The Moderating Influence of Service Use on Negative Caregiving Consequences This investigation adapts the social support conceptual framework to examine the moderating influence of community service use by impaired older persons on the negative consequences of caregiving for informal helpers. The model is modified by defining services as a type of social support that can counteract the stress associated with various care recipient impairments. Results from multivariate analyses of data from 401 caregivers suggest that certain services for care recipients can reduce the adverse effects of certain impairments on informal caregivers. The use of health care service by care recipients who are more disabled is related to lower levels of caregiver depression, health deterioration, and social isolation. Personal care service use consistently offsets the negative effects of care recipients' behavioral problems. Additionally, the use of household service when care recipients exhibit behavioral problems is associated with lower levels of caregiver depression. Read more
Service Use By Caregivers of Elders Receiving Case Management Although research on the effects of caregiver services has increased in recent years, the call for a research focus on the extent and predictors of their use has been largely ignored (Ory et al., 1985). The investigation described in this article addresses the gap in knowledge by examining the extent to which five types of caregiver services were used by study respondents: respite care, assistance finding or arranging for services, counseling or emotional support, education or training related to caregiving, and assistance with other responsibilities such as household tasks or child care. It also investigates the predictors of caregiver service use by applying a modified conceptual framework originally developed to examine factors influencing the use of health services (Andersen & Newman, 1973; Bass & Noelker, 1987). Read more
Influence of the Success of Psychoeducational Interventions on the Course of Family Care A reanalysis is presented of a previously reported study in order to investigate whether the short-term success of caregiver interventions is associated with positive longer-term outcomes. This new analysis focuses on whether or not families institutionalized their relative in the year following treatment, and the influence of response to treatment on the placement decision. Treatment outcomes (i.e., whether caregivers improved, failed to improve, or dropped out of treatment) were found to predict patient placement one year following initial assessment. Thus, caregiver interventions may have longer-term positive effects related to rates of patient institutionalization. Read more
Caregiving and its Social Support Social support is a feature of social relationships that can be discerned in many of the ordinary exchanges of daily social life but becomes especially prominent in the presence of adversity. However, despite its ubiquity, it is certainly no universal panacea. Not everyone has access to supportive relationships; people having such relationships do not necessarily benefit from them equally; and some adversities may be more resistant than others to the protective qualities of social support. These caveats notwithstanding, probably most people faced with difficult life exigencies have been the beneficiaries of social support, often without being aware of it. Indeed, individuals commonly confront unexpected and problematic junctures of the life course at which support goes beyond being merely useful and becomes, instead, a virtual requirement for the maintenance of well-being. Read more
The Interface Between Health and Social Services and Family Caregivers In the current debate over healthcare reform, an unresolved issue is Long Term-care coverage—whether it will be included in a reform package, and if so, to what extent, or whether deficit reduction and other economic considerations will make its cost prohibitive. Despite the uncertainty, extensive lobbying efforts continue to advocate linking acute and Long Term care in a reform package, and a number of plans to this effect have been proposed. The paradox is that while families currently are the unpaid yeomen of Long Term care and cost containment is a chief goal in healthcare reform, most plans ignore or give relatively little attention to the role of family caregivers. Read more
Falls Among Nursing Home Residents An Examination of Incident Resports Before and After Restraint Reduction Programs Objective: To examine changes in the rate of falling of an experimental group of restrained subjects who underwent restraint reduction, and to compare their rate of falling with a group of subjects who did not have restraint orders during the study period. Design: A quasi‐experimental, multiple time‐series study utilizing the principles of single‐subject design. Each subject was followed for 25 weeks before and 25 weeks after initiation of the intervention. Setting: Seven nursing homes. Intervention: Formal programs aimed at reducing all bed and chair restraints were initiated in all sites after staff received education and training. Multidisciplinary teams implemented the restraint reduction process on a case‐by‐case basis, beginning with 1 unit/floor at a time in each site. Most experimental subjects reached their optimum restraint‐elimination/reduced status within 2 weeks of intervention initiation. The implementation periods ranged from 4 months to more than a year. Participants: Subjects with chart orders for restraints at the start of the study comprised the experimental group and participated in the restraint reduction program (184 subjects). Subjects with no orders for restraints during the study period comprised the nonequivalent control group (111 subjects) and, therefore, did not undergo the intervention. Measurements: Incident reports documenting all falls during the study period were examined. Falls, the dependent variable, were classified as serious or nonserious. The independent variable (intervention) was the restraint reduction program offered to experimental subjects. Based on the principles of single subject design, the impact of the intervention on falls was calculated before and after the date the restraint reduction process was initiated for an individual (experimental group) subject. For the control group, the pre‐ and posttest period was calculated from the start date of the restraint reduction program on the unit on which each subject resided. Results: Serious falls did not increase, but nonserious falls increased significantly after restraints were removed or reduced in experimental subjects. The total mean weekly fall rate for this group increased from 1.87% of residents falling per week during preintervention to 3.01% during postintervention. The mean weekly fall rate of the control group was 3.18% at pretest and did not change statistically over time. Read more
Differences in Service Attitudes and Experiences Among Families Using Three Types of Support Services One goal of support services for family members of Alzheimer's patients is to facilitate the use of other formal services. Few existing studies empirically test the relationship between support service use and the use of other community or residential services. This research describes the relationship between support and other service use by comparing families who used three types of support services: • Information and referral • Educational programs; and • Support groups. Data from in-person interviews with 127 family caregivers showed that families who used one of the three support services differed in the use of other services, service attitudes, past service experiences, and reasons for support service use. Results profile the characteristics of families who turn to different types of support services and illustrate the importance of past service characteristics for explaining current and future utilization. Information and referral (I & R), educational programs, and support groups are commonly provided support services for family members of Alzheimer's disease victims. These three support services share the common goal of facilitating and encouraging the use of other formal services for Alzheimer patients and their family members. Despite this goal, research on support services has seldom considered whether their use is related to the use of other services. Read more
Analysis of Clustered Data in Community Psychology With an Example From a Worksite Smoking Cessation Project Although it is common in community psychology research to have data at both the community, or cluster, and individual level, the analysis of such clustered data often presents difficulties for many researchers. Since the individuals within the cluster cannot be assumed to be independent, the use of many traditional statistical techniques that assumes independence of observations is problematic. Further, there is often interest in assessing the degree of dependence in the data resulting from the clustering of individuals within communities. In this paper, a random-effects regression model is described for analysis of clustered data. Unlike ordinary regression analysis of clustered data, random-effects regression models do not assume that each observation is independent, but do assume data within clusters are dependent to some degree. The degree of this dependency is estimated along with estimates of the usual model parameters, thus adjusting these effects for the dependency resulting from the clustering of the data. Models are described for both continuous and dichotomous outcome variables, and available statistical software for these models is discussed. An analysis of a data set where individuals are clustered within firms is used to illustrate features of random-effects regression analysis, relative to both individual-level analyses which ignores the clustering of the data, and cluster-level analysis which aggregates the individual data. Read more
The Maturation of a Multiagency Computerization Effort for Alzheimer’s Respite Services This paper reports on a two-year project which developed a computerized multiagency database of respite service users. The project’s primary aim was to make seven non-profit respite programs technologically self-sufficient in terms of clinical information. The outcomes of computerization for these agencies are discusses, as well as modifications during the post-project period. Read more
