Kreitzer Natalie, Fink Stephanie, Adeoye Opeolu, Kurowski G Brad, Wade Shari, Sucharew Heidi, Bakas Tamilyn
Department of Emergency Medicine, University of Cincinnati, Medical Sciences Building Room 1654 231, Albert Sabin Way, PO Box 670769, Cincinnati, OH, 45267-0769, USA.
Department of Emergency Medicine, Washington University, 660 S. Euclid Ave., Campus Box 8072, Saint Louis, MO, 63110, USA.
Contemp Clin Trials Commun. 2024 Aug 24;41:101356. doi: 10.1016/j.conctc.2024.101356. eCollection 2024 Oct.
After injury, survivors of moderate to severe traumatic brain injury (msTBI) depend on informal family caregivers. Upwards of 77 % of family caregivers experience poor outcomes, such as adverse life changes, poor health-related quality of life, and increased depressive symptoms. Caregivers frequently report minimal support or training to prepare them for their new role. The majority of previously developed caregiver and caregiver/survivor dyad interventions after msTBI focus on providing information to either survivors only, or to long-term caregivers, rather than to the new caregiver. This manuscript describes the protocol of an ongoing randomized control trial, Caregiver Wellness after TBI (CG-Well), developed to provide education, support, and skill-building to caregivers of adults with msTBI, beginning when the survivor is early in the clinical course.
Within two weeks of admission to the ICU, participants are randomized to CG-Well online modules (intervention group, n = 50 dyads) or information, support, and referral (ISR) e-bulletins that exist in the public domain (control group, n = 50 dyads) over the first six months after their family member's msTBI. Both groups receive regular phone calls. The primary outcome is intervention satisfaction at six months.
Enrollment began in March 2022 and is projected to complete October 2024. We have enrolled approximately 70 % of participants at this time. Primary analysis completion is anticipated April 2025.
This RCT is designed to evaluate caregiver satisfaction by addressing the need for tailored supportive care for caregivers of msTBI beginning during the ICU admission.
Clinicaltrials. gov Registration Number: NCT05307640.
中度至重度创伤性脑损伤(msTBI)幸存者受伤后依赖非正式家庭照顾者。超过77%的家庭照顾者经历不良后果,如生活发生不利变化、健康相关生活质量差以及抑郁症状加重。照顾者经常报告在为新角色做准备时得到的支持或培训极少。此前大多数针对msTBI后照顾者及照顾者/幸存者二元组的干预措施,都只侧重于向幸存者或长期照顾者提供信息,而非新照顾者。本手稿描述了一项正在进行的随机对照试验——创伤性脑损伤后照顾者健康(CG-Well)的方案,该试验旨在为患有msTBI的成年人的照顾者提供教育、支持和技能培养,从幸存者处于临床病程早期时开始。
在入住重症监护病房(ICU)的两周内,参与者被随机分为CG-Well在线模块组(干预组,n = 50个二元组)或公共领域现有的信息、支持和转诊(ISR)电子公告组(对照组,n = 50个二元组),为期6个月,从其家庭成员发生msTBI后开始。两组都接受定期电话随访。主要结局是6个月时的干预满意度。
招募工作于2022年3月开始,预计2024年10月完成。目前我们已招募了约70%的参与者。预计2025年4月完成初步分析。
这项随机对照试验旨在通过满足对msTBI照顾者从入住ICU开始就提供量身定制的支持性护理的需求,来评估照顾者的满意度。
Clinicaltrials.gov注册号:NCT05307640。