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

NCT04759651 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1200

Last updated 2022-04-15

No results posted yet for this study

Summary

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.

Conditions

Interventions

OTHER

Functional Outcome of Sleep Questionnaire Turkish version (FOSQ-TR)

Sleep related quality of life questionnaire.

OTHER

Epworth Sleepiness Scale (ESS)

Subjective level of daytime sleepiness.

OTHER

Berlin Questionnaire

Evaluation of high-risk for Obstructive Sleep Apnea.

OTHER

Stop-Bang Questionnaire

Evaluation of high-risk Obstructive Sleep Apnea.

OTHER

Insomnia Questionnaire

Subjective evaluation of insomnia.

OTHER

Restless Leg Syndrome Questionnaire

Subjective evaluation of Restless Leg Syndrome.

OTHER

Zung Self-rating Depression Scale (SDS)

Subjective test for evaluation of depressive mood.

OTHER

Beck Anxiety Inventory

Subjective test for evaluation of anxiety.

Sponsors & Collaborators

  • Marmara University

    collaborator OTHER
  • Trakya University School of Medicine

    collaborator UNKNOWN
  • Istanbul Sureyyapasa Chest Diseases and Chest Surgery Training and Research Hospital

    collaborator OTHER
  • Yedikule Training and Research Hospital

    collaborator OTHER
  • Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey

    collaborator OTHER
  • Koç University

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-06-01
Primary Completion
2022-12-31
Completion
2023-06-30

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04759651 on ClinicalTrials.gov