ZASUSLocally Adapted Stroke Unit for Improved Outcomes in Lusaka, Zambia
This study aims to improve stroke outcomes by evaluating the proportion of clinical practice guidelines followed during your inpatient admission in a locally adapted stroke unit in Lusaka, Zambia.
Stroke Unit
Brain Diseases+4
+ Cardiovascular Diseases
+ Central Nervous System Diseases
Services Research Study
Summary
Study start date: October 25, 2024
Actual date on which the first participant was enrolled.This study aims to evaluate a new system of stroke care at the University Teaching Hospital in Lusaka, Zambia, to see if it can improve outcomes for people who have had a stroke. Stroke is a major health issue in Zambia and worldwide, especially in low- and middle-income countries where most stroke-related deaths and disabilities occur. The new system is designed to be locally relevant by considering unique risk factors and the resources available in Zambia. This research is important because it could lead to better stroke care and reduce deaths and disabilities in Zambia and potentially in other similar settings. Participants in this study will be adults who have experienced a stroke and are admitted to the hospital in Lusaka. The study will compare the results of stroke care under the new guidelines with past care practices to see if there is an improvement in the quality of care and patient outcomes. Researchers will look at how well the hospital follows the new stroke care guidelines and measure in-hospital and post-discharge mortality rates. The study does not involve any new drugs or acute stroke treatments but focuses on improving the organization and delivery of stroke care. If successful, the findings could help improve stroke care systems in other similar regions.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.300 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Services Research Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location