Pontiano Kaleebu
ID: UNCST-2021-R013577
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Formative Usability Study Protocol of the Panbio™ Dengue Duo test with Fingerstick Sample Collection
REFNo: HS7731ES
The primary objectives of this usability study are
• To evaluate Health Care Professional users’ Panbio™ Dengue Duo test labelling comprehension and the usability of the supplied components as describe in the IFU in a Point of Care setting. This will be assessed through the user questionnaire and observation sheets.
• To assess which lancet generates the correct volume of blood to enable to user to collect two samples from the same fingerstick.
• To identify the optimal instruction and technique for using the plastic capillary tube to collect the 30 µL from a fingerstick and to understand the impact of fingerstick on the usability of the sample collection tools.
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Uganda |
2026-06-11 12:06:13 |
2029-06-11 |
Medical and Health Sciences |
Non-Clinical Trial |
Non-degree Award |
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Rhona Mijumbi M
ID: UNCST-2023-R006843
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Learning together to advance Evidence and Equity in Policymaking to achieve the SDGs in Africa (Africa LEEPS)
REFNo: SS5344ES
The overall objective is to strengthen evidence pathways at regional and national levels to ensure timely access to relevant, contextualized evidence, including gender analysis, for policymaking that enhances population wellbeing.,4. To build a culture of sustained evaluation, knowledge exchange, and learning within the LEEPS partnership and the partners within the EARESI. ,3. To design a platform structures and processes to support timely access and use of evidence response at regional level for gender equity and inclusion in policymaking to enhance population wellbeing.,2. To strengthen the sustained capacity of individuals and organisations in applying evidence and gender equity and inclusion in policymaking to enhance population wellbeing,1. To strengthen evidence pathways at a regional policymaking to strengthen timely access to relevant and contextualised evidence, including gender analysis, for informing decisions to enhance population wellbeing,
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Uganda |
2026-06-11 12:04:48 |
2029-06-11 |
Social Science and Humanities |
Non-Clinical Trial |
Non-degree Award |
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Pauline Byakika-Kibwika
ID: UNCST-2019-R001206
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Platform Adaptive Randomised Trial for NEw and Repurposed Filovirus treatmentS
REFNo: HS7849ES
To evaluate the impact of potential treatments on mortality in patients with filovirus disease. ,
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Uganda |
2026-06-08 21:31:41 |
2029-06-08 |
Medical and Health Sciences |
Clinical Trial |
Non-degree Award |
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Derrick Abila Bary
ID: UNCST-2020-R014563
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Feasibility, acceptability, and preliminary outcomes of childhood cancer survivor-delivered nurse-facilitated peer support model on anxiety and depression among adolescents newly diagnosed with cancer at Uganda Cancer Institute (UCI), Uganda
REFNo: HS7533ES
1) To co-design with stakeholders the TOGETHER implementation strategies for adolescents newly diagnosed with cancer at UCI, Uganda,To evaluate the feasibility, acceptability, appropriateness, and preliminary outcomes of TOGETHER (a peer-support intervention delivered by childhood cancer survivors and nurse facilitators) on anxiety and depression among adolescents newly diagnosed with cancer at the Uganda Cancer Institute (UCI).
2) To pilot test the TOGETHER implementation strategies among adolescents newly diagnosed with cancer at UCI, Uganda, using a hybrid type II effectiveness implementation trial design.
3) To assess the perceived barriers and facilitators of a childhood cancer survivor (CCS) delivered nurse-facilitated peer support model (TOGETHER) for adolescents newly diagnosed with cancer at UCI, Uganda.
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Uganda |
2026-06-08 16:16:30 |
2029-06-08 |
Medical and Health Sciences |
Non-Clinical Trial |
Non-degree Award |
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Derrick Abila Bary
ID: UNCST-2020-R014563
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COMPARATIVE STUDY OF THE CERVICAL CANCER SCREENING FOR PREVENTION AND CONTROL PROGRAM: A CASE OF MBARARA MBARARA/CITY VS GULU DISTRICT/CITY
REFNo: HS7800ES
Main Objective
1. To evaluate the effectiveness of cervical cancer screening interventions at intervention sites compared with control sites in Gulu City and Gulu District during the same period.
Specific Objectives
1. To determine the number and proportion of precancerous lesions detected among women screened for cervical cancer in the intervention sites and compare these with the control sites.
2. To compare screen-positive treatment rates in the intervention and control sites before and after the intervention.
3. To assess the investments (costs) made to facilitate cervical cancer screening in the intervention sites compared with the control sites.
4. To compare the level of cervical cancer knowledge, awareness, and practices between the women in the communities in the intervention and control sites.
5. To explore stakeholder perspectives on the implementation, acceptability, barriers, facilitators, and sustainability of cervical cancer screening service delivery in the intervention and control sites.
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Uganda |
2026-06-08 16:04:57 |
2029-06-08 |
Medical and Health Sciences |
Non-Clinical Trial |
Non-degree Award |
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