- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05807269
Prevention and Rehabilitation of Stroke in Uganda
Stroke is increasing in low-income countries in Africa, and knowledge is lacking on risk factors and how to prevent stroke as well as how to best use the resources for rehabilitation after stroke which are very limited. Knowledge generation within this area is therefore urgently needed. This collaboration between the research group HELD (Health and Everyday Life among people with neurological Disorders), Karolinska Institutet (KI) and the research surveillant site Africa Medical and Behavioral Sciences Organization (AMBSO) population health surveillance (PHS), will create substantial research opportunities to develop and improve prevention and rehabilitation for stroke, which is in line with the sustainable development goals to reduce the prevalence and mortality rates due to NCDs. AMBSO is collecting data from 17 000 households on many potential risk factors for stroke. Questions about stroke primary and secondary prevention of stroke and impact of stroke or need of rehabilitation could be added to the existing questionnaires such as the validated Ugandan version of the Stroke Impact Scale. This is intended to fulfill the aim of the network which is to increase the knowledge of occurrence and consequences of NCDs with a specific focus on stroke, which will be valuable for the development of preventive healthcare policy documents and guidelines for appropriate prevention strategies and rehabilitation interventions.
Research questions in relation to NCDs with focus on stroke prevention and rehabilitation:
- How many cases (prevalence) are reported in the targeted study sites and what is the mortality rate (incidence) that can specifically relate to stroke?
- How does stroke and other NCDs affect and impact the quality of life for persons living in Uganda?
- Which factors impact the recovery process after stroke?
- What sort of rehabilitation is needed in the study areas for persons affected by stroke? In addition, risk factors of stroke such as diabetes and hypertension will be mapped.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Gunilla Eriksson, PhD
- Phone Number: +46702216924
- Email: gunilla.eriksson@ki.se
Study Locations
-
-
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Hoima, Uganda
- Recruiting
- AMBSO, Hoima
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Contact:
- Conrald Kalibagwa
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Kampala, Uganda
- Recruiting
- AMBSO, Wakiso
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Contact:
- Conrald Kalibagwa
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Stroke
- Risk factors for stroke: hypertension, diabetes, HIV, malaria, physical inactivity, obesity
Exclusion Criteria:
- Not having had stroke and/or having no risk factor for stroke
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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People with stroke
Participants with stroke or risk factors for stroke
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Stroke Impact Scale-16
Time Frame: At one assessment point during 2023-2024
|
Questionnaire comprising 16 statements concerning perceived impact of stroke.
Each item is rated on a scale from 0 (high impact) to 5 (no impact).
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At one assessment point during 2023-2024
|
Stroke Impact Scale, perceived recovery
Time Frame: At one assessment point during 2023-2024
|
Perceived recovery after stroke is rated on a visual analogue scale ranging from 0 (no recovery) to 100 (full recovery).
|
At one assessment point during 2023-2024
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Life Satisfaction Checklist (LISat-11)
Time Frame: At one assessment point during 2023-2024
|
Questionnaire that assesses life satisfaction with one global item "Life as a whole", and 9 domain-specific items.
Answering alternatives range from 1 (very dissatisfied) to 6 (very satisfied)
|
At one assessment point during 2023-2024
|
Patient Health Questionnaire-9
Time Frame: At one assessment point during 2023-2024
|
Questionnaire with nine items that inquire about the frequency of depressed mood and anhedonia over the past two weeks.
Score ranges from 0 (not at all) to 6 (nearly every day) where higher scores indicate higher frequency of depressed mood
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At one assessment point during 2023-2024
|
Generalized Anxiety Disorder Assessment-7
Time Frame: At one assessment point during 2023-2024
|
A questionnaire assessing generalized anxiety disorder.
The GAD-7 score is calculated by assigning scores of 0, 1, 2, and 3, to the response categories of 'not at all', 'several days', 'more than half the days', and 'nearly every day', respectively, and adding together the scores for the seven questions.
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At one assessment point during 2023-2024
|
Health Literacy Questionnaire
Time Frame: At one assessment point during 2023-2024
|
Questionnaire that assesses health literacy.
The Health Literacy Questionnaire contains 44 items, which are divided into nine areas of health literacy.
The first five scales are scored on a 4-point Likert scale (ranging from strongly disagree to disagree, agree, and strongly agree), building part I.
The other four scales, representing part II, are scored on a 5-point Likert scale where respondents are asked to rate the level of difficulty in undertaking a task (ranging from cannot do, always difficult, usually difficult, sometime difficult, usually easy, and always easy).
Higher scores indicate better health literacy.
In total six selected questions from part I and part II are used.
|
At one assessment point during 2023-2024
|
Use of health care services
Time Frame: At one assessment point during 2023-2024
|
Six questions on use of healthcare services, and information received on stroke and its consequences.
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At one assessment point during 2023-2024
|
Question about quality of life
Time Frame: At one assessment point during 2023-2024
|
The respondents are asked to rate their quality of life on a on a five-point scale from 1 (very poor) to 5 (very good)
|
At one assessment point during 2023-2024
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Gunilla Eriksson, PhD, Karolinska Institutet
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022-04303
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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