Description and predictors of self-determination in males and females with fragile X syndrome on the verge of adulthood

IF 2.1 2区 医学 Q1 EDUCATION, SPECIAL Journal of Intellectual Disability Research Pub Date : 2024-08-12 DOI:10.1111/jir.13182
L. Friedman, C. Moser, A. J. Thurman, J. L. Taylor, L. Abbeduto, J. Klusek
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Abstract

Background

Self-determination refers to setting goals and making decisions regarding one's own life with support from others as needed. Research on people with intellectual and developmental disabilities has established the importance of self-determination for quality of life outcomes, such as increased independence and life satisfaction. However, self-determination has not been characterised specifically in fragile X syndrome (FXS), the leading inherited cause of intellectual disability. Relative to youth with other forms of intellectual and developmental disabilities, youth with FXS may face exceptional barriers to the development of self-determined behaviour. In addition to intellectual disability, the FXS behavioural profile is characterised by high rates of autism and anxiety that may further limit opportunities for youth with FXS. The heritable nature of the condition can also yield a distinctive family environment, with siblings and parents also living with fragile X or its associated conditions. Considering these unique challenges, the present study examined self-determination in young adult males and females with FXS and explored whether factors such as language skills, adaptive behaviour and autism traits were associated with self-determination capacity and opportunities.

Methods

The present study included 9 females and 36 males with FXS between the ages of 17 and 25 years. Caregivers (mothers or fathers) completed the American Institute for Research Self-Determination Assessment, which is a questionnaire that yields three scores: self-determination capacity, opportunities for self-determination at home and opportunities for self-determination at school.

Results

Caregivers endorsed a wide range of self-determination capacity and opportunities, with ratings for opportunities at home and school exceeding ratings of capacity. Better adaptive behaviour skills were associated with more self-determination capacity, and the presence of more autism traits was associated with fewer opportunities at school.

Conclusions

Results from this study contribute to our understanding of avenues to best support young adults with FXS as they transition to adulthood. Our findings also have implications for practice, such that interventions targeting adaptive behaviours and self-determination may be an effective approach for promoting autonomy and independence for young adults with FXS. Additionally, caregivers and educators should continue to provide opportunities to practise self-determination, regardless of their perception of capacity.

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罹患脆性 X 综合征的男性和女性濒临成年时自我决定能力的描述和预测因素。
背景:自决是指在他人的必要支持下,为自己的生活设定目标并做出决定。对智力和发育障碍人士的研究已经证实,自我决定对提高生活质量具有重要意义,例如提高独立性和生活满意度。然而,对于脆性 X 综合症(FXS)这种导致智力残疾的主要遗传病因,人们还没有专门研究过他们的自决能力。与患有其他形式智力和发育障碍的青少年相比,患有脆性 X 射线综合症的青少年在发展自我决定行为方面可能面临特殊障碍。除智力障碍外,FXS 行为特征的另一个特点是自闭症和焦虑症的高发率,这可能会进一步限制 FXS 患者的机会。这种疾病的遗传性还可能导致独特的家庭环境,因为兄弟姐妹和父母也患有脆性 X 或相关疾病。考虑到这些独特的挑战,本研究考察了患有 FXS 的年轻成年男性和女性的自我决定能力,并探讨了语言技能、适应行为和自闭症特征等因素是否与自我决定能力和机会相关:本研究包括 9 名女性和 36 名男性 FXS 患者,年龄在 17 岁至 25 岁之间。照顾者(母亲或父亲)填写了美国研究所自决评估问卷,该问卷可得出三项评分:自决能力、在家中的自决机会和在学校的自决机会:照顾者对自决能力和自决机会的认可范围很广,对家庭和学校自决机会的评分超过了对自决能力的评分。较好的适应行为技能与较高的自决能力相关,而较多的自闭症特征与较少的在校机会相关:这项研究的结果有助于我们了解如何在 FXS 青少年向成年过渡的过程中为他们提供最佳支持。我们的研究结果还对实践产生了影响,例如,针对适应行为和自我决定的干预措施可能是促进 FXS 青少年自主和独立的有效方法。此外,照顾者和教育者应继续为他们提供实践自我决定的机会,无论他们对自己能力的认知如何。
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来源期刊
CiteScore
5.60
自引率
5.60%
发文量
81
期刊介绍: The Journal of Intellectual Disability Research is devoted exclusively to the scientific study of intellectual disability and publishes papers reporting original observations in this field. The subject matter is broad and includes, but is not restricted to, findings from biological, educational, genetic, medical, psychiatric, psychological and sociological studies, and ethical, philosophical, and legal contributions that increase knowledge on the treatment and prevention of intellectual disability and of associated impairments and disabilities, and/or inform public policy and practice. Expert reviews on themes in which recent research has produced notable advances will be included. Such reviews will normally be by invitation.
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