Investigation of the Effects of Tele-Yoga Training in Individuals With Lung Cancer Undergoing Lung Resection Surgery
The Effects of an 8-Week Tele-Yoga Program on Postoperative Recovery in Patients With Lung Cancer Undergoing Lung Resection
1 other identifier
interventional
40
1 country
1
Brief Summary
This randomized controlled clinical trial aims to evaluate the effects of an 8-week tele-yoga intervention in individuals with lung cancer who have undergone lung resection surgery. The intervention group will receive supervised yoga sessions via online synchronous video conferencing, while the control group will continue with standard post-operative care. The primary outcome is exercise capacity (6-minute walk test), with secondary outcomes including pulmonary function, respiratory and peripheral muscle strength, physical activity level, dyspnea, fatigue, sleep quality, anxiety and depression, and quality of life. It is hypothesized that tele-yoga will improve physical and psychological recovery post-surgery and may serve as a feasible home-based pulmonary rehabilitation alternative.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jun 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
May 23, 2025
CompletedFirst Posted
Study publicly available on registry
June 3, 2025
CompletedStudy Start
First participant enrolled
June 10, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 10, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 10, 2026
December 18, 2025
May 1, 2025
1 year
May 23, 2025
December 10, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The Six-Minute Walk Test (6MWT)
Distance walked in six minutes will be recorded. Test will be conducted according to the guideline of American Thoracic Society. Functional exercise capacity will be evaluated with the six-minute walk test. Patients will be walked in a 30-meter-long corridor for 6 minutes and the maximum walking distance will be measured. Before and after the test, heart rate, blood pressure and O2 saturation will be measured with pulse oximetry, and dyspnea and fatigue levels will be determined according to the Modified Borg scale.
Change from Baseline at 8 weeks
Secondary Outcomes (12)
Incremental Shuttle Walk Test (ISWT)
Change from Baseline at 8 weeks
6-Minute Pegboard and Ring Test (6PBRT)
Change from Baseline at 8 weeks
Pulmonary Function Tests (PFT)
Change from Baseline at 8 weeks
Respiratory Muscle Strength Test (MIP/MEP)
Change from Baseline at 8 weeks
Peripheral Muscle Strength (Handgrip Strength Test)
Change from Baseline at 8 weeks
- +7 more secondary outcomes
Study Arms (2)
Tele-Yoga Group
EXPERIMENTALParticipants in this arm will receive an 8-week supervised tele-yoga program delivered via real-time video conferencing.
Control Group
NO INTERVENTIONThe control group will not receive any intervention.
Interventions
The Tele-yoga group will participate in real-time yoga sessions three times a week for eight weeks, including individual sessions for the first two weeks and small group sessions for the remaining six weeks, with all sessions supervised by a certified instructor. Each session will last approximately 45-60 minutes and include a 5-10 minute warm-up, 15-20 minutes of yoga postures, 15-20 minutes of yogic breathing exercises, and 5-10 minutes of relaxation and meditation.
Eligibility Criteria
You may qualify if:
- Aged between 18 and 65 years,
- Histologically confirmed diagnosis of Stage I-IIIA lung cancer according to the 9th edition of the AJCC Cancer Staging Manual,
- Underwent lobectomy, pneumonectomy, segmentectomy, or wedge resection via thoracotomy or video-assisted thoracoscopic surgery (VATS),
- An estimated life expectancy of ≥6 months,
- Karnofsky Performance Status score greater than 80% at study entry,
- Possession of the necessary equipment and access to a stable internet connection to enable participation in online interventions.
You may not qualify if:
- History of receiving radiotherapy or chemotherapy prior to surgery,
- Presence of severe dysfunction in vital organs such as the heart, brain, kidneys, or others,
- Having any comorbid condition that contraindicates participation in an exercise training program,
- Presence of serious postoperative complications,
- Cognitive impairments that hinder effective communication,
- Current participation in a structured and regular exercise program,
- Missing three consecutive weeks of sessions or completing less than 75% of the prescribed exercises,
- Voluntary withdrawal from the study by the participant.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Thoracic Surgery, Cerrahpaşa Faculty of Medicine, Istanbul University-Cerrahpaşa
Istanbul, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Rengin Demir, Prof
Istanbul University - Cerrahpasa
- PRINCIPAL INVESTIGATOR
Akif Turna, Prof
Istanbul University - Cerrahpasa
- PRINCIPAL INVESTIGATOR
Sevde B Kara, PhD student
Istanbul University - Cerrahpasa
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- Outcome assessments will be performed by an investigator who is blinded to group allocation.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
May 23, 2025
First Posted
June 3, 2025
Study Start
June 10, 2025
Primary Completion (Estimated)
June 10, 2026
Study Completion (Estimated)
July 10, 2026
Last Updated
December 18, 2025
Record last verified: 2025-05
Data Sharing
- IPD Sharing
- Will not share