Support person

  • 文章类型: Randomized Controlled Trial
    移动健康(mHealth)具有从根本上改善健康行为和生活质量的潜力;但是,在了解如何优化移动健康参与方面仍然存在关键差距。大多数参与研究仅报告系统使用情况,而不考虑用户是否在认知上反思内容。尽管与mHealth的互动至关重要,认知投资对于有意义的行为改变也可能很重要。值得注意的是,设计为要求过多反射的内容可能会导致用户脱离接触。了解如何在反应负担和反思负担之间取得平衡,对于实现有效参与以影响预期结果至关重要。
    在这项观察性研究中,我们试图了解反应负担和反思负担之间的相互作用以及它们如何影响mHealth参与。具体来说,我们探讨了mHealth内容的响应和反射负担的变化将如何影响mHealth干预中用户的短信响应率。
    我们招募了糖尿病患者的支持人员进行一项随机对照试验,该试验评估了mHealth干预对糖尿病管理的影响。分配给干预的支持人员(n=148)完成了一项调查,并收到了9个月的短信。在为期2年的随机对照试验中,我们发送了4个版本的周刊,双向文本消息在反射负担(相对于其他消息的认知反射要求的水平)和响应负担(相对于其他消息的响应要求的信息水平)方面都有所不同。我们通过使用参与者级别的响应率来量化参与度。我们比较了每个文本的响应几率,并使用泊松回归来估计参与者特征和响应率之间的关联。
    无论响应负担如何,要求最多反思的文本的响应率最低(高反思和低响应负担:中位数为10%,IQR0%-40%;高反射和高响应负担:中位数23%,IQR0%-51%)。要求最少反射的文本的响应率最高(低反射和低响应负担:中位数90%,IQR61%-100%)对于要求中等反射的文本(中等反射和低响应负担:中位数75%,IQR38%-96%)。较低的反应几率与较高的反射负担相关(P<.001)。年轻的参与者和具有较低社会经济地位的参与者对具有更多反思负担的文本的响应率较低,相对于它们的对应物(所有P值均<.05)。
    随着反射负担的增加,参与度下降,我们发现不同参与者特征的参与度存在更多差异。鼓励适度反思的内容可能是实现认知投资和系统使用的理想选择。我们的发现为mHealth设计以及参与度和有效性的优化提供了见解。
    UNASSIGNED: Mobile health (mHealth) has the potential to radically improve health behaviors and quality of life; however, there are still key gaps in understanding how to optimize mHealth engagement. Most engagement research reports only on system use without consideration of whether the user is reflecting on the content cognitively. Although interactions with mHealth are critical, cognitive investment may also be important for meaningful behavior change. Notably, content that is designed to request too much reflection could result in users\' disengagement. Understanding how to strike the balance between response burden and reflection burden has critical implications for achieving effective engagement to impact intended outcomes.
    UNASSIGNED: In this observational study, we sought to understand the interplay between response burden and reflection burden and how they impact mHealth engagement. Specifically, we explored how varying the response and reflection burdens of mHealth content would impact users\' text message response rates in an mHealth intervention.
    UNASSIGNED: We recruited support persons of people with diabetes for a randomized controlled trial that evaluated an mHealth intervention for diabetes management. Support person participants assigned to the intervention (n=148) completed a survey and received text messages for 9 months. During the 2-year randomized controlled trial, we sent 4 versions of a weekly, two-way text message that varied in both reflection burden (level of cognitive reflection requested relative to that of other messages) and response burden (level of information requested for the response relative to that of other messages). We quantified engagement by using participant-level response rates. We compared the odds of responding to each text and used Poisson regression to estimate associations between participant characteristics and response rates.
    UNASSIGNED: The texts requesting the most reflection had the lowest response rates regardless of response burden (high reflection and low response burdens: median 10%, IQR 0%-40%; high reflection and high response burdens: median 23%, IQR 0%-51%). The response rate was highest for the text requesting the least reflection (low reflection and low response burdens: median 90%, IQR 61%-100%) yet still relatively high for the text requesting medium reflection (medium reflection and low response burdens: median 75%, IQR 38%-96%). Lower odds of responding were associated with higher reflection burden (P<.001). Younger participants and participants who had a lower socioeconomic status had lower response rates to texts with more reflection burden, relative to those of their counterparts (all P values were <.05).
    UNASSIGNED: As reflection burden increased, engagement decreased, and we found more disparities in engagement across participants\' characteristics. Content encouraging moderate levels of reflection may be ideal for achieving both cognitive investment and system use. Our findings provide insights into mHealth design and the optimization of both engagement and effectiveness.
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  • 文章类型: Journal Article
    目的:描述住院期间母乳喂养的每月趋势以及分娩期间妇女选择的伴侣的存在,以及关键区域响应者对支持人在场的同质性/异质性的看法,之前,期间(2020年2月至5月),在意大利一些地区的第一波COVID-19大流行浪潮之后。
    方法:两阶段研究。
    方法:分析了01.01.2019和31.03.2021之间六个意大利地区的意大利出生证明数据。对主要区域受访者进行了半结构化访谈。
    方法:将母乳喂养的频率分布和女性选择的伴侣的存在作为一个整体和每个地区进行计算。
    结果:在COVID-19大流行期间,婴儿喂养方式的变化小于分娩和分娩期间女性选择的伴侣,从2019年1月到2021年3月。所有地区的纯母乳喂养率最高的记录是在2020年9月(72.1%;95CI71.3-72.8)。而最低的是2021年3月(62.5%;95CI61.5-63.4)。在大流行期间,妇女在分娩和分娩期间选择的伴侣的存在减少,并且没有恢复到大流行前的水平。出生期间父亲的最高价值记录在2019年3月(59.0%;95CI58.2-59.8),而2020年4月最低(50.0%;95CI49.1-50.8)。新出现的主要主题是:国家的存在,区域和地方适应症;促进者(例如,爱婴医院倡议的实施,员工的强烈动机)和关键点(例如,对临床流行病学背景分析不足,不均匀的指征)支持人员存在的管理。
    结论:紧急情况改变了卫生服务的提供,而这些服务并不总能保证最佳实践的应用。希望能够评估出生证明数据的适当性,以收集更准确的信息并提供临床建议。
    to describe the monthly trend of breastfeeding during hospitalization and the presence of companion of woman\'s choice during labour and birth, and the key regional responders\' perspective of homogeneity/heterogeneity of the presence of the support person, before, during (February-May 2020), and after the first COVID-19 pandemic wave in a few Italian Regions.
    two-phase study.
    data from the italian birth certificate of six Italian Regions between 01.01.2019 and 31.03.2021 were analysed. Semi-structured interviews were conducted with the key regional respondents.
    the frequency distributions of breastfeeding and the presence of companion of woman\'s choice were calculated as a whole and for each Region.
    the infant feeding practices experienced smaller changes during COVID-19 pandemic than the presence of the companion of woman\'s choice during labour and birth, from January 2019 to March 2021. The highest value of exclusive breastfeeding was recorded in September 2020 (72.1%; 95%CI 71.3-72.8) in all Regions, while the lowest was recorded in March 2021 (62.5%; 95%CI 61.5-63.4). The presence of companion of woman\'s choice during labour and birth decreased during the pandemic and did not return to pre-pandemic levels. The highest value of presence of father during birth was recorded in March 2019 (59.0%; 95%CI 58.2-59.8), while the lowest in April 2020 (50.0%; 95%CI 49.1-50.8). The main emerging themes were: the existence of national, regional and local indications; the facilitators (e.g., Baby-Friendly Hospital Initiative implementation, strong motivation of the staff) and the critical points (e.g., inadequate analysis of the clinical-epidemiological context, inhomogeneous indications) of management of the support person presence.
    the emergency has changed the provision of health services that not always guaranteed the application of best practices. It would be desirable to work for assessing the appropriateness of the birth certificate data to collect more accurate information and to provide clinical recommendations.
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  • 文章类型: Randomized Controlled Trial
    目的:2型糖尿病自我管理发生在社会背景下。我们试图测试家庭/朋友激活对激励自我照顾(FAMS)的影响,通过手机提供的自我护理支持干预,关于糖尿病患者(PWD)及其支持者的社会心理结果。
    方法:在15个月的RCT中,PWD可以选择与朋友/家庭成员一起作为支持人员进行评估,以评估FAMS与增强常规护理的比较。FAMS包括每月9个月的电话辅导和对残疾人的短信支持,和短信支持注册的支持人员。
    结果:PWD(N=329)为52%的男性和39%的少数民族或种族;50%的人患有糖尿病恶化。支持人员(N=294)为26%的男性和33%的少数民族或族裔。在干预期间,FAMS改善了PWDs\'糖尿病困扰(d=-0.19)和全球幸福感(d=0.21),在少数群体中具有更大的影响。干预后和持续(15个月)的改善是由残疾人自我效能的变化驱动的,自我照顾行为,自治支持。在支持人员中,FAMS改善了有益的参与,而不会增加负担或有害的参与。
    结论:FAMS改善了PWD的社会心理幸福感,随着干预后的改善和自我效能感的持续改善,自我照顾,自治支持。支持人员增加了有益的参与而没有不利影响。
    OBJECTIVE: Type 2 diabetes self-management occurs within social contexts. We sought to test the effects of Family/friend Activation to Motivate Self-care (FAMS), a self-care support intervention delivered via mobile phones, on psychosocial outcomes for persons with diabetes (PWDs) and their support persons.
    METHODS: PWDs had the option to enroll with a friend/family member as a support person in a 15-month RCT to evaluate FAMS versus enhanced usual care. FAMS included 9 months of monthly phone coaching and text message support for PWDs, and text message support for enrolled support persons.
    RESULTS: PWDs (N = 329) were 52% male and 39% reported minoritized race or ethnicity ; 50% enrolled with elevated diabetes distress. Support persons (N = 294) were 26% male and 33% reported minoritized race or ethnicity. FAMS improved PWDs\' diabetes distress (d = -0.19) and global well-being (d = 0.21) during the intervention, with patterns of larger effects among minoritized groups. Post-intervention (9-month) and sustained (15-month) improvements were driven by changes in PWDs\' self-efficacy, self-care behaviors, and autonomy support. Among support persons, FAMS improved helpful involvement without increasing burden or harmful involvement.
    CONCLUSIONS: FAMS improved PWDs\' psychosocial well-being, with post-intervention and sustained improvements driven by improved self-efficacy, self-care, and autonomy support. Support persons increased helpful involvement without adverse effects.
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  • 文章类型: Randomized Controlled Trial
    探索以家庭为中心的沟通是否会影响决策并优化患者-伴侣-提供者的咨询。
    A平行线,我们进行了双臂随机对照试验,纳入了108例作为炎性关节炎患者或患者同伴的参与者.一对参加了模拟咨询,医生使用以家庭为中心或仅患者的交流来解释从生物起源到生物仿制药的变化。参与者报告了他们过渡的意愿,风险认知,理解和社会支持,并完成了各种量表,包括患者感知量表。访谈有助于了解对咨询的看法。
    与仅患者沟通相比,以家庭为中心的沟通不会影响改变意愿或认知风险观念。然而,它改善了情绪风险感知(p=0.047,科恩的d=.55)和沟通满意度(p=0.015,科恩的d=.71)。感觉解释令人放心与减少担忧有关(p=0.004)。接受情感支持(p=0.014)和同伴提出较少问题(p=0.046)与较高的召回率相关。干预改善了同伴参与(p<0.001,科恩的d=1.23)和支持(p=0.002,科恩的d=0.86)。采访表明,令人鼓舞的问题,包容的肢体语言,承认同伴促进了参与。
    以家庭为中心的沟通增加了患者-伴侣-提供者的接触,但不影响改变治疗的意愿。
    从业者在讨论生物仿制药时可以使用以家庭为中心的沟通,但应该提供保证,鼓励情感支持,并总结要点以增进理解。
    To explore whether family-centered communication impacts decisions and optimizes patient-companion-provider consultations.
    A parallel, two-arm randomized controlled trial was conducted with 108 participants acting as patients with inflammatory arthritis or companions. Pairs attended a mock consultation where a physician explained the change from a bio-originator to a biosimilar using family-centered or patient-only communication. Participants reported their willingness to transition, risk perceptions, understanding and social support, and completed various scales including the Patient Perception Scale. Interviews helped understand perceptions towards the consultation.
    Family-centered communication did not impact willingness to change or cognitive risk perceptions compared to patient-only communication. However, it improved emotional risk perceptions (p = 0.047, Cohen\'s d=.55) and satisfaction with communication (p = 0.015, Cohen\'s d=.71). Feeling the explanation was reassuring was associated with less worry (p = 0.004). Receiving emotional support (p = 0.014) and companions asking fewer questions (p = 0.046) were associated with higher recall. The intervention improved companion involvement (p < 0.001, Cohen\'s d= 1.23) and support (p = 0.002, Cohen\'s d=.86). Interviews showed that encouraging questions, inclusive body language, and acknowledging companions facilitated involvement.
    Family-centered communication augments patient-companion-provider encounters but does not influence willingness to change treatment.
    Practitioners can use family-centered communication when discussing biosimilars but should provide reassurance, encourage emotional support, and summarize key points to improve understanding.
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  • 文章类型: Journal Article
    背景:在西方国家,通常的做法是,妇女在分娩时得到信任的人的支持,通常是另一个父母。大量研究表明,这对女性对分娩过程和身体结果的满意度都有积极的影响。然而,关于伴侣的出生经历及其福祉的研究很少。这篇综述的目的是总结现有的关于合作伙伴经验的文献,考虑它的质量,并确定潜在的主题。
    方法:在三个数据库中进行系统的文献检索和手动检索,对于定性,定量,以及来自西方国家的混合方法研究,研究出生时伴侣的经历。
    结果:共纳入35项研究。只有一项研究包括同性伴侣(其他研究仅针对父亲的经历),并且只有一项经过验证的问卷调查了伴侣的出生经历。发现四个主要主题影响伴侣的出生经历:(1)强烈的感觉,(2)支持作用,(3)员工支持,(4)成为父亲。
    结论:在这种不熟悉的情况下,合作伙伴可能会感到非常脆弱和压力。他们需要员工的情感和非正式支持,想要积极参与,并为分娩妇女发挥重要作用。为了促进父母的良好依恋,系统地探索合作伙伴的需求对于积极的出生体验至关重要。由于家庭星座的多样性,所有合作伙伴都应纳入进一步研究,尤其是同性伴侣.
    BACKGROUND: In Western countries, it is common practice for a woman to be supported by a trusted person during childbirth, usually the other parent. Numerous studies have shown that this has a positive effect both on the woman\'s satisfaction with the birth process and on physical outcomes. However, there is little research on the birth experience of partners and their wellbeing. The aim of this review is to summarise the existing literature on partner experience, consider its quality and identify the underlying themes.
    METHODS: Both a systematic literature search in three databases and a manual search were conducted, for qualitative, quantitative, and mixed-methods studies from Western countries examining the experiences of partners present at a birth.
    RESULTS: A total of 35 studies were included. Only one study included same-sex partners (the other studies addressed fathers\' experiences only) and only one validated questionnaire examining partners\' birth experiences was identified. Four major themes were found to influence partners\' birth experiences: (1) intense feelings, (2) role of support, (3) staff support, and (4) becoming a father.
    CONCLUSIONS: Partners may feel very vulnerable and stressed in this unfamiliar situation. They need emotional and informal support from staff, want to be actively involved, and play an important role for the birthing woman. To promote good attachment for parents, systematic exploration of the needs of partners is essential for a positive birth experience. Because of the diversity of family constellations, all partners should be included in further studies, especially same-sex partners.
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  • 文章类型: Journal Article
    背景:多发性硬化症(MS)患者经常报告将饮食策略作为其个人健康计划的一部分;然而,关于MS患者健康行为改变的感知主题知之甚少。
    方法:对参加2项不同限制性饮食干预研究的20名MS女性及其18名自我确定的支持人进行了半结构的一对一访谈,其中包括伴侣和成年子女。采访被转录,编码,分类,分类然后分组为总结性主题。评估了被提及为饮食依从性的促进者或障碍的问题的频率,以确定在研究期间患有MS的女性与其支持者之间感知经验的可能差异。
    结果:确定了五个定性主题:(1)个人动机,(2)饮食成分,(3)时间,(4)支持,和(5)资源访问。饮食依从性的主要促进者来自支持人员和研究人员的积极支持,访问资源,症状改善,和个人动机。主要障碍包括研究饮食的新颖性,缺乏烹饪技能,症状没有变化或恶化,缺乏饮食知识,食物偏好和诱惑。症状严重程度更经常被报告为继发性进行性MS参与者的研究饮食依从性的障碍。
    结论:增强个人动机并确保支持者和研究人员的积极支持的方法可能会提高研究饮食依从性。由于MS患者面临的独特挑战,未来的研究应针对其独特的MS队列调整干预措施,以提高饮食依从性.
    BACKGROUND: People with multiple sclerosis (MS) frequently report implementing dietary strategies as part of their personal wellness programs; however, little is known about the perceived themes of healthy behavior change in people with MS.
    METHODS: Semistructured one-on-one interviews were conducted with 20 women with MS enrolled in 2 different restrictive dietary intervention studies and their 18 self-identified support persons consisting of partners and adult children. Interviews were transcribed, coded, categorized, and then grouped into summative themes. The frequency of issues being mentioned as facilitators of or barriers to diet adherence was evaluated to identify possible differences in perceived experiences between women with MS and their support persons during the studies.
    RESULTS: Five qualitative themes were identified: (1) personal motivation, (2) diet components, (3) time, (4) support, and (5) resource access. Major facilitators of dietary adherence were positive support from support persons and study staff, access to resources, symptom improvement, and personal motivation. Major barriers included the novelty of the study diet, lack of cooking skills, no change in or worsening of symptoms, lack of diet knowledge, and food preferences and temptations. Symptom severity was more frequently reported as a barrier to study diet adherence among participants with secondary progressive MS.
    CONCLUSIONS: Methods to enhance personal motivation and ensure positive support from support persons and study staff may improve study diet adherence. Due to the unique challenges faced by people with MS, future studies should tailor interventions to their unique MS cohort to increase diet adherence.
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  • 文章类型: Journal Article
    未经证实:痴呆症患者的照顾者会经历明显的身体,情感,和社会负担。需求评估可以提供重要信息,以协助服务机构为照顾者提供支持,以减轻这些负担。然而,很少有研究使用定量工具检查痴呆症患者护理人员所经历的未满足需求的患病率。这项研究旨在检查澳大利亚痴呆症患者护理人员所经历的未满足需求的患病率和类型。
    UNASSIGNED:这是一项针对照顾者的横断面调查,为居住在社区的痴呆症患者提供支持。护理人员是通过老年诊所招募的,老年护理提供者,支持服务和社区组织。同意的护理人员完成了一项调查,其中包括针对护理人员的80项研究特定的未满足需求工具(UNI-C)和社会人口统计学特征。描述性统计数据用于确定护理人员报告的最普遍的未满足需求。
    UNASSIGNED:共有169名护理人员(回应率为47%)完成了调查。大多数(87%)护理人员报告至少有一个未满足的需求。护理人员报告,在可能的80个未满足的需求中,中位数为16.0(IQR=24.0;max=58)。最常被认可的未满足的需求涵盖了一系列领域,包括情感健康,获得健康和老年护理服务,管理冷漠,寻找信息。
    UNASSIGNED:这项研究强调,很大一部分护理人员经历了与照顾痴呆症患者相关的未满足的需求。有必要制定并严格测试干预措施,以满足护理人员通常报告的未满足需求。
    Carers of people with dementia experience significant physical, emotional, and social burdens. Needs assessment can provide important information to assist services in providing support to carers to reduce these burdens. However, few studies have examined the prevalence of unmet needs experienced by carers of people with dementia using a quantitative instrument. This study aimed to examine the prevalence and type of unmet needs experienced by carers of people with dementia in Australia.
    This was a cross-sectional survey of carers providing support to community-dwelling individuals living with dementia. Carers were recruited through geriatric clinics, aged care providers, support services and community organisations. Consenting carers completed a survey including an 80-item study-specific unmet needs instrument for carers (UNI-C) and sociodemographic characteristics. Descriptive statistics were used to identify the most prevalent unmet needs reported by carers.
    A total of 169 carers (response rate 47%) completed the survey. Most (87%) carers reported at least one unmet need. Carers reported a median of 16.0 (IQR = 24.0; max = 58) out of a possible 80 unmet needs. The most frequently endorsed unmet needs spanned a range of areas including emotional wellbeing, accessing health and aged care services, managing apathy, and finding information.
    This study highlighted that a large proportion of carers experience unmet needs associated with caring for someone with dementia. Developing and rigorously testing interventions to meet carers\' commonly reported unmet needs are warranted.
    Supplemental data for this article is available online at https://doi.org/10.1080/13607863.2022.2053833 .
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  • 文章类型: Journal Article
    医疗保健提供者通常建议癌症患者参与肿瘤学护理的支持人员,以履行关键的支持角色。这项定性描述性研究从妇科癌症患者(n=18)的角度探讨了支持人参与肿瘤治疗就诊和癌症相关护理的三体看法的一致性。定期访问-出席支持人员(n=16),和医疗保健提供者(n=10),包括肿瘤学家,护士,和医疗助理。半结构化访谈(N=44)捕获了对肿瘤学提供者任命内外支持人员角色的促进和干扰的看法。专题分析揭示了支持人员的一致和分歧,信息性,和情感支持行为。关于同伴提供的支持功能的观点一致。然而,患者和支持者强调工具性支持的重要性,其次是信息和情感支持,而肿瘤学提供者强调了信息,其次是情感和工具支持。讨论提供了对三合会中每个角色观点的洞察。
    Health care providers routinely advise cancer patients to involve support persons in oncology care to fulfill critical support roles. This qualitative descriptive study explored alignment of triadic perceptions of support person involvement in oncology treatment visits and cancer-related care from the perspectives of patients with gynecologic cancer (n = 18), regular visit-attending support people (n = 16), and health care providers (n = 10), including oncologists, nurses, and medical assistants. Semi-structured interviews (N = 44) captured perceptions of facilitation and interference of support persons\' roles within and outside appointments with oncology providers. Thematic analyses revealed alignment and divergence regarding support persons\' instrumental, informational, and emotional support behaviors. Perspectives aligned regarding what support functions companions provide. However, patients and support persons emphasized the significance of instrumental followed by informational and emotional support, whereas oncology providers highlighted informational, followed by emotional and instrumental support. Discussion provides insight into each role\'s perspective in the triad.
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  • 文章类型: Journal Article
    Patient perceptions influence biosimilar uptake in non-mandatory transitions. Companions (support people) are often actively involved in the patient\'s medical journey and are likely to have unique perceptions of biosimilars, which may shape patient attitudes. This study explores the congruence between patient and companion perceptions towards biosimilars and their information needs. Patients taking bio-originators for rheumatic diseases (59% for rheumatoid arthritis) and their companions received an explanation about biosimilars. Participants (N = 78) completed questionnaires assessing their familiarity with biosimilars, perceptions, concerns, and benefits of being accompanied. Contingency tables and paired sample t-tests were used to explore differences in familiarity, confidence in knowledge, and perceptions. Intra-class correlation coefficients were calculated to assess the degree of congruence for perceptions towards biosimilars. Companions were significantly less familiar with biosimilars (p = 0.014, Cramer\'s V = 0.28) and reported lower confidence in their knowledge (p = 0.006, Cohen\'s d = 0.47) than patients. Companions and patients had moderate to good congruency for perceptions toward confidence in biosimilar use and safety, efficacy, and side-effect expectations (intra-class correlation coefficients ranging from 0.75 to 0.81). Companions and patients were most concerned about safety and effectiveness. Companions also reported concerns about cost savings driving the transition, while patients had concerns about uncertainty and testing. Patients reported the ability for discussion, improved understanding, and validation as benefits of being accompanied. Companions and patients have similar levels of perceptions and expectations towards biosimilars but report some unique information needs. Future educational interventions should involve companions and address their concerns to help improve biosimilar acceptance.
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  • 文章类型: Journal Article
    BACKGROUND: Involving patients in treatment decisions is commonplace in healthcare, and patients are frequently accompanied by a companion (support person). Companions are often actively involved in medical consultations, yet their impact on decisions to change medications is unknown.
    OBJECTIVE: This study examines the influence of companions on a patient\'s decision to transition from their bio-originator therapy to a biosimilar.
    METHODS: A parallel, two-arm randomized controlled trial was conducted with 79 patients taking a bio-originator for rheumatic diseases who regularly attend clinic with a companion. Patients were randomized to receive an explanation about a hypothetical transition to a biosimilar alone or with their companion. Patients reported willingness to transition, risk perceptions, difficulty understanding, social support, and completed the Decisional Conflict Scale and Satisfaction with Decision Scale.
    RESULTS: Companions did not influence decisions to transition to biosimilars or cognitive and affective risk perceptions. Accompanied patients reported more difficulty understanding the explanation (p = .006, Cohen\'s d = .64) but thought it was more important to receive information with companions (p = .023, Cohen\'s d = -.52). Companions did not impact decision satisfaction or decisional conflict. Receiving emotional, but not practical support, was associated with less decisional conflict in accompanied patients (p = .038, r  2 = 0.20).
    CONCLUSIONS: The presence of companions does not seem to influence risk perceptions or decisions about transitioning to biosimilars. Companions, however, impact the patient\'s reporting of their ability to understand treatment explanations. Providers should check understanding in all patients but may need to provide additional time or educational resources to accompanied patients and companions.
    BACKGROUND: Australian New Zealand Clinical Trial Registry: ACTRN12619001435178.
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