对“为青少年和青年设计积极的健康对话工具:一项混合方法研究”评论的回应。

IF 3.2 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES Health Expectations Pub Date : 2025-01-31 DOI:10.1111/hex.70159
Marja van Vliet, Machteld Huber, Sigrid van der Zanden
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引用次数: 0

摘要

我们很高兴有机会解决我们最近发表的“为青少年和年轻人设计一个积极的健康对话工具:一项混合方法研究”所引起的关注(健康预期,2024年10月;27(5):e70042)。我们重视建设性的反馈,并提供以下澄清。我们研究的定量方面涉及一个相对较小的样本(N = 118),如局限性部分所述。因此,这些发现应谨慎解释,不能推广到所有人群。我们的主要目标是将这一阶段作为探索性步骤,指导定性阶段(焦点小组和访谈),这是研究的基础。在定性研究中,N = 36的样本不算小;相反,数据深度和饱和度的实现是有效性的关键指标。此外,我们强调,这个针对青少年和年轻人的工具建立在成人和儿童版本开发过程中进行的严格研究的基础上。与从零开始相比,这些早期阶段需要不同的方法考虑。我们承认在我们的样本中存在性别失衡(79%为女性)。然而,我们的招聘策略优先考虑了诸如“患有疾病”和“教育水平”等因素,因为它们对健康观念有既定的影响,如文献报道(例如,[1,2])。这方面的性别差异往往不那么明显,正如以前的研究所指出的那样。我们同意有必要评估对话工具的长期影响,正如讨论部分所强调的那样。我们发表这篇文章的目的之一是鼓励未来的研究评估该工具的持续影响,就像对成人和儿童版本所做的那样(例如,[1,3,4])。鉴于这些早期版本的有希望的结果,我们预计这个版本也会有类似的积极结果。对话工具是专门为捕捉个人的主观经验而设计的,使自我报告数据成为这种情况下最合适的方法。对于需要更大客观性的评估,我们为成人版本开发了一个单独的测量工具[5,6]。为青少年和年轻人开发一个类似的工具将是合乎逻辑的下一步,并在我们的讨论部分推荐。这样才能达到科学评价的目的。尽管如此,这个对话工具的主要目标是促进对个人健康的主观理解,为就个人需求、优先事项和目标进行有意义的讨论提供基础。我们在方法考虑部分讨论了对普遍性的关注,具体讨论了其在不同文化和社会经济背景下的适用性。在我们之前的快速回顾bb0中也探讨了这个问题。有了这个特定的版本,我们的目标是促进对目标群体特异性的理解。进一步的研究计划在不同的群体中测试对话工具,以增强对工具本身的通用性的理解。我们相信这些澄清解决了所提出的担忧,并强调了我们对推进该领域研究的承诺。Marja van Vliet:写作-原稿。Machteld Huber和Sigrid van der Zanden:评论和编辑。作者声明无利益冲突。
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Response to Comments on “Designing a Positive Health Dialogue Tool for Adolescents and Young Adults: A Mixed Methods Study”

We appreciate the opportunity to address the concerns raised regarding our recent publication, “Designing a Positive Health Dialogue Tool for Adolescents and Young Adults: A Mixed Methods Study” (Health Expect. 2024 Oct;27(5):e70042). We value the constructive feedback and offer the following clarifications.

The quantitative aspect of our study involves a relatively small sample (N = 118), as acknowledged in the limitations section. These findings should, therefore, be interpreted with caution and are not generalisable to the entire population. Our main objective was to use this phase as an exploratory step, guiding the qualitative phase (focus groups and interviews), which forms the study's foundation. In qualitative research, a sample of N = 36 is not considered small; instead, the depth of data and achievement of saturation are critical indicators of validity.

Furthermore, we emphasise that this tool for adolescents and young adults builds upon rigorous research conducted during the development of both the adult and child versions. These earlier phases required distinct methodological considerations compared to starting from scratch.

We acknowledge the gender imbalance within our sample (79% female). However, our recruitment strategy prioritised factors such as ‘having a disease’ and ‘educational level’, given their established influence on health perceptions, as reported in the literature (e.g., [1, 2]). Gender differences in this context tend to be less pronounced, as also noted in previous studies.

We agree with the need to assess the long-term effects of the dialogue tool, as highlighted in the discussion section. One of our aims in publishing this article was to encourage future studies evaluating the sustained influence of the tool, as has been done for the adult and child versions (e.g., [13, 4]). Given the promising results of these earlier versions, we anticipate similar positive outcomes for this version.

The dialogue tool is specifically designed to capture an individual's subjective experience, making self-reported data the most appropriate method in this context. For evaluations requiring greater objectivity, we developed a separate measurement tool for the adult version [56]. Developing a similar tool for adolescents and young adults would be a logical next step and is recommended in our discussion section. This will enable scientific evaluation purposes.

Nevertheless, the main goal of this dialogue tool is to promote a subjective understanding of personal health, providing a foundation for meaningful discussions about individual needs, priorities, and goals.

We addressed concerns about generalisability in the methodological considerations section, specifically discussing its applicability across different cultural and socio-economic backgrounds. This issue was also explored in our earlier rapid review [1]. With this specific version, we aim to contribute to the understanding of specificity for targeted groups. Further research is planned to test the dialogue tool across various groups to enhance understanding of the generalisability of the tool itself.

We trust these clarifications address the concerns raised and underscore our commitment to advancing research in this area.

Marja van Vliet: writing–original draft. Machteld Huber and Sigrid van der Zanden: review and editing.

The authors declare no conflicts of interest.

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来源期刊
Health Expectations
Health Expectations 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.20
自引率
9.40%
发文量
251
审稿时长
>12 weeks
期刊介绍: Health Expectations promotes critical thinking and informed debate about all aspects of patient and public involvement and engagement (PPIE) in health and social care, health policy and health services research including: • Person-centred care and quality improvement • Patients'' participation in decisions about disease prevention and management • Public perceptions of health services • Citizen involvement in health care policy making and priority-setting • Methods for monitoring and evaluating participation • Empowerment and consumerism • Patients'' role in safety and quality • Patient and public role in health services research • Co-production (researchers working with patients and the public) of research, health care and policy Health Expectations is a quarterly, peer-reviewed journal publishing original research, review articles and critical commentaries. It includes papers which clarify concepts, develop theories, and critically analyse and evaluate specific policies and practices. The Journal provides an inter-disciplinary and international forum in which researchers (including PPIE researchers) from a range of backgrounds and expertise can present their work to other researchers, policy-makers, health care professionals, managers, patients and consumer advocates.
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