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NCT07388225Completed

The Effect of Preoperative Education on Recovery of Thoracic Surgery Patients

Source: ClinicalTrials.gov · Last updated 5 Feb 2026

Brief summary (registry, in English)

Brief Summary This randomized controlled study evaluated the effect of structured preoperative education on postoperative recovery outcomes in patients undergoing thoracic surgery for lung cancer. The study was conducted in a tertiary public hospital in Istanbul between June 2022 and December 2023 and included 100 adult patients who met the inclusion criteria. Participants were randomly assigned to an intervention group or a control group. Patients in the intervention group received structured, nurse-led preoperative education supported by a standardized patient education booklet, while the control group received routine hospital care. Recovery outcomes were assessed using physiological parameters, pulmonary function tests, shoulder joint range of motion measurements, pain intensity scores, and the Quality of Recovery-40 (QoR-40) questionnaire during the early postoperative period. The findings of this study aim to contribute evidence on the role of preoperative nursing education in improving functional recovery, reducing postoperative pain, and supporting respiratory function in patients undergoing thoracic surgery.

Status (registry)
Completed
Study type
Interventional
Enrollment
100 (actual)
First submitted
23 Jan 2026
Start date
1 Jun 2022
Primary completion date
31 Dec 2023
Lead sponsor
Başakşehir Çam & Sakura City Hospital
Diseases
Lung cancer
NCT number
NCT07388225

What you commit to

  • Study type: Interventional
  • Participants enrolled: 100
  • From 1 Jun 2022 to the primary completion date, 31 Dec 2023
  • 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.

Prior treatment

  • Patients with chronic pain in the preoperative period who are using analgesic medications for pain management
  • Patients receiving antineoplastic treatment

Other illness

  • Patients undergoing reoperation due to lung cancer
  • Patients diagnosed with metastatic lung cancer

Other

  • Patients with an ECOG performance status greater than 2
  • Patients with limited mobility in the preoperative period

Who the study is looking for

  • Patients diagnosed with lung cancer who are hospitalized for elective thoracic surgery
  • Aged 18 years and older
  • Able to read, write, and speak Turkish
  • Able to understand the information provided and without any condition that interferes with verbal communication
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2
  • Patients scheduled for lung resection via thoracotomy
  • Patients undergoing surgery under general anesthesia

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
Başakşehir Çam and Sakura City Hospital
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

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