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Intensive Care Unit Syndrome clinical trials

View clinical trials related to Intensive Care Unit Syndrome.

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NCT ID: NCT03828552 Completed - Clinical trials for Intensive Care Unit Syndrome

Parents' Experience of Their Children Stay in a Pediatric Intensive Care Unit.

VECUREA
Start date: March 4, 2019
Phase:
Study type: Observational

Children recovered in pediatric intensive care unit (PICU) suffer from severe conditions, sometimes life-threatening. Thus, priority is given to urgent somatic care, children medicalization is strong, invasive technics have to be used, and medical monitoring is close. A stay in PICU often leaves a painful memory to the child and family, and can lead to psychological morbidity such as post-traumatic stress disease. This study aims to assess parents' experience during their child hospitalization in PICU, and the impact of this stay on the entire family in the following month.

NCT ID: NCT03714399 Completed - Surgery Clinical Trials

Muscle Recovery Following Aortic Surgery Induced ICUAW.

VARIANCE
Start date: February 19, 2019
Phase:
Study type: Observational

To identify determinants of 'good and bad recovery' from ICUAW and build knowledge around the timing of these processes. Also, the investigators want to discover the effects of ICUAW on physical function and HRQoL following aortic surgery.

NCT ID: NCT03642249 Completed - Delirium Clinical Trials

Education for Recognition and Management of Delirium

Start date: November 5, 2019
Phase: N/A
Study type: Interventional

Delirium is a disturbance in consciousness with reduced ability to focus, sustain, or shift attention that occurs over a short period of time and tends to fluctuate over the course of the day. 50% to 81.7% had delirium during their ICU hospitalization. Delirium is associated with increased physical restraint, ventilation use, length of ICU stay, and mortality. However, there is no established delirium care pathway in target hospital. Chen et al. (2014) demonstrated that structured assessment stations with immediate feedback may improve overall learning efficiency over an EBP workshop alone. However, no published delirium care education study has used OSCEs as an intervention for healthcare professionals. The aim is to evaluate the effects of implementing a Scenario-based education intervention, including objective structured clinical examinations (OSCEs) on delirium care among healthcare professionals. This is a knowledge translation research, builds on eight years of delirium care research in University of Wollongong, Australia. The research will be undertaken at ICUs in a medical center in northern of Taiwan. There are two phases: (1) systematic review to identify delirium screen tool, and (2) a randomized controlled trial was conducted to determine the effects of implementing a Scenario-based education intervention, including OSCE (experimental group), and on-line education only (control group) focused on recognition and management of delirium. The hypothesis is: Scenario-based education intervention, including OSCE can increase the competence and self-efficacy among healthcare professionals in delirium care.

NCT ID: NCT03605407 Completed - Depression Clinical Trials

Patients Visit Prior to Hospital Admission & Intensive Care Unit

Start date: August 22, 2018
Phase: N/A
Study type: Interventional

The present study evaluates the effects of the visit prior to hospital admission on anxiety, depression and satisfaction of patients in an intensive care unit.

NCT ID: NCT03457376 Completed - Clinical trials for Intensive Care Unit Syndrome

Correlation of the Hand Grip Force With Maximum Inspiratory and Maximum Expiratory Pressure, in Critical Ill Patients

Start date: May 1, 2017
Phase: N/A
Study type: Observational

This study aimed to examine the relationship between Hand Grip Force (HGF), Maximum Inspiratory Pressure (PImax) and Maximum Expiratory Pressure (PEmax) in ICU tracheostomized patients. METHODS: All patients underwent assessment of PImax and PEmax by a membrane-type manometer, and for the measure of HGF an hydraulic hand dynamometer

NCT ID: NCT03392857 Completed - Clinical trials for Intensive Care Unit Syndrome

End Of Life in the Critically Ill patiEnt

EOLE
Start date: March 28, 2018
Phase:
Study type: Observational

The purpose of this multicentric study is to evaluate the perception of the quality of the end of life in intensive care units seen from the side of the caregivers, trough the CAESAR scale.

NCT ID: NCT03264365 Completed - Clinical trials for Intensive Care Unit Syndrome

The Effectiveness of a Post-ICU Recovery Program on Relatives

RAPIT-II
Start date: December 15, 2012
Phase: N/A
Study type: Interventional

Relatives of intensive care patients are at risk of developing symptoms of anxiety, depression and post-traumatic stress disorder resulting in impaired health-related quality of life (HRQOL). Recovery programs have been tested, but its effectiveness is sparse. The hypothesis is that relatives to former intensive care patients will improve their HRQOL one year after intensive care. We want to determine whether relatives to former intensive care patient's benefits from a recovery programme with improved HRQOL, Sense Of Coherence (SOC) and symptoms of anxiety, depression and PTSD compared to standard care one year after intensive care.

NCT ID: NCT03124342 Completed - Clinical trials for Intensive Care Unit Syndrome

Vanderbilt ICU Recovery Program Pilot Trial

VIP
Start date: May 1, 2017
Phase: N/A
Study type: Interventional

Every year, millions of Americans are admitted to the intensive care unit. Due to advances in critical care, mortality rates are decreasing, increasing the number of ICU survivors. Survivors of critical illness, however, often face physical, functional, and cognitive deficits that place them at risk for a cycle of re-hospitalization that frequently culminates in premature death. Moreover, post-ICU interventions may be resource-intensive and may be most cost-effective only in a subgroup of patients at highest risk. Whether a multi-disciplinary program to facilitate recovery from critical illness can prevent hospital readmission and improve quality of life among high-risk ICU survivors remains unknown. The primary aim of this pilot is to examine the feasibility of implementing a multidisciplinary ICU Recovery Program and the influence of such a program on process measures including contact with the ICU recovery team and attendance of ICU recovery clinic. The secondary aims are to compare the effect of an ICU Recovery Program on 30-day same-hospital readmission and other clinical outcomes.

NCT ID: NCT03055169 Completed - Hyperglycemia Clinical Trials

TCF7L2 Polymorphisms Influence on Glycemic Control in ICU Patients With Organ Failure

READIAB-G4
Start date: April 2012
Phase:
Study type: Observational

This study evaluates the link between genetic polymorphisms as r7903146, rs12255372 of TCF7L2 gene and the risk of developing hyperglycemia during Intensive care unit stay

NCT ID: NCT03050021 Completed - Delirium Clinical Trials

Risk Factors for Delirium in Critically Ill Surgical Patients

Start date: April 1, 2013
Phase: N/A
Study type: Observational

Delirium is characterized by changes in mental status, inattension, disorganized thinking, and altered consciousness. Prevalence of delirium in critically ill patients has varied from 20~80% depending on the severity of illness. Despite its high prevalence, delirium is often under-recognized by clinicians due to the difficulties in diagnosis and no interest. Delirium is associated with increased mechanical ventilation days, hospital length of stay, and mortality. The purpose of this study is to analyze the prevalence of delirium and risk factors for delirium in critically ill surgical patients.