Essential Acute Stroke Care in Low Resource Settings: a Pilot studY

NCT04157231 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2025-03-06

No results posted yet for this study

Summary

An investigator-initiated, evaluator-blinded, prospective, multi centre, before-and-after, effectiveness-implementation hybrid design study to assess the feasibility of essential acute stroke care in a low resource setting

Conditions

  • Acute Stroke

Interventions

OTHER

Acute stroke care Intervention arm

Training and education of the site staff about the treatment protocol for the different components of the management plan will be provided on two occasions. The aim of these sessions will be to educate stroke champions and other site staff on the management protocols. Available training resources will be accessed (including online materials) and simulation training will be used. New skills such as dysphagia assessment will be emphasized based on existing knowledge and competencies. After training, staff will have another assessment (Post-test) in order to determine whether they have been adequately trained and are able to adhere to the essential acute stroke care management plan. A standardised Power Point presentation and accompanying handouts will be made available for further use in the ward. Refresher training will be provided monthly during the intervention.

Sponsors & Collaborators

  • World Heart Federation

    collaborator UNKNOWN
  • The George Institute

    lead OTHER

Principal Investigators

  • Carlos Abanto, Dr · National Institute of Neurological Sciences, Lima, Peru

  • Kolawawole Wahab, Professor · University of Ilorin & University of Ilorin Teaching Hospital Ilorin, Nigeria

  • Hasan Farhan, Professor · President of Iraqi Scientific Council of Cardiology,Iraq

  • Yi Sui, Dr · Shenyang First People's Hospital Hospital Affiliated Brain Hospital

  • Saima Hilal, A/Professor · National University of Singapore

  • Lily Song, Dr · The George Institute of Global Health, China

  • Craig Anderson, Professor · Executive Director The George Institute for Global Health - China

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-12-30
Primary Completion
2027-06-30
Completion
2027-12-30

Countries

  • Nigeria
  • Peru

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04157231 on ClinicalTrials.gov