Determinants of Rehabilitation Outcomes in Survivors of Primary Subarachnoid Haemorrhage

Subarachnoid Hemorrhage, Spontaneous Clinical Trial

— DETERMINESAH  

Official title:

Determinants of Rehabilitation Outcomes in Survivors of Primary Subarachnoid

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04357626
• Other study ID #: DSRB 2019/00594
• Status: Completed
• Start date: August 6, 2019
• Est. completion date: September 15, 2019

Study information

• Verified date: April 2020
• Source: Tan Tock Seng Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

A retrospective, observational single centre study of electronic medical records of discharged patients who were admitted to from 1 January 2015 to 31 December 2018.

Period of data collection was from 5 August 2019 to 15 September 2019.

Description:

The objectives of this study were to describe a local cohort of acute SAH survivors during inpatient rehabilitation at a single tertiary rehabilitation centre in Singapore and identify early predictors impacting discharge rehabilitation outcomes.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 114
• Est. completion date: September 15, 2019
• Est. primary completion date: September 15, 2019
• Gender: All
• Age group: 21 Years to 85 Years

Eligibility

Inclusion Criteria:

• 1. Spontaneous, first-ever SAH diagnosed by admitting neurosurgeons and confirmed on neuroimaging (CT or magnetic resonance imaging) 2. Transferred from acute care facilities or admitted from clinics to TTSH RC 3. Ages between 21 - 85 years 4. Duration of SAH to rehabilitation admission =6 months

Exclusion Criteria:

• 1. No radiological evidence of SAH 2. Traumatic SAH 3. Previous diagnosis of SAH 4. Main reason for admission into TTSH RC was not for inpatient rehabilitation (e.g. wound care, medical or social admission)

Related Conditions & MeSH terms

• Hemorrhage
• Subarachnoid Hemorrhage
• Subarachnoid Hemorrhage, Spontaneous

Intervention

Other:
• Inpatient Rehabilitation
Observational electronic records review study during inpatient rehabilitation

Locations

Country	Name	City	State
Singapore	Tan Tock Seng Hospital	Singapore
Singapore	Tan Tock Seng Hospital Rehabilitation Centre	Singapore

Sponsors (1)

Lead Sponsor	Collaborator
Tan Tock Seng Hospital

Country where clinical trial is conducted

Singapore, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Functional Independence Measure (FIM score)	The FIM, scored between 18 - 126, comprises of 18 items (motor and cognitive sub scores) which assesses a patient's degree of disability and indicates the degree of assistance required for activities of daily living. FIM scoring is widely used for functional scoring in patients with neurologic pathologies such as stroke or traumatic brain injury. Studies on its utility have shown high reliability, validity, and sensitivity for measuring functional ability and high consistency with other functional scales such as the Barthel Index	Within 72 hours of discharge from rehabilitation
Secondary	FIM Change	Difference between FIM discharge and admission	Within 72 hours of admission and discharge from rehabilitation