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NCT07401056Not yet recruiting

Preoperative Structured Exercise Programme on Patients With Non-Small Cell Lung Cancer

The Effect of Preoperative Structured Exercise Programme on Postoperative Pain Severity, Recovery Level, Discharge Time and Quality of Life in Patients With Non-Small Cell Lung Cancer: Randomised Controlled Study

Source: ClinicalTrials.gov · Last updated 12 Feb 2026

Brief summary (registry, in English)

INTRODUCTION: Lung cancer is among the leading cancers, and surgery has a major role in treatment. Patients diagnosed with Non-Small Cell Lung Cancer (NSCLC) who are eligible for surgical treatment have a high risk of experiencing postoperative complications. Therefore, in recent years, the concept of prehabilitation has begun to gain importance. Within the scope of prehabilitation practices, patients are provided with programmes that include aerobic exercises and breathing exercises in the preoperative period. AIM: This study aims to evaluate the effects of a structured exercise programme, including aerobic exercises and breathing exercises in the preoperative period, on postoperative pain severity, surgical recovery level, length of hospital stays (LOS), and quality of life (QoL) in patients diagnosed with NSCLC and planned for surgical treatment. METHODS: The research is an experimental, parallel group-randomised controlled trial to be conducted with 62 participants followed in the Thoracic Surgery Outpatient Clinic of Dr. Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital and scheduled for surgery due to NSCLC. Patients will be equally assigned to the intervention and control groups using the block randomization method. In the intervention group, in the preoperative period, for two weeks and five days per week, at least 30 minutes of walking per day will be performed; in addition, for two weeks before surgery, throughout the entire week, during waking hours, 10 repetitions with incentive spirometer every hour, and daily four sessions of deep breathing \& coughing exercises will be performed as breathing exercises. In the control group, routine preoperative clinical procedures will be applied. In the postoperative period, pain severity, surgical recovery level, LOS, and QoL will be compared between the two groups. Data will be collected face-to-face by the researcher using the "Descriptive Characteristics Form", "EQ-5D-5L Quality of Life Scale", "Numeric Rating Scale (NRS)", and "Surgical Recovery Scale". Data on the length of hospital stay will be obtained from patient files. The data will be analysed using parametric and/or nonparametric tests through the SPSS. CONCLUSION: The findings of the study are expected to contribute to strengthening holistic care approaches for the preoperative period in surgical nursing practices and to improving patient outcomes.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
62 (estimated)
First submitted
3 Feb 2026
Start date
Feb 2026
Primary completion date
Feb 2027
Lead sponsor
Hacettepe University
Diseases
Lung cancer
NCT number
NCT07401056

What you commit to

  • Study type: Interventional
  • Planned participants: 62
  • From Feb 2026 to the primary completion date, Feb 2027
  • 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

  • Previous radiotherapy treatment prior to surgery.
  • Inability to complete the two-week structured exercise programme due to surgery being scheduled earlier or later than planned.
  • Complications resulting in prolonged (\>24 hours) intensive care unit stay after surgery.

Other illness

  • Diagnosis of recurrent lung cancer.
  • Any condition preventing walking or exercise (orthopedic, neurological, cardiovascular, metastatic, etc.).
  • Diagnosis of additional respiratory system disease such as COPD, asthma, or emphysema preventing breathing exercises.

Other

  • Inability to discontinue or continue the structured exercise programme at any stage.
  • Refusal to participate in the study.

Who the study is looking for

  • Age ≥ 18 years.
  • Ownership of a smartphone capable of tracking daily walking time.
  • Diagnosis of primary non-small cell lung cancer.
  • ASA (American Society of Anesthesiologists) classification I, II, or III.
  • Follow-up and treatment provided by the same surgical team.
  • No physical or cognitive impairment that would hinder participation in the study.

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
Hacettepe University, Ankara, Altındağ 06230
Coordinator of this site? Confirm its status
AnkaraTurkey (Türkiye)Unknown status

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