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Improving Antibiotic Stewardship for Children With Respiratory Illness Presenting to Village Health Workers in Uganda (STAR)

Primary Purpose

Respiratory Infections in Children

Status
Completed
Phase
Not Applicable
Locations
Uganda
Study Type
Interventional
Intervention
STAR Sick Child Job Aid
Sponsored by
University of North Carolina, Chapel Hill
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Respiratory Infections in Children focused on measuring Community health workers, C-reactive protein

Eligibility Criteria

2 Months - 5 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 2 months-5 years
  • Evaluated by a study VHW in one of the participating villages in Bugoye sub-county for acute respiratory illness defined as the following: fever (documented (temperature > 38°C) or subjective fever in the last seven days) AND fast breathing (respiratory rate > 30) OR cough

Exclusion Criteria:

  • Age > 5 years or < 2 months at time of presentation
  • Guardian not present to provide consent

Sites / Locations

  • Bugoye Health Center III

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control

Intervention

Arm Description

Children who present to a village health worker during a control period are evaluated and managed using the current standard of care per Uganda National Guidelines for Integrated Community Case Management (ICCM). Each village will experience both Control and Intervention conditions as the study employs a stepped wedge design.

Children who present to a village health worker during an intervention period are evaluated and managed using a modified ICCM algorithm that includes point-of-care C-reactive protein testing. Each village will experience both Control and Intervention conditions as the study employs a stepped wedge design.

Outcomes

Primary Outcome Measures

Antibiotic prescriptions at baseline visit
Proportion of children prescribed antibiotics by the village health worker at the baseline visit in the control as compared to the intervention condition.

Secondary Outcome Measures

Clinical Failure (Composite Outcome)
Proportion of children with one or more of the following outcomes in the control as compared to the intervention condition: persistence of fever at Day 7, development of danger signs as defined by local Integrated Community Care Management guidelines at any time during the seven-day follow-up period, need for hospitalization at any time during follow-up period, or death at any time during follow-up period.
Unexpected visits
Proportion of children brought to the village health worker during the seven-day follow-up period for persistent or worsening symptoms by their caregiver in the control as compared to the intervention condition.
Perceived improvement per caregiver
Proportion of caregivers who perceive that their child has clinically improved at the Day 7 follow-up assessment in the control as compared to the intervention condition.
Persistent fever
Proportion of children who have persistence of subjective or documented fever at the Day 7 follow-up assessment in the control as compared to the intervention condition.
Development of danger signs
Proportion of children who develop danger signs (as defined by local Integrated Community Care Management guidelines) during the seven-day follow-up period in the control as compared to intervention conditions.
Hospitalization
Proportion of children who require inpatient admission to a health facility during the seven-day follow-up period in the control as compared to intervention periods.
Death
Proportion of children who die during the seven-day follow-up period in the control as compared to intervention periods.
Antibiotic prescriptions during study follow-up
Proportion of children prescribed antibiotics by any provider either at the baseline visit or during the seven-day follow-up period in the control as compared to the intervention condition.

Full Information

First Posted
March 15, 2022
Last Updated
August 3, 2022
Sponsor
University of North Carolina, Chapel Hill
Collaborators
Thrasher Research Fund
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1. Study Identification

Unique Protocol Identification Number
NCT05294510
Brief Title
Improving Antibiotic Stewardship for Children With Respiratory Illness Presenting to Village Health Workers in Uganda
Acronym
STAR
Official Title
STewardship for Acute Respiratory Illness (STAR): a Stepped Wedge, Cluster Randomized Trial of Point-of-care Biomarker Testing by Village Health Workers
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
November 2, 2021 (Actual)
Primary Completion Date
May 30, 2022 (Actual)
Study Completion Date
May 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of North Carolina, Chapel Hill
Collaborators
Thrasher Research Fund

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a stepped wedge, cluster randomized study of a clinical algorithm that includes point-of-care C-reactive protein testing to inform antibiotic treatment decisions by village health workers for children presenting with acute respiratory illness in the Bugoye sub-county of the Kasese District in southwestern Uganda. The purpose of this study is to assess the impact of the algorithm on antibiotic use.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Infections in Children
Keywords
Community health workers, C-reactive protein

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Stepped wedge, cluster randomized trial with 5 clusters or treatment sequences of 3 villages each. Villages are first stratified by altitude, proximity to the local health center, and size (based on approximate number of children seen by the village health workers per year) into one of three strata: (1) low altitude, proximal, large, (2) low altitude, mid-distance, medium, (3) high altitude, distal, small. One village is then randomly selected from each strata for each of the 5 clusters. All clusters start in the control condition and one cluster crosses over from control to intervention each month.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1280 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Children who present to a village health worker during a control period are evaluated and managed using the current standard of care per Uganda National Guidelines for Integrated Community Case Management (ICCM). Each village will experience both Control and Intervention conditions as the study employs a stepped wedge design.
Arm Title
Intervention
Arm Type
Experimental
Arm Description
Children who present to a village health worker during an intervention period are evaluated and managed using a modified ICCM algorithm that includes point-of-care C-reactive protein testing. Each village will experience both Control and Intervention conditions as the study employs a stepped wedge design.
Intervention Type
Other
Intervention Name(s)
STAR Sick Child Job Aid
Intervention Description
The STAR Sick Child Job Aid is a modified ICCM protocol that includes the addition of a point-of-care C-reactive protein (CRP) test to inform antibiotic treatment decisions for children presenting with febrile acute respiratory illness who do not have any danger signs. If CRP ≥ 40 mg/L, the village health worker (VHW) will dispense amoxicillin per local guidelines. If CRP < 40 mg/L, the VHW will advise symptomatic care alone including acetaminophen for fever and additional fluids to maintain hydration.
Primary Outcome Measure Information:
Title
Antibiotic prescriptions at baseline visit
Description
Proportion of children prescribed antibiotics by the village health worker at the baseline visit in the control as compared to the intervention condition.
Time Frame
Baseline visit
Secondary Outcome Measure Information:
Title
Clinical Failure (Composite Outcome)
Description
Proportion of children with one or more of the following outcomes in the control as compared to the intervention condition: persistence of fever at Day 7, development of danger signs as defined by local Integrated Community Care Management guidelines at any time during the seven-day follow-up period, need for hospitalization at any time during follow-up period, or death at any time during follow-up period.
Time Frame
Between baseline visit and Day 7 follow-up assessment
Title
Unexpected visits
Description
Proportion of children brought to the village health worker during the seven-day follow-up period for persistent or worsening symptoms by their caregiver in the control as compared to the intervention condition.
Time Frame
Between baseline visit and Day 7 follow-up assessment
Title
Perceived improvement per caregiver
Description
Proportion of caregivers who perceive that their child has clinically improved at the Day 7 follow-up assessment in the control as compared to the intervention condition.
Time Frame
Day 7
Title
Persistent fever
Description
Proportion of children who have persistence of subjective or documented fever at the Day 7 follow-up assessment in the control as compared to the intervention condition.
Time Frame
Day 7
Title
Development of danger signs
Description
Proportion of children who develop danger signs (as defined by local Integrated Community Care Management guidelines) during the seven-day follow-up period in the control as compared to intervention conditions.
Time Frame
Between Day 1 and Day 7
Title
Hospitalization
Description
Proportion of children who require inpatient admission to a health facility during the seven-day follow-up period in the control as compared to intervention periods.
Time Frame
Between Day 1 and Day 7
Title
Death
Description
Proportion of children who die during the seven-day follow-up period in the control as compared to intervention periods.
Time Frame
Between Day 1 and Day 7
Title
Antibiotic prescriptions during study follow-up
Description
Proportion of children prescribed antibiotics by any provider either at the baseline visit or during the seven-day follow-up period in the control as compared to the intervention condition.
Time Frame
Between baseline visit and Day 7 follow-up assessment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Months
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 2 months-5 years Evaluated by a study VHW in one of the participating villages in Bugoye sub-county for acute respiratory illness defined as the following: fever (documented (temperature > 38°C) or subjective fever in the last seven days) AND fast breathing (respiratory rate > 30) OR cough Exclusion Criteria: Age > 5 years or < 2 months at time of presentation Guardian not present to provide consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emily J Ciccone, MD, MHS
Organizational Affiliation
University of North Carolina, Chapel Hill
Official's Role
Principal Investigator
Facility Information:
Facility Name
Bugoye Health Center III
City
Bugoye
State/Province
Kasese District
Country
Uganda

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Deidentified individual data that underlie the results will be shared beginning 9 to 36 months following publication provided the investigator who proposes to use the data has approval from an Institutional Review Board (IRB), Independent Ethics Committee (IEC), or Research Ethics Board (REB), as applicable, and executes a data use/sharing agreement with UNC.
IPD Sharing Time Frame
9 months to 36 months after publication
IPD Sharing Access Criteria
The investigator who proposes to use the data has approval from an IRB, IEC, or REB, as applicable, and an executed data use/sharing agreement with UNC

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Improving Antibiotic Stewardship for Children With Respiratory Illness Presenting to Village Health Workers in Uganda

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