NCT07441863

Brief Summary

This ambispective observational cohort study aims to evaluate age-related differences in clinical outcomes among patients undergoing lung cancer surgery who received a structured comprehensive in-patient physiotherapy (CIPT) program as part of standard postoperative care. The CIPT program includes patient education, chest physiotherapy, breathing exercises, airway clearance techniques, early mobilization, postural exercises, and upper- and lower-extremity range-of-motion exercises during the postoperative hospital stay. The primary outcome is hospital length of stay. Secondary outcomes include clinical parameters (blood pressure, resting heart rate, oxygen saturation, and respiratory rate), symptom-related outcomes (dyspnea, fatigue, and incisional pain), and inflammatory biomarkers (C-reactive protein, neutrophil-to-lymphocyte ratio, and albumin). Outcomes are analyzed according to predefined age groups (45-64 years and 65-90 years) to evaluate potential age-related differences.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jun 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2025

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

February 17, 2026

Completed
13 days until next milestone

First Posted

Study publicly available on registry

March 2, 2026

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 2, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 2, 2026

Completed
Last Updated

August 17, 2026

Status Verified

August 1, 2026

Enrollment Period

9 months

First QC Date

February 17, 2026

Last Update Submit

August 14, 2026

Conditions

Keywords

pulmonary physiotherapypulmonary rehabilitationlung cancerearly rehabilitationthoracic surgerylung cancer surgeryage-related outcomes

Outcome Measures

Primary Outcomes (3)

  • Length of Hospital Stay

    Length of hospital stay is defined as the number of days from postoperative admission to the ward until hospital discharge following lung cancer surgery.

    Postoperative period, from ward admission after surgery until hospital discharge (maximum 30 postoperative days)

  • C-reactive protein (CRP)

    Serum CRP levels (mg/L) will be measured to evaluate postoperative systemic inflammatory response.

    Postoperative Day 1 and at hospital discharge (up to 30 days after surgery)

  • Peripheral Oxygen Saturation (SpO₂)

    Peripheral oxygen saturation (%) will be measured using pulse oximetry to assess postoperative oxygenation status.

    Postoperative Day 1 and at hospital discharge (up to 30 days after surgery)

Secondary Outcomes (8)

  • Neutrophil-to-Lymphocyte Ratio (NLR)

    Postoperative Day 1 and at hospital discharge (up to 30 days after surgery)

  • Serum Albumin

    Postoperative Day 1 and at hospital discharge (up to 30 days after surgery)

  • Systolic Blood Pressure

    Postoperative Day 1 and at hospital discharge (up to 30 days after surgery)

  • Diastolic Blood Pressure

    Postoperative Day 1 and at hospital discharge (up to 30 days after surgery)

  • Heart Rate

    Postoperative Day 1 and at hospital discharge (up to 30 days after surgery)

  • +3 more secondary outcomes

Study Arms (2)

Middle-aged group (45-64 years)

Participants aged 45-64 years who underwent lung cancer surgery and received the comprehensive in-patient physiotherapy (CIPT) program as part of standard postoperative care during hospitalization. Outcomes were assessed during the postoperative inpatient period and compared with those of the older cohort.

Behavioral: Comprehensive In-Patient Physiotherapy (CIPT) Program

Older group (65-90 years)

Participants aged 65-90 years who underwent lung cancer surgery and received the comprehensive in-patient physiotherapy (CIPT) program as part of standard postoperative care during hospitalization. Outcomes were assessed during the postoperative inpatient period and compared with those of the middle-aged cohort.

Behavioral: Comprehensive In-Patient Physiotherapy (CIPT) Program

Interventions

The comprehensive in-patient physiotherapy (CIPT) program was provided as part of standard postoperative care following lung cancer surgery. The program included patient education, breathing exercises, incentive spirometry, airway clearance techniques, early mobilization, postural exercises, and upper- and lower-extremity range-of-motion exercises. It was initiated on the first day after transfer to the thoracic surgery ward and continued until hospital discharge. One session per day was supervised by a physiotherapist, with two additional sessions performed independently by the patient or with caregiver assistance

Middle-aged group (45-64 years)Older group (65-90 years)

Eligibility Criteria

Age45 Years - 90 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adults aged 45-90 years who underwent lung cancer surgery at Bezmialem Vakif University Hospital and received routine comprehensive in-patient physiotherapy (CIPT) as part of standard postoperative care. Eligible participants were hemodynamically stable during the early postoperative period and were classified into middle-aged (45-64 years) and older (65-90 years) cohorts for comparative analysis.

You may qualify if:

  • Patients aged 45 to 90 years
  • Undergoing lung cancer surgery (lobectomy, segmentectomy, or pneumonectomy)
  • Medically stable in the early postoperative period
  • Able to participate in a structured pulmonary physiotherapy program
  • Provided written informed consent

You may not qualify if:

  • Hemodynamic instability preventing mobilization
  • Severe cognitive impairment limiting cooperation
  • Neurological or orthopedic conditions restricting mobilization
  • Requirement for prolonged mechanical ventilation
  • Presence of another active malignancy
  • Any medical contraindication to physiotherapy as determined by the attending physician

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bezmialem Vakif University

Istanbul, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Lung Neoplasms

Condition Hierarchy (Ancestors)

Respiratory Tract NeoplasmsThoracic NeoplasmsNeoplasms by SiteNeoplasmsLung DiseasesRespiratory Tract Diseases

Study Officials

  • Ayşe Sena Manzak Dursun, Assistant Professor

    Bezmialem Vakif University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

February 17, 2026

First Posted

March 2, 2026

Study Start

June 1, 2025

Primary Completion

March 2, 2026

Study Completion

March 2, 2026

Last Updated

August 17, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Locations