Pinpointing the Factors Affecting Clinical Trial Experiences of Glioblastoma Patients
An In Depth Study Evaluating The Experiences of Patients In Glioblastoma Clinical Trials
1 other identifier
observational
500
0 countries
N/A
Brief Summary
Historically, clinical study participation has been biased toward certain demographics. However, there is a shortage of studies that delve into the underlying factors that influence patient participation, both positively and negatively. Several people will be invited to enroll in this study so that it may collect a variety of data about glioblastoma clinical trial experiences and identify barriers to participation as well as the causes of participants' failure or withdrawal. The data collected from this study will be analyzed and used to improve the experiences of future glioblastoma patients who are recruited for medical trials.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2024
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 4, 2023
CompletedFirst Posted
Study publicly available on registry
February 14, 2023
CompletedStudy Start
First participant enrolled
March 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2026
CompletedJune 12, 2023
June 1, 2023
1 year
February 4, 2023
June 9, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Number of patients who decide to participate in a glioblastoma clinical trial
3 months
Rate of patients who remain in glioblastoma clinical trial to trial completion
12 months
Eligibility Criteria
Glioblastoma patients who are actively considering enrolling in an observational clinical trial, but have not yet completed enrollment and randomization.
You may qualify if:
- Patient has self-identified as planning to enroll in a clinical trial
- Patient has been diagnosed with glioblastoma
- Patient is a minimum of 18 years or older
You may not qualify if:
- Patient does not understand, sign, and return consent form
- Inability to perform regular electronic reporting
- Patient is pregnant
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (3)
Wirsching HG, Galanis E, Weller M. Glioblastoma. Handb Clin Neurol. 2016;134:381-97. doi: 10.1016/B978-0-12-802997-8.00023-2.
PMID: 26948367BACKGROUNDOmuro A, DeAngelis LM. Glioblastoma and other malignant gliomas: a clinical review. JAMA. 2013 Nov 6;310(17):1842-50. doi: 10.1001/jama.2013.280319.
PMID: 24193082BACKGROUNDLuo C, Song K, Wu S, Hameed NUF, Kudulaiti N, Xu H, Qin ZY, Wu JS. The prognosis of glioblastoma: a large, multifactorial study. Br J Neurosurg. 2021 Oct;35(5):555-561. doi: 10.1080/02688697.2021.1907306. Epub 2021 Jul 8.
PMID: 34236262BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Michael B Gill
Power Life Sciences Inc.
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CROSSOVER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 4, 2023
First Posted
February 14, 2023
Study Start
March 1, 2024
Primary Completion
March 1, 2025
Study Completion
March 1, 2026
Last Updated
June 12, 2023
Record last verified: 2023-06