CTRI/2020/04/024681
Not yet recruiting
未知
Impact of improved diagnostic tools, practices,training and communication on acute fever case management and antibiotic prescriptions for children and adolescents presenting at outpatient facilities in the Community Clinics of ICMR-NICED, India - FIND
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: R509- Fever, unspecified
- Sponsor
- Foundation for Innovative New Diagnostics FIND
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •A.Patients with fever with no focus / RTI:
- •a.Children (6 months to \<14years) and adolescents (14 years to less than 18 years old) of both sexes.
- •b.Presenting with an acute febrile illness defined as temperature of \>37\.5°C (oral) or history of fever within the last 7 days with no focus or suspected RTI.
- •c.Parent/guardian providing written informed consent for their children aged less than 18 years of age.
- •d.Obtain assent for adolescent between 12 and less than 18 years old
- •e.Willing to provide blood (as well as urine, NP or throat swab if required) samples and adhere to study procedures explained in the consent forms following the protocol.
- •f. Available and willing to return for follow\-up visit at the health facility.
- •B.Training and communication (for those randomised to intervention arm):
- •a.Parent/guardian providing informed consent to participate in the training and communication component of the study. The same informed consent form will cover both populations adult caregivers and adolescents
- •b.Clinic staff who have provided written informed consent to participate in the training and communication as per randomisation protocol
Exclusion Criteria
- •Participants are excluded using the following exclusion criteria:
- •oChildren and adolescents from 6 months to less than 18 years old presenting with chronic febrile illness (fever lasting more than 7 days).
- •oPatients with acute febrile illness outside the allowed age range.
- •oSeverely ill patients requiring hospital admission or referral as assessed by the study clinicians.
- •oAnyone refusing consent to the study or not available for follow\-up (adults, the children of parents/guardians, or adolescents who refuse or are missed when asking for consent).
Outcomes
Primary Outcomes
Not specified
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