NCT02671916

Brief Summary

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. One year after the ICU stay patients will be send a Quality of Life questionnaire they need to fill out and return. All data will be evaluated together.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
55

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jan 2015

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2015

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

August 17, 2015

Completed
6 months until next milestone

First Posted

Study publicly available on registry

February 2, 2016

Completed
2.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2018

Completed
Last Updated

March 6, 2019

Status Verified

March 1, 2019

Enrollment Period

3.9 years

First QC Date

August 17, 2015

Last Update Submit

March 4, 2019

Conditions

Critically Ill

Keywords

QoL and Survival one year after ICU stay

Outcome Measures

Primary Outcomes (1)

  • Survival

    1 year after ICU discharge

Study Arms (1)

all patients

questionnaire for patients with ICU stay at least 5 days or longer without interruption at the ICU

Behavioral: questionnaire

Interventions

questionnaireBEHAVIORAL

Investigation on all study patients, no Intervention, no groups

all patients

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

all patients with conditions that lead to an ICU stay

You may qualify if:

  • patients who are at least 5 days or longer without interruption at the ICU

You may not qualify if:

  • patients with less than 4 days at the ICU

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Klinik Hirslanden

Zurich, Canton of Zurich, 8032, Switzerland

Location

MeSH Terms

Conditions

Critical Illness

Interventions

Surveys and Questionnaires

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Christoph Haberthür, MD

    Klinik Hirslanden, Zurich

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
1 Year
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Prof. Dr. med.

Study Record Dates

First Submitted

August 17, 2015

First Posted

February 2, 2016

Study Start

January 1, 2015

Primary Completion

December 1, 2018

Study Completion

December 1, 2018

Last Updated

March 6, 2019

Record last verified: 2019-03

Data Sharing

IPD Sharing
Will not share

Locations

CH(1)