Cardio-pulmonary Rehabilitation and Sleep Quality

December 8, 2023 updated by: Vidya Krishnan, MetroHealth Medical Center

Cardio-pulmonary Rehabilitation and Its Impact on Sleep Quality; a Prospective Analysis

In this prospective cohort study the investigators aim to evaluate the effect of pulmonary rehabilitation on sleep quality. Disturbed sleep is associated with, frequent exacerbations, increase in the severity of disease and increased mortality in chronic obstructive pulmonary disease (COPD). Sleep quality is a good predictor of quality of life in patients with stable COPD. However, there has been little investigation into non-pharmacological methods to improve sleep quality in patients with COPD and heart failure. It is also uncertain, how long the beneficial effects of cardio-pulmonary rehabilitation on sleep quality, if any, usually last. Due to lack of robust data, the investigators sought to find the effect of cardio-pulmonary rehabilitation on sleep quality.

Study Overview

Detailed Description

Sleep disorders including poor quality of sleep are common in patients with heart failure, chronic obstructive pulmonary disease (COPD) and, possibly, other chronic lung disorders. These patients complain of difficulty sleeping and sleep fragmentation, often related to symptoms such as cough, sputum production or shortness of breath. Patients with COPD and heart failure commonly have other abnormalities such as nocturnal oxygen desaturation that may further worsen sleep disturbances. Moreover, sleep disordered breathing (SDB), like obstructive sleep apnea syndrome (OSA), has been linked to higher morbidity and mortality if COPD is present (known as Overlap syndrome). In patients with COPD and heart failure, cardio-pulmonary rehabilitation has important health benefits such as improvement in disease related symptoms, exercise tolerance, and health-related quality of life. However, the effect of cardio-pulmonary rehabilitation on sleep quality is controversial. Disturbed sleep is associated with frequent exacerbations, increase in the severity of disease and increased mortality in COPD and heart failure patients.

The investigators hypothesize that cardio-pulmonary rehabilitation results in improved sleep quality in patients with chronic lung disease and heart failure, this may be an important contributor to improved health outcomes after completion of cardio-pulmonary rehabilitation program.

The study will use data from questionnaires filled by the patients before and after completion of cardio-pulmonary rehabilitation. A 3-month follow up survey using the same questionnaires will be conducted to determine the longevity of improved sleep quality (if present). The questionnaires that will be used include Pittsburgh sleep quality index (PSQI), Epworth sleepiness scale (ESS), Berlin questionnaire, COPD assessment test (CAT) for COPD patients, Kansas city cardiomyopathy questionnaire (KCCQ) for heart failure patients, hospital induced anxiety and depression scale (HADS) and insomnia severity index (ISI).

Study Type

Observational

Enrollment (Estimated)

30

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Ohio
      • Cleveland, Ohio, United States, 44109
        • MetroHealth Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Setting: Outpatient

The study cohort will include patients will chronic lung and heart diseases who meet the inclusion criteria and are to undergo cardiopulmonary rehabilitation in a safety net hospital.

Description

Inclusion Criteria:

  • Age > 18 years
  • Patient who are willing to participate in follow-up survey 3 months after completion of pulmonary rehabilitation.
  • Patients who complete rehabilitation for at least 8 weeks.

Exclusion Criteria:

• Not meeting inclusion criteria

Study Plan

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

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Patient with chronic lung or cardiac diseases

This study will focus on patients with obstructive or restrictive lung diseases eligible for pulmonary rehabilitation.

Patient with cardiac disease such as heart failure, coronary artery disease or cardiomyopathies who are eligible for cardiac rehabilitation will also be included.

Patients will undergo standardized cardio-pulmonary rehabilitation program.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Improvement in sleep quality using Pittsburgh sleep quality index
Time Frame: 8 weeks on average

Pittsburgh sleep quality index is validated questionnaire and will be used to determine improvement in sleep quality before and after completion of cardiopulmonary rehabilitation. Pittsburgh sleep quality index comprises of seven components. Each component is marked from 0 to 3, with a maximum total score of 21 and a minimum total score of 0. A score of less than 5 indicates good overall sleep quality and a score of 5 and more indicates poor sleep quality.

From literature review using Pittsburgh sleep quality index, minimal clinically important difference was determined to be 3 between before and after measurements.

8 weeks on average
Sleep apnea screening using Berlin questionnaire.
Time Frame: Through study completion which is approximately one year.
Berlin questionnaire will be used to screen for sleep apnea in individuals who are to begin cardiopulmonary rehabilitation and do not have a known diagnosis of sleep apnea. Investigators will specifically look for the percentage of patients who are at high risk for sleep apnea based on Berlin questionnaire (positive score on 2 out of 3 categories of the questionnaire) in the cardio-pulmonary cohort.
Through study completion which is approximately one year.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Effect of cardio-pulmonary rehabilitation on disease specific health related quality of life.
Time Frame: 8 weeks

Hospital anxiety and depression scale is self-reported questionnaire tool to screen for anxiety and depression with two subscales (one of anxiety and one for depression). Each subscale has a minimum score of 0 and maximum score of 21. A cut-off of 11 or more indicates probable mood disorder.

COPD assessment test will be used for COPD patients. COPD assessment test consists of 8 items with a minimum score of 0 and a maximum score of 40. A score of 10 or more suggests presence of significant lung disease.

Kansas city cardiomyopathy questionnaire consists of 23 items with a minimum score of 0 and a maximum score of 100. A score of less than 25 signifies presence of poor heart function.

Change in mean scores before and after rehabilitation will be determined and paired student t-test will be used to determine if the change in scores is significant.

8 weeks
Correlation between sleep quality and disease specific health related quality of life.
Time Frame: 8 weeks
Correlation between change in disease specific health status as determined by the questionnaires (HADS, CAT and KCCQ) after cardio-pulmonary rehabilitation and change in sleep quality as determined by Pittsburgh sleep quality index will be determined by using Pearson's correlation coefficient (r).
8 weeks
Change in insomnia severity index
Time Frame: 8 weeks.
Insomnia severity index will be determined before and after cardiopulmonary rehabilitation. Insomnia severity index consists of 7 items with a minimum total score of 0 and maximum total score of 28 with a score of 8 or more suggesting presence of insomnia. A 6 point change is considered significant (minimum significant important difference) as determined by literature. Paired student t-test will be used to compare means before and after cardio-pulmonary rehabilitation
8 weeks.
Longevity of sleep improvement
Time Frame: 3 months.
Pittsburgh sleep quality index questionnaire will be administer 3-months after completion of cardio-pulmonary rehabilitation if there is improvement in sleep quality at the end of cardio-pulmonary rehabilitation. The mean scores from end of rehabilitation and 3-months after completion of cardio-pulmonary rehabilitation will be compared using paired student t-test.
3 months.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Vidya Krishnan, MD, MetroHealth Medical Center

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 11, 2020

Primary Completion (Estimated)

October 11, 2024

Study Completion (Estimated)

October 11, 2024

Study Registration Dates

First Submitted

October 7, 2020

First Submitted That Met QC Criteria

December 13, 2020

First Posted (Actual)

December 16, 2020

Study Record Updates

Last Update Posted (Actual)

December 12, 2023

Last Update Submitted That Met QC Criteria

December 8, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

No current plan to share individual participant data at this time.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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