NCT07197229

Brief Summary

This study evaluates the effect of a structured three-month pulmonary rehabilitation (PR) program, delivered both in-hospital and at home, on exercise capacity, respiratory symptoms, and functional status in stable COPD patients.

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
20mo left

Started Apr 2026

Status
not yet 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 Progress1%
Apr 2026Dec 2027

First Submitted

Initial submission to the registry

September 20, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

September 29, 2025

Completed
7 months until next milestone

Study Start

First participant enrolled

April 30, 2026

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 30, 2027

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2027

Last Updated

September 29, 2025

Status Verified

September 1, 2025

Enrollment Period

1.5 years

First QC Date

September 20, 2025

Last Update Submit

September 20, 2025

Conditions

Keywords

COPD

Outcome Measures

Primary Outcomes (1)

  • Six-Minute Walk Test (6MWT)

    Measures the distance (in meters) a patient can walk in six minutes as a marker of exercise capacity and functional endurance.

    12 weeks

Study Arms (1)

patients diagnosed with moderate-to-severe COPD (confirmed by spirometry) who are clinically stable

EXPERIMENTAL

Participants undergo a 12-week structured PR program including both hospital-based sessions (education, structured exercise, nutrition counseling, smoking cessation) and home-based exercises (daily walking, strength training progression).

Behavioral: Pulmonary Rehabilitation

Interventions

A tailored pulmonary rehabilitation program combining hospital-based and home-based components over 12 weeksParticipants undergo a 12-week structured PR program including both hospital-based sessions (education, structured exercise, nutrition counseling, smoking cessation) and home-based exercises (daily walking, strength training progression

patients diagnosed with moderate-to-severe COPD (confirmed by spirometry) who are clinically stable

Eligibility Criteria

Age40 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Stable COPD patients diagnosed based on spirometry (post-bronchodilator FEV1/FVC \<70%)
  • Age \> 40 years
  • Moderate to severe COPD stage
  • Able and willing to participate in rehabilitation program

You may not qualify if:

  • Age \< 40 years
  • Current acute COPD exacerbation at enrollment
  • Significant comorbid conditions limiting participation (e.g., uncontrolled diabetes mellitus, uncontrolled hypertension, left-sided heart failure, renal failure, liver cell failure)
  • Neuromuscular diseases, severe cognitive impairment, or psychiatric disturbance
  • Pregnant patients
  • Unwilling to participate in the rehabilitation program

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (1)

  • Arnold MT, Dolezal BA, Cooper CB. Pulmonary Rehabilitation for Chronic Obstructive Pulmonary Disease: Highly Effective but Often Overlooked. Tuberc Respir Dis (Seoul). 2020 Oct;83(4):257-267. doi: 10.4046/trd.2020.0064. Epub 2020 Aug 10.

    PMID: 32773722BACKGROUND

MeSH Terms

Conditions

Pulmonary Disease, Chronic Obstructive

Condition Hierarchy (Ancestors)

Lung Diseases, ObstructiveLung DiseasesRespiratory Tract DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: ince this is a quasi-experimental single-arm study, there is only one intervention group the Pulmonary Rehabilitation Group: Participants undergo a 12-week structured PR program including both hospital-based sessions (education, structured exercise, nutrition counseling, smoking cessation) and home-based exercises (daily walking, strength training progression).
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
resident at the chest department

Study Record Dates

First Submitted

September 20, 2025

First Posted

September 29, 2025

Study Start

April 30, 2026

Primary Completion (Estimated)

October 30, 2027

Study Completion (Estimated)

December 30, 2027

Last Updated

September 29, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share