Completed

Barriers to Patient Enrollment Onto Frontline Therapeutic Clinical Trials and Development of Intervention Strategies to Increase the Proportion of Enrollment

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What is being collected

Procedure Data

+ procedure Data

Procedure
Who is being recruted

Urogenital Diseases+87

+ Genital Diseases

+ Adnexal Diseases

Until 21 Years
See all eligibility criteria
How is the trial designed

Observational
Study Start: February 1992
See protocol details

Summary

Principal SponsorChildren's Oncology Group
Last updated: February 14, 2014
Sourced from a government-validated database.Claim as a partner

Study start date: February 1, 1992

Actual date on which the first participant was enrolled.

OBJECTIVES: I. Identify prospectively physician and patient factors associated with reasons why patients who are eligible for Pediatric Oncology Group therapeutic protocols are not enrolled onto such studies. II. Provide information that may be used to develop intervention strategies to decrease barriers to patient enrollment, thus increasing enrollment in therapeutic protocols. OUTLINE: This is a case-control, multicenter study. Case patients are stratified. Stratum 1 comprises patients for whom there is an appropriate Pediatric Oncology Group (POG) frontline therapeutic protocol that has not yet been submitted to, disapproved by, or approved by the Institutional Review Board (IRB). Stratum 2 comprises patients for whom there is an appropriate POG frontline therapeutic protocol that has been approved by the IRB. Physicians complete an IRB submission form for their patients on stratum 1. Patients/parents on stratum 2 who refused enrollment and their primary physicians complete questionnaires that address reasons for nonenrollment. Control patients/parents who consented to enrollment complete questionnaires that address reasons for enrollment. Demographic information, including the size of the treating institution and the annual number of patients enrolled onto its protocols, is collected. Additional demographic information regarding the patient and his or her family is collected. PROJECTED ACCRUAL: A total of 595 case patients (12 with soft tissue sarcoma, 34 with osteosarcoma, 19 with brain tumors, 32 with Hodgkin's disease, 60 with non-Hodgkin's lymphoma, 278 with acute lymphoblastic leukemia, 65 with acute non-lymphoblastic leukemia, 56 with neuroblastoma, 14 with hepatoblastoma, and 25 with germ cell tumors) will be accrued for this study within 7 years. Corresponding control patients will be accrued for this study.

NCT00002485
Principal SponsorChildren's Oncology Group
Last updated: February 14, 2014
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

359 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Until 21 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Urogenital DiseasesGenital DiseasesAdnexal DiseasesBrain DiseasesBrain NeoplasmsCentral Nervous System DiseasesCerebral Ventricle NeoplasmsCranial Nerve DiseasesCranial Nerve NeoplasmsDigestive System DiseasesDigestive System NeoplasmsDNA Virus InfectionsEndocrine System DiseasesEndocrine Gland NeoplasmsEye DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsGenital Diseases, FemaleGenital Diseases, MaleGenital Neoplasms, FemaleGenital Neoplasms, MaleGliomaGonadal DisordersHematologic DiseasesHemic and Lymphatic DiseasesHerpesviridae InfectionsImmune System DiseasesImmunoproliferative DisordersInfectionsLeukemia, LymphoidLiver DiseasesLymphatic DiseasesLymphoma, Non-HodgkinLymphoproliferative DisordersMeningeal NeoplasmsNeoplasmsNeoplasms by Histologic TypeNeoplasms by SiteNeoplasms, Connective TissueNeoplasms, Germ Cell and EmbryonalNeoplasms, Glandular and EpithelialNeoplasms, Nerve TissueNeoplasms, Vascular TissueNervous System DiseasesNervous System NeoplasmsOptic Nerve DiseasesOvarian DiseasesPathologic ProcessesPeripheral Nervous System NeoplasmsPathological Conditions, Signs and SymptomsTesticular DiseasesTumor Virus InfectionsUrogenital NeoplasmsVirus DiseasesHistiocytosisHistiocytic Disorders, MalignantLymphoma, B-CellNeuroectodermal TumorsNeoplasms, Complex and MixedNeoplasms, Connective and Soft TissueNeoplasms, Bone TissueNeuroectodermal Tumors, Primitive, PeripheralNeuroectodermal Tumors, PrimitiveNeoplasms, NeuroepithelialOptic Nerve NeoplasmsEpstein-Barr Virus InfectionsDisease AttributesFemale Urogenital DiseasesMale Urogenital DiseasesAstrocytomaBurkitt LymphomaLeukemiaLiver NeoplasmsLymphomaMedulloblastomaMeningiomaNeuroblastomaOligodendrogliomaOvarian NeoplasmsRecurrenceSarcomaOsteosarcomaTeratomaTesticular NeoplasmsCentral Nervous System NeoplasmsChoroid Plexus NeoplasmsHepatoblastomaRhabdoid TumorOptic Nerve GliomaPrecursor Cell Lymphoblastic Leukemia-LymphomaDendritic Cell Sarcoma, Interdigitating

Criteria

DISEASE CHARACTERISTICS: Case or control patient clinically eligible for a Pediatric Oncology Group (POG) frontline therapeutic protocol, whether or not the protocol was submitted to or approved by the physician's Institutional Review Board Case patients must not have enrolled on the POG frontline protocol due to decision by the physician or patient/parent Control patients must have been enrolled on the POG frontline protocol Ineligible if offered treatment on an in-house therapeutic protocol (institutional review board-approved) rather than the POG protocol PATIENT CHARACTERISTICS: Age: 21 and under Performance status: Not specified Life expectancy: Not specified Hematopoietic: Not specified Hepatic: Not specified Renal: Not specified PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: Not specified Endocrine therapy: Not specified Radiotherapy: Not specified Surgery: Not specified

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 31 locations

University of California Davis Medical Center

Sacramento, United StatesOpen University of California Davis Medical Center in Google Maps

Shands Hospital and Clinics, University of Florida

Gainesville, United States

Sylvester Cancer Center, University of Miami

Miami, United States

CCOP - Florida Pediatric

Tampa, United States
Completed31 Study Centers