NCT06998550

Brief Summary

The PRETTY Study aims to evaluate patient satisfaction with pulmonary rehabilitation (PR) services across Türkiye and to investigate how satisfaction levels are related to the organizational structures and team compositions of the PR programs. This national, multicenter, cross-sectional observational study will also identify structural and organizational factors that may enhance patient-centered care and promote the standardization of PR services.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
384

participants targeted

Target at P75+ for all trials

Timeline
1mo left

Started Jul 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress92%
Jul 2025Jun 2026

First Submitted

Initial submission to the registry

May 22, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

May 31, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

July 29, 2025

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Last Updated

September 9, 2025

Status Verified

September 1, 2025

Enrollment Period

10 months

First QC Date

May 22, 2025

Last Update Submit

September 2, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • Patient Satisfaction Questionnaire

    An online survey designed to assess patient experiences and satisfaction levels with pulmonary rehabilitation (PR) programs. The questionnaire covers aspects such as accessibility, communication, program structure, perceived outcomes, and overall satisfaction. It is administered via Google Forms and completed voluntarily by patients who have completed a PR program.

    Within 4 weeks after completion of the pulmonary rehabilitation program

  • Institutional Survey on PR Program Structure and Team Composition

    A structured online questionnaire completed by the designated PR program coordinator or team member. It includes questions on organizational features of the PR program, such as team composition, session frequency, assessment tools, referral and admission criteria, and program setting (inpatient, outpatient, or home-based). This survey aims to document the structural diversity of PR services across different healthcare institutions.

    Within 4 weeks after completion of the pulmonary rehabilitation program

Study Arms (2)

PatiePatient Group: Individuals Who Completed a Pulmonary Rehabilitation Programnts

Adult patients with a respiratory disease who have completed a pulmonary rehabilitation (PR) program, regardless of the setting (inpatient, outpatient, or home-based).

Other: Patient Satisfaction Questionnaire

Institutional Representative Group: Pulmonary Rehabilitation Program Coordinators

Healthcare professionals (e.g., physiotherapists, pulmonologists, or allied health staff) who are designated as coordinators or key team members responsible for organizing and managing the pulmonary rehabilitation program in their institution.

Other: Institutional Survey on PR Program Structure and Team Composition

Interventions

An online survey designed to assess patient experiences and satisfaction levels with pulmonary rehabilitation (PR) programs. The questionnaire covers aspects such as accessibility, communication, program structure, perceived outcomes, and overall satisfaction. It is administered via Google Forms and completed voluntarily by patients who have completed a PR program.

PatiePatient Group: Individuals Who Completed a Pulmonary Rehabilitation Programnts

A structured online questionnaire completed by the designated PR program coordinator or team member. It includes questions on organizational features of the PR program, such as team composition, session frequency, assessment tools, referral and admission

Institutional Representative Group: Pulmonary Rehabilitation Program Coordinators

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Group/Cohort 1 (Label): Patient Group Description: Adults with respiratory disease who have completed a PR program and will complete the Patient Satisfaction Questionnaire. Group/Cohort 2 (Label): Program Coordinator Group Description: Healthcare professionals responsible for PR program coordination who will complete the Institutional Survey Form about organizational and team structures.

You may qualify if:

  • 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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Saglik Bilimleri Universitesi

Istanbul, Üsküdar, 34668, Turkey (Türkiye)

RECRUITING

MeSH Terms

Conditions

Lung Diseases

Condition Hierarchy (Ancestors)

Respiratory Tract Diseases

Central Study Contacts

Esra Pehlivan, Assoc Professor

CONTACT

Fulya Senem Karaahmetoğlu, PT

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
5 Days
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD

Study Record Dates

First Submitted

May 22, 2025

First Posted

May 31, 2025

Study Start

July 29, 2025

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

June 1, 2026

Last Updated

September 9, 2025

Record last verified: 2025-09

Locations