OBJECTIVES: Parents of children with autism spectrum disorder (ASD) face competing demands when caring for their child and fulfilling family commitments. It remains unknown whether family obligations and parental stress might decrease the use of intervention services for young children with ASD.
METHODS: The current study is a secondary analysis of baseline date from a published randomized control trial with 147 low-resourced caregiver-child dyads. Demographic information, data on service use, maternal employment, parent’s perception of their child’s development, and parental stress were collected for primary caregivers of 2- to 5-year-old children with ASD from 5 sites. Multiple logistic regressions of accessing any intervention services or more than 1 services on familial characteristics were performed, controlling for demographic and contextual variables.
RESULTS: Twenty-five percent of children were receiving no intervention service; 26% were receiving 1 service; and 49% were receiving 2 or more services. Perceived developmental delay and not having a sibling in the home were associated with higher odds of receiving intervention services. Children were more likely to receive more than 1 service if their parents had at least a college education and low levels of stress.
CONCLUSIONS: Factors including perceived developmental level, parental stress, and caring for siblings may play a role in accessing services for children with ASD. Results reveal that competing family needs may be barriers to service use. Mothers of children with ASD with multiple children in the home, low levels of education, and high levels of stress may need additional supports or alternative service delivery models.
- ASD —
- autism spectrum disorder
- OR —
- odds ratio
- SES —
- socioeconomic status
Early referral for and enrollment in autism spectrum disorder (ASD) specialized services is critical, as behavioral and educational interventions can improve outcomes for children in cognitive, language, and social domains.1 Professional guidelines recommend parental involvement in their children’s intervention services to ensure optimal health and developmental outcomes.1 These recommendations are significant for children’s development and growth because there is evidence that children whose parents are involved in intervention show improvements in important areas, including cognitive skills.2 Although parental involvement in interventions may be a key component of acquisition and generalization of skills into the home context, the time required to maintain high parent involvement may compete with other family needs. This is particularly important to consider with parents of children with ASD because some effective interventions for young children with ASD are demanding and time intensive,3 requiring parents to take on multiple roles, including coordinators of different services4 and deliverers of the intervention itself.1,5,6
The influence of parental involvement in intervention services on the family is particularly important to examine in parents of children with ASD because they exhibit unique patterns of stress. Mothers of children with ASD are at risk for experiencing greater parental stress than mothers of typically developing children6,7 and mothers of children with other disabilities.8,9 Furthermore, parents of children with ASD exhibit similar cortisol levels to those of combat soldiers, parents who have a child with cancer, and individuals who suffer from posttraumatic stress disorder.10 Mothers of children with ASD consistently report high levels of psychological distress, including parental stress, depressive symptoms, and social isolation.11,12 Approximately 40% of such mothers report clinically significant levels of parenting stress, and between 33% and 59% report depressive symptoms warranting psychiatric evaluation.13,14 These depressive symptoms are associated with decreased energy, concentration, and lack of motivation, and can adversely affect maternal functioning as well as a mother’s capacity to manage the health needs of her children.15–18 In this population, parental stress can also result from the patterns of behavior that children with ASD exhibit, specifically related to deficits in social and communication skills and the presence of restricted interests and repetitive behaviors. Not only do these behaviors themselves influence parents’ stress,12,13 but acquiring and coordinating the sometimes multitude of intervention services needed for children with ASD places a significant strain on a family’s time and financial resources.19
Some evidence suggests that parents may experience improvements in their own mental health and sense of competency when their child begins receiving intervention services,20,21 especially when those services directly target parent needs for information and specific help for their child.22 However, there is also evidence suggesting that enrollment in intervention services may raise additional, unintended challenges for the family unit. In a recent analysis of the National Survey of Children with Special Health Care Needs, the authors showed that families of children with ASD may face higher levels of financial and employment burden than families of other children with special health care needs; specifically, avoiding job changes to maintain health insurance, paying higher out-of-pocket expenses, experiencing financial problems, spending a substantial amount of time each week coordinating care, and reducing or ending employment.23 Recently, authors of a qualitative study described the challenges faced by parents of children with ASD and found that most parents reported having to adapt their employment and child care conditions to accommodate time-consuming intervention schedules.4 These findings are consistent with previous studies in which authors showed that mothers of children with ASD are less likely to be employed24 and more likely to face problems with employment because of child care arrangements.25,26 In children with ASD, when intervention attendance (as measured by the percentage of sessions completed) was examined in families in 1 study, parents from a lower socioeconomic status (SES) background were less likely to attend intervention sessions as compared with parents from a higher SES background.27 The importance of insurance coverage and SES reveals that further understanding is needed surrounding the relation between familial characteristics and service use in parents of children with ASD.
Given the challenges that are often associated with accessing services for ASD (eg, obtaining an individualized education plan through a school district), family burden is an important factor to consider when evaluating the extent to which underserved children with ASD are receiving appropriate services. The current study used baseline data from a multisite randomized controlled trial for children with ASD to examine the association among familial characteristics and the odds of accessing ASD-targeted therapies inside and outside of school.28 In the context of previous literature demonstrating family burden associated with ASD, we sought to investigate whether familial characteristics such as maternal employment, parental stress, and additional family and child characteristics were associated with the use of intervention services at the time of entry into the study. We sought to examine intervention use in underserved children with ASD who are 5 years old and younger, because this age group represents children eligible for early intervention services and early childhood special education.
The current study is a secondary analysis of baseline date from a previously published randomized controlled intervention study.28 Children with an existing diagnosis of ASD were recruited from the following 5 study centers across the United States participating in the Autism Intervention Research Network for Behavioral Health: University of Washington, University of Michigan, Kennedy Krieger Institute, Florida State University, and University of California, Los Angeles. Institutional review board approval was obtained at all 5 sites and all caregivers consented to their family’s participation in the study. To be eligible for the main study, children must have had a diagnosis of ASD, as confirmed with the Autism Diagnostic Observation Schedule,29 were between 2 and 5 years of age, and have had a reported lack of resources as defined by receiving government assistance, such as Medicaid health insurance or difficulty accessing services for ASD. Recruitment occurred over 23 months (from August 2009 through July 2011). For the current analysis, we examine data from the 147 primary caregivers (83% mothers) across 5 sites who completed self-report measures on demographics, family resources, family stress, and service use at study entry.
Our outcome of interest in this analysis was whether the child was receiving intervention services before study entry. Parents reported on all services the child was receiving (ie, speech language therapy, occupational therapy, special education, behavioral therapy, biomedical treatments, and other treatments or therapies) and whether the services were received inside school, outside of school, or both. We then compared children who were receiving no intervention services to children who were receiving at least 1 intervention service and, separately, children who were receiving only 1 intervention service to children who received more than 1 intervention service.
Independent Variables and Covariates
Caregivers completed self-report measures related to their family’s demographic information, their perceptions of their child’s developmental level, and their own parental stress.
Caregivers completed a self-report form, which asked them to report on familial characteristics including maternal employment, whether there was more than 1 child living in the home, child’s age, child’s sex, child’s race and ethnicity, language the child hears most at home, mother’s education, and household income. Because this was a multisite study, the study site was entered as a covariate into the model. All variables were selected for their potential to impact service use and entered into the model simultaneously, and there was no evidence of multicollinearity between variables. Caregivers completed questionnaires to collect information about their child’s background and their own background. The number of adults in the home was asked inconsistently across study sites; therefore, we were not able to use the presence of adults (second parents or other caregivers) in our analyses. However, single mothers were eligible for enrollment in the study. The child’s age was calculated in months from date of birth to date of entry into the study. Caregivers were asked to select any number of options to report on their child’s race and ethnicity and these categories were collapsed into white, African American, Hispanic, Asian American, and other (American Indian and Pacific Islander were placed into the “other” category). Caregivers were asked to select the child’s mother’s level of education from 7 categories and this variable was then categorized as high school diploma or less, some college, college degree, or more than college. Caregivers were asked to report the primary language the child hears most at home, and this variable was coded as “English” or “not English.” Caregivers were asked to list the number of children in the home, and this covariate was dichotomized to reflect whether the study participant had siblings living in the home or no siblings living in the home. Given that mothers are typically involved with intervention services, we elected to use maternal employment and education in our model.
Perceptions of Child’s Developmental Level
Caregivers were asked whether they perceived their child’s development to be “behind age level,” “at age level,” or “above age level.” This variable was dichotomized as “behind age level” or “at age level or above.”
Parental stress was measured with the Parenting Daily Hassles survey30 (internal consistency reliability α = .81–.90). This is a 20-item measure of typical everyday events in parenting and parent-child interactions. Parents were asked to rate (1) how often these events occur in their daily life (frequency), and (2) how much of a hassle they feel these events are (intensity). For the frequency subscale, in response to each item, the caregiver rates the frequency of occurrence on a 5-point scale (never = 0, rarely = 1, sometimes = 2, a lot = 3, constantly = 4). A frequency scale score is calculated as the sum of the frequency ratings on all 20 items and treated as a continuous variable in the analysis. A frequency scale score of 37 (SD = 7) is considered average. We elected to use the frequency subscale of the Parenting Daily Hassles survey because we were interested in the frequency with which parents experience challenges with their children.
All analyses were performed by using R version 3.3.2 statistical programming language (R Foundation for Statistical Computing, Vienna, Austria). For our primary analysis we conducted multiple logistic regressions to examine whether familial characteristics influence the odds of receiving any intervention services. As a secondary analysis, we also sought to determine if any familial characteristics were associated with accessing fewer intervention services among those families who successfully accessed at least 1 service. We therefore restricted the next analysis to families who had accessed intervention services and conducted a separate multiple logistic regression of accessing more than 1 intervention service, compared with accessing only 1 service, controlling for the covariates described above. Missing data represented at most 20% of the sample in which parents did not return the demographic form. Significance was determined at P < .05, and moderate significance was determined as P range between .05 and .1.
Demographic characteristics of the children and families included in the study sample are presented in Table 1. Twenty-five percent were receiving no services or interventions on entry to the study, 26% were receiving 1 service or intervention, and 49% were receiving 2 or more services. All parents reported on services that children received inside and/or outside of school. Fourteen percent of the sample was Hispanic, and 14% of participants spoke a language other than English at home. In addition, 21% of mothers had a high school diploma or General Equivalency Diploma or less. Of the 147 caregiver-child dyads, 112 caregivers provided complete data (“completers”) on all the variables of interest and 35 caregivers did not provide complete data (“noncompleters”). A detailed analysis was performed to determine if completers and noncompleters differ in the variables of interest. There were no significant differences between completers and noncompleters in any variables of interest.
Logistic regression of maternal employment on accessing any intervention services revealed that children whose mothers perceived delays in their child’s development had higher odds of accessing services for their children compared with those whose mothers did not feel that their child’s development was delayed (odds ratio [OR] = 0.22, P = .05). Maternal employment was not associated with the odds of receiving intervention services, nor were any other familial characteristics. Additionally, having a sibling was associated with lower odds of accessing any intervention services (OR = 0.26, P = .05). Among children who had received at least 1 intervention service, higher maternal education was associated with higher odds of accessing more than 1 service (OR = 6.86, P = .04 for some college versus high school or less; OR = 11.23, P = .03 for postcollege versus high school or less; see Fig 1A); whereas, higher parental stress was associated with lower odds of accessing more than 1 intervention service (OR = 0.92, P < .01; see Fig 1B). Again, maternal employment was not significantly associated with the odds of receiving more than 1 intervention service, nor were any other familial characteristics.
These results suggest that parental stress, whether there is another sibling in the household, and a parents’ perception of their child’s development are significantly associated with accessing intervention services for a child with ASD. Both having a mother who is experiencing high stress and having another sibling in the home were associated with lower odds of receiving intervention services. With these findings, we demonstrate the difficulty parents of children with ASD face in addressing competing needs in the family. Conversely, caregivers who perceived that their child’s development was behind his or her chronological age were more likely to access intervention services for their child as compared with caregivers who did not perceive delays in their child’s development. Taken together, these results highlight the critical role caregivers play in accessing and coordinating service delivery for children with ASD. It was somewhat surprising that maternal employment was not associated with the odds of receiving intervention services; however, this may be because the reason behind maternal employment level was not collected. That is, mothers were not asked to report whether they were unemployed by choice, or unemployed because they were unable to find work. Future studies could examine the reasons behind maternal employment as a possible means of determining its relation to receipt of ASD services.
Ideally, access to intervention services should be determined by how likely the child is to benefit from these services; however, our findings suggest that specific familial characteristics should be targeted to enhance service use. Intervention providers might consider the extra demands on parents who have more than 1 child and are experiencing high levels of parental stress. Although the type of intervention service received was not examined as a part of this study, because many interventions include some level of parent involvement,5,31 we must consider the different effects of this involvement. Recently, efficacy studies of parent-delivered interventions have become increasingly popular because they are cost-effective, and intervention techniques continue to be taught in the home when the parent and child are together.28,32,33 Parents and therapists collaborate in helping their children improve communication and social skills. Although an efficacious means of delivering intervention services, if children whose parents have more than 1 child have greater difficulty accessing these services, they may need additional supports at home and work to meet their competing demands. The current study provides an important first step in understanding the challenges that parents may face when confronted with the reality of enrolling their children in intervention programs.
The current study has several limitations, which should be examined further in the future. Although our sample size is considerably larger than many studies of children with ASD, our relatively small sample prevented us from a deep dive into the complexities of paternal employment versus maternal, and single versus 2-parent families. Authors of future studies could examine whether differences exist in the services children receive inside of school or outside of school, because the coordination of services outside of school may require a higher level of maternal involvement. Additionally, the options caregivers were given to describe their child’s development were broad, and future studies could examine this in a more nuanced manner. All families enrolled in the main study were considered low-resourced and results should be interpreted in light of the study population. The ways in which parents navigate their living situations and also care for a child who needs additional services and specialized schooling is a critical topic as ASD becomes more prevalent in the population. Although ASD services are becoming more available to all families, the ability to obtain those services, advocate for your child and maintain your own household duties are likely critical concerns of mothers and fathers alike. Interventions developed for children with ASD should consider familial characteristics and may serve children better if real-world considerations for involving parents are included.
Despite a relatively small sample, the current study revealed important relations between number of children living in the household, parental stress, maternal education, and the likelihood that young children will receive interventions. Intervention providers, as well as policy makers and grant-funding agencies may need to consider additional supports for children with ASD who have difficulty accessing intervention services. Raising a child with special needs places extra demands on families: financially, emotionally and logistically. With these findings, we suggest that our current service delivery system might place parents in the difficult position of choosing between caring for a sibling and ensuring that their child with ASD accesses appropriate services to reach their full developmental potential. To complement this model, parents may need additional supports to enroll and maintain services for their children. Future studies should examine what structural changes can be made to increase the likelihood that parents are able to enroll their children and maintain them in intervention services.
We acknowledge Vani Nimbal, MPH for her assistance with preliminary data cleaning of this data set and Lynette Lau, PhD for her assistance in the preparation of this manuscript. We would like to acknowledge the Autism Intervention Research Behavioral Network (PI: Kasari), who conceived of and collected data for the original study from which participants were drawn for the current study. Autism Intervention Research Behavioral Network members include Connie Kasari, PhD, Catherine Lord, PhD, Bryan King, MD, Amy Wetherby, PhD, and Rebecca Landa, PhD. We also express our sincere gratitude to the families who participated in the original study.
- Accepted September 26, 2017.
- Address correspondence to Elizabeth A. Karp, MS, Department of Psychology, University of Washington, Box 351525, Seattle, WA 98195. E-mail:
FINANCIAL DISCLOSURE: The authors have indicated they have no financial relationships relevant to this article to disclose.
FUNDING: Supported by the Maternal and Child Health Bureau (MCHB) Autism Intervention Research Behavioral Network (UA3MC11055; principal investigator [PI]: Kasari) and further supported by an MCHB R40 Secondary Data Analysis Study (R40MC22642; PI: Kuo). Drs Lau and Kuo are also supported by the MCHB Health Care Transitions Research Network (UA3MC27364; PI: Kuo).
POTENTIAL CONFLICT OF INTEREST: The authors have indicated they have no potential conflicts of interest to disclose.
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