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NCT Number: NCT07610239

Evaluation of an Information Management and Communication System for Population-wide Point-of-Care Infant Sickle Cell Disease Screening

A cluster randomized trial (CRT) of the novel sickle cell disease (SCD), M-health based SCD Information Management and Communication system SIMCS vs routine new born screening strategy in health care centres in Uganda to evaluate impact on access screening, coordination of care and clinical outcomes

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Nalufenya Childrens

Jinja, Uganda

Location status: Recruiting

Location contact

Emmanuel Tenywa

CONTACT

[email protected]

0703672573

Nelson Sewankambo

PRINCIPAL_INVESTIGATOR

Ruth Namazzi

SUB_INVESTIGATOR

About this study

We will conduct a cluster randomized trial (CRT) of the novel SCD SIMCS and utilize a logical framework of measurable indicators of barriers, utilization, mediating factors, and clinical outcomes of SCD screening and care to evaluate its impact. We will randomize health facilities rather than individual patients because it would be impossible to avoid contamination if we randomized individuals. This design is ideal for evaluating the effectiveness of systems level interventions.

Study procedures Trial Intervention. SCD SIMCS APP, which is an AI-enhanced mobile platform that captures, interprets and relays results of point of care tests for SCD to health care providers and to a centralised public data server at the Uganda Ministry of Health. The SCD SIMCS app prototype consists of four modules: (1) ID module - captures child's demographic and biometric data and builds a printable QR-code; (2) Assay module - captures HemoTypeSCTM and the Sickle Scan TM test image, interprets, and transmits results to the CPHL data centre; (3) Education module - stores and plays back short educational videos for pre- and post-screening counselling; (4) SCD e-Passport module - entry and display of child's longitudinal salient clinical information.

Baseline assessment; following stratified purposive sampling and consent from community leaders, Control and Experimental HCs will undergo baseline evaluation with regards to current resources and childcare visit workflows and the availability of the data sources and measurable indicators of interest. A baseline assessment of resources, workflows, and routine source data collection systems at the centres will facilitate implementation planning for the proposed SCD SIMCS and accurate measurement of its impact on the HCs.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Providers of child health and maternity services at selected hospitals Infants born or attending child health and maternity services at selected hospitals . Infants are the targeted age-group in this study because this is the ideal age to screen for SCD and prevent complications and mortality that generally occurs early, by 5 years old. The infants will be recruited at birth or at vaccination visits

Exclusion criteria

  • Decline of inability to provide informed consent

Treatment and study plan

Sickle Cell Disease screening information management and communication system

Other

Mobile Health information managment system

Primary outcomes

  1. Improved number and timeliness of refferal of infants with sickle cell disease for care

    Time frame: 12 months

    proportion with positive sickle cell disease screen recievign conformatory SCD test,penicillin , hydroxyurea

  2. Ajusted Mortality Rate of children with sickle cell disease

    Time frame: 18 months

    Evaluate the impact of the SCD SIMCS on access to screening.

Study contacts

Contact information is provided by the study sponsor or research team.

Mwanje Kavuma Mwanje

CONTACT

[email protected]

+256783132151

Sponsors and collaborators

Lead sponsor

Makerere University

Other

Collaborators

  • National Institutes of Health (NIH)

Registry information

Acronym: SMICS

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
May 27, 2026
Registry last updated
May 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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