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Sleep Disorders in Patients With Suspected Lung Cancer Before and After Thoracic Surgery

K

Koç University

Status

Unknown

Conditions

Lung Cancer

Treatments

Other: Epworth Sleepiness Scale (ESS)
Other: Insomnia Questionnaire
Other: Restless Leg Syndrome Questionnaire
Other: Zung Self-rating Depression Scale (SDS)
Other: Functional Outcome of Sleep Questionnaire Turkish version (FOSQ-TR)
Other: Beck Anxiety Inventory
Other: Stop-Bang Questionnaire
Other: Berlin Questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT04759651
2020.482.IRB1.172

Details and patient eligibility

About

The main aim of this study is to prospectively evaluate the occurrence of sleep disorders in patients undergoing thoracic surgery due to the preliminary diagnosis of lung cancer. Secondary aims include anxiety, depressive mood and functional outcomes before and 3 months after the intervention.

Full description

Cancer surgery is one of the traumas that affect human life, starting from diagnostic procedures, along with the recovery process. Although 5-year survival in lung cancer has increased to 60%, there is a general prejudice that lung cancer has a poor prognosis. A preliminary diagnosis of a such condition has consequently a negative effect on the mood and sleep patterns of the patients, starting already from the beginning of the diagnostic procedures. In our study, we want to evaluate the occurrence of sleep disorders, anxiety, depressive mood and functional outcomes before and 3 months after the surgical intervention. This would also help us to better identify the patients in need for professional support for sleep disorders as well as psychiatric conditions, and thus, a better management of patients with lung cancer.

Enrollment

1,200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who will undergo lung resection with a pre-diagnosis of lung cancer
  • Being literate or having the physical strength to answer questions.

Exclusion criteria

  • The patient has a chronic disease such as dementia or treatment-resistant schizophrenia in which reality assessment is impaired.
  • Patients who have received chemotherapy and / or radiotherapy due to their previous disease.

Trial contacts and locations

1

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Central trial contact

Hale Yapıcı Eser, MD; Suat Erus, MD

Data sourced from clinicaltrials.gov

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