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NCT06593080Recruiting

The DECIDE-TB Trial; Validation of Treatment Decision Algorithms for Childhood Tuberculosis

Validation of Treatment Decision Algorithms for Childhood Tuberculosis at District Health Care Levels in Mozambique and Zambia - the Decide-TB Cluster-randomized Pragmatic Trial

Source: ClinicalTrials.gov · Last updated 24 Mar 2026

Brief summary (registry, in English)

The Decide-TB project aims to generate evidence for the implementation of a comprehensive Treatment Decision Algorithms (TDA) based approach for TB in children living in high TB burden and resource-limited countries, at District Hospital (DH) and Primary Health Centre (PHC) levels, and to facilitate the integration of this evidence within practices and policies. This programmatic pilot led by the National TB Programs (NTP) will test a TDA-based approach integrating TB screening, diagnosis, treatment decision-making, and disease severity assessment for shorter treatment eligibility, for use at a lower level of healthcare. This TDA-based approach will be evaluated in a hybrid effectiveness implementation study based on a pragmatic stepped wedge cluster-randomized trial. The Decide TB project will be implemented at the district level, targeting five districts in each country. Each cluster in a district will be made up of one district hospital and six primary health centers. The study will develop a Clinical Decision Support System (CDSS) to operationalize the use of TDAs, and strengthen District Health Information Systems (DHIS2) to collect individual data, which will contribute to monitoring and evaluation, clinical mentoring, and supervision by the country's NTPs.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
30240 (estimated)
First submitted
1 Aug 2024
Start date
1 Jun 2024
Primary completion date
31 Aug 2027
Lead sponsor
Chishala Chabala
Diseases
Tuberculosis, HIV
NCT number
NCT06593080

What you commit to

  • Study type: Interventional
  • Planned participants: 30240
  • From 1 Jun 2024 to the primary completion date, 31 Aug 2027
  • 29 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • There will be no exclusion criteria for the programmatic pilot: all children will be offered the intervention.

Who the study is looking for

  • The effectiveness assessment will be conducted using aggregated or individual data from direct beneficiaries of the intervention:
  • All sick children aged below 15 years entering the selected health facilities (DH and PHC) at either outpatient (OPD) or inpatient (IPD) departments, including children from high-risk groups, as well as children identified as contact of TB cases through community- or facility-based household contact tracing.
  • Children with presumptive TB.
    • The WHO definition of presumptive TB will be used, as defined in the 2022 WHO Operational Handbook, namely: children are classified as having presumptive TB if they have unremitting symptoms lasting more than 2 weeks (any one of cough, fever, not eating well or anorexia, weight loss or failure to thrive, fatigue, reduced playfulness or decreased activity) .
    • The definitions of presumptive TB have been adapted locally for the programmatic pilot. All children with presumptive TB as defined locally will be considered in the intervention and in secondary effectiveness and sub-group analyses.
    • High-risk group will be defined using the definition in WHO-suggested TDAs A\&B as children younger than 2 years, CLHIV or children with SAM. CLHIV will be defined per national testing strategy including positive PCR test for children below the age of 18 months. Children will be considered to have SAM (and thereby be eligible for the TB-Speed SAM algorithm) using WHO criteria. These include being \<5 years with a weight-for-height Z score (WHZ) \< -3 SDs or mid-upper arm circumference (MUAC) \< 115 mm (in children over 6 months) or clinical signs of bilateral pitting oedema, and being aged ≥5 years with a body mass index (BMI) for age Z-score \< -3SD.

Age in the registry: - to 14 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (29)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chiwempala Urban Health Centre
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ChingolaZambiaRecruiting
Kabundi East Urban Health Clinic
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ChingolaZambiaRecruiting
Nchanga 1 Urban Health Centre
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ChingolaZambiaRecruiting
Nchanga North Referal Hospital
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ChingolaZambiaRecruiting
Chawama Urban Health Centre
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ChingolaZambiaRecruiting
Kasompe Urban Health Centre
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ChingolaZambiaRecruiting
Muchinshi Rural Health Centre
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ChingolaZambiaRecruiting
Lusitu Rural Health Centre
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ChirunduZambiaRecruiting
Jamba Rural Health Centre
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ChirunduZambiaRecruiting
Chipepo Rural Health Centre
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ChirunduZambiaRecruiting
Sikoongo Rural Health Centre
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ChirunduZambiaRecruiting
Mtendere Mission Referal hospital
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ChirunduZambiaRecruiting
Hachipilika Rural Health Centre
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ChirunduZambiaRecruiting
Kapululira Rural Health Centre
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ChirunduZambiaRecruiting
Namwianga Urban Health Centre
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KalomoZambiaRecruiting
Habulile Rural Health Centre
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KalomoZambiaRecruiting
Kalomo District Hospital
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KalomoZambiaRecruiting
Kalomo Urban Health Centre
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KalomoZambiaRecruiting
Siachitema Rural Health Centre
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KalomoZambiaRecruiting
Mawaya Urban Health Centre
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KalomoZambiaRecruiting
Nkandanzovu Rural Health Centre
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KalomoZambiaRecruiting
Roan Antelope General Hospital
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LuanshyaZambiaRecruiting
Malaika Urban Health Centre
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LuanshyaZambiaRecruiting
Chaisa Urban Health Centre
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LuanshyaZambiaRecruiting
Fisenge Urban Health Centre
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LuanshyaZambiaRecruiting
Thomson District Hospital
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LuanshyaZambiaRecruiting
Kawama Urban Health Centre
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LuanshyaZambiaRecruiting
Allessandras Urban Health Centre
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LuanshyaZambiaRecruiting
Mikomfwa Urban Health Centre
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LuanshyaZambiaRecruiting

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This page is information, not medical advice. Discuss any trial with your doctor.