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

dc.contributor.authorKhan, Sikandar
dc.contributor.authorBiju, Ashok
dc.contributor.authorWang, Sophia
dc.contributor.authorGao, Sujuan
dc.contributor.authorIrfan, Omar
dc.contributor.authorHarrawood, Amanda
dc.contributor.authorMartinez, Stephanie
dc.contributor.authorBrewer, Emily
dc.contributor.authorPerkins, Anthony
dc.contributor.authorUnverzagt, Frederick W.
dc.contributor.authorLasiter, Sue
dc.contributor.authorZarzaur, Ben
dc.contributor.authorRahman, Omar
dc.contributor.authorBoustani, Malaz
dc.contributor.authorKhan, Babar
dc.contributor.departmentMedicine, School of Medicineen_US
dc.date.accessioned2018-07-20T19:05:36Z
dc.date.available2018-07-20T19:05:36Z
dc.date.issued2018-02-07
dc.description.abstractBACKGROUND: 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.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationKhan, S., Biju, A., Wang, S., Gao, S., Irfan, O., Harrawood, A., … Khan, B. (2018). Mobile critical care recovery program (m-CCRP) for acute respiratory failure survivors: study protocol for a randomized controlled trial. Trials, 19, 94. http://doi.org/10.1186/s13063-018-2449-2en_US
dc.identifier.urihttps://hdl.handle.net/1805/16752
dc.language.isoen_USen_US
dc.publisherBioMed Centralen_US
dc.relation.isversionof10.1186/s13063-018-2449-2en_US
dc.relation.journalTrialsen_US
dc.rightsAttribution 3.0 United States
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/
dc.sourcePMCen_US
dc.subjectCognitive impairmenten_US
dc.subjectCognitive trainingen_US
dc.subjectCritical careen_US
dc.subjectDeliriumen_US
dc.subjectICU survivorshipen_US
dc.subjectPhysical activityen_US
dc.subjectPost-intensive care syndromeen_US
dc.subjectQuality of lifeen_US
dc.titleMobile critical care recovery program (m-CCRP) for acute respiratory failure survivors: study protocol for a randomized controlled trialen_US
dc.typeArticleen_US
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