Development and psychometric properties of the Clinical Anxiety Scale for People with Intellectual Disabilities (ClASP-ID)

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY Journal of Neurodevelopmental Disorders Pub Date : 2024-07-27 DOI:10.1186/s11689-024-09554-9
Jessica Eliza Mingins, Joanne Tarver, Effie Pearson, Georgina Edwards, Megan Bird, Hayley Crawford, Chris Oliver, Lauren Shelley, Jane Waite
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Abstract

There is a critical need for the development of dependable and valid anxiety assessment tools suitable for people with moderate to severe intellectual disabilities, particularly those who speak few or no words. Distinguishing anxiety from distress caused by physical discomfort (pain) or characteristics associated with autism, prevalent in this population, necessitates specialised assessment tools. This study (a) developed a parent-report anxiety questionnaire tailored for individuals with severe to moderate intellectual disabilities, potentially with a co-diagnosis of autism, and (b) evaluated the psychometric attributes of this novel measure. A comprehensive approach involving literature reviews, inspection of existing tools, and interviews with clinicians and parents guided the creation of the Clinical Anxiety Scale for People with Intellectual Disabilities. The tool was completed by parents or caregivers (N = 311) reporting on individuals aged 4 or older with intellectual disabilities. Exploratory factor analysis indicated a four-factor structure encompassing anxiety, pain, low energy/withdrawal, and consolability. The anxiety factor explained the most variance in scores (26.3%). The anxiety, pain, low energy/withdrawal subscales demonstrated robust internal consistency (α = 0.81-0.92), and convergent, divergent, and discriminant validity. Robustness of these subscales was further evidenced by test-retest reliability (ICC = 0.79-0.88) and inter-rater reliability (ICC = 0.64-0.71). Subgroup analyses consistently demonstrated strong psychometric properties among individuals diagnosed with non-syndromic autism (N = 98), children (N = 135), adults (N = 175), and across diverse communication abilities within the sample. Moreover, individuals diagnosed with both autism and anxiety exhibited significantly higher scores on the anxiety subscale compared to those without an anxiety diagnosis, while showing no difference in autism characteristic scores. The findings indicate that the Clinical Anxiety Scale for People with Intellectual Disabilities is a promising measure for use across diverse diagnostic groups, varying communication abilities, and with people with moderate to severe intellectual disabilities.
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智障人士临床焦虑量表(ClASP-ID)的开发与心理测量特性
目前亟需开发可靠有效的焦虑评估工具,以适用于中重度智障人士,尤其是那些很少说话或不会说话的智障人士。要将焦虑与因身体不适(疼痛)或自闭症相关特征(在这类人群中普遍存在)引起的困扰区分开来,就必须使用专门的评估工具。本研究(a)为重度至中度智障人士(可能合并自闭症诊断)量身定制了家长报告焦虑问卷,(b)评估了这一新型测量工具的心理测量属性。通过文献综述、对现有工具的检查以及对临床医生和家长的访谈等综合方法,我们设计出了 "智障人士临床焦虑量表"。该工具由报告 4 岁或 4 岁以上智障人士情况的家长或照顾者(N = 311)完成。探索性因子分析显示,该量表具有四因子结构,包括焦虑、疼痛、低能量/退缩和可安慰性。焦虑因子解释了最大的分数差异(26.3%)。焦虑、疼痛、低能量/退缩子量表显示出很强的内部一致性(α = 0.81-0.92),以及收敛效度、发散效度和区分效度。测试再测信度(ICC = 0.79-0.88)和评分者间信度(ICC = 0.64-0.71)进一步证明了这些子量表的稳健性。在被诊断为非综合症自闭症患者(98 人)、儿童(135 人)、成人(175 人)以及样本中不同沟通能力的人群中,分组分析一致显示出较强的心理测量特性。此外,与未被诊断出焦虑症的患者相比,同时被诊断出患有自闭症和焦虑症的患者在焦虑分量表上的得分明显更高,而在自闭症特征得分上则没有差异。研究结果表明,智障人士临床焦虑量表是一种很有前途的量表,可用于不同诊断群体、不同沟通能力以及中重度智障人士。
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来源期刊
CiteScore
7.60
自引率
4.10%
发文量
58
审稿时长
>12 weeks
期刊介绍: Journal of Neurodevelopmental Disorders is an open access journal that integrates current, cutting-edge research across a number of disciplines, including neurobiology, genetics, cognitive neuroscience, psychiatry and psychology. The journal’s primary focus is on the pathogenesis of neurodevelopmental disorders including autism, fragile X syndrome, tuberous sclerosis, Turner Syndrome, 22q Deletion Syndrome, Prader-Willi and Angelman Syndrome, Williams syndrome, lysosomal storage diseases, dyslexia, specific language impairment and fetal alcohol syndrome. With the discovery of specific genes underlying neurodevelopmental syndromes, the emergence of powerful tools for studying neural circuitry, and the development of new approaches for exploring molecular mechanisms, interdisciplinary research on the pathogenesis of neurodevelopmental disorders is now increasingly common. Journal of Neurodevelopmental Disorders provides a unique venue for researchers interested in comparing and contrasting mechanisms and characteristics related to the pathogenesis of the full range of neurodevelopmental disorders, sharpening our understanding of the etiology and relevant phenotypes of each condition.
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