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FAMS-T1D移动健康干预对1型糖尿病青少年成人优化自我调节和社会调节的可接受性与可行性

Acceptability and feasibility of FAMS-T1D mHealth intervention to optimize self- and social regulation for emerging adults with type 1 diabetes.

作者信息

Mayberry Lindsay S, Wiebe Deborah J, Parks Makenzie, Campbell MaryJane S, Beam Aislinn B, Berg Cynthia A

机构信息

Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, 37203, USA.

Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, USA.

出版信息

Pilot Feasibility Stud. 2024 Apr 30;10(1):68. doi: 10.1186/s40814-024-01497-1.

Abstract

BACKGROUND

Among emerging adults with type 1 diabetes (T1D), self-regulation and social regulation skills can help avoid high A1c and diabetes distress. FAMS (Family/friend Activation to Motivate Self-care) is mobile phone-delivered intervention that supports development of these skills and is efficacious among adults with type 2 diabetes. However, the acceptability and feasibility of the FAMS intervention among emerging adults with T1D are unknown.

METHODS

Therefore, we adapted FAMS for in a new disease context and developmental stage and then conducted a 3-month mixed-methods pre-post pilot study. Participants were emerging adults with T1D and a friend/family member enrolled as a support person (optional). Feasibility/acceptability outcomes and associated progression thresholds were recruitment (≥ 70% eligible emerging adults), retention (≥ 85%), intervention engagement (≥ 70%), and satisfaction (≥ 70%). We also collected qualitative feedback to determine if the intervention addressed relevant needs and explored changes in outcomes of interest (family/friend involvement, self-efficacy, self-management, distress, A1c).

RESULTS

Recruitment rates indicate recruitment of emerging adults with T1D (n = 30) and their support persons (n = 20) is feasible - 79% of emerging adults who screened as eligible enrolled and 70% of enrolled emerging adults invited a support person. Emerging adults completed 98% of coaching sessions, and response rates to automated text messages were median 85% IQR [68%, 90%]. Changes in selected measures for outcomes of interest were in expected directions suggesting sensitivity to changes occasioned by the intervention in a future evaluative trial. Emerging adults said FAMS-T1D helped with setting realistic goals, motivated them to prioritize diabetes goals, and increased support, indicating acceptability of the intervention in this new disease and developmental context.

CONCLUSIONS

Findings suggest potential for FAMS-T1D to engage emerging adults and their support persons and feasibility for an evaluative trial examining effects on self-regulation (self-efficacy, self-management), social regulation (family/friend involvement), and outcomes (diabetes distress, A1c).

TRIAL REGISTRATION

We did not register this study on ClinicalTrials.gov because the purpose of the study was to assess the feasibility and acceptability of the intervention and study procedures and measures in preparation for a future trial. The purpose of that future trial will be to evaluate the effect of the intervention on health-related biomedical and behavioral outcomes, and that trial will be registered accordingly.

摘要

背景

在患有1型糖尿病(T1D)的青年成年人中,自我调节和社会调节技能有助于避免糖化血红蛋白(A1c)水平过高和糖尿病困扰。FAMS(家庭/朋友激活以促进自我护理)是一种通过手机提供的干预措施,可支持这些技能的发展,并且在患有2型糖尿病的成年人中具有疗效。然而,FAMS干预措施在患有T1D的青年成年人中的可接受性和可行性尚不清楚。

方法

因此,我们将FAMS调整应用于新的疾病背景和发育阶段,然后进行了一项为期3个月的混合方法前后对照试点研究。参与者为患有T1D的青年成年人以及作为支持人员(可选)登记的朋友/家庭成员。可行性/可接受性结果及相关进展阈值包括招募(≥70%符合条件的青年成年人)、留存率(≥85%)、干预参与度(≥70%)和满意度(≥70%)。我们还收集了定性反馈,以确定该干预措施是否满足相关需求,并探索了感兴趣的结果(家人/朋友参与、自我效能感、自我管理、困扰、A1c)的变化。

结果

招募率表明,招募患有T1D的青年成年人(n = 30)及其支持人员(n = 20)是可行的——79%筛查合格的青年成年人登记入组,70%登记入组的青年成年人邀请了一名支持人员。青年成年人完成了98%的辅导课程,对自动短信的回复率中位数为85%,四分位距为[68%,90%]。感兴趣的结果的选定测量指标的变化方向符合预期,表明在未来的评估试验中对干预引起的变化具有敏感性。青年成年人表示,FAMS-T1D有助于设定现实的目标,促使他们将糖尿病目标列为优先事项,并增加了支持,表明该干预措施在这种新的疾病和发育背景下具有可接受性。

结论

研究结果表明,FAMS-T1D有潜力吸引青年成年人及其支持人员参与,并且对于一项评估其对自我调节(自我效能感、自我管理)、社会调节(家人/朋友参与)和结果(糖尿病困扰、A1c)影响的评估试验具有可行性。

试验注册

我们未在ClinicalTrials.gov上注册本研究,因为该研究的目的是评估干预措施以及研究程序和测量方法的可行性和可接受性,为未来的试验做准备。未来试验的目的将是评估该干预措施对与健康相关的生物医学和行为结果的影响,并且该试验将相应地进行注册。

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