Clinical trials: Post ICU Discharge
Family Resilience, Parent-Infant Bonding
Development and Evaluation of an Intelligent Parent-Infant Connection-Based Intervention to Strengthen Family Resilience in Preterm Infant Care
This study aims to develop, optimize, and evaluate the effectiveness of a family resilience intervention centered on intelligent parent-infant connection for parents of preterm infants.
- Conditions
- Family Resilience, Parent-Infant Bonding, Parents of Premature Infants, Intelligent Intervention
- Trial name
- NCT07373002
- Testing
- Intelligent Intervention to enhance Parent-Infant Connection and Family Resilience, Routine Care
- Volunteers
- 300 people, healthy volunteers welcome
- Sponsor
- National Defense Medical Center, Taiwan
Morbid Obesity in Cardiac Surgery Patients, Postoperative Respiratory Dysfunction
Prophylactic Use of APRV Before Extubation in Morbidly Obese Patients After Cardiac Surgery.
Morbidly obese patients undergoing open heart surgery are at increased risk of breathing problems after removal of the breathing tube due to reduced lung function and chest wall restriction following surgery.
- Conditions
- Morbid Obesity in Cardiac Surgery Patients, Postoperative Respiratory Dysfunction, Mechanical Ventilation Strategies
- Trial name
- APRV-OBESE-CS (NCT07409324)
- Testing
- Airway Pressure Release Ventilation (APRV), Conventional Lung-Protective Mechanical Ventilation
- Volunteers
- 180 people
- Sponsor
- Ain Shams University
COVID-19 Pandemic, ICU
Chronic Pain in COVID-19 Patients Discharged From Intensive Care Unit
More than six million French were affected by SARS-COV2 epidemic. About 20% of infected peoples were hospitalized, and about 5% were admitted to the intensive care units (ICU) for severe SARS-COV2 acute respiratory distress…
- Conditions
- COVID-19 Pandemic, ICU, Pain, Chronic, Post Intensive Care Unit Syndrome
- Trial name
- NCT04940208
- Testing
- Pain and neuropsychological questionnaires, Quantitative Sensory testing
- Where
- 3 sites in France
- Volunteers
- 143 people
- Sponsor
- Mikhail Dziadzko, MD, PhD
In-Hospital Mortality, Number of ICU Readmission
To Survive After ICU Discharge
Many factors before and after ICU stay determine the outcome of patients at ICU discharge, the type of illness, physical dependence and other sequelae can be a trigger for complications in hospital ward which can induce ICU…
- Conditions
- In-Hospital Mortality, Number of ICU Readmission, Number of Warnings On-duty
- Trial name
- NCT02599636
- Testing
- None intervention
- Where
- Spain
- Volunteers
- 1,200 people
- Sponsor
- Althaia Xarxa Assistencial Universitària de Manresa
Quality of Life, Post ICU Discharge
Study in Intensive Care Follow-up Programme in Improving Long-term Outcomes of ICU Survivors
Study Hypothesis: Critical illness is associated with long-term medical and psychological sequelae that can impact the professional and private life.
- Trial name
- SUIVI-REA (NCT01796509)
- Testing
- Medical, psychological, social
- Where
- France
- Volunteers
- 545 people
- Sponsor
- Assistance Publique - Hôpitaux de Paris
Adult Patients, Intensive Care Unit
Functional Recovery Over the First Year After ICU Discharge
Intensive Care Unit Acquired Delirium (ICU-AD) and Intensive Care Unit Acquired Weakness (ICU-AW) are common in critically ill, mechanically ventilated adult patients.
- Trial name
- NCT04206306
- Where
- Taiwan
- Volunteers
- 407 people
- Sponsor
- National Taiwan University Hospital
Sepsis, Post Intensive Care Unit Syndrome
Accelerating Recovery After ICU Admission: Post-discharge Supplementation With Pasteurized Akkermansia Muciniphila.
The goal of this clinical trial is to learn if daily oral supplementation with pasteurized Akkermansia muciniphila (PAM), an EFSA-approved food supplement, can support recovery in adults who have recently been treated in the ICU…
- Conditions
- Sepsis, Post Intensive Care Unit Syndrome, Critical Illness, Microbiome Dysbiosis
- Trial name
- PAM-ICU (NCT07295353)
- Testing
- Pasteurized Akkermansia muciniphila
- Volunteers
- 50 people
- Sponsor
- Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Critical Illness
User Experience of a Telemedicine Platform for the Follow-up of Post Intensive Care Syndrome (PICS)
Survivors of critical illness may present with a set of physical, emotional and cognitive sequelae, known as Post Intensive Care Syndrome (PICS).
- Trial name
- NCT06438380
- Volunteers
- 14 people
- Sponsor
- Corporacion Parc Tauli
Critical Illness, Mechanical Ventilation Complication
A Problem Solving Intervention for Post-ICU Cognitive Impairment in Older Adults
This study will apply an evidence based program to assist ICU survivors to overcome cognitive problems as a result of their critical illness.
- Conditions
- Critical Illness, Mechanical Ventilation Complication, Delirium, Cognitive Impairment
- Trial name
- PIC-UPS (NCT03972384)
- Testing
- Post-ICU Problem Solving
- Where
- United States
- Volunteers
- 19 people
- Sponsor
- Ohio State University
ICU Acquired Weakness, Intensive Care Neuropathy
Predictive Validity of the Chelsea Critical Care Physical Assessment Tool (CPAx) for Regaining Autonomy Three Months After ICU Discharge
This single-center observational study aims to explore the relationship between the CPAx score (Chelsea Critical Care Physical Assessment Tool), measured at ICU discharge, and the 6-minute walk test (6MWT) distance performed 3…
- Trial name
- CPAx-Predict (NCT07167121)
- Testing
- CPAx
- Where
- France
- Volunteers
- 29 people
- Sponsor
- Centre Hospitalier Intercommunal Elbeuf-Louviers-Val de Reuil
Post Intensive Care Unit Syndrome, Covid19
CPAx for Assessing Functional Status of COVID-19 Patients After Intensive Care Unit Discharge
The present assessment tools for assessing physical function after intensive care unit (ICU) can be categorized as (1) functional tests (2) walk tests (3) strength test (4) Health-related quality of life (HRQOL).
- Trial name
- NCT04762056
- Testing
- Chelsea Critical Care Physical Assessment Tool
- Where
- 2 sites in Turkey (Türkiye)
- Volunteers
- 16 people
- Sponsor
- Gaziosmanpasa Research and Education Hospital
Hospital Mortality
International Multicenter Study of In-hospital Outcome of Patients After ICU Discharge
Several patients die in the intensive care unit (ICU) due to their acute disease and comorbid conditions. Moreover, after ICU discharge, some ICU survivors still die in the wards.
- Trial name
- NCT02347150
- Where
- 3 sites in Portugal
- Volunteers
- 3,000 people
- Sponsor
- Hospital Vila Franca de Xira
Critical Care
Strengthening Hope After ICU Discharge
The goal of this clinical trial is to evaluate an interventional program that aims to strengthen hope in intensive care unit (ICU) patients in the rehabilitation phase.
- Trial name
- NCT06569901
- Testing
- Hope Intervention
- Where
- 3 sites in Norway
- Volunteers
- 75 people
- Sponsor
- Oslo University Hospital
Anemia, Post ICU Syndrome
Iron Deficiency at ICU Discharge
IRON-RECOVERY is a prospective, multicenter, observational cohort study designed to determine the prevalence of iron deficiency at intensive care unit (ICU) discharge and to evaluate its association with post-ICU clinical…
- Conditions
- Anemia, Post ICU Syndrome, Red Blood Cell Transfusions, Iron Deficiencies
- Trial name
- IRON-ICU (NCT07781540)
- Testing
- transferrin saturation
- Where
- 4 sites in Belgium, Italy
- Volunteers
- 462 people
- Sponsor
- Università degli Studi di Ferrara
Post Intensive Care Unit Syndrome
Feasibility of a Physiotherapy-led Follow-up Programme in Adult Critical Illness Survivors
Survivors of critical illness might suffer from ongoing physical, cognitive and emotional impairments after being discharged home. Furthermore, several studies have shown that these patients might have a need for ongoing support.
- Trial name
- NCT04175717
- Testing
- physiotherapy-led follow-up programme
- Where
- Switzerland
- Volunteers
- 3 people
- Sponsor
- Kantonsspital Winterthur KSW
Prematurity
Post-Discharge Growth of Infants Who Received Donor Human Milk Products in the Neonatal Intensive Care Unit (NICU)
Human milk feeding is associated with great benefits to the health and development of infants, especially in premature infants. Some mothers are unable or unwilling to provide breast milk to their infant.
- Trial name
- NICU (NCT01483079)
- Where
- United States
- Volunteers
- 51 people
- Sponsor
- Baylor College of Medicine
Critical Illness, Transitions of Care
Evaluating the Effectiveness of an Electronic Medical Transfer Tool to Improve Communication During Transfers From ICU
The transfer of patients from the intensive care unit (ICU) to a medical or surgical hospital ward is a particularly high risk transfer that may expose patients to complications or adverse events if there are communication…
- Trial name
- NCT03590002
- Testing
- Electronic ICU Medical Transfer Tool
- Where
- 4 sites in Canada
- Volunteers
- 1,751 people
- Sponsor
- Henry T. Stelfox, MD PhD
Critical Illness
Reducing Post-traumatic Stress Disorder After ICU Discharge With the IPREA3 Program
Reducing discomfort in the intensive care unit (ICU) should be beneficial to longterm outcomes. This study assesses whether a tailored multicomponent program for discomfort reduction may be effective in reducing post-traumatic…
- Trial name
- PTSD-REA (NCT03991611)
- Testing
- Administration of the IPREA3 questionnaire, Immediate feedback through electronic reminder messages, Targeted interventions in each ICU to reduce discomforts
- Where
- 33 sites in France
- Volunteers
- 3,312 people
- Sponsor
- Centre Hospitalier of Chartres
Critically Ill
Health and Quality of Life One Year After Discharge From the Intensive Care Unit (ICU)
The goal is to capture the Quality of life and survival of patients one year after the stay at ICU. Data will be collected during the stay in the ICU and evaluated.
- Trial name
- QoL_ICU (NCT02671916)
- Testing
- questionnaire
- Where
- Switzerland
- Volunteers
- 55 people
- Sponsor
- Prof. Dr. med. Cristoph Haberthür
Covid19, Neurocognitive Dysfunction
Long-term Neurocognitive and Psychiatric Consequences in Severe COVID-19 Survivors.
Long-term neurocognitive and psychiatric consequences of COVID-19 remain mostly unknown to date. It has been reported that coronaviruses cause direct central nervous system infection (Needham et al. 2020).
- Trial name
- NPQCOVID (NCT05019300)
- Testing
- Exposure: COVID-19 severity
- Where
- Chile
- Volunteers
- 80 people
- Sponsor
- Pontificia Universidad Catolica de Chile