Clinical Trials Directory

Trials / Unknown

UnknownNCT05826756

Project PEER: Understanding the Lung Cancer Patient ExperiEnce in the Real-World Setting

Status
Unknown
Phase
Study type
Observational
Enrollment
1,300 (estimated)
Sponsor
LUNGevity Foundation · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

LUNGevity Foundation, a non-profit lung cancer organization, wants to learn about living with lung cancer from the point of view of people with lung cancer and their family and friends who provide care. To do this, we have an online study designed to better understand how treatments people living with lung cancer receive impact their quality of life. Participants will complete surveys once a month for 12 months. What does participation involve? 1. Emailing the study team to learn more and get access to the study website. 2. Once a month for 12 months you will receive a survey by email. 3. Complete these surveys on a smartphone, tablet, or computer at your convenience and receive an e-gift card for your time.

Detailed description

PEER is an international study, that is Institutional Review Board (IRB) approved and General Data Protection Regulation (GDPR) compliant. The study objective is to collect longitudinal data to facilitate a rigorous understanding of the diagnostic and treatment experiences of people diagnosed with lung cancer and to identify determinants of treatment heterogeneity. Study data will be used to understand the diagnostic and treatment pathways, explore patient-experience data in different domains (financial impact/quality of life/symptoms) and test the hypothesis that different classes of therapies (chemotherapy/ immunotherapy/ targeted therapy/ surgery/ radiation) impact patient experience (eg., physical function). Study participants will consent and register for the study and complete an initial baseline survey. They will then be followed for 12 months and receive a monthly survey (11 surveys in total) via email. The development of the surveys was guided by input from patients, clinicians, FDA experts, and incorporates questions from existing patient-reported outcomes (PRO) measures. Summarized study results will also be posted on LUNGevity's website. External researchers will be able to apply to have limited access to de-identified data.

Conditions

Interventions

TypeNameDescription
OTHERThere are no interventions in this study. All participants complete online surveys.There are no interventions in this study. All participants complete online surveys.

Timeline

Start date
2020-08-15
Primary completion
2024-12-01
Completion
2025-12-01
First posted
2023-04-24
Last updated
2023-04-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05826756. Inclusion in this directory is not an endorsement.