are some helpful resources from independent sources. Always remember that a clinical research study is research, not treatment.

Know Who to Contact

  • Eligibility: For questions about a specific study and who is eligible to participate, call or email the contact person listed for that study.
  • Your Rights: For questions about your rights as a research participant, contact the UF Institutional Review Boards at 352-273-9600.
  • Feedback: For general questions or feedback about study listings, email the UF Clinical and Translational Science Institute at CTSI-Studies-L@lists.ufl.edu.

Other Resources

  • HealthStreet: Health-focused services, classes and events, and opportunities to participate in research.
  • ResearchMatch.org: Join a national registry of volunteers willing to be contacted about research studies.

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