Turkish Nijmegen Questionnaire Validation for COPD Assessment
This study aims to validate the Turkish version of the Nijmegen Questionnaire as a tool for assessing COPD (Chronic Obstructive Pulmonary Disease) in the Turkish population.
Data Collection
Collected from today forward - ProspectiveChronic Disease+5
+ Lung Diseases
+ Lung Diseases, Obstructive
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: January 30, 2026
Actual date on which the first participant was enrolled.This study focuses on patients with clinically stable COPD, a condition that affects breathing. The main goal is to validate the Nijmegen Questionnaire in Turkish, ensuring it's culturally appropriate and effective for Turkish-speaking COPD patients. This is important because it will help healthcare providers better understand and assess the symptoms of COPD in this population, potentially improving care and treatment. The study follows international guidelines for patient-reported outcome measures to ensure accuracy and reliability. The study involves two main phases. First, the Nijmegen Questionnaire is translated and adapted to Turkish, a process that includes forward and back-translation, review, and cognitive debriefing with patients. Once the Turkish version (NQ-TR) is ready, it's given to eligible participants twice, with a one-week gap, to assess its consistency. The study also evaluates how well the NQ-TR aligns with other established clinical measures for COPD, such as the COPD Assessment Test (CAT), Modified Medical Research Council (mMRC) Dyspnea Scale, Hospital Anxiety and Depression Scale (HADS), and Dyspnea-12 (D-12). This helps to ensure the questionnaire's validity and reliability.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.90 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 75 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria