College of Education

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    THE EDUCATIONAL EFFECTS FOR PEDIATRIC RESIDENTS OF A COMPUTER- BASED TRAINING ABOUT THE PART C EARLY INTERVENTION PROGRAM
    (2011) Pettko, Regina; Lieber, Joan; Special Education; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    This study examined knowledge gains about early intervention programs using a computer-based training with pediatric residents. Fourteen pediatric residents at the University of Maryland School of Medicine were pre-tested, provided with training, and post-tested. Given in a computer lab, the training was part of the residency education program. Results showed a statistically significant increase in test scores post- intervention. The training was more effective in teaching about early intervention law, philosophy, and recommendations for physician screenings than it was in teaching best practices for making referrals to the early intervention program. Findings were consistent with past studies on computer trainings in other medical topics. Limitations included small sample size and lack of a control group or follow-up assessment to measure maintenance and generalization of knowledge gained. Further investigation should look into the kinds of learning for which a computer is suitable versus the kinds that require more personal teacher-student relationships.
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    CASE STUDY OF A CARIBBEAN FAMILY'S PERCEPTIONS OF CULTURALLY APPROPRIATE AND FAMILY CENTERED SERVICE PROVISION
    (2007-01-08) Joseph, Lenisa Nicole; Cooper, David; Special Education; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    This case study explores a Caribbean family's perceptions of the cultural appropriateness and the family-centeredness of services they received from their service providers. Families' cultural beliefs and the mandates of early intervention services under the Individuals with Disabilities Education Improvement Act are sometimes very different. Researchers have done well to highlight issues of importance to many cultural groups; however, there is as yet no record of Caribbean families' experience. This qualitative study collected data over a two-month period through interviews, observations and document analysis. The constant comparative method was used to analyze the data, resulting in the themes used to describe the phenomenon. The number of years this family lived in the US seems to have resulted in acculturation to the point where their experiences were similar to that of an American family. They perceived the services they received to be family centered.
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    An Investigation of State-Level Child Find and Public Awareness Campaigns to Promote Early Intervention to the Medical Community
    (2006-06-21) Fulton, Jody Lynn; Lieber, Joan; Special Education; Digital Repository at the University of Maryland; University of Maryland (College Park, Md.)
    The Individuals with Disabilities Education Improvement Act requires States, through their Child Find Program, to locate, evaluate, and provide services to all children with delays. The purpose of this research was to investigate what the States are doing to promote Child Find to the medical community, how they evaluate the effectiveness of their efforts, and what, if any barriers prohibit these efforts. Three data collection methods were used: 1) an analysis of each State's policy as it relates to Child Find and the medical community, 2) an analysis of public awareness plans as they relate to Child Find and the medical community, and 3) a survey sent to each of the Part C lead agency coordinators in each State and US territory investigating Child Find efforts to the medical community. The results of this research reveal that most States have vague or ambiguous objectives in their policies related to Child Find and public awareness to the medical community. However, States' public awareness plans contain more detail about these objectives. The majority of States are working in collaboration with the medical community, as 85% had a member of the medical community serving on the State Interagency Coordinating Council. Ninety-one percent of the respondents reported their State collects data on how many referrals to early intervention they receive each year, and 100% of the people who responded reported collecting data on where these referrals come from. Only 56% collect referral data from the NICUs; however 94% collect data on referrals from other medical related institutions. Seventy percent have a public awareness plan and 53% routinely collaborate with the Local Education Agencies (LEA) on the effectiveness of this plan. In spite of plans, policies, and collaborative efforts, the States are still experiencing barriers in their efforts to reach out to the medical community. Lack of staff, lack of time, and difficult accessing the medical community were the three most frequently cited barriers. Limitations of this research, as well as suggestions for future research and practice are presented.