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Brazilian Intervention to Increase Evidence Usage in Practice - Stroke (BRIDGE-Stroke) (BRIDGEStroke)

H

Hospital do Coracao

Status

Completed

Conditions

Acute Ischemic Stroke

Treatments

Behavioral: Multifaceted Strategy

Study type

Interventional

Funder types

Other

Identifiers

NCT02223273
BRIDGE-Stroke

Details and patient eligibility

About

Phase 1: An observational study ( registry) will be conducted with the objective of documenting the practice of stroke treatment in brazilian and latin american hospitals.

Phase 2: A cluster randomized trial aiming to evaluate the effect of a multifaceted strategy to increase evidence based treatments usage for stroke patients. The hospitals will be randomized into two groups: the multifaceted strategy group and the usual care group.

Full description

Study Objective: The purpose of this study is to evaluate a multifaceted strategy to increase evidence based therapies for patients with acute ischemic stroke.

Study Population; Patients with suspected stroke or transient ischemic attack (TIA) with symptoms lasting up to 24h hours.

Quality Improvement Multifaceted Intervention: The strategy includes a simulation based team training, case manager, check lists, reminders and educational material.

Enrollment

1,624 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Patient Eligibility Criteria

Inclusion Criteria:

  • Patients over 18 years old, diagnosed with ischemic stroke (including transient ischemic attack) with symptoms lasting up to 24 hours.

Exclusion Criteria:

  • Patients with signs of hemorrhagic stroke, expansive lesions, central nervous system infections, and those coming from institutions that did not provide institutional approval form signed by the patients' guardians.

Cluster Eligibility Criteria

Inclusion Criteria:

  • Hospitals with a emergency department, with available tomography, neurologist and alteplase

Exclusion Criteria:

  • Hospitals that don't provide Institutional Authorization Form

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

1,624 participants in 2 patient groups

Multifaceted Strategy
Experimental group
Description:
Multifaceted Intervention 1. Simulation Based Team Training 2. Case Manager 3. Check lists 4. Reminders 5. Educational Materials
Treatment:
Behavioral: Multifaceted Strategy
Usual Care
No Intervention group
Description:
Hospital Standard Treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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