Actively Recruiting

Age: 18Years - 70Years
All Genders
ID06727370

Cognitive Screening in Lung Cancer Patients

Led by European Institute of Oncology · Updated on 2024-12-10

200

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating how lung cancer and its treatments may affect thinking and memory in patients with both small-cell lung cancer (SCLC) and non-small-cell lung cancer (NSCLC). This observational study aims to understand the occurrence of cognitive impairment during the first year after patients join the study. The European Institute of Oncology is leading this research to better understand cognitive changes in lung cancer patients. The study includes patients diagnosed with lung cancer across all stages (I to IV). There are no drug treatments or interventions involved since this is an observational study, meaning researchers will monitor and assess participants without giving any new treatments. Participants will be observed and evaluated during the first year after enrollment to track cognitive changes. Participants will undergo comprehensive neuropsychological assessments to measure thinking and memory abilities at different times over one year. Researchers will also look for risk factors that might affect cognitive function in lung cancer patients. The study excludes patients with brain metastases, brain radiotherapy, or other neurological or psychiatric disorders. The total time of involvement is up to 12 months, during which participants will complete cognitive tests and other assessments.

CONDITIONS

Brief Title

Cognitive Screening in Lung Cancer Patients

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of small-cell or non-small-cell lung cancer (stage I, II, III, or IV)
  • Age 18 years or older
  • Ability to speak and read the local language fluently
  • Willingness to provide signed informed consent
Not Eligible

You will not qualify if you...

  • Age 70 years or older
  • Presence of brain metastases
  • Having neurological or psychiatric disorders
  • Receiving brain radiotherapy
  • Previous diagnosis of lung cancer

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 12 months

Participants are observed to assess cognitive impairment and risk factors over time.

Visits occur at baseline and periodically up to 12 months

Trial Site Locations

Total: 1 location

1

Istituto Europeo di Oncologia

Milan, Italy, 20141

Actively Recruiting

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Research Team

G

Gabriella Pravettoni

L

Lorenzo Conti

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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