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Clinical Trials/NCT00982384
NCT00982384
Completed
Not Applicable

Comprehensive Disease Management Program in COPD Patients in the Community: Randomized Controlled Trial

Sheba Medical Center2 sites in 1 country1,202 target enrollmentOctober 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Obstructive Pulmonary Disease (COPD)
Sponsor
Sheba Medical Center
Enrollment
1202
Locations
2
Primary Endpoint
Hospital admission for acute exacerbation of COPD or all-cause mortality
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to determine whether comprehensive disease management program combined with best care recommended in clinical guidelines, is more effective than best care alone in patients with advanced chronic obstructive pulmonary disease (COPD).

Detailed Description

The study objective is to evaluate the effectiveness of a comprehensive program among patients with advanced COPD, implemented by a multi-disciplinary team. The program consists of best care recommended in clinical guidelines, combined with disease management, compared to best care only. The program will include designated COPD centers operated by multi-disciplinary teams (pulmonologists, nurse practitioners, physiotherapists, social workers and dietitians). Disease management will be provided in these centers by qualified designated nurses.

Registry
clinicaltrials.gov
Start Date
October 2009
End Date
December 2014
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ofra Kalter-Leibovici MD

Director of the Unit of Cardiovascular Epidemiology, Gertner Institute.

Sheba Medical Center

Eligibility Criteria

Inclusion Criteria

  • Age 40 years or older
  • Advanced COPD

Exclusion Criteria

  • Permanent tracheostomy
  • Heart failure with significant left-ventricular dysfunction
  • Severe other chronic disease
  • Significant cognitive impairment, Drug or alcohol abuse, inability to cooperate
  • No telephone or permanent address
  • Refusal to use telemonitoring equipment
  • Participation in another clinical trial

Outcomes

Primary Outcomes

Hospital admission for acute exacerbation of COPD or all-cause mortality

Time Frame: Within 2 to 5 years after randomization

Secondary Outcomes

  • Depression(Within 2 to 5 years after randomization)
  • Functional capacity(Within 2 to 5 years after randomization)
  • Spirometry parameters(Within 2 to 5 years after randomization)
  • Total days of hospitalization for acute exacerbations of COPD(Within 2 to 5 years after randomization)
  • Total number of acute exacerbations of COPD(Within 2 to 5 years after randomization)
  • Quality of life(Within 2 to 5 years after randomization)

Study Sites (2)

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