Mobile critical care recovery program (m-CCRP) for acute respiratory failure survivors: study protocol for a randomized controlled trial

被引:13
作者
Khan, Sikandar [1 ,2 ]
Biju, Ashok [2 ]
Wang, Sophia [3 ,4 ,5 ]
Gao, Sujuan [6 ]
Irfan, Omar [7 ]
Harrawood, Amanda [2 ]
Martinez, Stephanie [2 ]
Brewer, Emily [2 ]
Perkins, Anthony [4 ,6 ]
Unverzagt, Frederick W. [3 ]
Lasiter, Sue [8 ]
Zarzaur, Ben [9 ]
Rahman, Omar
Boustani, Malaz [2 ,4 ,5 ,10 ]
Khan, Babar [1 ,2 ,5 ]
机构
[1] Indiana Univ Sch Med, Dept Med, Div Pulm Crit Care Sleep & Occupat Med, Indianapolis, IN 46202 USA
[2] Regenstrief Inst Hlth Care, IU Ctr Aging Res, Indianapolis, IN 46202 USA
[3] Indiana Univ Sch Med, Dept Psychiat, Indianapolis, IN 46202 USA
[4] Ctr Translat Sci & Innovat, Ctr Hlth Innovat & Implementat Sci, Indianapolis, IN USA
[5] Eskenazi Hosp, Sandra Eskenazi Ctr Brain Care Innovat, Indianapolis, IN USA
[6] Indiana Univ Sch Med, Dept Biostat, Indianapolis, IN 46202 USA
[7] Aga Khan Univ, Karachi, Pakistan
[8] Univ Missouri, Sch Nursing & Hlth Studies, Kansas City, MO 64110 USA
[9] Indiana Univ Sch Med, Dept Surg, Indianapolis, IN 46202 USA
[10] Indiana Univ Sch Med, Dept Internal Med, Div Geriatr & Gen Internal Med, Indianapolis, IN 46202 USA
关键词
Delirium; Physical activity; Cognitive training; Cognitive impairment; Critical care; ICU survivorship; Quality of life; Post-intensive care syndrome; QUALITY-OF-LIFE; TERM COGNITIVE IMPAIRMENT; INTENSIVE-CARE; CRITICAL ILLNESS; COLLABORATIVE CARE; PHYSICAL REHABILITATION; DISTRESS-SYNDROME; UNIT SURVIVORS; DEPRESSION; OUTCOMES;
D O I
10.1186/s13063-018-2449-2
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Patients admitted to intensive care units (ICU) with acute respiratory failure (ARF) face chronic complications that can impede return to normal daily function. A mobile, collaborative critical care model may enhance the recovery of ARF survivors. Methods: The Mobile Critical Care Recovery Program (m-CCRP) study is a two arm, randomized clinical trial. We will randomize 620 patients admitted to the ICU with acute respiratory failure requiring mechanical ventilation in a 1: 1 ratio to one of two arms (310 patients per arm)-m-CCRP intervention versus attention control. Those in the intervention group will meet with a care coordinator after hospital discharge in predetermined intervals to aid in the recovery process. Baseline assessments and personalized goal setting will be used to develop an individualized care plan for each patient after discussion with an interdisciplinary team. The attention control arm will receive printed material and telephone reminders emphasizing mobility and management of chronic conditions. Duration of the intervention and follow-up is 12 months post-randomization. Our primary aim is to assess the efficacy of m-CCRP in improving the quality of life of ARF survivors at 12 months. Secondary aims of the study are to evaluate the efficacy of m-CCRP in improving function (cognitive, physical, and psychological) of ARF survivors and to determine the efficacy of m-CCRP in reducing acute healthcare utilization. Discussion: The proposed randomized controlled trial will evaluate the efficacy of a collaborative critical care recovery program in accomplishing the Institute of Healthcare Improvement's triple aims of better health, better care, at lower cost. We have developed a collaborative critical care model to promote ARF survivors' recovery from the physical, psychological, and cognitive impacts of critical illness. In contrast to a single disease focus and clinic-based access, m-CCRP represents a comprehensive, accessible, mobile, ahead of the curve intervention, focused on the multiple aspects of the unique recovery needs of ARF survivors.
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页数:11
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