(Cost-)Effectiveness Interdisciplinary Community-based COPD Management Program (INTERCOM)
Primary Purpose
Pulmonary Disease, Chronic Obstructive
Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
INTERdisciplinary COMmunity-based COPD management (INTERCOM)
Sponsored by
About this trial
This is an interventional treatment trial for Pulmonary Disease, Chronic Obstructive
Eligibility Criteria
Inclusion Criteria:
- Moderate to severe COPD according to the recent GOLD guidelines
- Reduced exercise capacity during an incremental exercise test of less than 70% of predicted normal values
Exclusion Criteria:
- Lack of motivation to participate in the treatment program
- Other pathologic conditions unabling participation in the training program (e.g. coronary, orthopaedic, neurological or severe endocrine disorders)
- participation in other pulmonary rehabilitation projects
Sites / Locations
- Catharina Hospital
- Maxima Medical Centre
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Intercom
Usual Care
Arm Description
INTERdisciplinary COMmunity-based COPD management (INTERCOM)
Outcomes
Primary Outcome Measures
The two primary outcomes are disease-specific quality of life assessed with the St. George's Respiratory Questionnaire (SGRQ) and the total number of exacerbations
Secondary Outcome Measures
dyspnea, quality of life, exercise performance measures, body composition measures and lung function
Full Information
NCT ID
NCT00840892
First Posted
February 10, 2009
Last Updated
February 16, 2018
Sponsor
Maastricht University Medical Center
Collaborators
Maxima Medical Center, Erasmus Medical Center, The Netherlands Asthma Foundation, Stichting Astma Bestrijding, The Netherlands, Nutricia Netherlands, PICASSO: Partners in Care Solutions for COPD
1. Study Identification
Unique Protocol Identification Number
NCT00840892
Brief Title
(Cost-)Effectiveness Interdisciplinary Community-based COPD Management Program (INTERCOM)
Official Title
Randomized Controlled Trial to Establish the (Cost-)Effectiveness of an Interdisciplinary Community-based COPD Management Program Relative to Usual Care.
Study Type
Interventional
2. Study Status
Record Verification Date
February 2009
Overall Recruitment Status
Completed
Study Start Date
January 2002 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
March 2007 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Maastricht University Medical Center
Collaborators
Maxima Medical Center, Erasmus Medical Center, The Netherlands Asthma Foundation, Stichting Astma Bestrijding, The Netherlands, Nutricia Netherlands, PICASSO: Partners in Care Solutions for COPD
4. Oversight
5. Study Description
Brief Summary
There is growing evidence that COPD is a multi-organ system disease. Besides impaired lung function, skeletal muscle weakness and weight loss are important determinants of impaired exercise performance, decreased quality of life and increased mortality. Based on earlier succesful intervention studies in pulmonary rehabilitation settings, Máxima Medical Centre developed an integrated, inter-disciplinary approach to the management of COPD including physical exercise, nutritional therapy, education, smoking cessation and psychological consultation. This COPD management program consists of a set of protocols that cover patient recruitment, diagnostic testing, treatment, follow-up and communication between professionals.
The exercise program and the nutitional therapy are carried out by local physiotherapists and dieticians working outside but in conjunction with the hospital. A program in such a setting could be substantially less expensive and certainly more easily accessible for many more patients than an inpatient or hospital-based outpatient rehabilitation program, as it is offered close to a patient's home. This study investigates the (cost-)effectiveness of the COPD management program compared to usual care in a randomized controlled trial.
Patients with moderate to severe COPD and a reduced exercise capacity during an incremental exercise test of less than 70% of predicted, are randomised to a treatment or a control group. The treatment group will participate in the COPD management program during the first 4 months after which they will be followed up for the remaining months. Both groups (n=100) are followed for 2 years and outcomes will be assessed at the beginning of the program, after 4, 12 and 24 months by disease-specific and generic measures of health status, body composition, skeletal muscle function and exercise capacity. A cost-effectiveness and cost-utility analysis with a two-year time horizon will be performed. The analysis is conducted from a societal perspectice, including the program costs and all COPD-related direct costs within and outside the healthcare sector ans costs of lost productivity.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Disease, Chronic Obstructive
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
199 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Intercom
Arm Type
Experimental
Arm Description
INTERdisciplinary COMmunity-based COPD management (INTERCOM)
Arm Title
Usual Care
Arm Type
No Intervention
Intervention Type
Other
Intervention Name(s)
INTERdisciplinary COMmunity-based COPD management (INTERCOM)
Intervention Description
The INTERCOM program consisted of exercise training, education, nutritional therapy and smoking cessation support offered by local physiotherapists and dieticians in the proximity of the patient's home and by respiratory nurses in the hospital. The program was divided in a 4-month intensive intervention phase, followed by a 20-month maintenance phase.
Primary Outcome Measure Information:
Title
The two primary outcomes are disease-specific quality of life assessed with the St. George's Respiratory Questionnaire (SGRQ) and the total number of exacerbations
Secondary Outcome Measure Information:
Title
dyspnea, quality of life, exercise performance measures, body composition measures and lung function
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Moderate to severe COPD according to the recent GOLD guidelines
Reduced exercise capacity during an incremental exercise test of less than 70% of predicted normal values
Exclusion Criteria:
Lack of motivation to participate in the treatment program
Other pathologic conditions unabling participation in the training program (e.g. coronary, orthopaedic, neurological or severe endocrine disorders)
participation in other pulmonary rehabilitation projects
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Annemie MWJ Schols, Prof PhD
Organizational Affiliation
Maastricht University Medical Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Catharina Hospital
City
Eindhoven
Country
Netherlands
Facility Name
Maxima Medical Centre
City
Veldhoven/Eindhoven
Country
Netherlands
12. IPD Sharing Statement
Citations:
PubMed Identifier
20188315
Citation
van Wetering CR, Hoogendoorn M, Broekhuizen R, Geraerts-Keeris GJ, De Munck DR, Rutten-van Molken MP, Schols AM. Efficacy and costs of nutritional rehabilitation in muscle-wasted patients with chronic obstructive pulmonary disease in a community-based setting: a prespecified subgroup analysis of the INTERCOM trial. J Am Med Dir Assoc. 2010 Mar;11(3):179-87. doi: 10.1016/j.jamda.2009.12.083. Epub 2010 Feb 4.
Results Reference
derived
PubMed Identifier
19703824
Citation
van Wetering CR, Hoogendoorn M, Mol SJ, Rutten-van Molken MP, Schols AM. Short- and long-term efficacy of a community-based COPD management programme in less advanced COPD: a randomised controlled trial. Thorax. 2010 Jan;65(1):7-13. doi: 10.1136/thx.2009.118620. Epub 2009 Aug 23.
Results Reference
derived
PubMed Identifier
19574331
Citation
Hoogendoorn M, van Wetering CR, Schols AM, Rutten-van Molken MP. Is INTERdisciplinary COMmunity-based COPD management (INTERCOM) cost-effective? Eur Respir J. 2010 Jan;35(1):79-87. doi: 10.1183/09031936.00043309. Epub 2009 Jul 2.
Results Reference
derived
Learn more about this trial
(Cost-)Effectiveness Interdisciplinary Community-based COPD Management Program (INTERCOM)
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