Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden.
Theme of Women's Health and Allied Health Professionals, Karolinska University Hospital, Stockholm, Sweden.
Health Expect. 2024 Oct;27(5):e70057. doi: 10.1111/hex.70057.
Care transitions from hospital to home are a critical period for patients and their families, especially after a stroke. The aim of this study was to assess the feasibility, fidelity and acceptability of a co-designed care transition support for stroke survivors.
A non-randomised controlled feasibility study recruiting patients who had had stroke and who were to be discharged home and referred to a neurorehabilitation team in primary healthcare was conducted. Data on the feasibility of recruitment and fidelity of the intervention were collected continuously during the study with screening lists and checklists. Data on the perceived quality of care transition were collected at 1-week post-discharge with the Care Transition Measure. Data on participant characteristics, disease-related data and outcomes were collected at baseline (hospitalisation), 1 week and 3 months post-discharge. Data on the acceptability of the intervention from the perspective of healthcare professionals were collected at 3 months using the Normalisation Measure Development Questionnaire.
Altogether, 49 stroke survivors were included in the study: 28 in the intervention group and 21 in the control group. The recruitment and data collection of patient characteristics, disease-related data, functioning and outcomes were feasible. The fidelity of the intervention differed in relation to the different components of the co-designed care transition support. The intervention was acceptable from the perspective of healthcare professionals. Concerns were raised about the fidelity of the intervention. A positive direction of effects of the intervention on the perceived quality of the care transition was found.
The study design, data collection, procedures and intervention were deemed feasible and acceptable. Modifications are needed to improve intervention fidelity by supporting healthcare professionals to apply the intervention. The feasibility study showed a positive direction of effect on perceived quality with the care transition, but a large-scale trial is needed to determine its effectiveness.
Stroke survivors, significant others and healthcare professionals were involved in a co-design process, including the joint development of the intervention's components, contextual factors to consider, participant needs and important outcomes to target.
ClinicalTrials.gov ID: NCT0292587.
患者及其家属从医院到家庭的过渡期是一个关键时期,特别是在中风之后。本研究旨在评估为中风幸存者设计的过渡护理支持的可行性、保真度和可接受性。
本研究是一项非随机对照可行性研究,招募的患者中风后出院并被转介到初级保健中的神经康复团队。在研究过程中,通过筛查清单和检查表连续收集有关干预措施可行性和保真度的数据。在出院后 1 周,使用护理过渡测量表收集对护理过渡质量的感知数据。在基线(住院)、出院后 1 周和 3 个月时收集参与者特征、疾病相关数据和结局的数据。在 3 个月时,使用正常化措施开发问卷收集医护人员对干预措施的可接受性数据。
共有 49 名中风幸存者参与了这项研究:干预组 28 名,对照组 21 名。患者特征、疾病相关数据、功能和结局的数据收集具有可行性。干预措施的保真度因合作设计的过渡护理支持的不同组成部分而有所不同。从医护人员的角度来看,干预措施是可以接受的。人们对干预措施的保真度表示担忧。干预措施对护理过渡质量的感知有积极的影响。
研究设计、数据收集、程序和干预措施被认为是可行和可接受的。需要进行修改,以通过支持医护人员应用干预措施来提高干预措施的保真度。可行性研究表明,护理过渡的感知质量有积极的影响,但需要进行大规模试验来确定其效果。
中风幸存者、重要他人和医护人员参与了合作设计过程,包括联合开发干预措施的组成部分、考虑的背景因素、参与者的需求和要针对的重要结果。
ClinicalTrials.gov ID:NCT0292587。