Determining Clinical Trial Experiences of Lung Cancer Patients
An Observational Study to Determine Experience Patterns in Participants of Lung Cancer Clinical Trials
1 other identifier
observational
500
0 countries
N/A
Brief Summary
Participation in medical trials usually favors a particular demographic group. But there is limited research available to explain what trial attributes affect the completion of these specific demographic groups. This trial will admit a wide range of data on the clinical trial experience of lung cancer patients to determine which factors prevail in limiting a patient's ability to join or finish a trial. It will also try to analyze data from the perspective of different demographic groups to check for recurring trends which might yield insights for the sake of future lung cancer patients.
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
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 25, 2023
CompletedFirst Posted
Study publicly available on registry
March 8, 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 5, 2023
June 1, 2023
1 year
February 25, 2023
June 2, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Number of lung cancer patients who decide to enroll in a clinical trial
3 months
Rate of patients who remain in a lung cancer clinical trial to trial completion
12 months
Eligibility Criteria
Lung cancer patients who are actively considering participating in a clinical trial, but have not yet completed enrollment and randomization.
You may qualify if:
- Patient has been diagnosed with lung cancer
- Patient has self-identified as planning to enroll in an observational clinical trial
- Patient is a minimum of 18 years or older
You may not qualify if:
- Pregnant or nursing patients
- Inability to perform regular electronic reporting
- Patient does not understand, sign, and return consent form
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (3)
Menis J, Besse B, Lacombe D. Methodology of clinical trials in lung cancer. Chin Clin Oncol. 2015 Dec;4(4):44. doi: 10.3978/j.issn.2304-3865.2015.11.03.
PMID: 26730756BACKGROUNDSchulkes KJ, Nguyen C, van den Bos F, van Elden LJ, Hamaker ME. Selection of Patients in Ongoing Clinical Trials on Lung Cancer. Lung. 2016 Dec;194(6):967-974. doi: 10.1007/s00408-016-9943-7. Epub 2016 Sep 20.
PMID: 27650509BACKGROUNDSchulkes KJ, Nguyen C, van den Bos F, Hamaker ME, van Elden LJ. Patient-Centered Outcome Measures in Lung Cancer Trials. Lung. 2016 Aug;194(4):647-52. doi: 10.1007/s00408-016-9903-2. Epub 2016 Jun 10.
PMID: 27287676BACKGROUND
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 25, 2023
First Posted
March 8, 2023
Study Start
March 1, 2024
Primary Completion
March 1, 2025
Study Completion
March 1, 2026
Last Updated
June 5, 2023
Record last verified: 2023-06