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Predictors of the Long-term Functional Benefits of a Pulmonary Rehabilitation Program?

Predictors of the Long-term Functional Benefits of a Pulmonary Rehabilitation Program?

Status
Suspended
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02528487
Enrollment
360
Registered
2015-08-19
Start date
2015-05-31
Completion date
2023-03-31
Last updated
2019-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease

Keywords

Pulmonary Rehabilitation, Chronic Obstructive Pulmonary Disease, Psychiatric Disorders

Brief summary

The present study aims to assess the prevalence and impact of comorbid psychiatric disorders among patients with chronic obstructive pulmonary disease (COPD) undergoing pulmonary rehabilitation (PR), in order to determine the effects of psychiatric comorbidity on exercise tolerance and physical activity post-PR and HRQoL, as well as to determine the processes by which these psychiatric disorders may impact on these patient behaviours.

Interventions

None listed

Sponsors

Mount Sinai Rehabilitation Hospital
CollaboratorOTHER
Hopital Charles Lemoyne
CollaboratorOTHER
Centre hospitalier de l'Université de Montréal (CHUM)
CollaboratorOTHER
Jewish Rehabilitation Hospital
CollaboratorOTHER
Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

1. Patients over the age of 40 will be eligible if 2. they are diagnosed with moderate-severe COPD, 3. currently participate to a PR program, and 4. agree to participate.

Exclusion criteria

They will be excluded if: 1. they have any comorbidity that is more important (i.e., more likely to cause morbidity or mortality) than COPD (e.g., active cancer), 2. they have contraindications to exercise (though they will not likely be referred to PR), 3. they have participated in a PR program in the past year, 4. and if they are unable to provide informed consent due to language difficulties or cognitive impairment.

Design outcomes

Primary

MeasureTime frameDescription
The change in exercise tolerance at 1-year post-PRParticipants will be evaluated at 3 time points: (1) post-PR; (2) at 6-mo; (3) at 12-mo follow-up.Exercise tolerance will be measured with the 6-minute walking test (6MWT).

Secondary

MeasureTime frameDescription
The change in health-related quality of life (HRQoL) at 1-year post-PRParticipants will be evaluated at 3 time points: (1) post-PR; (2) at 6-mo; (3) at 12-mo follow-up.HRQoL will be measured with the 12-Item Short Form Survey and the COPD Assessment Test

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026