Caregivers' attitudes toward their family members' participation in Alzheimer disease research: implications for recruitment and retention.
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Benefits and Risks in Secondary Use of Digitized Clinical Data: Views of Community Members Living in a Predominantly Ethnic Minority Urban Neighborhood.Understanding recruitment and retention in neurological research.Learning from recruitment challenges: barriers to diagnosis, treatment, and research participation for Latinos with symptoms of Alzheimer's disease.Barriers to participation in mental health research: are there specific gender, ethnicity and age related barriers?Family caregiving and emotional strain: associations with quality of life in a large national sample of middle-aged and older adults.Diagnostic labels, stigma, and participation in research related to dementia and mild cognitive impairment.Barriers and facilitators of African American participation in Alzheimer disease biomarker research.Recruitment of a community-based cohort for research on diversity and risk of dementia.The feasibility of cell phone based electronic diaries for STI/HIV researchAddressing the challenges to successful recruitment and retention in Alzheimer's disease clinical trialsExploring the reasons urban and rural-dwelling older adults participate in memory research.An interdisciplinary outreach model of African American recruitment for Alzheimer's disease research.Researchers' perspectives on the role of study partners in dementia research.Degradation of misfolded proteins in neurodegenerative diseases: therapeutic targets and strategies.More than Tuskegee: understanding mistrust about research participationClinical research participation among aging adults enrolled in an Alzheimer's Disease Center research registry.Ethical issues in naturalistic versus controlled trials"I Kept Coming for the Love": Enhancing the Retention of Urban African Americans in Diabetes Education.Differences between African American and White research volunteers in their attitudes, beliefs and knowledge regarding genetic testing for Alzheimer's diseaseRecruiting Community-Based Dementia Patients and Caregivers in a Nonpharmacologic Randomized Trial: What Works and How Much Does It Cost?A model for the design and implementation of a participant recruitment registry for clinical studies of older adults.I'd Do Anything for Research, But I Won't Do That: Interest in Pharmacological Interventions in Older Adults Enrolled in a Longitudinal Aging Study.Diversity and disparity in dementia: the impact of ethnoracial differences in Alzheimer diseaseStigmatization in Alzheimer's disease research on African American elders.African Americans with memory loss: findings from a community clinic in Lexington, KentuckyFamily first: the development of an evidence-based family intervention for increasing participation in psychiatric clinical care and research in depressed African American adolescents.Recruitment and retention of older adults in aging research"Mama just won't accept this": adult perspectives on engaging depressed African American teens in clinical research and treatmentFacilitating Alzheimer disease research recruitment.Supporting Healthy Dementia Culture: An Exploratory Study of the Church.Dealing with daily challenges in dementia (deal-id study): process evaluation of the experience sampling method intervention 'Partner in Sight' for spousal caregivers of people with dementia.Recruitment of pregnant women to an exercise-intervention study.Establishing the motivations of patients with dementia and cognitive impairment and their carers in joining a dementia research register (DemReg).Identifiable Characteristics and Potentially Malleable Beliefs Predict Stigmatizing Attributions Toward Persons With Alzheimer's Disease Dementia: Results of a Survey of the U.S. General Public.To test or not to test: interest in genetic testing for Alzheimer's disease among middle-aged adults.Knowledge and perceptions of dementia and Alzheimer's disease in four ethnic groups in Copenhagen, Denmark.Overcoming barriers to conducting an intervention study of depression in an older African American population.Patient involvement in research: an audit of study feedback to participants.The UP-TECH project, an intervention to support caregivers of Alzheimer's disease patients in Italy: preliminary findings on recruitment and caregiving burden in the baseline population.What motivates women to take part in clinical and basic science endometriosis research?
P2860
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P2860
Caregivers' attitudes toward their family members' participation in Alzheimer disease research: implications for recruitment and retention.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
2001年论文
@zh
2001年论文
@zh-cn
name
Caregivers' attitudes toward t ...... for recruitment and retention.
@en
type
label
Caregivers' attitudes toward t ...... for recruitment and retention.
@en
prefLabel
Caregivers' attitudes toward t ...... for recruitment and retention.
@en
P2093
P1476
Caregivers' attitudes toward t ...... for recruitment and retention.
@en
P2093
P304
P356
10.1097/00002093-200107000-00005
P407
P577
2001-07-01T00:00:00Z