- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07371741
PICS Clinic Attendance and Recovery Engagement (PICS-CARE)
February 10, 2026 updated by: Claudia Spies, Charite University, Berlin, Germany
To identify relevant factors influencing attendance at appointments at the PICS outpatient clinic after intensive care treatment in order to derive targeted measures to increase the participation rate or send more targeted invitations.
Study Overview
Status
Recruiting
Conditions
Detailed Description
This retrospective study examines which factors influence patient attendance at structured follow-up appointments after intensive care treatment in the PICS outpatient clinic at Charité.
The focus is on analyzing demographic, clinical, and care-related factors that influence actual participation in follow-up care after intensive care treatment.
Study Type
Observational
Enrollment (Estimated)
2500
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Claudia Spies, MD, Prof.
- Phone Number: +49 30 450 551102
- Email: claudia.spies@charite.de
Study Locations
-
-
-
Berlin, Germany, 13353
- Recruiting
- Department of Anesthesiology and Intensive Care Medicine (CCM/CVK), Charité - Universitätsmedizin Berlin
-
Contact:
- Claudia Spies, MD. Prof.
- Phone Number: +49 30 450 55 11 02
- Email: claudia.spies@charite.de
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Principal Investigator:
- Claudia Spies, MD, Prof.
-
Sub-Investigator:
- Nicolas Paul, MD, Prof.
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Sub-Investigator:
- Björn Weiß, MD, Prof.
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Sub-Investigator:
- Désirée Boehnke, MD
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Sub-Investigator:
- Claudia Denke
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Sub-Investigator:
- Frédéric Schwarz
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
Intensive Care unit patients, who were invited for follow-up care by the PICS outpatient clinic of the Department of Anesthesiology and Intensive Care Medicine (CCM/CVK)
Description
Inclusion Criteria:
- Patients who, between January 1, 2021, and December 31, 2025:
- were invited for follow-up care by the PICS outpatient clinic of the Department of Anesthesiology and Intensive Care Medicine (CCM/CVK)
- were ≥18 years old at the time of the appointment.
Exclusion Criteria:
- none
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Intensive care unit patients
Intensive care unit patients, which are invited in the post-intensive care outpatient clinic
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Follow-up appointment
Time Frame: 01.01.2021- 31.12.2025
|
Participation in the first scheduled follow-up appointment at the post-intensive care syndrome (PICS) outpatient clinic (binary: attended vs. did not attend) is measured by medical record review.
|
01.01.2021- 31.12.2025
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cancellation of a scheduled follow-up appointment.
Time Frame: 01.01.2021- 31.12.2025
|
Cancellation of a scheduled follow-up appointment is measured by medical record review.
|
01.01.2021- 31.12.2025
|
|
Reasons for canceling a scheduled appointment.
Time Frame: 01.01.2021- 31.12.2025
|
Reasons for canceling a scheduled appointment is measured by medical record review.
|
01.01.2021- 31.12.2025
|
|
Failure to attend a scheduled follow-up appointment.
Time Frame: 01.01.2021- 31.12.2025
|
Failure to attend a scheduled follow-up appointment is measured by medical record review.
|
01.01.2021- 31.12.2025
|
|
Death after discharge from the intensive care unit until the first follow-up appointment.
Time Frame: 01.01.2021- 31.12.2025
|
Death after discharge from the intensive care unit until the first follow-up appointment is measured by medical record review.
|
01.01.2021- 31.12.2025
|
|
Death between the first and second follow-up appointments.
Time Frame: 01.01.2021- 31.12.2025
|
Death between the first and second follow-up appointments is measured by medical record review.
|
01.01.2021- 31.12.2025
|
|
Scheduling a second follow-up appointment after initial presentation at the outpatient clinic.
Time Frame: 01.01.2021- 31.12.2025
|
Scheduling a second follow-up appointment after initial presentation at the outpatient clinic is measured by medical record review.
|
01.01.2021- 31.12.2025
|
|
Attendance at the second scheduled follow-up appointment after initial presentation at the outpatient clinic.
Time Frame: 01.01.2021- 31.12.2025
|
Attendance at the second scheduled follow-up appointment after initial presentation at the outpatient clinic is measured by medical record review.
|
01.01.2021- 31.12.2025
|
|
Scheduling a third follow-up appointment after initial presentation at the outpatient clinic.
Time Frame: 01.01.2021- 31.12.2025
|
Scheduling a third follow-up appointment after initial presentation at the outpatient clinic is is measured by medical record review.
|
01.01.2021- 31.12.2025
|
|
Attendance at the third scheduled follow-up appointment after initial presentation at the outpatient clinic.
Time Frame: 01.01.2021- 31.12.2025
|
Attendance at the third scheduled follow-up appointment after initial presentation at the outpatient clinic is measured by medical record review.
|
01.01.2021- 31.12.2025
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Claudia Spies, MD, Prof., Charite University, Berlin, Germany
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 10, 2026
Primary Completion (Estimated)
February 1, 2027
Study Completion (Estimated)
February 1, 2027
Study Registration Dates
First Submitted
January 19, 2026
First Submitted That Met QC Criteria
January 19, 2026
First Posted (Actual)
January 28, 2026
Study Record Updates
Last Update Posted (Actual)
February 12, 2026
Last Update Submitted That Met QC Criteria
February 10, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PICS-CARE
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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