INPUT: Integrating Pediatric TB Services Into Child Healthcare Services in Africa

Sponsor
Elizabeth Glaser Pediatric AIDS Foundation (Other)
Overall Status
Completed
CT.gov ID
NCT03862261
Collaborator
UNITAID (Other), University of Sheffield (Other), Kenya Ministry of Health (Other), Cameroon Ministry of Public Health (Other)
1,715
12
2
31.7
142.9
4.5

Study Details

Study Description

Brief Summary

Under-diagnosis of TB in children is a critical gap to address. The INPUT study is a multinational stepped-wedge cluster-randomized intervention study aiming to assess the effect of integrating TB services into child healthcare services on TB diagnosis capacities in children under 5 years of age.

Condition or Disease Intervention/Treatment Phase
  • Other: Integrated pediatric TB services
N/A

Detailed Description

Study clusters (district-level hospitals and their health centers) will start under standard-of-care and transition to the intervention at randomly assigned time points.

In this study two strategies will be compared: i) The standard of care, offering pediatric TB services based on current routine approach; ii) The intervention, with pediatric TB services integrated into child healthcare services.

The primary objective will be to assess the effect of the intervention compared to standard of care on the proportion of TB cases diagnosed among children <5 years old (that is the number of children who are clinically or bacteriologically diagnosed with TB over the total number of children attending the child healthcare services). Secondary objectives are detailed in the protocol.

Study sites will include six hospital in each participating country (Cameroon and Kenya) along with selected attached health centers.

The study population will be children aged less than five years of age with a presumptive diagnosis of TB.

Study enrollment will start in March 2019, last enrollments until July 2020 and follow up will be completed by August 2021.

Study Design

Study Type:
Interventional
Actual Enrollment :
1715 participants
Allocation:
Randomized
Intervention Model:
Sequential Assignment
Intervention Model Description:
Cluster-randomized stepped-wedge model, where intervention will be randomly allocated to the different study sites at different time points.Cluster-randomized stepped-wedge model, where intervention will be randomly allocated to the different study sites at different time points.
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Integrating Pediatric TB Services Into Child Healthcare Services in Africa. A Cluster-randomized Stepped-wedge Trial
Actual Study Start Date :
May 10, 2019
Actual Primary Completion Date :
Jun 30, 2021
Actual Study Completion Date :
Dec 31, 2021

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Standard-of-Care

Pediatric TB services based on current routine approach (national standard of care)

Experimental: Intervention

Integrated pediatric TB services

Other: Integrated pediatric TB services
pediatric TB services will be integrated into key child healthcare services: maternal neonatal and child health (MNCH) services, under-5 clinic, pediatric outpatient services, nutrition services, pediatric antiretroviral therapy (ART) services and primary health care: Integration of the screening into all the child health care services with introduction of a specific case detection tool and updated presumptive TB register. Improvement of diagnosis capacities and their integration in all levels of care and all services.

Outcome Measures

Primary Outcome Measures

  1. Proportion of children diagnosed with active TB [up to two months]

    Number of pediatric TB cases diagnosed (bacteriologically confirmed and/or clinically diagnosed) over the number of children attending the child healthcare services during the study period.

Secondary Outcome Measures

  1. Proportion of children screened for TB [one month]

    Number of children screened for TB over the number of children attending the child healthcare services during the study period

  2. Proportion of screened children who have a sample collected [up to three months]

    Proportion of children who have a sample collected for microbiologic diagnosis among those screened positive for TB (i.e. presumptive TB cases)

  3. Proportion of children diagnosed with TB among presumptive TB cases [up to two months]

    Proportion of children diagnosed with TB (bacteriologically or clinically) among presumptive TB cases, overall and disaggregated by HIV status and nutrition status

  4. Time from screening to clinical or bacteriologic diagnosis [up to three months]

    For children finally diagnosed with TB, time elapsed from presumptive to confirmed TB case

  5. Time from diagnosis to treatment initiation [up to three months]

    For children diagnosed with TB, time elapsed to initiate treatment after active TB is confirmed

  6. Proportion of cases with a bacteriologically confirmed diagnosis [up to three months]

    Proportion of cases with a bacteriologically confirmed diagnosis among children diagnosed with TB

  7. Proportion of children who initiate TB treatment among those diagnosed [up to two months]

    Proportion of children who initiate TB treatment among those diagnosed will give treatment coverage

  8. Treatment outcome [8 to 14 months (2 months after treatment completion)]

    Treatment outcomes for patients initiated on treatment according to WHO categories: treatment success, treatment failed, died, lost to follow-up, and not evaluated.

  9. Adherence to the TB treatment [6 to 12 months (at treatment completion)]

    Adherence documented by seven-day recall and counting of pills

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A to 5 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Children < 5 years old.

  • TB diagnosis investigations initiated.

  • Other infectious diseases are not suspected or have already been ruled out.

  • Commitment to take treatment in the clinic of enrolment or another INPUT study site.

  • Parental/caregiver consent for the child to participate in the study.

Exclusion Criteria:
  • Children who are TB contacts but without symptoms or signs of active TB

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hopital de District Akonolinga Akonolinga Centre Cameroon
2 Hopital de District Soa Soa Centre Cameroon
3 Hopital de District Loum Loum Littoral Cameroon
4 Hopital de District Foumban Mbanga Littoral Cameroon
5 Hopital de District Dschang Dschang West Cameroon
6 Hopital de District Mbouda Mbouda West Cameroon
7 Kendu Sub County Hospital Kendu Bay Homa Bay Kenya
8 Ndhiwa Sub county Hospital Ndhiwa Homa Bay Kenya
9 Kakuma Mission Hospital Kakuma Turkana Kenya
10 Lokitaung sub-county hospital Lokitaung Turkana Kenya
11 Lopiding Sub County Hospital Lopiding Turkana Kenya
12 Homa Bay County Referral Hospital Homa Bay Kenya

Sponsors and Collaborators

  • Elizabeth Glaser Pediatric AIDS Foundation
  • UNITAID
  • University of Sheffield
  • Kenya Ministry of Health
  • Cameroon Ministry of Public Health

Investigators

  • Principal Investigator: Appolinaire Tiam, MBChB, MMed, Elizabeth Glaser Pediatric AIDS Foundation

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Elizabeth Glaser Pediatric AIDS Foundation
ClinicalTrials.gov Identifier:
NCT03862261
Other Study ID Numbers:
  • EG0214
First Posted:
Mar 5, 2019
Last Update Posted:
Mar 23, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 23, 2022