Position Statement on Therapies and Interventions, Updated July 2022

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Therapies and Interventions,  including Early Intensive Behavioural Therapies (EIBIs) and Applied Behaviour Analysis (ABA)

POSITION STATEMENT

UPDATED: July 2022

Summary

Reframing Autism acknowledges that many therapies have the potential to be beneficial for Autistic people at certain stages across their lifespan.

Psychology, Occupational Therapy, Speech and Language Therapy, Music, Art, and Physical Therapies, and supports enabling communication through the provision of alternative means such as AAC or sign language, may be intrinsic to helping Autistic individuals to manage the challenges inherent in living in a world that is not oriented to an Autistic neurology. We endorse the use of these therapies when they are approached from the strengths-based, citizenship, human rights framework that is fundamental to the social model of disability, and when they are utilised to support an Autistic individual to be their best Autistic self.

As an organisation, however, Reframing Autism has grave concerns about the provision of any therapy or intervention which “normalises” Autistic people or suppresses intrinsic Autistic behaviours.

We also reject any intervention which suggests (whether tacitly or explicitly) that a non-autistic neurology is superior or even preferable to an Autistic one.

Reframing Autism specifically rejects the use of any therapy or intervention which are intensive in nature, or which utilises a system of rewards and punishments to modify Autistic behaviours and train Autistic individuals to act and perform non-autistically.

Early Intensive Behaviour Intervention (EIBI) and Applied Behaviour Analysis (ABA)

1. EIBIs and ABA as Evidence-Based Practices

We note that, in Australia, many families are being recommended ABA as the “only” evidence-based, effective “treatment” or intervention for Autism (Lizard Centre, 2017; Autism Partnership Australia, 2013), with ABA offered as a family’s best hope of setting their child up for a successful and ordinary, independent life (Grasswill, 2014). For example, on the new Autism: What Next? website, a key takeaway for EIBIs/ABA is that “there are more than three decades of research demonstrating the effectiveness of the principles and techniques of ABA for teaching children with autism a range of new skills, and helping to reduce challenging behaviours”. The recommendation for families to embark on EIBI is coming from some paediatric and diagnostic teams, as well as some service providers themselves (e.g., AEIOU, 2019).

Reframing Autism has severe concerns with the framing of this recommendation, including:

  • the weak evidence demonstrating the efficacy of ABA and EIBIs (e.g., Magiati, Charman & Howlin, 2007; Howlin, Magiati & Charman, 2009; Reichow et al., 2018);
  • the inherent conflict of interest in ABA providers prescribing intensive ABA to families;
  • the existence of other, non-intensive, non-behavioural therapies that are evidenced to have positive outcomes for Autistic individuals (Lindgren & Doobay, 2011);
  • diagnosticians, and ABA and EIBI providers, often present families with only worst-case scenarios about a child’s future, exploiting vulnerable parents with “apocalyptic” conjecturing, into committing to expensive and time-intensive interventions (Lilley, 2011; see testimonials below);
  • the lack of balanced information given to families regarding EIBIs,
  • in advocating for intensive interventions as optimal for children, practitioners of EIBIs ignore the “inconsistent findings” linking intervention amount to child outcomes (Trembath et al., 2021) and risk failing to individualise or personalise the intervention, as is recommended practice (Trembath et al., 2022), and
  • the lack of genuine choice offered to families at their child’s diagnosis, at which families are often given no choices (ABA is presented as the “only” effective choice), or are given a bewildering array of choices and rely on their own research to make decisions about their child’s therapy (Deyro, Simon & Guay, 2016).

We also note that families usually make decisions about interventions and therapies for their Autistic child shortly after an official diagnosis. Research shows that official diagnoses are often accompanied by dire predictions for a child’s future life outcomes (Chamak & Bonniau, 2013; Laser Beak Man, 2019; Chan, 2019), and parents report pressure to make intervention decisions immediately without delay to get the best outcomes for their child, citing a “window of opportunity” for early intervention (Edwards et al., 2017).

Reframing Autism does not wish to engage here extensively with the claim of an “evidence-base” for EIBIs. It should be noted, however, that a comprehensive 2018 Cochrane review cites significant reservations about the extant evidence for the efficacy of EIBIs, concluding that “there is weak evidence that EIBI may be an effective behavioral treatment for some children with ASD” (Reichow et al., 2018; emphasis added). Indeed, the 2022 edition of The Wiley-Blackwell Handbook of Childhood Social Development concludes that “in terms of the effectiveness of ABA approaches, research suggests that intervention effects do not generalise beyond the intervention environment, and […] there is inadequate collective evidence for change on any selected outcome” (Davis et al., 2022).

Research also challenges the oft-cited evidence that ABA promotes Autistic learning and engagement, suggesting that in fact it exacerbates hyper-specificity and undermines organic Autistic processes of learning (Harris et al., 2015).

More recently, in a report to Congress dated October 25, 2019, the United States Department of Defense stated about its Autism Care Demonstration package, that after a year of ABA treatment, 76% of Autistic participants showed “little to no change in symptom presentation” and, in fact, 9% demonstrated “worsening symptoms”. Equally, Hassiotis et al. (2018), documents no reduction in “challenging” behaviours in clients with intellectual disability receiving reward-based behavioural interventions.

Moreover, there is no evidence to indicate that EIBIs are effective for non-traditionally communicating, specifically nonspeaking, Autistic children (Sandoval-Norton, Shkedy & Shkedy, 2021). Conversely, prompt-dependency, reward-expectation, reduced performance quality, difficulty generalising, unquestioning compliance, and learned helplessness characterise the adult Autistic population exposed to EIBIs as children (Sandoval-Norton & Shkedy, 2019). Whilst compliance might superficially seem like a reasonable goal for children, conditioning already vulnerable Autistic individuals to be unquestioningly compliant puts them at even greater increased risk for emotional, physical and sexual abuse (Weiss & Fardella, 2018).

We also note the existence of research which suggests that EIBIs misinterpret and thus exacerbate self-injurious behaviours in children (Shkedy, Shkedy & Sandoval-Norton, 2019), that they stifle organic communication preferences. Indeed, such intensive “therapisation” of the home detrimentally affects the mental health and quality of life outcomes not only for Autistic children, but for their whole family by sacrificing the sense of “intactness” that is fundamental to an individual’s feelings of self-worth, self-efficacy, and self-determination (Turnbull et al., 1999).

2. Stated Outcomes of EIBIs

With these reservations about the evidenced limitations of EIBIs stated, we wish to engage with the exact outcomes that EIBIs are ostensibly evidenced to produce in Autistic individuals.

ABA and other EIBIs have, as their purpose, the “recovery” of Autistic children who become “indistinguishable from their peers” as a result of behavioural intervention (a sentiment first expressed by ABA’s creator, Ole Ivar Løvaas).

EIBIs are thus ostensibly evidenced to decrease Autistic “symptomology”, to “improve” Autistic behaviours, and to decrease “challenging”, “undesirable”, “problem”, “interfering”, “non-functional”, “maladaptive” behaviours (Odom et al., 2010; National Autism Center, 2015; Prior & Roberts, 2012).

Such goals, however, reward and promote the concealment or suppression of authentic Autistic self-expression, punish organic Autistic behaviours, demean Autism, and frame Autism as a disease or deviance to be cured or treated (Shyman, 2016). As Milton (2018) notes, EIBIs are “highly normative, and unsympathetic to a social model of disability”, which disregards the recommendation for supports and goals to be neuro-affirming (Trembath et al., 2022).

Take, for example, self-stimulatory behaviours (“stimming”), which are often pathologised as deviant or problematic behaviour in EIBIs. As Sandoval-Norton and Shkedy (2019) observe, EIBIs often punish stimming or reward the suppression of stimming. Given the importance of stimming to Autistic self-regulation and organic communication as a form of Autistic body language (Kapp et al., 2019), Sandoval-Norton and Shkedy (2019) are confident in asserting that:

“A lifetime of being punished for certain movements, and being forced to engage in eye contact despite the physiological pain and discomfort of doing so, is psychological and physical abuse. A lifetime of being forced to sit still with no regard for actual cognitive abilities can create further emotional and psychological harm” (p. 4; emphasis added).

As Ne’eman (2021) suggests, interventions which target or seek to extinguish stigmatised, but not intrinsically harmful or personally distressing disability-related traits, often fail to address more meaningful and relevant, person-centred goals.

3. Ethical Congruence: A Requirement for EBPs

Reframing Autism also notes that for practices to be considered “evidence-based”, they need to correspond with the values, preferences and ethical ideologies of parents, care providers and the Autistic individual (National Autism Center, 2015).

That is, evidence-based practices (EBPs) need to epitomise the social and ethical ideologies of Autistic clients, their parents and other stakeholders (such as the NDIS), and it is recommended that practitioners have an understanding of the views and preferences of the Autistic community in terms of supports (Trembath et al., 2022).

We question how EIBIs are consistent with the ideologies of the Autistic community, given the significant and global Autistic protest to EIBIs (Ask an Autistic, 2019).

We equally question how EIBIs are consistent with the NDIS ideology of choice and control, and adherence to the social model of disability.

As Shyman (2016) notes, ABA is inherently tied to the medical model of disability; it strips the Autistic individual of all choice and control since parent and therapist are placed in the position of absolute power to define the deviant (often organically Autistic) behaviour and eliminate it.

As Tim Chan, an Autistic adult and ABA recipient, notes, the basis of ABA and other EIBIs is the medical model in which Autism is viewed as a disorder and a diseased condition, with the onus on Autistic individuals to conform and adhere to social norms, expectations and conventions. This “ableist” perspective does not respect or embrace neurodivergent functioning, and “normalism” is used mainly as a disciplining, repressive force (Waldschmidt, 2005).

That is, non-autistic behavioural therapists decide arbitrarily which behaviours are, and are not, functional or problematic, and seek to apply homogenous neuro-normative values to Autistic behaviours, without an adequate understanding of Autism or Autistic neurology.

4. Undertrained Practitioners

In this context, then, we also note that ABA practitioners (including Board Certified Behaviour Analysts) need not have specific training in Autism itself, with professional development concentrating on behaviour analysis, education or psychology. That is, ABA practitioners are not specialists in Autism, nor do they necessarily have qualifications or even basic training in Autism.

Moreover, EIBIs are highly reliant on sourcing junior therapists to provide the intervention for the majority of the 30-40 hour per week program. Such junior therapists are usually only given a few days of training before they begin working directly with Autistic children; they need no other formal or informal qualifications. This reality contravenes the recommendation that “practitioners should have relevant qualifications, [and] be regulated” (Trembath et al., 2022).

5. Potential to Do Harm

Most importantly, ABA and EIBIs are not evidenced to improve wellbeing, or to decrease mental illness or distress, or to increase self-determination, resilience, long-term independence or communication, or to boost family quality of life outcomes.

Conversely, there is emerging evidence to suggest that ABA and other “normalising” EIBIs decrease wellbeing and increase mental illness, including severe psychiatric distress like posttraumatic stress symptoms (PTSS; Kupferstein, 2018; 2019).

Whilst further longitudinal study is indicated, Kupferstein’s initial research suggests that exposure to ABA significantly increases posttraumatic stress disorder (PTSD) in Autistic individuals, with nearly 1 in 2 Autistic individuals exposed to ABA presenting with PTSD, and with extreme levels of trauma severity in half of these affected individuals. Autistic adults have a 41%, and Autistic children a shocking 130%, increased chance of meeting PTSD criteria after exposure to ABA. Autistic adults and children not exposed to ABA have a 72% chance of reporting no PTSS.

Importantly, there is currently no evidence to prove that ABA and EIBIs are psychologically safe for Autistic individuals or their families. Indeed, the National Autism Center’s report (2015) expressly states that it is not concerned with identifying or documenting “any adverse intervention effects” (p. 31), and Dawson and Fletcher-Watson (2022) note that there is “a pervasive failure to consider harms” in the research into ABA, which has been “flagged as a violation of research ethics” (p. 564). Indeed, bioethicists Daniel Wilkenfeld and Allison McCarthy (2020), argue from a bioethical perspective that “ABA violates the principles of justice and nonmaleficence and, most critically, infringes on the autonomy of children and (when pushed aggressively) of parents as well” (p. 31). This is concerning, given the current strong recommendation for supports to be ethical to protect the rights of children and families (Trembath et al., 2022).

With this in mind, then, we note that there does exist evidence to indicate the very real and significant potential for “adverse effects”, which contravenes the strong recommendation for supports for Autistic children to lay “the foundation for a positive future, including optimum health… and wellbeing” (Trembath et al., 2022).

Recently, claims have been made that concerns about EIBIs and their connection to trauma and mental harm reflect a “woke” agenda of late-diagnosed Autistic adults. In response to these claims, we refer to the qualitative study by McGill and Robinson (2021) which accessed the views of Autistic adults who had experienced more than 6 months of ABA as a child. The dominant themes expressed by the Autistic participants in that study who had experience ABA in childhood, were ABA’s predominantly detrimental impact, and its hidden harms, on their childhood. Participants described ABA creating a painful lived experience, eroding their sense of self, having a causal impact on their continued negative mental health, engendering self-loathing, and resulting a loss of self-agency.

Additionally, we acknowledge that a significant and large body of anecdotal evidence exists to speak to the potential harm that EIBIs pose to Autistic individuals from individuals who have experience EIBIs in childhood.

We hold that it is inherently ableist to ignore this immense body of anecdotal evidence because it is not peer-reviewed research (Ask an Autistic, 2019; ABA Controversy Autism Discussion, 2017; Davison, 2018).

As a society, we have an absolute duty to listen to Autistic voices, who are the only real experts in what they have experienced when exposed to EIBIs.

6. Fidelity 

We also wish to question whether the principles encoded in peer-reviewed research are echoed in the reality of service provision. Given that Hassiotis et al. (2018) cite “intervention fidelity” (or, more rightly, a lack of intervention fidelity across clinicians) as a major concern, it is apposite to question how closely interventions mirror researched practice. Indeed, parent and Autistic testimony indicates a significant disparity between research and practice (Kupferstein, 2019).

Conclusion

Reframing Autism advocates for families to be given accurate information about the evidence-base for – and against – ABA and EIBIs. In the draft national guidelines for supporting the learning, participation, and wellbeing of Autistic children and their families in Australia, it is recommended that “parents should have the information they need to make informed choices about supports” (Trembath et al., 2022). Reframing Autism wholly endorses this recommendation and calls on all practitioners to provide families with full and frank disclosure, to ensure informed choice is possible.

Just as any practitioner has a duty of care to disclose risks and benefits of any intervention, so too, disclosure of the risks of ABA (including the lack of Autism-specific training for practitioners, and the significant risk of PTSS/PTSD) should be disclosed prior to commencement or exposure to ensure proper informed consent requirements.

Furthermore, Reframing Autism advocates that the burden of proof lies with proponents of ABA and EIBIs to prove through co-produced research that these interventions are not psychologically harmful.

Reframing Autism calls on the medical professionals who have a duty of care, including the NDIS and other related funding bodies, to question whether it is responsible to recommend or to fund a potentially harmful, restrictive practice, especially given that EIBIs are antithetical to a social model of disability and can offer no proof of long-term safety (Sandoval-Norton & Shkedy, 2019).

We ask whether the majority of the goals of EIBIs – to suppress Autistic neurology and eliminate authentic self-expression – align with the NDIS principles for choice and control.

The Australian Autistic population is experiencing a mental health crisis, with mortality rates 2.06 times that of the general population, and with suicide a leading cause of premature death.

Research shows that concealment (as promoted by EIBIs), and stigmatisation (as is communicated by the promotion of neuro-normative performance over Autistic neurology within EIBI frameworks), are key to the dire mental health statistics of the Autistic population (Hwang et al., 2019).

Reframing Autism understands that parents of Autistic children are operating from a motivation of wanting the very best for their child. Families are a vulnerable population, susceptible to being oversold EIBIs as “cures” without due understanding of the significant risks associated with these interventions.

As a society, we need to ensure safe, effective, viable and respectful information and provision of alternative service models to EIBIs, to counter the pervasive stigmatisation of Autism and to change the narrative for the benefit of the Autistic community and our families and allies.

References

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The Reframing Autism team would like to acknowledge the Traditional Owners of the lands on which we have the privilege to learn, work, and grow. Whilst we gather on many different parts of this Country, the RA team walk on the land of the Birpai, Awabakal, Wattamattagal, Whadjak, Amangu, Bunurong and Kaurna Yarta peoples.

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