Clinical trial Recruiting at 1 site Observational Ages 18 to 80

How team organization affects patient experience in pulmonary rehabilitation in Türkiye

Official title: Patient Experiences and the Role of Team Structures in Pulmonary Rehabilitation in Türkiye: The PRETTY Study - A National, Multicenter, Cross-Sectional Observational Study

Run by Saglik Bilimleri Universitesi · NCT06998550 · Data updated 2026-11-12

This project will ask adults in Türkiye who completed pulmonary rehabilitation to see if different program team setups are linked to their satisfaction.

Quick facts

Study typeObservational
Ages18 Years to 80 Years
SexAll
Enrollment384 (estimated)
SponsorSaglik Bilimleri Universitesi
Academic / other
Locations1 site (Istanbul, Üsküdar)
StatusRecruiting
StartedJuly 29, 2025
Main results expectedJune 1, 2026
Study endsJune 1, 2026
Registry record updatedSeptember 9, 2025
Trial IDNCT06998550 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (≥18) in Türkiye with a diagnosed respiratory condition who have completed a structured pulmonary rehabilitation program and can complete the online questionnaire are ideal candidates.

Probably not a fit

People still enrolled in a PR program, or those unable to complete the questionnaire without caregiver help because of cognitive or language barriers, will not be included and therefore will not directly benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This national, multicenter, cross-sectional observational project will collect patient-reported satisfaction data and institutional information from pulmonary rehabilitation (PR) centers across Türkiye. Adults who have completed a structured PR program will complete an online Patient Satisfaction Questionnaire, and designated PR coordinators will complete an Institutional Survey on team composition and service delivery. The analysis will look for associations between organizational features (such as multidisciplinary staffing, coordinator roles, and service models) and reported patient satisfaction. Results aim to identify structural factors that support patient-centered care and inform standardization of PR services nationwide.

Why it matters

Potential benefit: If successful, the work could point to specific team and organizational changes that improve patient satisfaction and help standardize pulmonary rehabilitation services in Türkiye.

How similar studies have gone: Similar cross-sectional surveys in other countries have found links between rehabilitation team composition and patient satisfaction, but comprehensive national multicenter data from Türkiye are limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Patient Inclusion Criteria:

* Age ≥18 years
* Diagnosed with a respiratory condition (e.g., COPD, interstitial lung disease, asthma, bronchiectasis, etc.)
* Completed a structured PR program (minimum duration and frequency as defined by national guidelines or center-specific protocols)
* Willing and able to complete the online Patient Satisfaction Questionnaire
* Able to provide informed consent

Patient Exclusion Criteria:

* Ongoing participation in a PR program (only completed cases will be included)
* Inability to complete the questionnaire due to cognitive or language barriers without a caregiver

Coordinator Inclusion Criteria:

* Officially designated as the PR program coordinator or responsible team member
* Affiliated with a healthcare institution (public, university-affiliated, or private) in Türkiye that provides PR services
* Willing to complete the Institutional Survey Form regarding team structure, service delivery, and organizational characteristics
* Authorized by the institution to provide structural data related to the PR unit

Coordinator Exclusion Criteria:

* PR services provided on an informal or ad-hoc basis without a designated team or structure
* Institutions not offering a structured PR program

Where it's running

  • Saglik Bilimleri Universitesi
    Istanbul, Üsküdar, Turkey (Türkiye)
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.