scholarly journals Treating specific phobias in young people with autism and severe learning difficulties

2017 ◽  
Vol 10 ◽  
Author(s):  
Phillippa Burton ◽  
Anna Palicka ◽  
Tim I. Williams

AbstractAnimal phobias in young people with autism spectrum disorders (ASD) and intellectual disability (ID) can provoke behaviours that put them at risk and impede access to the community. Previous studies suggest that cognitive behavioural therapy including systematic desensitization and modelling are effective for people with ID, including those with comorbid ASD. Methods of adapting such treatment to people with little spoken language are not well described, and ethical issues concerning both young people and animals during treatment have not been addressed. The aim of this study was to describe, using a case series of consecutive referrals: (1) adaptations to systematic desensitization when communication of the young person is impaired, and (2) the ethics of involving animals in therapeutic interventions. Treatment was planned based on the use of systematic desensitization with a hierarchy of feared situations using visual symbols and schedules to communicate with the participants. Five young people with ASD, severe ID and minimal language were successfully treated for dog phobia. Modifications to treatment included both the use of non-verbal means of communication including printed symbols and graded activities such as jigsaw puzzles and picture matching to present information to clients in a more finely graded format. The treatment of specific phobias is possible with the use of minimal language provided that a variety of individualized stimuli approximating to the feared objects are developed and the safety of all participants is respected. Further work is required to develop sufficiently flexible treatment protocols, which in turn would enable a randomized controlled trial.

2019 ◽  
Vol 13 (2) ◽  
pp. 307-319
Author(s):  
Íbis Ariana Peña Moraes ◽  
Carlos Bandeira de Mello Monteiro ◽  
Talita Dias da Silva ◽  
Thais Massetti ◽  
Tânia Brusque Crocetta ◽  
...  

F1000Research ◽  
2018 ◽  
Vol 7 ◽  
pp. 1864
Author(s):  
Jeanne Wolstencroft ◽  
William Mandy ◽  
David Skuse

Turner Syndrome (TS) is a sex chromosome aneuploidy (45,X) associated with social skill difficulties. Recent clinical care guidelines recommend that the Program for the Education and Enrichment of Relational Skills (PEERS) social skills intervention programme be trialled in this population. PEERS has been successfully used in adolescents with autism spectrum conditions without intellectual disabilities. The PEERS program will be piloted with adolescents and young women with TS aged 16-20 using an uncontrolled study trial with a multiple-case series design. The program will be delivered face to face and online. The assessment battery is designed to measure social skills comprehensively from diverse informants (parent, teacher young person). It includes measures of social performance, social knowledge and social cognition. Parents and young people taking part in the intervention will also feedback on the acceptability and feasibility of the pilot. The outcomes of this small scale pilot (n=6-10) will be used to adapt the programme based on feedback and estimate the sample for a future randomised controlled trial.


2020 ◽  
Vol 19 (6) ◽  
pp. 438-455
Author(s):  
Rosanna Chapman ◽  
Bethan Evans

Anxiety is a common experience for young people with an autism spectrum condition (ASC). This article describes the use of Acceptance and Commitment Therapy (ACT) through the medium of art to increase well-being for a young woman with ASC and significant anxiety. An ACT art protocol was delivered over 8-weekly sessions with outcome measured administered at baseline, pre-, mid- and post-intervention. Follow-up data were also obtained 3 months after the intervention. It was found that the young person experienced improvements in measures of well-being and psychological flexibility. Importantly, these were seen to translate to increased engagement in activities that were in line with the young person’s values. This demonstrates that using third-wave approaches for young people with ASC can result in improvements in well-being and quality of life, but that adaptations in line with person-centered care are crucial to facilitate engagement and produce meaningful change.


2020 ◽  
Author(s):  
Daniel Vella Fondacaro ◽  
Nigel Camilleri

Abstract Background: Young people (YP) with autism spectrum disorder (ASD) may prefer individual to group physical activity (PA). Levels of PA may differ with disorder severity and age. This study explores parents’ experiences with YP suffering from ASD when choosing between group and individual PA.Method: Retrospective case note reviews identified 701 new referrals received by the National Child and Young People’s Services, Malta, between 2016 to 2017. Of them, 24 received a diagnosis of ASD without co-morbidities and 10 were chosen via purposive random sampling. An 11-component semi-structured interview guide was created specifically for use in this study. Parents were interviewed and a thematic analysis was carried out.Results: Only one young person carried out PA which met the World Health Organisation recommendations. More parents (group only: n=3; 30%, both: n=6 ; 60%) preferred group PA for their children, while more YP (individual only: n=4; 40%, both: n=4 ; 40%) preferred individual PA. Parents described both group and individual PA having benefits. Most parents felt ‘misrepresented' and wanted to have more ASD-friendly sports facilities developed in for YP in Malta. Long hours of screen time was also a major parental concern. Younger age and more severe ASD were associated with higher levels of PA. Lower levels of PA, older age and milder ASD were associated with higher use of technology.Conclusion: This study reported on the parents’ perceptions on PA and discusses a possible link between ASD severity, PA, age and technological devices. The recommendations from this study are aimed at informing the development of sport services to be outsized as a form of therapy in Malta.


2021 ◽  
Vol 11 ◽  
Author(s):  
Jan Scott ◽  
Thomas D. Meyer

Attempts to increase early identification of individuals in the early stages of bipolar disorders (i.e., individuals at high risk of bipolar disorders and/or experiencing a subthreshold syndrome with bipolar symptoms) have highlighted the need to develop high benefit-low risk interventions. We suggest that any new psychological therapy should (i) be acceptable to young people seeking help for the first time, (ii) be applicable to “at risk” conditions and sub-syndromal states and (iii) consider pluripotent factors that may be linked to illness progression not only for bipolar disorders specifically but also for other potential disease trajectories. However, evidence indicates that current interventions for youth with emerging mood disorders mainly represent approaches abbreviated from “disorder-specific” therapies used with older adults and are primarily offered to first episode cases of bipolar disorders who are also receiving psychotropic medication. This brief report discusses empirical findings used to construct core targets for therapeutic interventions that might reduce or delay transition to full-threshold bipolar disorders. We describe an intervention that includes strategies for problem-solving, reducing sleep-wake cycle disturbances, self-management of rumination and that addresses the needs of individuals with “sub-threshold” presentations who are probably at risk of developing a bipolar or other major mental disorders. Outcome data from a case series of 14 youth indicates that the intervention appears to demonstrate a relatively high benefit-to-risk ratio, promising levels of engagement with the therapy modules, and the therapy appears to be acceptable to a wide range of help-seeking youth with early expressions of bipolar psychopathology.


2018 ◽  
Vol 22 (12) ◽  
pp. 1-222 ◽  
Author(s):  
David J Cottrell ◽  
Alex Wright-Hughes ◽  
Michelle Collinson ◽  
Paula Boston ◽  
Ivan Eisler ◽  
...  

BackgroundSelf-harm in adolescents is common and repetition rates high. There is limited evidence of the effectiveness of interventions to reduce self-harm.ObjectivesTo assess the clinical effectiveness and cost-effectiveness of family therapy (FT) compared with treatment as usual (TAU).DesignA pragmatic, multicentre, individually randomised controlled trial of FT compared with TAU. Participants and therapists were aware of treatment allocation; researchers were blind to allocation.SettingChild and Adolescent Mental Health Services (CAMHS) across three English regions.ParticipantsYoung people aged 11–17 years who had self-harmed at least twice presenting to CAMHS following self-harm.InterventionsEight hundred and thirty-two participants were randomised to manualised FT delivered by trained and supervised family therapists (n = 415) or to usual care offered by local CAMHS following self-harm (n = 417).Main outcome measuresRates of repetition of self-harm leading to hospital attendance 18 months after randomisation.ResultsOut of 832 young people, 212 (26.6%) experienced a primary outcome event: 118 out of 415 (28.4%) randomised to FT and 103 out of 417 (24.7%) randomised to TAU. There was no evidence of a statistically significant difference in repetition rates between groups (the hazard ratio for FT compared with TAU was 1.14, 95% confidence interval 0.87 to 1.49;p = 0.3349). FT was not found to be cost-effective when compared with TAU in the base case and most sensitivity analyses. FT was dominated (less effective and more expensive) in the complete case. However, when young people’s and caregivers’ quality-adjusted life-year gains were combined, FT incurred higher costs and resulted in better health outcomes than TAU within the National Institute for Health and Care Excellence cost-effectiveness range. Significant interactions with treatment, indicating moderation, were detected for the unemotional subscale on the young person-reported Inventory of Callous–Unemotional Traits (p = 0.0104) and the affective involvement subscale on the caregiver-reported McMaster Family Assessment Device (p = 0.0338). Caregivers and young people in the FT arm reported a range of significantly better outcomes on the Strengths and Difficulties Questionnaire. Self-reported suicidal ideation was significantly lower in the FT arm at 12 months but the same in both groups at 18 months. No significant unexpected adverse events or side effects were reported, with similar rates of expected adverse events across trial arms.ConclusionsFor adolescents referred to CAMHS after self-harm, who have self-harmed at least once before, FT confers no benefits over TAU in reducing self-harm repetition rates. There is some evidence to support the effectiveness of FT in reducing self-harm when caregivers reported poor family functioning. When the young person themselves reported difficulty expressing emotion, FT did not seem as effective as TAU. There was no evidence that FT is cost-effective when only the health benefits to participants were considered but there was a suggestion that FT may be cost-effective if health benefits to caregivers are taken into account. FT had a significant, positive impact on general emotional and behavioural problems at 12 and 18 months.LimitationsThere was significant loss to follow-up for secondary outcomes and health economic analyses; the primary outcome misses those who do not attend hospital following self-harm; and the numbers receiving formal FT in the TAU arm were higher than expected.Future workEvaluation of interventions targeted at subgroups of those who self-harm, longer-term follow-up and methods for evaluating health benefits for family groups rather than for individuals.Trial registrationCurrent Controlled Trials ISRCTN59793150.FundingThis project was funded by the NIHR Health Technology Assessment programme and will be published in full inHealth Technology Assessment; Vol. 22, No. 12. See the NIHR Journals Library website for further project information.


F1000Research ◽  
2019 ◽  
Vol 7 ◽  
pp. 1864
Author(s):  
Jeanne Wolstencroft ◽  
William Mandy ◽  
David Skuse

Turner Syndrome (TS) is a sex chromosome aneuploidy (45,X) associated with social skill difficulties. Recent clinical care guidelines recommend that the Program for the Education and Enrichment of Relational Skills (PEERS) social skills intervention programme be trialled in this population. PEERS has been successfully used in adolescents with autism spectrum conditions without intellectual disabilities. The PEERS program will be piloted with adolescents and young women with TS aged 16-20 using an uncontrolled study trial with a multiple-case series design. The program will be delivered face to face and online. The assessment battery is designed to measure social skills comprehensively from diverse informants (parent, teacher young person). It includes measures of social performance, social knowledge and social cognition. Parents and young people taking part in the intervention will also feedback on the acceptability and feasibility of the pilot. The outcomes of this small scale pilot (n=6-10) will be used to adapt the programme based on feedback and estimate the sample for a future randomised controlled trial.


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