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Volume 87, Issue 3, Pages 343-350 (March 2006)


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Social Support, Social Problem-Solving Abilities, and Adjustment of Family Caregivers of Stroke Survivors

Joan S. Grant, DSNaCorresponding Author Informationemail address, Timothy R. Elliott, PhDb, Michael Weaver, PhDa, Gerald L. Glandon, PhDc, James L. Raper, DSN, CRNPd, Joyce N. Giger, EdDe

Abstract 

Grant JS, Elliott TR, Weaver M, Glandon GL, Raper JL, Giger JN. Social support, social problem-solving abilities, and adjustment of family caregivers of stroke survivors.

Objective

To determine contributions of social support and social problem-solving abilities in prediction of adjustment of family caregivers of stroke survivors.

Design

Descriptive.

Setting

Two rehabilitation facilities (1 private, 1 state) in the southeastern United States.

Participants

Fifty-two family caregivers (46 women, 6 men) of stroke survivors (28 women, 24 men).

Interventions

Not applicable.

Main Outcome Measures

Predictor variables were social support and social problem-solving abilities. Outcome measures of caregiver adjustment were depressive symptomatology, well-being, and general health. Participants completed these measures 1 to 2 days before discharge from inpatient rehabilitation and at 5, 9, and 13 weeks postdischarge in the home.

Results

Trajectory analysis indicated higher levels of social support were associated with lower levels of caregiver depressive symptomatology and higher levels of well-being and general health, independent of social problem solving. A greater negative problem orientation was associated with higher levels of depressive symptomatology and lower levels of well-being. A more positive problem orientation was associated with greater increases in general health. The strength or slope of this positive relation lessened over time.

Conclusions

Social support and the emotion-focused component of social problem solving, problem orientation, independently contribute to caregiver adjustment. Interventions that provide social support and assist caregivers to develop more adaptive abilities toward problem solving may be beneficial.

Article Outline

Abstract

Methods

Participants

Procedure

Predictor Variables

Demographic data

Social support

Social problem-solving abilities

Criterion Variables

Depressive symptomatology

Well-being

General health

Statistical Analyses

Results

Caregiver Depressive Symptomatology

Caregiver well-being

Caregiver Health

Discussion

Conclusions

References

Copyright

STROKE IS THE UNITED STATES’S third leading cause of death and a major cause of long-term disability. Family members, typically a spouse or other family member, often provide assistance with activities of daily living (ADLs).1 Unfortunately, family members often experience depressive symptomatology in caring for stroke survivors, with rates ranging from 34% to 52%2, 3, 4, 5 or even higher in the first 3 months after return to the community.6

The extant literature also indicates negative effects on caregivers’ well-being and general health.7 Family-caregiving literature concerning stroke survivors is reflective of much of this research. Caregivers often experience fatigue, inadequate rest, and mental and emotional strain.8, 9 Caregivers vary, however, in the way they adjust to their role. In fact, some persons thrive and report a heightened sense of well-being and personal meaning over time.10, 11

However, very few of these studies examine factors associated with positive adjustment among caregivers, so little is known about the personal and social characteristics of persons who are able to adjust and adapt to the caregiver role. Studies that distinguish characteristics of caregivers who do and do not adjust well are important so appropriate interventions can be strategically provided to persons at risk for poor adjustment.12

Although extant literature suggests social support promotes caregiver adjustment in other populations,13, 14 published studies examining this problem in family caregivers of stroke survivors are relatively few and components of clinical interventions remain unclear.15 Review of these cross-sectional studies suggests social support is a significant predictor of depression and life satisfaction at the onset of the caregiver role.16, 17 Furthermore, these benefits may extend long-term, generating better energy, mental health, physical function, general health, quality of life, and less pain.18

Although these studies indicate that social support is a significant predictor of caregiver adjustment in this population, other variables such as social problem-solving abilities may be better in predicting caregiver depressive symptomatology and health.19 Furthermore, research also suggests that effective problem-solving abilities are associated with caregiver well-being.1 In fact, caregivers of family members with acquired disabilities who possess ineffective problem-solving abilities are more likely to experience depressive symptomatology, anxiety, and ill health in the initial year of caregiving.20

Several other studies support the value of social problem-solving interventions in treating depressive symptomatology and distress and improving self-regulation. Social problem-solving abilities consist of 2 components: problem orientation and problem-solving skills. Problem orientation represents a cognitive emotional set of beliefs, appraisals, and feelings people have about how they view problems as well as how effectively they can solve them. Problem orientation serves as a motivator (either negative or positive) in managing problems. Problem-solving skills refer to cognitive and behavioral strategies persons use to better understand and systematically manage problems.21 Those effective interventions can be easily implemented in primary-care settings22 and home-based training programs to assist caregivers.23

Although social support and social problem-solving abilities are important predictors of caregiver adjustment, theoretical bases for and characteristics of social support and social problem-solving clinical interventions are significantly different. It is critical, then, to examine changes in caregiver social support and social problem-solving abilities over time and to link these changes to trajectories of caregiver adjustment. Therefore, the purpose of this study was to determine the unique contributions of social support and social problem-solving abilities in prediction of adjustment of family caregivers of stroke survivors during the first few months of caring for a stroke survivor. Predictor variables were social support and social problem-solving abilities. Caregiver adjustment measures were depressive symptomatology, well-being, and general health.

Methods 

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A descriptive design was used in this study. Data for these analyses were drawn from a 3-group repeated-measures experimental study that examined the impact of social problem-solving telephone partnerships on primary family-caregiver outcomes after stroke survivors were discharged home from a rehabilitation facility. Only sham intervention and control group (but not the intervention group) data were used for this examination because no differences were found between those 2 groups on major study outcomes across the 4 time points analyzed in the current study. A more detailed description of the intervention and corresponding protocols is available.23

Participants 

Caregivers of stroke survivors who had an admitting diagnosis of ischemic stroke (including brain infarction) caused by either thrombi or emboli were entered into the study. Given the high incidence of stroke recurrence (about 25% of stroke survivors will have another stroke within 5 years), this study was not restricted to caregivers of first-time stroke survivors.24

We controlled for number of strokes and subsequent functional deficits that can affect caregiver outcomes by selecting stroke survivors with the FIM instrument25 scores ranging between 36 to 96 (mean, 68) or moderate disability.26 A history of diseases such as dementia or schizophrenia, as defined by the Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, served as an exclusion criterion for both caregivers and stroke survivors.

Procedure 

A trained research nurse contacted family caregivers and stroke survivors at least twice to confirm eligibility criteria, explain the study, and obtain informed consent. The study was approved by an institutional review board for the protection of human rights. Instruments were administered in random order, initially 1 to 2 days before discharge of the stroke survivor in a quiet conference room and at 5, 9, and 13 weeks postdischarge in the home of either the stroke survivor or primary family caregiver.

Predictor Variables 

Demographic data 

Bivariate associations between each of the criterion variables (depressive symptomatology, well-being, general health) and each of the available demographic variables were examined to identify potential covariates to include within the regression model. Pearson product-moment or Spearman correlations were calculated for interval and ordinal demographic variables, respectively. Analysis of variance (ANOVA) was used to estimate ω2, a measure of relation between nominal and interval variables and test for significance of the relation. Although all demographic variables that had a bivariate relation that was either .20 or greater (using P=.10) were made available for the regression model (table 1), only those that maintained a statistically significant relation or whose removal appreciably degraded model fit were retained within the model. As a result, only stroke survivor age was incorporated into the models, which was consistent with our previous experience.

Table 1.

Associations Between Caregiver and Stroke Survivor Demographic and Criterion Variables (n=52)

Demographic VariableCriterion Variable
CES-DGeneral Well-BeingMental Health
Family caregiver’s age.21(P=.13)−.28(P=.05)−.09(P=.53)
Family caregiver’s sex−.14(P=.30)−.11(P=.42)−.05(P=.70)
Family caregiver’s race−.20(P=.16).04(P=.76).12(P=.40)
Family caregiver’s education.05(P=.71)−.18(P=.19).11(P=.44)
No. of other family members who assisted in caregiving−.19(P=.20).20(P=.18).18(P=.23)
No. of hours spent (daily) in caregiving by caregiver.18(P=.22).07(P=.65)−.18(P=.23)
No. of hours spent weekly by other family members in caregiving−.13(P=.39)−.23(P=.13).01(P=.95)
Stroke survivors’ age.09(P=.54)−.20(P=.15)−.01(P=.95)
Stroke survivors’ sex−.02(P=.91).14(P=.33).17(P=.22)
Stroke survivor’s race−.22(P=.12).06(P=.69).12(P=.41)
Stroke survivors’ educational level.04(P=.80)−.20(P=.15)−.03(P=.83)
Total number of strokes.04(P=.76)−.04(P=.75).11(P=.44)
Location of stroke−.06(P=.66)−.27(P=.07).17(P=.24)
Type of stroke−.19(P=.17)−.30(P=.03).03(P=.24)
Stroke survivors’ marital status.01(P=.88).02(P=.99).18(P=.47)
Family caregiver’s relationship to stroke survivor.21(P=.53).09(P=.95).27(P=.30)

Abbreviation: CES-D, Center for Epidemiologic Studies Depression Scale.

Measure of association is ω2.

Measure of association is the Pearson r.

Measure of association is the Spearman ρ.

The reliability of all instruments was examined before beginning the study by using a similar sample of 19 family caregivers of stroke survivors. Reliability coefficients concerning internal consistency and homogeneity were at acceptable levels (ie, α range, .71–.91; r range, .81–.89).

Social support 

The 30-item, Interpersonal Support Evaluation List (ISEL) was used to measure social support and its subscales, appraisal, belonging, and tangible support.27 Empirical evidence supports its validity and reliability, with α coefficients ranging from .88 to .91. The total ISEL score was used in the present study; lower scores indicate greater social support.28, 29

Social problem-solving abilities 

The sixth-grade version of the Social Problem Solving Inventory–Revised,30 a 52-item, Likert-type scale, was used to measure social problem solving in this study. Positive and negative problem orientation scales assess a general orientation toward problem solving, whereas the other 3 scales, rational problem solving, impulsivity and carelessness, and avoidance, assess general problem-solving styles.30

People who have higher scores on the problem-orientation scale are more optimistic, have greater confidence in themselves, are more motivated toward problem solving, and experience less frustration when confronted with problems. Furthermore, persons with positive orientations believe problems are a part of everyday life and tend to be more objective in analyzing factors that contribute to problems. In contrast, people who have higher scores on the negative orientation scale tend to be less optimistic and more pessimistic, have less confidence in themselves, are less motivated toward problem solving, and experience more frustration when confronted with problems. Persons with negative orientations doubt their ability to effectively solve problems and try to avoid solving them. Persons with negative orientations also personalize problems, commonly attributing them to “less than ideal behaviors” they showed.30

Rational problem solving represents a constructive problem-solving style of effective problem-solving abilities and how people use them. Persons who have higher scores on rational problem solving systematically identify problems, generate potential solutions, and implement and evaluate best solutions to problems. Reflective of their name, impulsivity and carelessness and avoidance styles are dysfunctional patterns in which people use impetuous, imprecise, and evasive methods for managing problems The impulsivity and carelessness scale assesses dispositions toward solving problems in impulsive and haphazard manners, whereas the avoidance scale assesses dysfunctional problem solving characterized by putting problems off. Internal consistency and test-retest coefficients range from .76 to .92 and .72 to .88, respectively.30

Criterion Variables 

Depressive symptomatology 

The Center for Epidemiologic Studies Depression Scale (CES-D)31 was used to assess caregiver depressive symptomatology. The instrument has 20 items that are rated on a 5-point, Likert-type scale. The CES-D has been used in numerous studies with various populations, including family caregivers of stroke survivors, that support adequate psychometric properties.32, 33 Higher scores indicate more depressive symptomatology.

Well-being 

Caregiver well-being was assessed with the mental health scale of the Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36). Internal consistency reliabilities for this dimension range from .67 to .95, with test-retest coefficients ranging from .75 to .80. Higher scores on this 5-item scale reflect a sense of peacefulness and happiness while lower scores imply unhappiness, distress, and nervousness.34

General health 

Caregiver general health was assessed with the 5-item general health dimension of the SF-36. Internal consistency and test-retest reliabilities for this dimension range from .78 to .95 and .80 to .83, respectively. Higher scores indicate a greater sense of personal health, whereas lower scores reflect ill health. The recommended algorithm to transform scores to a 0 to 100 scale was used for both well-being and general health.34

Statistical Analyses 

Linear mixed-model analyses were used to explore how social support and social problem-solving abilities as predictor variables relate over time to trajectories of depressive symptomatology, well-being, and general health. Models containing time (0, 5, 9, 13wk) as a within-subjects random effect, care recipient age as a covariate, social support (ISEL), and problem-solving (positive orientation, negative orientation, rational problem solving, impulsivity and carelessness, avoidance) variables were examined for each response variable. A variance-components repeated-measures structure was used because that form produced the best fit. Interaction effects between time and each predictor were examined initially and nonsignificant interactions removed from the model.

Linear mixed models allow modeling of time effects as a random variable, enabling individualized estimation of changes over time, whereas more traditional analyses (eg, repeated-measures ANOVA) do not provide that capability. Additionally, this approach offers the ability to model repeated-measures dependencies, producing appropriate error terms and P-value estimates. Standard linear model-type techniques entail listwise deletion (ie, all data from a subject would be excluded if even a single observation on a dependent variable or covariate used in the repeated-measures analysis were missing). However, linear mixed-models estimation can use all data available without imposing the heavy penalty of listwise deletion.

The use of a linear mixed-model approach provided 177 observations (because of each repeated measure for each of the 52 independent subjects) for each linear mixed model. For the largest models (composed of 14 predictors, including time interactions), this was only slightly above the bare minimum observation per predictor ratio (ie, 10) required for stable parameter estimates. Population effect sizes (R2) of at least .10 for tests of the largest full models and .09 for the smaller, final models were required to produce a power of 80%, and effect sizes (f2) of at least .05 were required to have 80% power for tests of individual parameters. From this standpoint, only relatively strong interaction effects were able to be identified as statistically significant and retained from analyses of the largest models; validation of these findings is needed with larger samples. Although no directly comparable studies were found in the literature, the required effect sizes were analogous to relations among similar variables reported in studies involving caregiving.17

Results 

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Research participants were 52 family caregivers (46 women, 6 men) who ranged in age from 25 to 74 years, with a mean age ± standard deviation of 55.6±11.6 and 57.2±13.6 years, respectively. The caregivers primarily were women (88%) who were spouses (n=21 [40.4%]) or daughters (n=18; 35%), were related by blood or marriage, and provided unpaid assistance to stroke survivors at least 6 hours a day in ADLs and instrumental ADLs after discharge from a rehabilitation facility. Most were married (n=37 [73%]) and either completed high school (n=28 [54%]) or college (n=17 [33%]); there were more whites (n=37 [71%]) than blacks (n=15 [29%]).

Stroke survivors ranged in age from 37 to 92 years, with nearly equal numbers of women (n=28) and men (n=24), with a mean age of 74.2±12.6 and 74.0±9.4 years, respectively. Most were either married (n=27 [52%]) or widowed (n=21 [40%]), and their ethnicity was identical to that of the caregivers. The majority either completed the eighth grade (n=14 [27%]) or high school (n=20 [39%]). Their median income was less than $20,000 per year. The number of strokes for each person ranged from 1 to 5 (average, 2) strokes. More stroke survivors had left-sided (n=31 [60%]) than right-sided (n=17 [32%]) hemispheric strokes, whereas 2 (4%) had bilateral strokes and 2 (4%) were unknown.

Caregiver Depressive Symptomatology 

Table 2 provides a model predicting risk for caregiver depressive symptomatology, well-being, and general health. Significant variance of random time coefficients (σ2=.225, z=2.03, P=.021) supported modeling the time slope as a random effect. The fixed effect for time was not significant, indicating (on average) no change in caregiver depressive symptomatology over time.

Table 2.

Model Predicting Risk for Caregiver Depressive Symptomatology, Well-Being, and General Health

Variable EffectβdftP
Depression
Intercept27.910503.20.002
Positive orientation−0.27872−1.08.285
Negative orientation0.537724.30<.001
Rational problem-solving−0.03272−0.35.728
Impulsivity/carelessness−0.00272−0.02.986
Avoidance−0.04372−0.20.840
Social support−0.76472−5.13<.001
Care recipient age0.093721.24.220
Time−0.09946−0.88.382
Well-being
Intercept13.567501.18.242
Positive orientation0.486721.18.242
Negative orientation−0.88372−3.83<.001
Rational problem-solving0.198721.46.148
Impulsivity/carelessness0.111720.57.568
Avoidance0.281720.79.434
Social support0.619722.51.014
Care recipient age0.143721.11.270
Time2.853452.93.005
Care recipient age by time−0.03972−2.81.006
General health
Intercept62.102503.37.002
Positive orientation1.015701.54.128
Negative orientation0.259701.01.314
Rational problem-solving0.128700.68.400
Impulsivity/carelessness0.121700.42.679
Avoidance−0.65170−1.39.169
Social support0.671702.70.009
Care recipient age−0.40870−2.01.048
Time0.083460.15.885
Positive orientation by time−0.14870−2.36.021
Rational problem-solving by time0.032701.85.069

NOTE. Error degrees of freedom computed by the containment method,61 which results in error degrees of freedom for linear mixed models that are different from traditional fixed linear models N–k–1 (independent subjects – number of predictors – 1).

Not statistically significant, but removal degraded model fit.

Statistically significant.

Furthermore, removing the set of problem-solving variables from the full model significantly degraded model performance (F5,72=8.30, P<.01), as did removing the social support variable (F1,72=26.35, P<.01), indicating that problem solving and social support were independently related to depressive symptomatology. However, removing the set of 4 nonsignificant problem-solving variables (ie, positive orientation, rational problem solving, impulsivity and carelessness, avoidance styles) did not degrade model explanatory power (F4,72=.66, not significant [NS]). Therefore, negative orientation was primarily responsible for the association between social problem solving and caregiver depressive symptomatology.

Caregiver well-being 

Significant variability of the random time coefficient (σ2=.844, z=2.75, P=.003) supported modeling the time slope as a random effect. The fixed effect for time was statistically significant, indicating (on average) an increase in caregiver well-being over time. Caregiver well-being declined faster over time when caring for older stroke survivors than when caring for younger stroke survivors.

Removing the set of problem-solving variables from the full model degraded model performance significantly (F5,72=9.34, P<.01) as did removing the social support variable (F1,72=6.32, P<.05), indicating that problem solving and social support were independently related to well-being. However, removing the set of 4 nonsignificant problem-solving variables (ie, positive orientation, rational problem solving, impulsivity and carelessness, avoidance styles) did not degrade model explanatory power (F4,72=2.08, NS). Therefore, negative orientation was primarily responsible for the association between social problem-solving abilities and caregiver well-being.

Caregiver Health 

The interaction between rational problem solving and time was not statistically significant. However, it was retained because removing it reduced model performance. Variability of the coefficient for the random time effect was not significant (σ2=.277, z=1.01, P=.156), indicating that there was not significant individual variability in the time coefficient. A more parsimonious model, using only an intercept as a random effect, was indicated.

Removing the set of problem-solving variables (including the interactions between positive orientation and rational problem solving with time) from the full model significantly degraded model performance (F7,70=2.44, P<.05), as did removing the social support variable (F1,70=7.28, P<.01). There was a significant interaction between positive orientation with time (P=.021). However, removing the set of 3 nonsignificant problem-solving variables (ie, negative orientation, impulsivity and carelessness, avoidance style) did not significantly degrade model explanatory power (F3,70=.70, P=.56). Although not statistically significant, removal of the rational problem solving by time and interaction effect did degrade model fit. Whether this observation represents an actual effect or an artifact of the values observed in this particular sample needs to be addressed further in independent, larger samples.

Discussion 

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Our results support social support, and the emotion-focused component of social problem solving, problem orientation, independently contributes to caregiver adjustment. Trajectory analysis indicated that higher levels of social support were associated with lower levels of caregiver depressive symptomatology and higher levels of well-being and general health, independent of social problem solving. A greater negative problem orientation was related to higher levels of depressive symptomatology and lower levels of well-being. A more positive problem orientation was associated with smaller decreases in general health. The strength or slope of this positive relation lessened over time.

Consistent with prior research, declines in social support are linked intricately with family-caregiver adjustment, and these associations are evident soon after their return to the community.35 The present study shows the dynamic association between social support and caregiver adjustment the first 3 months after stroke, affecting depressive symptomatology, well-being, and general health.

Social support often erodes over time for many caregivers who assist family members with chronic health conditions.36 Caregivers who are at risk for complicated adjustment have social and individual characteristics reflective of their constellation of supportive networks under routine and stressful situations. Distressed persons tend to seek support and alienate supportive people over time.37 Conversely, persons who are more likely to thrive in the caregiver role may be buffered by social support. We suspect this trend would continue throughout the year, based on prior modeling of the social support−caregiver adjustment relation after the onset of severe disability in family members.35

A negative orientation toward solving problems can disrupt individual abilities to regulate mood, think rationally,21 and effectively perform complex learning tasks.38 Therefore, caregivers with a lower negative orientation tend to be less pessimistic and more open to positive aspects of caregiving. More succinctly, caregivers with a lower negative orientation are more likely to interpret stressful aspects of caregiving in a more benign manner than those prone to a higher negative orientation. A greater negative orientation is associated with a low sense of preparation for caregiving roles and duties23 and may contribute to higher levels of caregiver depressive symptomatology and lower levels of well-being in the first months of caring for a stroke survivor.

People with positive orientations perceive they will be successful in their problem-solving efforts and manage problems effectively, experiencing improved health over time.39 Other empirical data support the importance of a positive problem orientation in general health. For example, structural equation modeling techniques support an indirect association between a positive constructive problem-solving style and psychologic adjustment, with greater adherence to human immunodeficiency virus antiretroviral medication regimens.40 Similarly, a positive problem orientation is associated with greater life satisfaction in patients with spinal cord injury41 and other chronic diseases.42 A challenge in examining the theoretical link between a positive problem orientation and general health in this and other studies is a pragmatic one. Changes in general health occur over time. The current study was limited to 3 months. However, longitudinal studies examining this relation are essential.

In this study, caregivers of older stroke survivors had declines in their well-being faster over time than caregivers of younger stroke survivors. This finding is in contrast to other studies that report no significant differences between stroke survivor age and caregiver well-being, after controlling for survivor functional deficits,43 as in this study. Stroke survivors in this analysis, however, had moderate levels of disability. The higher degree of homogeneity regarding functional deficits in this sample may contribute to differences in findings. The sample size also limits examining the potentially moderating or mediating effect of other variables on family adjustment as well as other study findings.

These results suggest that social support and positive problem orientation and the interaction with time are independent predictors of general health. Our findings suggest a moderating effect of positive problem orientation on change in general health over time so that caregivers with higher levels of social support and positive problem orientation experienced smaller decreases in their general health over time than did caregivers with lower levels of social support and positive problem orientation.

These results also indicate that both social support and problem orientation may be important in family caregiver adjustment. Therefore, health care professionals should explore strategies to provide these components. Although empirical literature examining the effect of problem orientation, itself, is absent, problem-solving training that incorporates both problem orientation and systematic problem-solving skills is used in home family-education programs44 by videophones45 and telephone.23, 46, 47 Although these studies are still limited in number, these problem-solving training programs provide support while decreasing caregiver depressive symptomatology and increasing wellness and perceptions of preparedness. These training programs also improve other aspects of caregiver health by increasing vitality and social functioning and lessening role limitations related to emotional problems.23

Health professionals face many challenges and opportunities in meeting the full array of unmet needs of stroke survivors and their caregivers. Although our research reveals the importance of social support and problem orientation, health care providers can assist caregivers to obtain and maintain social support to sustain them in challenges they face. Health care professionals can provide this assistance by developing a proactive approach as they interact with caregivers.

Assessment of caregivers’ networks of social support includes determining availability of family and friends who are willing and able to provide support. Other important considerations are caregivers’ comfort and ability to specifically identify needed assistance in meeting long-term needs of family members poststroke, the ability to ask others for assistance, and the investigation of potential resources of support. Health care professionals, working in tandem with medical social workers, can assist caregivers by providing them with a list of available local, regional, and national resources. Although many caregivers are savvy in using and accessing resources via certain modes (eg, face-to-face and telephone contacts), other caregivers may admit they are uncomfortable accessing resources using other modes (eg, accessing resources via electronic devices).

Through appropriate social support referrals, health care professionals can assist caregivers to adjust positively to this role. The following organizations may be useful in caregivers’ quests for social support outside immediate family and network of friends: Stroke Awareness for Everyone Inc,48 the Stroke Information Directory,49 American Stroke Association,50 National Stroke Association,51 Pediatric Stroke Network,52 Lexi-Comp Inc Stroke Explained,53 Different Strokes,54 Strokesurvivors International,55 and the Internet Stroke Center.56

The Support Team Network57 is an example of a nationally available resource that uses an empirically based team approach to create social support for care recipients and their caregivers in the community. In the past 55 years, more than 10,000 teams provided support to over 25,000 people and their families across the United States and southern Africa through this organization’s efforts. Volunteers, typically associated with churches and community organizations, use a coordinated, built-in support system to sustain their efforts. Support-team volunteers offer practical, tangible, emotional, and spiritual support and assistance based on their unique skills. Although there are many ways to organize a team, the “basic model” usually meets a variety of needs for 1 person or family and the team approach allows that flexibility. Although support teams cannot do everything for stroke survivors and their caregivers, they can improve their quality of life.

Typically, support-team activities include providing rides to health care providers or grocery stores, helping with household or yard chores, running errands, cooking or delivering meals, visiting or making telephone calls, or offering caregivers a brief time away or break from their daily routine through respite. Some support-team volunteers also share prayer or communion, based on the mutual needs and desires of a person or caregiver. A support team generally has 3 major boundaries: money, medicine, and medical care. The support team does not loan or give money, dispense prescription medications, or offer medical care. In addition to referring persons to existing support teams, health care professionals can serve as the impetus for the creation of local support teams. An initiative typically consists of a 1-year partnership between a community (eg, 1–10 congregations, agencies, and organizations) and the support team network to teach volunteers how to develop support teams. The 5 phases of development of the partnership result in an ability to develop support teams.

There are also useful techniques we, as clinicians, can use with family caregivers to strengthen social problem solving. During hospitalization, provide both oral and written information to reinforce components and steps of social problem solving. In introducing social problem solving, share how emotions affect how caregivers view problems. Furthermore, emphasize knowing a systematic process for managing problems also influences emotions. Initially, assist families to identify a variety of potential solutions for problems that commonly occur on discharge home.47 For example, problems may include assuring safety and managing ADLs and cognitive, behavioral, and emotional changes of stroke survivors.58

Provide laminated handouts for use after discharge and posters for display on walls to remind caregivers of key problem orientation components and social problem-solving steps. In problem orientation, emphasize the following: (1) problems are a part of everyday life; (2) they are capable of solving these problems by using appropriate resources; (3) some problems will be solved rather quickly, whereas others will be solved more slowly; and (4) they choose how to view problems, which will influence their feelings toward and effectiveness in solving problems. In the problem-solving component, accentuate the following key steps: identify and define the problem, identify possible solutions to the problem, choose and test the best solution, and evaluate outcomes of problem solving. In addition, provide examples that show how to apply problem orientation and problem-solving steps. Initially, make examples simple and only address 1 problem. Later, provide situations that show how to apply problem orientation and problem-solving steps in more complex situations (eg, assure safety in managing physical, cognitive, and behavioral problems).47

Some investigators59, 60 suggest people tend to view situations from 3 possible explanatory styles: assigning an internal or external cause to a problem, assessing whether the problem has affected specific (ie, some) or global (ie, all) areas of their lives, and examining whether the problem has transient or enduring effects on their lives. Persons with negative orientations tend to personalize problems, ascribing internal, enduring, and global attributes to situations, while ignoring other perspectives.

Although it seems almost automatic to enhance correct explanatory styles in problem orientation, successful programs strengthen these skills in both problem orientation and problem solving. Problem orientation and problem solving overlap so that orientation influences problem solving and vice versa. For example, in identifying problems, their associated feelings, and possible causes of problems, caregivers enhance their positive problem orientation and lessen their negative problem orientation while strengthening systematic problem solving.

Health care practitioners should encourage caregivers to identify specific problems (rather than global problems that often are unwieldy and unmanageable), external causes of problems they can realistically change, and practical solutions. Internal feelings also should be explored, assisting them to recognize situations they have limited control over, except how they are viewed and managed. Positive self-reinforcement also should be inherent in the process (eg, throw rugs on floors and weakness of my _______’s leg make me afraid of falls, safety issues that occur from throw rugs on floors are common after a stroke, removing the throw rugs will solve this problem quickly and also make me feel less anxious, I feel good I solved this problem). Over time, applying these skills enhances viewing problems less negatively and more positively, which our study findings suggest are both essential in improving outcomes related to depressive symptomatology, well-being, and general health.

Conclusions 

return to Article Outline

Social support and the emotion-focused component of social problem solving, problem orientation, independently contribute to caregivers’ adjustment after their return to the community with stroke survivors. Higher levels of social support were associated with lower levels of caregiver depressive symptomatology and higher levels of well-being and general health, independent of social problem solving. A greater negative problem orientation was associated with higher levels of depressive symptomatology and lower levels of well-being. A more positive problem orientation was associated with greater increases in general health. The strength or slope of this positive relation lessened over time. Although social support is independently associated with general health, the influence of a positive problem orientation on this outcome, over time, is tenuous and should be explored further. Interventions that provide social support and assist caregivers to develop a more adaptive orientation toward problem solving may benefit family caregivers after their return to the community.

References 

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a School of Nursing, University of Alabama, Birmingham, AL

b Department of Psychology, University of Alabama, Birmingham, AL

c Department of Health Services Administration, University of Alabama, Birmingham, AL

d Department of Medicine-Infectious Diseases, University of Alabama, Birmingham, AL

e School of Nursing, University of California, Los Angeles, CA.

Corresponding Author InformationReprint requests to Joan S. Grant, DSN, RN, CS, University of Alabama, School of Nursing, NB #407, 1701 University Blvd, Birmingham, AL 35294-1210

 Supported by the National Institute of Nursing Research (grant no. 1R15NR04724-01), the University of Alabama at Birmingham, and the Neuroscience Nursing Foundation of the American Association of Neuroscience Nurses.

No commercial party having a direct financial interest in the results of the research supporting this article has or will confer a benefit upon the author(s) or upon any organization with which the author(s) is/are associated.

PII: S0003-9993(05)01282-7

doi:10.1016/j.apmr.2005.09.019


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