the Incidence and the Association Between Motor Subtypes and Outcome of Delirium in Ischemic Stroke Patients

Delirium Clinical Trial

Official title:

the Prospective Study on the Incidence and the Association Between Motor Subtypes and Outcome of Delirium in Ischemic Stroke Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03317106
• Other study ID #: 2017-07-058
• Status: Completed
• Start date: August 8, 2017
• Est. completion date: August 31, 2018

Study information

• Verified date: July 2021
• Source: Chungnam National University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

this study examines the incidence of newly developed delirium in patients who admit to university hospital stroke unit for cerebral infarction, and analyze the association between delirium motor subtypes and short-term outcome in post-stroke delirium patients.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 943
• Est. completion date: August 31, 2018
• Est. primary completion date: March 31, 2018
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• All cerebral infarction patients who admit to stroke unit Chungnam National University Hospital.

Exclusion Criteria:

• Any patients who refuse to enroll the study.
• Any patients who admit to Intensive Care Unit(ICU), because ICU is well-known for precipitating delirium.

Related Conditions & MeSH terms

• Cerebral Infarction
• Delirium
• Infarction

Locations

Country	Name	City	State
Korea, Republic of	Chungnam National University Hospital	Daejeon	Munhwa-ro 282, Jung-gu

Sponsors (1)

Lead Sponsor	Collaborator
Chungnam National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	mean K-DRS-R98 score	mean score of delirium severity rating scale during follow up period. Detailed information about scale: Korean Version of the Delirium Rating Scale-Revised-98(K-DRS-R98) DRS-R98 proved to be a valid and reliable instrument for the assessment of delirium severity and distinguish patients with delirium from non-delirious patients including dementia. The scale is composed of two sections. The first section is the severity scale, which consists of 13 items that are scored from 0 to 3 according to a Likert scale that is anchored by descriptions of phe-nomenology. The second section consists of three diagnostic items that are scored from 0 to 2 or 3. These items include temporal onset of symptoms, fluctuation of symptom severity and physical disorder. The total scale is comprised of 16 items. The total score is the sum of the scores for each item and the higher the score, the greater the severity.	3 weeks