Alaska Native Parkinson's Disease Registry

Abstract

This registry initiates a program of epidemiological assessments of PS among Alaska Natives to study the natural history and clinical management of PS and establishes a database of Alaska native people with PS for public health research and educational purposes. As feasible the prevalence of PS in Alaska Natives may be estimated as well. This registry not only would facilitate future research into PS ebology but also guide health care planning and community education efforts in this population. The proposal takes advantage of a case control study of PS that is commencing in the same population. The registry is designed in two phases. Phase I is a developmental period and is well underway at this time. During this phase we are establishing the data collection and dissemination protocols regulatory submissions are under review for the registry to obtained necessary approvals the registry database is under development and a pilot project in Anchorage will be initiated pending approvals. Phase 2 has not yet begun. It is a period of educational outreach and active statewide data collection on prevalent and incident cases of PS. After Phase 2 ends the registry will be sustained through the Alaska Native Medical Center.

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Document Details

Document Type
Technical Report
Publication Date
Nov 01, 2007
Accession Number
ADA478553

Entities

People

  • Brian A. Trimble

Organizations

  • Alaska Native Tribal Health Consortium

Tags

DTIC Thesaurus Topics

  • Communities
  • Databases
  • Dementia
  • Diseases And Disorders
  • Education
  • Health
  • Health Care
  • Health Services
  • Medical Personnel
  • Movement Disorders
  • Natural History
  • Parkinson'S Disease
  • Public Health
  • Therapy

Fields of Study

  • Medicine

Readers

  • Canadian European Scientific Immigration and Epilepsy Clearance Studies
  • Clinical Trial Research.