NCT05778045

Brief Summary

Medical study participation percentages haven't always been fully representative of a given demographic. The goal is to find out which aspects of a clinical trial may make it more difficult for patients to take part or see it through. Participating in an observational clinical trial may help patients with non-small cell lung cancer since it advances medical knowledge and may improve treatment choices in the future.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
0mo left

Started Apr 2024

Typical duration for all trials

Status
not yet recruiting

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

Study Progress97%
Apr 2024Jun 2026

First Submitted

Initial submission to the registry

March 10, 2023

Completed
11 days until next milestone

First Posted

Study publicly available on registry

March 21, 2023

Completed
1 year until next milestone

Study Start

First participant enrolled

April 1, 2024

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2025

Completed
1.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Expected
Last Updated

March 21, 2023

Status Verified

March 1, 2023

Enrollment Period

1.1 years

First QC Date

March 10, 2023

Last Update Submit

March 10, 2023

Conditions

Keywords

non-small cell lung cancer

Outcome Measures

Primary Outcomes (2)

  • Rate of patients who decide to enroll in a non-small cell lung cancer clinical study.

    3 months

  • Number of non-small cell lung cancer patients who remain in clinical trial until completion.

    12 months

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Non-small cell lung cancer patients who are actively considering involvement in an observational clinical trial, but have not yet completed enrollment and registration.

You may qualify if:

  • Participant has a diagnosis of non-small cell lung cancer
  • Patient has self-identified as planning to enroll in a clinical trial for non-small cell lung cancer
  • Patient is at least 18 years of age

You may not qualify if:

  • Inability to perform regular electronic reporting
  • Any mental or medical condition that prevents the patient from giving informed consent or participating in the trial
  • Pregnant or lactating woman

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (3)

  • Kayser G. [Non-small cell lung cancer. New biomarkers for diagnostics and therapy]. Pathologe. 2015 Nov;36 Suppl 2:189-93. doi: 10.1007/s00292-015-0084-1. German.

    PMID: 26391246BACKGROUND
  • Dufraing K, Van Casteren K, Breyne J, D'Haene N, Van Campenhout C, Vander Borght S, Zwaenepoel K, Rouleau E, Schuuring E, von der Thusen J, Dequeker E. Molecular pathology testing for non-small cell lung cancer: an observational study of elements currently present in request forms and result reports and the opinion of different stakeholders. BMC Cancer. 2022 Jul 6;22(1):736. doi: 10.1186/s12885-022-09798-5.

    PMID: 35794532BACKGROUND
  • Simeone JC, Nordstrom BL, Patel K, Klein AB. Treatment patterns and overall survival in metastatic non-small-cell lung cancer in a real-world, US setting. Future Oncol. 2019 Oct;15(30):3491-3502. doi: 10.2217/fon-2019-0348. Epub 2019 Sep 9.

    PMID: 31497994BACKGROUND

MeSH Terms

Conditions

Carcinoma, Non-Small-Cell Lung

Condition Hierarchy (Ancestors)

Carcinoma, BronchogenicBronchial NeoplasmsLung NeoplasmsRespiratory Tract NeoplasmsThoracic NeoplasmsNeoplasms by SiteNeoplasmsLung DiseasesRespiratory Tract Diseases

Study Officials

  • Michael B Gill

    Power Life Sciences Inc.

    STUDY DIRECTOR

Central Study Contacts

Michael B Gill

CONTACT

Study Design

Study Type
observational
Observational Model
CASE CROSSOVER
Time Perspective
PROSPECTIVE
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 10, 2023

First Posted

March 21, 2023

Study Start

April 1, 2024

Primary Completion

May 1, 2025

Study Completion (Estimated)

June 1, 2026

Last Updated

March 21, 2023

Record last verified: 2023-03