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Most of us鈥攁t least those of us who lack scientific training鈥攁ssociate clinical research with the second definition of clinical: cool, analytical, dispassionate. Talk to Marie Cox, D.N.P., clinical assistant professor in the , though, and it is apparent that her clinical research is anything but dispassionate.

Dr. Cox studies Huntington鈥檚 disease, but not from the point of view of its victims. Rather, she looks at the quality of life of their caregivers. She became interested in the field in the early 2000s when, as the research nurse coordinator in neuroscience at Northwell Health (formerly North Shore-LIJ Health System), she worked on research trials for patients with Parkinson鈥檚 disease and Huntington鈥檚 disease. She subsequently worked as a nurse practitioner treating patients with these conditions and similar ones.

Huntington鈥檚 disease has been called the disease of families. If one of your parents has Huntington鈥檚, you have a 50 percent chance of inheriting the gene. There is no known cure, and the disease, which usually sets in during one鈥檚 30s or 40s, is devastating. Nerve cells in the brain break down over a 10- to 20-year period, resulting in a gradual decline in the ability to reason, walk and speak.

Caring for the patient often falls to a family member and the burden can be enormous. The disease is relatively rare鈥攖here are about 30,000 cases in the United States鈥攁nd the victims are often too young to go into traditional nursing homes. Add to that the pain of knowing that a victim鈥檚 offspring also have a high likelihood of carrying the gene.

As she began to work in the area, Dr. Cox noticed that 鈥渨hen someone is diagnosed with the disease, it was really the family member that needed a lot of attention鈥攁s much as the person diagnosed themselves.鈥�

The observation led her to study the quality of life of Huntington鈥檚 disease caregivers. A 2009 survey she conducted among caregivers at four sites indicated a lack in social support services, both for Huntington鈥檚 victims and the people鈥攗sually family members鈥攚ho care for them.

That conclusion led Dr. Cox and a colleague, Carol Moskowitz, a consultant at Terence Cardinal Cooke Health Care Center鈥攁 skilled nursing facility for Huntington鈥檚 disease care鈥攖o design their latest study: in-depth interviews with a smaller number of caregivers. 鈥淲e鈥檙e going to ask them questions such as, 鈥榃hat works? What do you do to keep that person with Huntington鈥檚 disease at home?鈥欌�� Dr. Cox said. Their ultimate goal is to share the results with families, nurses and other healthcare providers to help them care for persons with Huntington鈥檚 disease in the community. They also hope to find ways to reduce unnecessary healthcare expenses by keeping people well supported in the community.

Lowering healthcare costs ties in closely with New York State Governor Andrew Cuomo鈥檚 recently announced $45 million Vital Access/Safety Net Provider Program to improve community care for the most vulnerable members of the population.

鈥淵ou never know what鈥檚 going to come out of鈥� qualitative interviews, Dr. Cox said. She is excited by the endless possibilities and the promise of finding 鈥渟ome helpful information to share with the Huntington鈥檚 disease community to at least put some comfort into other people鈥檚 lives.鈥�