Key Longitudinal Associations With Risk and Glioblastoma Outcomes
NCT ID: NCT06625684
Last Updated: 2026-01-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
200 participants
OBSERVATIONAL
2024-12-10
2029-12-10
Brief Summary
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The main questions it aims to answer are:
* How do genetic and immune system factors impact survival and quality of life in GBM patients?
* What occupational and medical history factors are linked to the risk of getting GBM?
Participants will:
* Fill out an online survey about their medical history and lifestyle.
Participants will have the chance to give a blood sample (from the outer arm) for genetic and immune system testing. Blood samples will be given using a home collection kit provided by the study team.
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Detailed Description
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The study employs a case-only design where participants will be followed over time to observe how different factors affect their health outcomes. Participants will be selected based on their diagnosis of glioblastoma and will be included in the study regardless of current treatment status or disease stage.
Findings from this study are expected to provide valuable insights into the factors affecting glioblastoma outcomes and may contribute to the development of personalized treatment strategies and risk assessment tools for better management of the disease.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Adults with Glioblastoma
This group consists of adults diagnosed with glioblastoma, a type of aggressive brain tumor. Participants are observed to identify factors influencing their outcomes, including genetic, immunologic, and personal medical history factors. The study aims to explore how these factors impact survival rates and quality of life in this patient population. There are no specific interventions. Instead, the focus is on analyzing survey data and biological samples to understand risk factors and disease progression.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Pathologically-confirmed diagnosis of glioblastoma multiforme (GBM) or grade 4 brain tumor
* Participant is accessible for follow-up (has a working email address)
* Participant is willing and able to comply with the study requirements
Exclusion Criteria
* Those who cannot view an online survey
18 Years
ALL
No
Sponsors
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Glioblastoma Research Organization
UNKNOWN
StacheStrong
UNKNOWN
Duke University
OTHER
Responsible Party
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Principal Investigators
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Quinn Ostrom, PhD
Role: PRINCIPAL_INVESTIGATOR
Duke University
Locations
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Duke University
Durham, North Carolina, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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Pro00114859
Identifier Type: -
Identifier Source: org_study_id
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