Publication | Closed Access

PRO Data Collection in Clinical Trials Using Mixed Modes: Report of the ISPOR PRO Mixed Modes Good Research Practices Task Force

Clinical Trial DesignMeta-analysisHealth PolicyClinical Trial ManagementPro Data CollectionClinical EndpointClinical TrialsPatient-reported OutcomeRandomized Controlled TrialDrug TrialPublic HealthClinical Trial EvaluationHealth InformaticsHealth Sciences