Using Technology to Deliver Multi-Disciplinary Care to Individuals with Parkinson Disease in Their Homes
Background: Parkinson disease is a chronic condition that affects ~500,000 Americans. Individuals diagnosed with Parkinson disease require specialized care for their condition from a neurologist. However, 40% of current Medicare beneficiaries with Parkinson disease either do not have access to or do not utilize a neurologist. Those who do not see a neurologist are ~20% more likely to fracture a hip, to be placed in a skilled nursing home facility, and to die. Simple, inexpensive web-based video conferencing software, akin to Skype, can connect patients in their homes to neurologists at centers of excellence, which are medical institutions supported by the National Parkinson Foundation. In two previous research studies, we demonstrated that providing remote medical care (telemedicine) is feasible, comparable to in-person care, and saves patients and caregivers time and travel. However, the feasibility and value of telemedicine has not yet been demonstrated on a national level.
Objectives: We are conducting a national, randomized study aimed at comparing the effectiveness of using telemedicine to deliver multidisciplinary specialty care to that of a patient’s usual care enhanced with educational materials. In this study, we aim to do the following:
- To demonstrate the feasibility of using telemedicine to deliver care into the homes of individuals with Parkinson disease who have limited access to care;
- To show that such an approach can improve quality of life;
- To establish that the telemedicine can enhance the quality of care; and
- To demonstrate that this remote approach to care saves time, reduces travel, and decreases caregiver burden.
Methods: The study will be a 12-month, 200-person randomized research study of individuals with Parkinson disease and limited access to care. Individuals will be randomized to receive care in their homes from specialists, nurses, and other professionals at centers of excellence via web-based video conferencing or to receive their usual care, supplemented by patient-centered educational resources.
Patient Outcomes: Feasibility of conducting remote assessments will be determined by the percentage of patients who complete at least one telemedicine visit. Quality of life for the patient will be measured by the Parkinson Disease Questionnaire 39, and quality of care for the patient will be measured by the Patient Assessment of Care for Chronic Conditions. Time and travel will be assessed using a patient survey, and caregiver burden will be assessed using the Zarit Burden Interview. We aim to provide evidence that will help change the current model of care to one that allows anyone anywhere with a chronic condition to receive the care that he or she needs.
Dorsey ER, Achey MA, Beck CA, Beran DB, Biglan KM, Boyd CM, Schmidt PN, Simone R, Willis AW, Galifianakis NB, Katz M, Tanner CM, Dodenhoff K, Ziman N, Aldred J, Carter J, Jimenez-Shahed J, Hunter C, Spindler M, Mari Z, Morgan JC, McLane D, Hickey P, Gauger L, Richard IH, Bull MT, Mejia NI, Bwala G, Nance M, Shih L, Anderson L, Singer C, Zadikoff C, Okon N, Feigin A, Ayan J, Vaughan C, Pahwa R, Cooper J, Webb S, Dhall R, Hassan A, Weis D, DeMello S, Riggare SS, Wicks P, Smith J, Keenan HT, Korn R, Schwarz H, Sharma S, Stevenson EA, Zhu W. National Randomized Controlled Trial of Virtual House Calls for People with Parkinson's Disease: Interest and Barriers. Telemed J E Health. 2016 Jul;22(7):590-8. doi: 10.1089/tmj.2015.0191. Epub 2016 Feb 17. PubMed PMID: 26886406; PubMed Central PMCID: PMC4939367 [Available on 2017-07-01]. (Abstract only available)
Can Virtual House Calls Provide More Patients with High-Quality Parkinson Disease Care? - A narrative on bringing care into the homes of patients with Parkinson disease using simple videoconferencing software.