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Sponsored by: |
Alzheimer's Association |
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Information provided by: | National Institute on Aging (NIA) |
ClinicalTrials.gov Identifier: | NCT00059410 |
The TIPS Study, or Treatment and Illness Perceptions Survey, is a study funded by the national Alzheimer's Association to learn more about differences between African Americans' and Whites' attitudes, beliefs, and experiences related to Alzheimer's disease (AD). The study involves a one-time 30-minute telephone survey in which participants are asked about a range of topics related to AD, including their personal experiences, their beliefs about the disease's symptoms and risk factors, and their attitude toward possible future treatment options. Information from the survey will be used to develop more culturally sensitive health education and healthcare services for persons with AD.
Condition |
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Alzheimer Disease |
Study Type: | Observational |
Study Design: | Prospective |
Official Title: | Alzheimer's Disease Treatment and Illness Perceptions Survey (TIPS) II |
Estimated Enrollment: | 210 |
Study Start Date: | January 2003 |
Estimated Study Completion Date: | September 2005 |
The main goal of the Boston University's TIPS II project is to examine differences in Alzheimer's disease (AD) illness perceptions between African Americans and Whites in order to better understand attitudes and beliefs and to develop more culturally sensitive health services for AD. This 30-minute telephone survey will include a total of 140 first-degree relatives and caregivers of people with AD, as well as a comparison group of 70 adults without family history. The researchers will assess 1) beliefs about AD; 2) the perceived threat it poses; 3) sources of information about AD; 4) knowledge of basic facts about AD; 5) appraisal of AD treatments; and 6) intentions regarding current and emerging care options. Based on preliminary data, this study hypothesize that, as compared to Whites, African Americans will report lower levels of perceived threat, fewer sources of information, less awareness of facts, and less interest in care options. Focus group interviews with African American participants will help interpret study findings and inform recommendations for health education interventions.
Findings will inform the development of a set of recommendations for AD health educators that will help them tailor their interventions to African Americans. Such educational programs promote increased use of assessment, treatment, and caregiver assistance services. Results will also be used as pilot data in a proposal for a national survey of caregivers and relatives. This program of research will address a growing need for increased understanding of beliefs, knowledge, and intentions regarding AD. A total of 210 participants are being sought (105 African Americans, and 105 Whites). Participants who complete the survey will be given a $10.00 check, plus informational brochures on AD and the latest newsletter from the Boston University Alzheimer's Disease Center.
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Three groups of participants are sought to take part in the survey:
Exclusion Criteria:
United States, Massachusetts | |
Boston University School of Medicine, Alzheimer's Disease Center | |
Boston, Massachusetts, United States, 02118 |
Study Director: | Scott Roberts, PhD | Boston University Alzheimer's Disease Center |
Study ID Numbers: | IA0045, NIRG-02-3712, BUMC 2002-308 |
Study First Received: | April 24, 2003 |
Last Updated: | February 15, 2008 |
ClinicalTrials.gov Identifier: | NCT00059410 |
Health Authority: | Unspecified |
Alzheimer disease Caregivers African Americans Perceptions Cultural Competency |
Delirium, Dementia, Amnestic, Cognitive Disorders Mental Disorders Alzheimer Disease Central Nervous System Diseases Neurodegenerative Diseases |
Brain Diseases Dementia Cognition Disorders Delirium |
Nervous System Diseases Tauopathies |