Clinical trials

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Condition / disease
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Status: Not yet recruiting

The Feasibility and Acceptability of a Post-tuberculosis Lung Disease Diagnostic Algorithm in Uganda.

The goal of this clinical trial is to determine whether a structured diagnostic algorithm improves the identification and referral of people with post-tuberculosis lung disease (PTLD) in primary healthcare facilities in Uganda. The clinical trial will, in addition, assess how feasible and acceptable it is for health workers to use this algorithm as part of routine care. The main trial questions are: * Does the diagnostic algorithm increase identification and referral of patients with suspected PTLD compared to standard care? * Is the algorithm feasible to implement and acceptable to health providers and patients in real-world primary health care settings? The research team will compare four health centre level III (HCIII) facilities ( two using the diagnostic algorithm and two using standard care) to see if the algorithm helps with early diagnosis and referral of PTLD. Health centre level III in Uganda are the primary health facilities and have provision for tuberculosis treatment. Participants will be screened for PTLD at the time they complete tuberculosis treatment at their local health facility. At intervention sites, participants will undergo assessment using a structured PTLD diagnostic algorithm developed in earlier stages of this research. The algorithm will be based on a symptom questionnaire and clinical criteria. At control sites, participants will be evaluated using standard practices (consensus clinical definition only). Participants clinically suspected to have PTLD. will be referred to Mbarara Regional Referral Hospital. Primary care health facilities will: * Be randomly assigned to use either the diagnostic algorithm or standard care. * Receive a baseline training on PTLD and ongoing support through monthly video conference * Submit triplicate referral forms to track referrals.

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Mbarara University of Science and TechnologyUpdated: Jul 16, 2025Locations: 1
Eligibility criteria

Located within a 10 km radius of Mbarara Regional Referral Hospital (MRRH). [+8]

It declines to participate or cannot commit to consistent follow-up activities. [+5]

Status: Recruiting

A Social Media Intervention to Improve Retention in Care for Adolescents and Young Adults With HIV in Uganda

Adolescents and young adults with HIV (AYWH) aged 15- 24 years are the fastest-growing population of people living with HIV worldwide. AYWH have worse outcomes along the HIV continuum of care than adults with HIV; HIV/AIDS is the second leading cause of mortality and the fourth leading cause of disability among AYWH worldwide. This study will develop a youth-friendly, mobile health (mHealth) intervention to improve retention in care that has the potential to improve AIDS-related mortality and morbidity among AYWH and decrease onward new transmission, thus contributing towards ending the HIV/AIDS pandemic.

Participants needed: 105
Trial details
Age: 15+Biological sex: AllType: InterventionalSponsor: Mbarara University of Science and TechnologyUpdated: May 18, 2025Locations: 1
Eligibility criteria

AYWH who are aged 15-24 [+3]

Clinic counsellors who are ≥18 years [+1]

Status: Recruiting

Mobile Health Intervention (Support-moms) in Antenatal Care to Improve Maternal Health in Uganda

High maternal mortality is a major public health problem in many settings. Because of low antenatal care (ANC) and skilled birth usage, Ugandan women and their children suffer from high maternal and perinatal mortality. The investigators developed a promising intervention (Support-Moms app) that shares targeted health information, and engages social support networks through scheduled reminders to help support pregnant women to utilize maternity services in rural Uganda. The investigators now propose to test and implement the Support-Moms intervention and hypothesize that Support-Moms will be feasible and cost-effective in improving utilization of available maternity care services, and ultimately reduce maternal and perinatal mortality.

Participants needed: 1,680
Trial details
Age: 10-65Biological sex: AllType: InterventionalSponsor: Mbarara University of Science and TechnologyUpdated: Aug 5, 2024Locations: 2
Eligibility criteria

are in the first trimester of pregnancy who have not yet presented for ANC [+6]

do not own a cell phone for personal use with reported reliable reception [+6]