Self Injury - Autism Research Institute https://autism.org/category/self-injury-2/ Advancing Autism Research and Education Sun, 28 Apr 2024 21:01:17 +0000 en-US hourly 1 https://wordpress.org/?v=6.5.3 Treating autism with contingent electric shock: Are all possible options really considered? https://autism.org/treating-autism-with-electric-shock/ Fri, 16 Dec 2022 18:27:59 +0000 https://last-drum.flywheelsites.com/?p=15873 The use of punishment to treat severe behavioral challenges in autistic children was first introduced nearly 60 years ago. Although most people in the autism community strongly disagree with using any form of punishment as a therapeutic approach, aversives continue to be a source of discussion and controversy. Recently, the

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The use of punishment to treat severe behavioral challenges in autistic children was first introduced nearly 60 years ago. Although most people in the autism community strongly disagree with using any form of punishment as a therapeutic approach, aversives continue to be a source of discussion and controversy. Recently, the Association for Behavior Analysis International, a renowned professional organization established in 1974, asked its members to vote on whether contingent electric shock should be entirely ruled out or be appropriate in some cases. Given the recent renewed interest in aversives, I thought it would be timely to share my thoughts on this topic.

Over the past 50+ years, much has been written about using aversive interventions to treat those on the autism spectrum. Aversives involve mild to severe degrees of discomfort or pain, from saying the word “no” or making a loud noise to more extreme forms such as forced ammonia inhalation, blindfolding, and electric shock [1-3].

Although aversives can be moderately effective in reducing challenging behaviors, such as self-injurious behavior (SIB) and aggression toward others, critics often use the words “cruel” and “torture” to describe extreme forms of aversives. However, some forms of aversives are currently accepted by the general professional community. For instance, aversives, including contingent electric shock (CES), are sometimes employed to treat addictions in the general population, including alcoholism, gambling, and smoking [4-6].

In this editorial, I will address CES given a legal decision rendered last year (July 2021) [7]. Basically, a judge allowed the utilization of CES for clients who engaged in severe challenging behaviors potentially leading to harm to others or to themselves. This ruling applies only to clients at the Judge Rotenberg Educational Center in Canton, Massachusetts. The ruling affects about one-fifth of the approximately 300 clients at the center. However, this decision can now be referred to in other legal cases involving similar situations.

CES should not be confused with electroconvulsive therapy (ECT). The former is applied immediately, usually within seconds, after a challenging behavior, such as self-harming behavior or aggression. The latter, ECT, involves administering electric current into the brain to induce a brief seizure. ECT has been given to some individuals on the spectrum to treat severe self-injurious behavior [8] and catatonia [9].

Research on CES started in the mid-1960s, soon after autism was recognized as a biological condition as opposed to a condition caused by emotional neglect by parents. Early studies typically involved single-subject controlled experiments. Over the years, few studies have been reported in the literature.

Today, CES is, for the most part, not considered a viable form of intervention within the autism community. In addition, the Food and Drug Administration banned CES in the United States [10], and the United Nations has stated that CES is dehumanizing and abusive [11].

The use of CES over the decades was never widespread; however, it was sometimes employed as a last resort since SIB can lead to severe self-inflicted harm, such as lacerations, bone fractures, and concussions. There are also reports of individuals blinding themselves in addition to biting off their fingers or part of their tongue. One rationale people have used when condoning CES is to avoid other “less desirable” options, including long-term sedation or restraint.

Several methods have been used to deliver CES, including (1) an electrical prod, (2) an electrical grid embedded in the floor, (3) a remote-controlled device activated by a therapist, and (4) an automated movement sensor. Regarding the latter, the Self-Injurious Behavior Inhibiting System (SIBIS) was created to control head-banging by placing a sensor on the child’s head that would deliver a signal to activate a shock to the arm or leg [12].

How should we approach the treatment of severe challenging behaviors?

Edward Carr, one of the leading experts in treating challenging behaviors, would often tell a heart-wrenching story about the time he attempted to treat a young man on the spectrum who engaged in severe SIB [13]. Dr. Carr’s team developed a behavioral strategy that involved giving CES immediately after the man engaged in head-hitting. The intervention was moderately successful in that the frequency of head-hitting decreased but was not entirely eliminated. Later, the team learned that the man suffered from migraine headaches. One could imagine how an individual would feel when experiencing both a severe head pain and electric shock.

In a recent interview in the Boston Globe, a father described his son who had blinded himself in one eye and exhibited numerous challenging behaviors (August 1, 2021) [14]. After receiving CES, he stopped poking his other eye. Other benefits seen in the child were also attributed to the CES, including improvements in communication and self-help skills.

However, it is important to mention that one research study demonstrated a dramatic reduction in eye-poking behavior in a group of autistic children after receiving liquid calcium [15]. This is because some-to-many individuals who exhibit this type of behavior suffer from hypocalcemia. One possible explanation for eye-poking is that low calcium levels are associated with dry eye syndrome, which may lead to inflammation on the surface of the eyes and/or the eyelids as well as cause a burning sensation [16, 17]. Thus, giving an individual a simple nutritional supplement may be beneficial when treating behavior directed toward the eyes. Unfortunately, this treatment is not well-known among clinicians.

The use of CES, as almost always argued, is considered after attempting all other possible options for intervention. Although this may sound convincing and commendable, the term “all” can be considered a misnomer because this really depends on the knowledge-base as well as the training of the members of the clinical team as well as outside consultants. Given the limited amount of research and the lack of widespread knowledge about the biology of challenging behaviors, one can easily question whether the decision to administer electric shock is truly reasonable and thorough.

There is mounting evidence indicating that internal discomfort or pain may be associated with SIB. Unfortunately, many individuals on the autism spectrum have impaired communication skills. As a result, they often cannot express their feelings of discomfort and pain. Comorbidities associated with SIB include gastrointestinal problems [18], immune system issues [19], metabolic problems [20], seizures [21], abnormal sensory processing [22], nutritional issues [23], anxiety [24], and sleep problems [25].

Obviously, it can be a daunting task to assess all possibilities when determining the underlying reasons for a severe behavior, but it is crucial that an all-out effort be made.

The Autism Research Institute recently launched a new webpage, www.Self-InjuriousBehavior.com, designed to assist professionals and parents in identifying treatments that may reduce or eliminate self-injurious behavior. After answering questions regarding the location of the injury as well as related factors, users are directed to a description of possible underlying causes for the behavior. In addition, online links are presented with respect to understanding and treating the behavior.

A large parent survey that collected data on almost 40,000 individuals with ASD indicated that 9% engaged in SIB, 19% engaged in aggression, and 19% engaged in both behaviors (data collected by the Autism Research Institute between 1964 and 2006). Given that nearly half of individuals on the spectrum exhibit one or both of these challenging behaviors, we urge the autism community to work collaboratively to establish a consensus report on treating challenging behaviors. The goal of such an effort would be to recommend a number of behavioral, sensory, medical, and biomedical approaches that could help to identify the underlying reasons for the behaviors of interest, pointing to the most appropriate treatments. We hope that the autism community will welcome such a challenge and support such an endeavor.

References are available at www.ARRIReferences.org.

This editorial originally appeared in Autism Research Review International, Vol. 36, No. 4, 2022

Past issues of Autism Research Review International are available online at 

ARI’s Latest Accomplishments

April 15th, 2024|News|

Connecting investigators, professionals, parents, and autistic people worldwide is essential for effective advocacy. Throughout 2023, we continued our work offering focus on education while funding and support research on genetics, neurology, co-occurring medical

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Autismo y el Procesamiento Sensorial: Estrategias Prácticas para Usar en Casa https://autism.org/autismo-y-el-procesamiento-sensorial/ Tue, 13 Sep 2022 17:34:00 +0000 https://last-drum.flywheelsites.com/?p=15097 Printable handouts are available online HERE (.pdf) Moira Peña, BScOT, MOT, OT Reg (Ont.), discusses sensory processing strategies for home. She describes how atypical sensory processing affects lived experiences of individuals with autism and outlines three sensory profiles. Peña dives into the sensory diet approach noting short- and long-term goals

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Printable handouts are available online HERE (.pdf)

Moira Peña, BScOT, MOT, OT Reg (Ont.), discusses sensory processing strategies for home. She describes how atypical sensory processing affects lived experiences of individuals with autism and outlines three sensory profiles. Peña dives into the sensory diet approach noting short- and long-term goals and the importance of the “power senses.” She provides examples of strategic sensory schedules and environmental adaptations and emphasizes the importance of co-regulating and leisure activities. Peña celebrates individual differences in autism and suggests that productive failures are part of the process. She provides more resources and tools before opening the question-and-answer session.

Ms. Peña offers a presentation on this topic in English HERE

About the Speaker

Moira Peña, BScOT, MOT, OT Reg. (Ont.) is an experienced occupational therapist working with children and youth on the autism spectrum at Holland Bloorview Kids Rehabilitation Hospital in Toronto, Ontario, Canada. She is an Expert Hub Team member of the ECHO Ontario Autism Program which aims to further develop pediatricians’, school psychologists’ and teachers’ skills to best support autistic children and youth and their families. A published researcher, she has presented nationally and internationally to parents, teachers, occupational therapy practitioners and other health care professionals. Moira is also the proud creator and host of Holland Bloorview’s Autism Summit.

Take the knowledge quiz

Can’t see the quiz below? Take it online HERE

Effective Coping Strategies for Sensory Differences and Executive Function

January 30th, 2024|Adults on the Spectrum, Anxiety, Autism Spectrum Disorders, Self Care, Sensory, Social Skills, Ways to Help, Webinar|

Drs. Greg Wallace and Goldie McQuaid share their research on strategies autistic adults develop to compensate for non-social challenges they experience, including sensory sensitivities and executive function differences. Handouts are

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Meltdowns & Calming Techniques in Autism https://autism.org/meltdowns-calming-techniques-in-autism/ Tue, 28 Jun 2022 17:58:21 +0000 https://last-drum.flywheelsites.com/?p=15253 Meltdowns and tantrums present with similar characteristics and are challenging to navigate; however, the root causes of tantrums and meltdowns are very different, and it is crucial to manage them accordingly. Understanding these differences is especially important for individuals with autism spectrum disorder and their caregivers. This article defines meltdowns and tantrums,

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Meltdowns and tantrums present with similar characteristics and are challenging to navigate; however, the root causes of tantrums and meltdowns are very different, and it is crucial to manage them accordingly. Understanding these differences is especially important for individuals with autism spectrum disorder and their caregivers. This article defines meltdowns and tantrums, describes how they differ and provides calming techniques and resources for more information. 

Meltdowns vs. Tantrums 

A tantrum is an emotional outburst with a specific goal or function. It is a learned behavioral response used to attain the desired outcome (e.g. , get out of an activity, get a toy). Tantrums happen deliberately, and the individual maintains control of their body and mind the entire time. Outbursts generally stop after the desired outcome, so recovery is nearly instant. 

Contrastingly, meltdowns are involuntary responses to a nervous system overload. They are the physical manifestation of neurobiological chaos caused by a perceived threat to life. Meltdowns are not behavioral responses and generally aren’t used to attain a specific outcome. The reaction is involuntary and cannot be controlled as intense emotions take over, and tension build-up is released via stimming, repetitive movements, zoning out, screaming, crying, stomping, etc. Once individuals have reached that state, they cannot usually respond to standard behavioral calming cues or techniques. Recovery time for meltdowns can last up to 20 minutes or more after removing the stressor. 

Nervous system overload and sensory processing

Difficulties with sensory processing can trigger nervous system overload. Sensory inputs are the first way we interact with and understand the world around us. Our sensory systems (e.g.., touch, smell, sound, sight) automatically process and translate input into meaningful information; however, individuals with impaired nervous systems experience and use sensory inputs differently. 

Sensory inputs are perceived and interpreted in the lower part of the brain (brain stem), where our most basic human responses are regulated (i.e., instinct, survival, arousal). The brain perceives highly dysregulated sensory inputs as a literal threat to survival which initiates the fight, flight, freeze response. At that point, sensory information stops transmitting to the emotional processing (limbic system) or analytical (neocortex) parts of the brain, making it very difficult to think about the situation at hand.  

Meltdowns and Autism

Many core symptoms of autism are related to sensory processing, communication, and emotional regulation. Differences in brain function and neuron pathway connections may predispose individuals with autism to dysregulated sensory input. 

Watch one of our free webinars for more information on sensory processing and emotional regulation in autism: 

Sensory Processing and Autism (2019) with Virginia Spielman, MSOT

Emotional Regulation in Autism Spectrum Disorder with Dr. Carla Mazefsky

Sensory Processing and Autism (2015) with Lucy Jane Miller, Ph.D., OTR

Calming and Recovery Techniques

Meltdowns continue until the individual feels safe and calm. They can be challenging to navigate for everyone involved, and it is essential to know what to do when these situations occur. Meltdowns can create uncomfortable or dangerous situations if the stressor continues and proper recovery time isn’t possible. As a parent or caretaker, it is essential to remember that your loved one is experiencing difficulty with their emotions and that they may look to you for support or assistance. Try to take each incident as it comes, and remember to stay calm and provide meaningful support. 

Keeping yourself regulated and alert is essential for ensuring your safety and the safety of the individual experiencing dysregulation. You need to meet the individual at their energy level and react quickly to their needs, recognizing when to call for help. A positive response to meltdowns can be simplified into three steps: regulate, relate, and reason. 

Regulate

During meltdowns, the emotional part of the brain takes over, and it may be difficult for the individual to listen while they are experiencing it since explanations and logic may not be clearly understood and may add to sensory overload. In these cases, it is best for an individual to self-regulate. Body-based regulations like stimming, jumping, etc., are often purposeful and used as coping mechanisms for sensory imbalances. Use as few words as possible and provide reassurance through self-regulation and calming tools. 

It is crucial to stay present with your patient or loved one throughout the entire experience. Some practitioners advise parents to meet their child on their level – if they are jumping and screaming, you can start doing the same thing–sometimes meeting them where they are creates an easier connection. Other times it is best to allow them space for self-regulation. Containment strategies are suggested to defuse meltdowns – mainly when others in the area are in danger. There is no single way to regulate, but maintaining your self-regulation and creating an understanding and supportive presence is important. 

Relate

It is equally important to show love and engage your loved one in a supportive situation where they feel safe. Maintain respect and keep in mind that a person in meltdown may be experiencing some trauma from losing control of themselves. It can be an embarrassing and frustrating experience. Let them rest and give them time to calm down and relax. If speaking is possible, tell them it’s okay to feel this way and that it will go away soon. It is essential to be empathetic, validate the experience, and make sure they know they are not alone. If physical contact is okay, tactile, comforting techniques like hugs, weighted blankets, a favorite plush, or a cozy sweater can create a comfortable and safe environment. 

Reason

When they have calmed enough to talk (if verbal), try discussing what happened and remind them they are safe. Working through the logic of what happened can help with emotional regulation and personal understanding. Note that this is not a time for lecturing. Remember that a person recovering from a meltdown has just experienced a perceived threat to life and help them to understand what may have triggered that response. 

For more tips and resources on sensory supports and meltdown recovery, watch one of these free webinars:

Supporting Sensory Needs with Lindsey Biel, MA, OTR/L

Major Meltdowns: Factors Leading to Emotional Dysregulation in ASD from the Johnson Center

Tantrums and Meltdowns, Oh My! from the Johnson Center

Prevention Strategies and Treatments

Contemporary meltdown treatment and prevention strategies include various therapy and medical techniques. Many approaches incorporate behavioral and physical therapies to help with bodily autonomy and emotional control. Before any treatment or prevention plans are created, your patient/loved one will likely need to complete a Functional Behavior Assessment (FBA) or a similar screening process to identify the functionality of meltdown symptoms. 

Creating a behavior log to find patterns in context and surroundings leading up to meltdowns can help the evaluation. Behavior logs also assist parents and caretakers in understanding signs leading up to meltdowns. Learning these timelines allows greater insight into what sensory issues or comorbid conditions may cause meltdowns. Once the context is better understood, you can begin to practice calming techniques before meltdowns occur and teach your loved one or patient to identify their feelings before they happen. 

Treating underlying comorbid conditions associated with autism is also essential. Sensory or emotional issues are often the result of uncommunicated pain or discomfort related to such conditions (e.g., GI disruption, anxiety, sleep disorders, etc.). If you have tried cognitive behavioral therapy and meltdown severity or prevalence hasn’t decreased, consider speaking with a gastroenterologist, psychologist, or other medical specialists to address underlying issues. 

Watch one of our free webinars to learn more about prevention and treatment techniques:

ABC’s of Behavioral Support in 2021 with Melissa Olive, Ph.D., BCBA-D

Assessing and Treating Challenging Behaviors with Lauren Moskowitz, Ph.D.

Hippotherapy for Autism Spectrum Disorders with Chelsea Whitaker, OTR/L, founder and COO of Taking the Lead

Article: Treating Challenging Behaviors

Article: Supporting Jeremy Home and Community

 

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Handouts are online at: https://ariconference.com/webinars/optimistic.pdf Certificates of Participation are available upon successful completion of a knowledge quiz following the webinar at: https://www.classmarker.com/online-test/start/?quiz=9fd5511d23657ccc Challenging behaviors continue to top the list of concerns for

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Causes and Interventions for Self-Injury in Autism https://autism.org/causes-and-interventions-for-self-injury-in-autism/ Wed, 02 Sep 2020 17:20:12 +0000 https://last-drum.flywheelsites.com/?p=11457 Strictly speaking, self-injury is not a symptom of autism. However, certain symptoms, situations, and comorbidities related to ASD can lead some people with autism to engage in self-injurious behavior. Treating underlying disorders and helping the individual to learn additional communication and coping skills can enable them to avoid self-injury and minimize the

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Strictly speaking, self-injury is not a symptom of autism. However, certain symptoms, situations, and comorbidities related to ASD can lead some people with autism to engage in self-injurious behavior. Treating underlying disorders and helping the individual to learn additional communication and coping skills can enable them to avoid self-injury and minimize the long-term effects of this behavior. 

With contributions from the leading experts in research and treatment, Understanding and Treating Self-Injurious Behavior (2016) provides a comprehensive analysis of this poorly understood behavior in people with Autism Spectrum Disorder (ASD) or related developmental disabilities, and the different methods available to treat them. The book is edited by ARI’s executive director, Stephen M. Edelson, and past ARI Board member, Jane B. Johnson, and consists of chapters written by leading experts in the autism field. Learn More

What is self-injurious behavior

It is important to remember that individuals may engage in self-injury for many reasons. This article deals specifically with self-injury co-occurring with autism. However, people with other conditions may also engage in self-injury. 

Any behavior that causes physical harm to the individual is classified as self-injurious. This could include: 

  • Slapping
  • Scratching
  • Headbanging
  • Biting
  • Pinching

To address these behaviors, caregivers must first understand the underlying issues that may be causing them. 

Why do some people with autism engage in self-injury? 

People often view self-injury in terms of its effects. A child may suffer a lasting injury, and a parent may feel demoralized or overwhelmed, and strangers may not understand. While these effects can grab attention, focusing on them is unlikely to address the underlying issue. Parents and clinicians aiming to help a person diagnosed with autism who is engaged in self-injury should start by investigating triggers that lead to the behavior.  Often self-injury can begin accidentally and, when it’s inadvertently reinforced, it can become a learned behavior.

In many cases, self-injury serves as a means of communication. Often a child is trying to convey a feeling or idea they may not be able to express in words. Biting, headbanging or other self-injurious behaviors are a means of getting their needs met and may be their urgent need to express pain, fear, displeasure, or anxiety.  They may be trying to say, for example, “I’m scared, I want to get out of here” or “this is too hard, I don’t want to do this” or “Play with me!” or “Look at me!” or “My head hurts, it feels better when I bang it,” etc.

Self-injury can also be a form of sensory stimulation. An individual with autism may self-injure as a way to increase or decrease their level of arousal. 

Often, self-injury is a learned behavior. Parents certainly don’t intend to teach children to engage in self-injury, but they may unintentionally reinforce the behaviors. If the child engages in self-injury and the parent or teacher hands them a preferred toy, the child quickly learns that self-injury leads to their favorite toy. On the other hand, if the child engages in self-injury, and the parent immediately removes them from an overstimulating environment, they learn that self-injury can help them avoid uncomfortable situations. 

Lauren Moskowitz, Ph.D., explores the motivations and reasons for such behaviors in her webinar Assessing and Treating Challenging Behavior in Individuals with ASD

It is important to remember that the child is not acting with malice, and neither is the parent or caregiver. In both cases, the child is attempting to communicate very real wants and needs. When the behavior achieves the result they wanted, they learn to associate self-injury with a positive result. Their goal is not to anger or manipulate. Instead, they are attempting to communicate. If self-injury achieves their goals, they are likely to continue the behavior. 

Other factors that may be associated with self-injury include biochemistry in the brain, seizure activity, genetic factors, a pain response, or frustration. Dr. Stephen M. Edelson explores the research behind these factors in his article on Understanding and Treating Self-Injurious Behavior

Identifying the causes of self-injury

Before you and your care team can identify interventions that are likely to address self-injury, you will need to understand the reasons and motivations for the behavior. What does the child need or want? What communication barriers do they face that led them to initiate the behavior? When you identify situations or stimuli that are likely to trigger episodes of self-injury, you can begin to understand what the individual is attempting to communicate. 

Parents and caregivers can keep a journal to track instances of self-injury, including where it occurred, what was happening, who was present, what occurred immediately before, what occurred immediately after – e.g., how did other people react/respond, did the child get to avoid or escape or leave or delay a difficult situation – etc. Written records are more reliable than emotionally charged recollections, and can help you notice details you might otherwise have passed over. 

Your clinician may use a functional behavioral assessment (FBA) to help identify the function of self-injurious behavior for the individual. This process includes: 

  1. Defining the behavior: using specific, observable language to describe what the self-injury looks like
  2. Gathering and analyzing information: exploring when, where, and how the behavior is occurring, the consequences of the behavior, and the people and situations that seem to be related. 
  3. Identifying reasons or causes: making an informed hypothesis about what might be causing the behavior or what the child is trying to communicate.
  4. Making a plan to address the situation: specifying actions and interventions to help improve communication or reduce trigger events. 

Teachers and school officials also use this method to identify ways to better support students. The result is a behavior intervention plan (BIP) that guides them to teach and reward positive behaviors. 

Interventions to address self-injury

The most important thing you can do is teach the child to communicate

Once you understand what is causing the behavior, you can work with your clinician and make a plan to address it.  

If the self-injury is related to anxiety or discomfort in certain situations, social stories and priming may help ease transitions. Social stories help children practice before a situation occurs in real life, and priming provides the child with information about what will happen next to reduce their anxiety. Providing choices can also give the child a venue to communicate needs and preferences. Anything that makes situations more predictable, such as priming and social stories, can be helpful in reducing self-injury for those people with ASD for whom unpredictability serves as a trigger for the self-injury.

Teaching an alternative behavior to replace the self-injury to help the child get their wants and needs met in another way is crucial. For example: if a child bites his hand and, subsequently, his parents leave him alone whenever he bites his hand (i.e., the self-injury serves an escape function), then the most important intervention is to teach the child the words to use instead. Teaching him to say “leave me alone,” or something equivalent to that – either verbally or through sign language or with PECS or an ACC device, etc. – empowers him to have his needs met in a safer way.

The second most important thing is to remove or alter the triggers. Social stories and priming can help make things more predictable if the trigger is unpredictability, but if the trigger is – for example – a math assignment that is too hard for the child, then you need to make the math assignment easier or provide more help.

The third most important thing you can do is reinforce the child for displaying communication instead of self-injury… and/or reinforce the child for periods of time in which he/she displays reduced occurrences and, eventually, no self-injury.

Treating physical ailments

In some cases, children will engage in self-injury to communicate that they are feeling physical pain or discomfort. For example, you might assume that a person may bang their head because they have a headache. However, sometimes the action and the pain are not so closely related. Headbanging can be a sign of gastrointestinal issues or other discomforts as well. A careful medical examination with a physician who is knowledgeable about autism and its co-occurring conditions is crucial to identifying physical ailments that may be an underlying cause of the behavior. 

Exploring psychological causes

Anxiety and depression are both common comorbidities of autism. Look for other signs like changes in sleep, mood, or energy that may indicate a psychological comorbidity. Treating these disorders may help to minimize or prevent self-injury.

Behavior therapy

If the self-injury has become a habit, then behavioral therapy may help children replace old self-injurious patterns with new skills and strategies. By rewarding positive behaviors and teaching new communication and coping skills, behavior therapy may help some children cease self-injurious behavior. 

For a deeper look at self-injurious behavior, its causes, and its interventions, explore this article from Stephen M. Edelson, Ph. D.

ARI thanks Lauren Moskowitz, PhD, for her contributions to this article. 

Introducing: ARI’s Understanding and Treating Self-Injurious Behavior Tool

This free resource provides deeper insight into understanding and treating self-injurious behavior in autism. It is designed to assist professionals and parents in identifying treatments that may reduce or eliminate self-injurious behaviors (SIB) in clients or children. Filling out the questionnaire may provide insight into one or more possible reasons why an individual engages in SIB. Links to published studies on causes as well as appropriate interventions, are also provided.

Visit the tool

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