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Turkish Nijmegen Questionnaire Validation for COPD Assessment

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Study Aim

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.

What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Chronic Disease+5

+ Lung Diseases

+ Lung Diseases, Obstructive

From 18 to 75 Years
+12 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: January 2026
See protocol details

Summary

Principal SponsorSaglik Bilimleri Universitesi
Study ContactEsra PehlivanMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitleTurkish Validation of the Nijmegen Questionnaire in COPD
Principal SponsorSaglik Bilimleri Universitesi
Study ContactEsra PehlivanMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

90 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

Chronic DiseaseLung DiseasesLung Diseases, ObstructivePathologic ProcessesRespiratory Tract DiseasesPathological Conditions, Signs and SymptomsDisease AttributesPulmonary Disease, Chronic Obstructive

Criteria

5 inclusion criteria required to participate
Adults aged 18 years and older

Diagnosis of COPD confirmed according to GOLD criteria

Clinically stable disease (no acute exacerbation or hospitalization within the last 4 weeks)

Ability to read and understand Turkish

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7 exclusion criteria prevent from participating
Acute COPD exacerbation or respiratory infection within the previous 4 weeks

Presence of severe cardiac, neurological, or systemic disease affecting questionnaire responses

Coexisting pulmonary conditions such as bronchiectasis, lung cancer, prior pulmonary tuberculosis, pleural disease, or history of lung surgery

Moderate to severe cognitive impairment or communication difficulties

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Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.
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