Comparison of Early Postoperative Functional Capacity and Kinesiophobia in Patients Undergoing Thoracic Surgery Via Thoracotomy or VATS
1 other identifier
observational
18
1 country
1
Brief Summary
This observational cross-sectional study aims to compare early postoperative functional capacity and kinesiophobia in patients undergoing thoracic surgery via thoracotomy or video-assisted thoracic surgery (VATS). Patients aged 18-75 years who underwent thoracic surgery and agreed to participate will be evaluated during the early postoperative period, after chest tube removal and before hospital discharge. Functional capacity will be assessed using the 1-minute sit-to-stand test. Kinesiophobia will be evaluated using the Tampa Scale for Kinesiophobia. Pain, dyspnea, fatigue, and coronavirus-related anxiety will also be assessed using validated scales and questionnaires. The study will investigate the relationship between kinesiophobia and postoperative functional and symptom-related outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started May 2021
1 active site
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
May 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2022
CompletedFirst Submitted
Initial submission to the registry
June 10, 2026
CompletedFirst Posted
Study publicly available on registry
June 15, 2026
CompletedJune 15, 2026
June 1, 2026
1 year
June 10, 2026
June 10, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Kinesiophobia
Kinesiophobia will be assessed using the Tampa Scale for Kinesiophobia. The scale consists of 17 items scored on a 4-point Likert scale. Total scores range from 17 to 68, with higher scores indicating greater fear of movement.
Early postoperative period, after chest tube removal and before hospital discharge, approximately postoperative days 2-10
Secondary Outcomes (5)
Functional Capacity
Early postoperative period, after chest tube removal and before hospital discharge, approximately postoperative days 2-10
Pain Level
Early postoperative period, after chest tube removal and before hospital discharge, approximately postoperative days 2-10
Dyspnea
Early postoperative period, after chest tube removal and before hospital discharge, approximately postoperative days 2-10
Fatigue
Early postoperative period, after chest tube removal and before hospital discharge, approximately postoperative days 2-10
Coronavirus-related Anxiety
Early postoperative period, after chest tube removal and before hospital discharge, approximately postoperative days 2-10
Study Arms (2)
Thoracotomy Group
Patients aged 18-75 years who underwent thoracic surgery via thoracotomy and agreed to participate in the study.
VATS Group
Patients aged 18-75 years who underwent thoracic surgery via video-assisted thoracic surgery and agreed to participate in the study.
Eligibility Criteria
Patients aged 18-75 years who underwent thoracic surgery via thoracotomy or video-assisted thoracic surgery at the Department of Thoracic Surgery, Hacettepe University, and agreed to participate in the study.
You may qualify if:
- Undergoing thoracic surgery via thoracotomy or video-assisted thoracic surgery
- Aged between 18 and 75 years
- Volunteering to participate in the study
- Providing informed consent
You may not qualify if:
- Presence of cooperation or communication problems that prevent assessment
- History of previous thoracic surgery
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
HAcettepe University
Ankara, Altındağ, 06100, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 10 Days
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MsC PT
Study Record Dates
First Submitted
June 10, 2026
First Posted
June 15, 2026
Study Start
May 1, 2021
Primary Completion
May 1, 2022
Study Completion
July 1, 2022
Last Updated
June 15, 2026
Record last verified: 2026-06