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Improving Patient-Centered Care Delivery Among Patients With Chronic Obstructive Pulmonary Disease (BREATHE)

Johns Hopkins University logo

Johns Hopkins University

Status

Completed

Conditions

Chronic Obstructive Pulmonary Disease

Treatments

Other: BREATHE program
Other: Usual Care

Study type

Interventional

Funder types

Other

Identifiers

NCT02036294
NA_00090518
IH-1304-7118 (Other Identifier)

Details and patient eligibility

About

This study involves development and testing of a patient and family-centered transitional care program for patients who are hospitalized with Chronic Obstructive Pulmonary Disease (COPD) exacerbations. The study intervention includes tailored services to address individual patients' biopsychosocial needs, starting early during hospital stay and continuing for 3 months post hospital discharge.

The study hypothesis is that compared to usual care, the study intervention will : a) Improve patient health- related quality of life and survival, and reduce use of hospital and emergency room visits; b) result in improved patient experience, self- confidence, and self-care behaviors; c) result in improved family caregivers coping skills, self-confidence, and problem solving skills to address patient barriers to care and treatment.

Full description

This study evaluates using a randomized controlled trial design the impact of a patient and family-centered transitional care program named the BREATHE program. The BREATHE program stands for 'Better Respiratory Education and Treatment Help Empower'. The BREATHE program offers the following:

  1. Individualized transition support services to help ensure that the patient (and family caregiver if available) are prepared for discharge, understand the discharge plan of care, and receive post discharge follow up to help meet their needs
  2. Tailored COPD self-management education and support program that starts during the hospital stay and continues post discharge in the community setting
  3. Facilitated access to community based services.

The intervention is delivered by a new team member called "COPD Nurse Transition Guide". The new team member works with both the hospital and outpatient care teams, is a registered nurse with homecare services experience, and have received additional training in COPD self-management and motivational interviewing. The nurse meets participants in the hospital and then follows up with them via home visits and phone calls.The intervention involves both patients and family caregivers (if available), is literacy adapted, and follows a tailored approach based on patient needs, priorities, and preferences.

Enrollment

240 patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Admitted to the hospital with a diagnosis of an acute COPD exacerbation; OR has a previous COPD diagnosis* AND receiving treatment to control COPD symptoms - (e.g. nebulizer treatment, prednisone course, ...) in the current hospitalization
  • Age > 40 and >10 pack-yrs smoking
  • English speaking
  • Anticipated discharge back to home (rather than to Hospice or long term nursing home placement)

Exclusion criteria

  • Severe cognitive dysfunction
  • Terminal illness (less than 6 months life expectancy) that is non-COPD related
  • Homeless (no home address)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

240 participants in 2 patient groups

Usual Care
Other group
Description:
Usual Care: Standard healthcare services will be received. Study participants in this arm will not receive any additional study interventions.
Treatment:
Other: Usual Care
BREATHE program
Experimental group
Description:
Study participants randomized to this arm will be offered the BREATHE program an integrated multifaceted intervention that includes comprehensive biopsychosocial assessment, a tailored treatment plan, a tailored disease management program, and care management support services .
Treatment:
Other: BREATHE program

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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