Validation of the Food Safe Zone questionnaire for families of individuals with Prader-Willi syndrome.

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY
Elisabeth M Dykens, Elizabeth Roof, Hailee Hunt-Hawkins, Theresa V Strong
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引用次数: 0

Abstract

Background: Prader-Willi syndrome (PWS), a genetic neurodevelopmental disorder, is characterized by hyperphagia and significant behavioral problems. Hyperphagic individuals with PWS are chronically hungry yet rarely feel sated, and often engage in food-seeking behaviors. To avoid life-threatening obesity in their children, families implement food security strategies (e.g., locking food sources, constant supervision around food, alerting others). Although widely used, these strategies have yet to be systematically examined. We thus developed and analyzed the psychometric properties of a new measure of these diverse strategies, the Food Safe Zone, and evaluated them in relation to hyperphagic symptoms and demographic variables. In doing so, we also shine a light on the extraordinary efforts of families in managing their children's hyperphagia.

Methods: Our team developed 20 FSZ items that were revised for clarity and completeness in an iterative feedback process with stakeholders, including parents, PWS specialists, and individuals with PWS. The FSZ was pilot tested, descriptive findings were reviewed by additional stakeholders, and then administered to 624 parents in a large-scale study. Based on an open-ended question, "Is there anything else you do to ensure food safety?" two additional items were added and evaluated in a follow-up study.

Results: Principal component analyses revealed that 21 FSZ items loaded onto 5 factors that were readily interpretable, accounting for 67% of test variance: Alerting Others and Food Supervision in the Community; Locking or Restricting Food Sources; Checking for Food; At Home Supervision and Meals; and Avoiding Food Settings. Internal consistency and test-rest reliability were robust. Convergent validity analyses revealed that parents implemented FSZ strategies in response to the severity of their child's hyperphagia, and not their child's age, gender or PWS genetic subtype.

Conclusions: The psychometrically sound FSZ holds promise for future research, especially on the effects of food safety tactics on family members. In future clinical trials, the FSZ could also be used to help parents think critically about their food safety tactics in relation to their child's hyperphagia, or as an exploratory endpoint; if hyperphagia is lessened, so too may food safety tactics, thereby enhancing familial quality of life.

Prader-Willi综合征患者家庭食品安全问卷的验证。
背景:Prader-Willi综合征(PWS)是一种遗传性神经发育障碍,以嗜食和显著的行为问题为特征。患有PWS的贪食症患者长期处于饥饿状态,但很少感到满足,并且经常从事寻找食物的行为。为避免儿童罹患危及生命的肥胖,各家庭实施粮食安全战略(例如,锁定食物来源、不断监督食物、提醒他人)。这些策略虽然被广泛使用,但尚未得到系统的审查。因此,我们开发并分析了这些不同策略的一种新措施的心理测量特性,即食品安全区,并评估了它们与贪食症状和人口变量的关系。在这样做的过程中,我们也揭示了家庭在管理孩子的贪食症方面所做的非凡努力。方法:我们的团队开发了20个FSZ项目,并在与利益相关者(包括家长、PWS专家和PWS患者)的迭代反馈过程中进行了修订,以确保其清晰和完整。FSZ进行了试点测试,描述性结果由其他利益相关者审查,然后在一项大规模研究中对624名家长进行了管理。在一个开放式问题“你们还做了什么来确保食品安全?”的基础上,又增加了两个项目,并在后续研究中进行了评估。结果:主成分分析显示,21个FSZ项目加载到5个易于解释的因子上,占检验方差的67%:警示他人和社区食品监管;锁定或限制食物来源;检查食物;在家监护和膳食;避免食物设置。内部一致性和test-rest信度是稳健的。收敛效度分析显示,父母采用FSZ策略是针对孩子贪食症的严重程度,而不是孩子的年龄、性别或PWS基因亚型。结论:从心理测量学角度来看,FSZ具有良好的研究前景,特别是在食品安全策略对家庭成员的影响方面。在未来的临床试验中,FSZ也可以用来帮助父母批判性地思考与孩子贪食有关的食品安全策略,或者作为一个探索性终点;如果暴食症减少,食品安全策略也会减少,从而提高家庭生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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