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Study Type(s)

Topic Area(s)

Document Type(s)

Study Method(s)

Document Method(s)

PROBeX: Source Documentation and Participant Source File SOP (1282)

PROBeX SOPTB/Coinfection Studies PROBeXClinical HIV DataInformationParticipantProcedureTestingResultsRecords Drug ARTTreatment Africa SourceTuberculosisDiagnosis XDRDocumentationResistanceBedaquilineGeneticMechanismsInteractionsPharmakineticSynthesisMedicationsRitonavirLopinavir FileInternational 2020PRO-Document MethodsClinicalChart ExtractionCommunity HealthImmunologyVirologyGeneticsClinicalProspective Cohort StudyQuantitativeClinical

Source documentation and participant source file SOP in PROBeX study.

TRAX: Source Documentation SOP (1255)

TRAX SOP TRAXTB/Coinfection StudiesContact Data FormTestingCommunityResourceRecords SocialQuestionnaire Rural DrugIntervention DAIDSTransmissionNetwork AfricaCluster SourceTracingResistantGenotypeTuberculosisMortalityPatternsEpidemiologyLimitedCo-infection SouthHospitalsImmunocompromisedCongregateInteractionSettingsDocumentationInternational 2014TRAX-Document MethodsChart ExtractionClinicalPreventionCommunity HealthBehavioralHealth EquityVirologyGeneticsClinicalCross Sectional StudyClinicalChart ExtractionQualitative

Source documentation protocol for TRAX study staff.

Le Kip Kip: Protocol (1201)

Le Kip KipProtocolsLe Kip KipPrevention Data PrEPPopulationAdherenceBackgroundAssuranceControl DesignProceduresQualityReferencesPersistenceTimeline Social Access Uptake Female WomenInterventionObjectivesStatisticalEconomic HumanInfluence PeerOutcomesTransmissionProtectionSubjects YoungInfectionOptimizationScale-upEmpower AfricaMultiphaseMOST FrameworkEvaluationStrategyModification ActorIntensityDurationClusterProgramExistingInfrastructureEffectiveness CostModelingAdoptionAdolescentAdvertising Worker SexCampaignCondoms Girls RefillRationaleConsiderations SourceInternational 2023PreventionCommunity HealthBehavioralImplementationClinicalStandard RCTClinicalImplementation ScienceQual + Quant

Protocol for Le Kip Kip, includes; key roles, background and rationale, objectives, study design, study population, study procedures, statistical considerations, access to source data/documents, quality control and quality assurance, protection of human subjects, timeline, references.