2017
DOI: 10.1037/rep0000110
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African American Dementia Caregiver Problem Inventory: Descriptive analysis and initial psychometric evaluation.

Abstract: The descriptive analysis of the types and frequency of problems of African American dementia caregivers coupled with the outcomes of the psychometric evaluation bode well for the adoption of the DCPI-A in clinical settings. (PsycINFO Database Record

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Cited by 9 publications
(6 citation statements)
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References 50 publications
(67 reference statements)
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“…Dementia caregivers find it difficult to attend any form of group intervention, even locally, due to high costs of and logistical problems in obtaining respite care and transportation (Scott et al, 2016). Sociocultural barriers are also a significant obstacle in translating CBI-based treatment (Wells et al, 2017). Individuals tend to be somewhat mistrustful of providers and interventions originating outside their locale, and this is particularly the case when the provider and/or the treatment approach appear to conflict with their family and religious values (e.g., Glueckauf et al, 2012; Glueckauf & Lustria, 2008; Glueckauf et al, 2005).…”
Section: Introductionmentioning
confidence: 99%
“…Dementia caregivers find it difficult to attend any form of group intervention, even locally, due to high costs of and logistical problems in obtaining respite care and transportation (Scott et al, 2016). Sociocultural barriers are also a significant obstacle in translating CBI-based treatment (Wells et al, 2017). Individuals tend to be somewhat mistrustful of providers and interventions originating outside their locale, and this is particularly the case when the provider and/or the treatment approach appear to conflict with their family and religious values (e.g., Glueckauf et al, 2012; Glueckauf & Lustria, 2008; Glueckauf et al, 2005).…”
Section: Introductionmentioning
confidence: 99%
“…Findings from both reviewers were compared, and areas of disagreement were discussed until consensus was achieved. (1) Were telecommunication-based randomized controlled trials which focused on at least one caregiver outcome (i.e., health behaviors, psychosocial functioning, health service utilization, and cost or clinical outcomes) (2) Used at least one telehealth component in 50% of caregiver training sessions (e.g., service delivery over the Internet, telephone, videophone, point-to-point videoconference, and/or chat) (3) Were primarily focused on family caregiver intervention (may also include a care recipient training component) (4) The care recipient had a chronic medical condition (e.g., HIV/AIDs, progressive dementia, heart failure, psychiatric disabilities, and traumatic brain injury)…”
Section: Coding Of Intervention Characteristicsmentioning
confidence: 99%
“…It is commonplace for family caregivers to prioritize the needs of their loved ones with chronic illnesses above their own personal concerns and lifestyle preferences. Although they often verbalize the importance of health-promoting activities, many caregivers find it challenging to create time for self-care opportunities, to attend doctors' appointments, and to ask for caregiving assistance from other family members [3,4]. Caregivers often report substantial declines in social activities, disrupted familial relationships, financial problems, and deterioration in physical and mental health [5].…”
Section: Introductionmentioning
confidence: 99%
“…Practitioners can use assessment measures to assess the level of stress, burden, emotional distress, and relational difficulties of caregivers and be aware of effective interventions for these difficulties, such as support groups and trainings for caregivers (Qualls, 2016). Measures available for practitioners to use to assess caregivers’ coping abilities and level of distress include the Zarit Burden Interview (Zarit, Reever, & Bach-Peterson, 1980), the African American Dementia Caregiver Problem Inventory (Wells et al, 2017), the Coping Orientation to Problems Experienced Inventory (Carver, Scheier, & Weintraub, 1989), and the Maslach Burnout Inventory (Maslach, Jackson, & Leiter, 2017), among others.…”
Section: The Importance Of Supporting Caregiversmentioning
confidence: 99%