NCT07070310

Brief Summary

In this longitudinal cohort study the incidence of delirium is assessed for all patients being admitted to the acute intensive neurological-neurosurgical rehabilitation over 3 years. Delirium assessment will be performed daily from admission to discharge. Patients will be divided into 3 groups, according to the presentation of delirium on admission, during the course or not any during the stay in acute rehabilitation and compared regarding the treatment and outcome.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
210

participants targeted

Target at P75+ for all trials

Timeline
34mo left

Started Aug 2025

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress21%
Aug 2025Feb 2029

First Submitted

Initial submission to the registry

July 8, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

July 17, 2025

Completed
29 days until next milestone

Study Start

First participant enrolled

August 15, 2025

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 15, 2028

Expected
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

February 15, 2029

Last Updated

July 22, 2025

Status Verified

July 1, 2025

Enrollment Period

3 years

First QC Date

July 8, 2025

Last Update Submit

July 17, 2025

Conditions

Neurological Conditions

Outcome Measures

Primary Outcomes (1)

  • incidence of delirium

    3 years

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients in Neurosurgical rehabilitation

You may qualify if:

  • Any patient admitted to acute neurological-seurosurgical rehabilitation

You may not qualify if:

  • : patients with level of consciousness of coma or vegetative state

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Herz-Kreislauf-Zentrum Klinikum Hersfeld Rotenburg GmbH, Klinik für Neurologie und Neurologische Rehabilitation

Rotenburg an der Fulda, 36199, Germany

Location

Central Study Contacts

Caroline Renner, Priv.-Doz. Dr. med

CONTACT

+49-6623-88-0c.renner@hkz-rotenburg.de

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Head of Clinical Research Institute

Study Record Dates

First Submitted

July 8, 2025

First Posted

July 17, 2025

Study Start

August 15, 2025

Primary Completion (Estimated)

August 15, 2028

Study Completion (Estimated)

February 15, 2029

Last Updated

July 22, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

Locations

DE(1)