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NCT07754409Recruiting

Aspects of Quality of Life During Adjuvant Oncological Treatment for Locally Advanced Lung Cancer Which Include Immune Checkpoint Inhibitor.

Self-reported Health During Adjuvant Immunotherapy for Locally Advanced Lung Cancer - the ImmLungCare Project.

Source: ClinicalTrials.gov · Last updated 2 Sept 2026

Brief summary (registry, in English)

Current oncological treatment for patients with locally advanced lung cancer comprise adjuvant immunotherapy (immune checkpoint inhibitors-ICI) as an additional one-year treatment after chemoradiotherapy which increases overall survival and progression-free survival. Patients with lung cancer have a high burden of distressful symptoms at diagnosis and during chemoradiotherapy. Side-effects from immunotherapy differs, they are unspecific and may develop at any point during treatment. However, it is not investigated thoroughly during adjuvant treatment in locally advanced lung cancer. As new oncological treatments are being introduced, focus must be placed on patients quality of life and how patients endure treatment to be able to know how to best support patients during this treatment. The knowledge gained from this project include how adjuvant immunotherapy treatment impacts health. This knowledge is sparse due to the novelty of the treatment.

Status (registry)
Recruiting
Study type
Observational
Enrollment
75 (estimated)
First submitted
27 Jul 2026
Start date
1 Sept 2026
Primary completion date
31 Dec 2028
Lead sponsor
Göteborg University
Diseases
Lung cancer
NCT number
NCT07754409

What you commit to

  • Study type: Observational
  • Planned participants: 75
  • From 1 Sept 2026 to the primary completion date, 31 Dec 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • diseases or comorbidities that may have significant impact on the outcome variables

Other

  • limited understanding of the Swedish language preventing the possibility to give oral and written informed consent.

Who the study is looking for

  • Patients with locally advanced non-small lung cancer
  • cared for at either one of two specialized oncology centres
  • ≥ 18 years of age
  • planned for concurrent chemoradiotherapy including ICI for 12 months
  • performance status 0-2.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Department of Oncology, Sahlgrenska University Hospital
Coordinator of this site? Confirm its status
GothenburgSwedenRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.