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The goal of this research study is to learn about: The effect of enrolling in the YOLC program on patient satisfaction with care provided, The needs of patients younger than 50 with lung cancer and their family, and The impact of participating in peer support networks on these patients.
Primary Objectives: 1. To determine whether enrollment in a dedicated program (YOLC) results in improved patient satisfaction with care provided. 2. To characterize the distinct needs of patients under age 50 diagnosed with lung cancer as well as those of their families, and how these needs may change over time throughout the care pathway. 3. To evaluate the impact of participation in peer support networks and whether it has a beneficial effect on the primary and secondary endpoints. Secondary Objectives: 1. To determine whether enrollment in a dedicated program (YOLC) results in improved patient satisfaction with care provided. 2. To characterize the distinct needs of patients under age 50 diagnosed with lung cancer as well as those of their families, and how these needs may change over time throughout the care pathway. 3. To evaluate the impact of participation in peer support networks and whether it has a beneficial effect on the primary and secondary endpoints. 4. Overall survival, defined by time from diagnosis to death from any cause 5. Clinical trial enrollment, defined by participation in any therapeutic clinical trial related to lung cancer treatment after diagnosis 6. Completion of multi-disciplinary consultations, defined by patients completing consultations with at least one other specialist other than a thoracic medical oncologist or thoracic surgeon from time of initial consultation for the YOLC Program 7. Quality of life, as defined by FACT-LUNG 8. Financial toxicity, as defined by patient-reported financial burden, including out-of-pocket costs, insurance coverage issues, and impact of overall financial well-being (measured using validated financial toxicity scale such as COST-FACIT
Age
18 - 50 years
Sex
ALL
Healthy Volunteers
No
The University of Texas M. D. Anderson Cancer Center
Houston, Texas, United States
Start Date
September 25, 2025
Primary Completion Date
May 31, 2029
Completion Date
May 31, 2031
Last Updated
October 23, 2025
75
ESTIMATED participants
Survey
OTHER
Lead Sponsor
M.D. Anderson Cancer Center
NCT06498635
NCT06305754
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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