Reeves Mathew J, Hughes Anne K, Woodward Amanda T, Freddolino Paul P, Coursaris Constantinos K, Swierenga Sarah J, Schwamm Lee H, Fritz Michele C
Department of Epidemiology and Biostatistics, College of Human Medicine, Michigan State University, B601 West Fee Hall, East Lansing, MI, 48824, USA.
School of Social Work, College of Social Science, Michigan State University, East Lansing, MI, USA.
BMC Neurol. 2017 Jun 17;17(1):115. doi: 10.1186/s12883-017-0895-1.
For some stroke patients and caregivers, navigating the transition between hospital discharge and returning home is associated with substantial psychosocial and health-related challenges. Currently, no evidence-based standard of care exists that addresses the concerns of stroke patients and caregivers during the transition period. Objectives of the Michigan Stroke Transitions Trial (MISTT) are to test the impact of a social worker home-based case management program, as well as an online information and support resource, on patient and caregiver outcomes after returning home.
The Michigan Stroke Transitions Trial is a randomized, pragmatic, open (un-blinded), 3-group parallel designed superiority trial conducted in 3 Michigan hospitals. Eligible participants are adult acute stroke patients discharged home directly or within 4 weeks of being discharged to a rehabilitation facility. The patient's primary caregiver is also invited to participate. Patients are randomized on the day they return home using a randomized block design. Consented patients discharged to a rehabilitation facility who do not go home within 4 weeks are dropped from the study. The 2 study interventions begin within a week of returning home and conclude 3 months later. The 3-group design compares usual care to either a home-based social worker stroke case management (SWSCM) program, or a combination of the SWSCM program plus access to an online information and support resource (MISTT website). Outcomes data are collected at 7-days and 90-days by trained telephone interviewers. Primary patient outcomes include the PROMIS global 10 score (a generic Quality of Life scale), and the Patient Activation Measure (PAM). Caregiver outcomes include the Bakas Caregiving Outcomes Scale. Final analysis will be based on 214 randomized acute stroke patients. To accommodate subjects excluded due to prolonged rehabilitation stays, as well as those lost-to-follow-up, up to 315 patients will be consented.
The MISTT study will determine if a home-based case management program designed around the needs and preferences of stroke patients and caregivers, alone or in combination with a patient-centered online information and support resource can improve stroke survivor and caregiver outcomes 3 months after returning home.
ClinicalTrials.gov: NCT02653170 (Protocol ID: 135457). Registered April 9, 2015.
对于一些中风患者及其护理人员而言,在医院出院和回家之间的过渡阶段面临着诸多重大的社会心理和健康相关挑战。目前,尚无基于证据的护理标准来解决中风患者及其护理人员在过渡期间的担忧。密歇根中风过渡试验(MISTT)的目标是测试一项由社会工作者提供的居家病例管理计划以及一个在线信息与支持资源对患者及其护理人员回家后的结局的影响。
密歇根中风过渡试验是一项在密歇根州的3家医院进行的随机、务实、开放(非盲法)、3组平行设计的优效性试验。符合条件的参与者为成年急性中风患者,他们直接出院回家或在出院后4周内转入康复机构。患者的主要护理人员也被邀请参与。患者在回家当天采用随机区组设计进行随机分组。同意参与研究但出院后转入康复机构且4周内未回家的患者将被排除在研究之外。两项研究干预措施在回家后一周内开始,并在3个月后结束。3组设计将常规护理与居家社会工作者中风病例管理(SWSCM)计划,或SWSCM计划与访问在线信息和支持资源(MISTT网站)的组合进行比较。结局数据由经过培训的电话访问员在第7天和第90天收集。主要患者结局包括PROMIS全球10分评分(一种通用的生活质量量表)和患者激活量表(PAM)。护理人员结局包括巴卡斯护理结局量表。最终分析将基于214名随机分组的急性中风患者。为了纳入因长期康复住院而被排除的受试者以及失访者,将同意多达315名患者参与研究。
MISTT研究将确定一项围绕中风患者及其护理人员的需求和偏好设计的居家病例管理计划,单独或与以患者为中心的在线信息和支持资源相结合,是否能够改善中风幸存者及其护理人员回家3个月后的结局。
ClinicalTrials.gov:NCT02653170(方案编号:135457)。于2015年4月9日注册。