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Recruiting NCT05912413

Predicton of Sepsis Recovery Performance Subtypes Pilot Study

Observational Sepsis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: there is no intervention.
Who it may be relevant to
Registry conditions: Sepsis. Basic parameters: 18 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Prediction of Sepsis Recovery Physical Performance Subtypes: A Pilot Study

Overview

This study addresses critically ill sepsis patients' current literature reports of ongoing post-hospital discharge weakness and hospital readmissions. This study is aimed at capture and interpretation of a complex set of tests, administered during a subject's sepsis functional recovery trajectory, particularly capturing hospital readmission's effects on survivors' physical function recovery.

Detailed description

Patients with Sepsis who require ICU care, experience frequent weakness, physical dysfunction, fatigue, difficulty concentrating, poor memory, and mental morbidity that persists after hospital discharge. This syndromic pattern has been labeled as Post Intensive Care Syndrome (PICS) or Post Sepsis Syndrome (PSS). These patients are at increased risk of rehospitalization (up to 40% at 6 months). Studies have pointed out that sepsis survivors recover within several different recovery patterns or trajectories. Unfortunately there are no objective biomarkers early in these patients' hospitalizations, to predict which physical function trajectory a sepsis survivor will experience. However, a very common, unifying symptom of sepsis survivors is weakness. The literature maintains that an intervention of exercise rehabilitation remains a safe and potential therapy for sepsis survivors. It is important to note that as of yet, there has been no benefit demonstrated when highly heterogeneously functioning survivors are included in studies of a uniform rehabilitation intervention. However, for the future designs of ICU and post-hospital ICU Survivor exercise-rehab trials, the field is in need of information on how to label sepsis patients by their predicted outpatient recovery trajectory group, and to be able to do so very proximally in their course, prior to hospital discharge. The intent of this study is to closely track and characterize physical function recovery trajectory groups as a means of informing strategies for effective future study design.

Interventions

  • Other there is no intervention
    there is no intervention

Primary outcome measures

  • Short Performance Physical Battery [Time frame: 3 months post hospital discharge]

Eligibility criteria

Inclusion criteria

  • Sepsis requiring organ support in an ICU setting

Exclusion criteria

  • inability to obtain informed consent
  • the attending physician reports that the patient's goals of care are transitioning to palliation/withdrawal of life-sustaining therapy
  • recent cancer therapy in the last 12 months
  • age >80
  • plans to be discharged on mechanical ventilation to a Long Term Acute Care Hospital
  • planned discharge to rehabilitation facility, long-term hospital or nursing home.
  • Pregnancy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • University of Alabama at Birmingham (UAB) Hospital — Birmingham

Identifiers

NCT: NCT05912413 · IRB-300010502-003 · CTSA

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗