search
Back to results

A Structured Lifestyle Intervention on Daily Physical Activity Level in COPD (COACH)

Primary Purpose

Chronic Obstructive Pulmonary Disease (COPD)

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Coach, using a stepcounter with exercise counseling
Sponsored by
Groningen Research Institute for Asthma and COPD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Chronic Obstructive Pulmonary Disease (COPD) focused on measuring COPD, Lifestyle, Pedometer

Eligibility Criteria

40 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 40-80 years
  • COPD GOLD stage I-IV
  • Written informed consent

Exclusion Criteria:

  • Comorbidity, like serious cardiovascular problems, serious limitations in neuromuscular performance and exacerbations in the previous two months, which can effect the outcome of the study.

Sites / Locations

  • Wilhelmina Ziekenhuis
  • Delfzicht ziekenhuis
  • University Medical Centre Groningen
  • Diaconessenhuis

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

1

2

Arm Description

5 counseling meetings of 30 min in the first 3 months. In counseling, patients will be stimulated individually to enhance a physically active lifestyle.

daily physical activity is assessed at baseline, 3 months, 9 months and 15 months. No counseling.

Outcomes

Primary Outcome Measures

Daily physical activity in steps counts a day

Secondary Outcome Measures

Personal characteristics
Body Mass Index
Fat Free Mass
Lung function (FEV1)
Physical fitness (arm strength, leg strength, respiratory muscle strength, 6MWT)
COPD related costs
Type of activity, attitude towards physical activity, health status, physical fitness, psychological factors (self-efficacy, depression), quality of life, fatigue.

Full Information

First Posted
January 31, 2008
Last Updated
March 23, 2012
Sponsor
Groningen Research Institute for Asthma and COPD
search

1. Study Identification

Unique Protocol Identification Number
NCT00614796
Brief Title
A Structured Lifestyle Intervention on Daily Physical Activity Level in COPD
Acronym
COACH
Official Title
A Study Evaluating the Effects of a Structured Lifestyle Intervention on Daily Physical Activity Level of COPD Patients in the First, Second and Third Echelon.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2010
Overall Recruitment Status
Completed
Study Start Date
November 2006 (undefined)
Primary Completion Date
August 2009 (Actual)
Study Completion Date
November 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Groningen Research Institute for Asthma and COPD

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Chronic Obstructive Pulmonary Disease (COPD) is increasing in the Netherlands. COPD is characterized by a deterioration of lung function, a lowering physical activity level and a low state of quality of life. The aim of this randomized controlled study is to investigate the effects of a structured lifestyle program compared with usual care (in the first, second and third echelon) on the physical activity level of COPD patients. 150 COPD patients (GOLD I-IV) will be included, aged between 40 and 80 years. In each echelon 25 patients will participate in a structured lifestyle program and 25 patients will be treated with usual care. In the structured lifestyle program, patients will be stimulated individually to enhance a physically active lifestyle. The primary outcome parameter is daily physical activity (steps/ day) assessed with a pedometer. According to the study protocol patients in the experimental group and the control group participate in four measurement sessions distributed over 15 months. In each assessment a physical fitness test, lung function and questionnaires are taken. Patients of the experimental group participate in five individual counseling sessions and one telephonic counseling.
Detailed Description
Background of the study: Chronic Obstructive Pulmonary Disease (COPD) is increasing in the Netherlands. The incidence of COPD is about 2-3 per 1000 and the prevalence of 12-19 per 1000 patients in the Dutch primary health care. The World Health Organization (WHO) states that its prevalence in 2020 will be on the fourth rank of death and the fifth rank of causes of disability-adjusted life years lost worldwide. COPD is characterized by a deterioration of lung function, a lowering physical activity level and a low state of quality of life. Objective of the study: The aim of the study is to investigate the effects of a structured lifestyle program (in the first, second and third echelon) on the physical activity level of COPD patients Study design: It concerns a randomized controlled study. In this study a structured lifestyle program will be compared with usual care in the first, second and third echelon of the health care. Study population: 150 COPD patients (GOLD I-IV) will be included, aged between 40 and 80 years. In each echelon 25 patients will participate in a structured lifestyle program and 25 patients will be treated with usual care. Intervention: A structured lifestyle program, based on the COACH method, will be used. This method was developed by the Institute of Human Movement Sciences of the University of Groningen (RUG). Using COACH, patients will be stimulated individually to enhance a physically active lifestyle. Primary study parameters/outcome of the study: Daily physical activity (steps/ day) Secondary study parameters/outcome of the study: Personal characteristics, Body Mass Index, Fat Free Mass, lung function (FEV1), physical fitness (arm strength, leg strength, respiratory muscle strength, 6MWT), COPD related costs, ADL activities, type of activity, attitude towards physical activity, health status, physical fitness, psychological factors (self-efficacy, depression), quality of life, fatigue. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: According to the study protocol patients in the experimental group and the control group participate in five measurement sessions. In each assessment a physical fitness test, lung function, questionnaires is taken. Al participants wear a pedometer to registrate the number of steps a day during 2 weeks after each appointment. Patients of the experimental group participate in five individual counseling sessions and one telephonic counseling. As a result of the type of assessments used, the study has a very low risk profile.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease (COPD)
Keywords
COPD, Lifestyle, Pedometer

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
155 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
5 counseling meetings of 30 min in the first 3 months. In counseling, patients will be stimulated individually to enhance a physically active lifestyle.
Arm Title
2
Arm Type
No Intervention
Arm Description
daily physical activity is assessed at baseline, 3 months, 9 months and 15 months. No counseling.
Intervention Type
Behavioral
Intervention Name(s)
Coach, using a stepcounter with exercise counseling
Other Intervention Name(s)
COACH
Intervention Description
5 counseling meetings of 30 min in the first 3 months. In counseling, patients will be stimulated individually to enhance a physically active lifestyle.
Primary Outcome Measure Information:
Title
Daily physical activity in steps counts a day
Time Frame
Experimental group: assessment during first 3 months, 2 week assessment at 6 months, 9 months and 15 months. Control group: 2 weeks assessment at baseline, 3 months, 9 months and 15 months
Secondary Outcome Measure Information:
Title
Personal characteristics
Time Frame
assessment at baseline
Title
Body Mass Index
Time Frame
assessment at baseline, 3 months, 9 months and 15 months
Title
Fat Free Mass
Time Frame
assessment at baseline, 3 months, 9 months and 15 months
Title
Lung function (FEV1)
Time Frame
assessment at baseline, 3 months, 9 months and 15 months
Title
Physical fitness (arm strength, leg strength, respiratory muscle strength, 6MWT)
Time Frame
assessment at baseline, 3 months, 9 months and 15 months
Title
COPD related costs
Time Frame
assessment at 3 months, 9 months and 15 months
Title
Type of activity, attitude towards physical activity, health status, physical fitness, psychological factors (self-efficacy, depression), quality of life, fatigue.
Time Frame
assessment at baseline, 3 months, 9 months and 15 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 40-80 years COPD GOLD stage I-IV Written informed consent Exclusion Criteria: Comorbidity, like serious cardiovascular problems, serious limitations in neuromuscular performance and exacerbations in the previous two months, which can effect the outcome of the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Johan B Wempe, Phd, MD
Organizational Affiliation
University Medical Center Groningen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wilhelmina Ziekenhuis
City
Assen
Country
Netherlands
Facility Name
Delfzicht ziekenhuis
City
Delfzijl
Country
Netherlands
Facility Name
University Medical Centre Groningen
City
Groningen
ZIP/Postal Code
9700 RB
Country
Netherlands
Facility Name
Diaconessenhuis
City
Meppel
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
25499548
Citation
Altenburg WA, ten Hacken NH, Bossenbroek L, Kerstjens HA, de Greef MH, Wempe JB. Short- and long-term effects of a physical activity counselling programme in COPD: a randomized controlled trial. Respir Med. 2015 Jan;109(1):112-21. doi: 10.1016/j.rmed.2014.10.020. Epub 2014 Nov 22.
Results Reference
derived
PubMed Identifier
23810269
Citation
Altenburg WA, Bossenbroek L, de Greef MH, Kerstjens HA, ten Hacken NH, Wempe JB. Functional and psychological variables both affect daily physical activity in COPD: a structural equations model. Respir Med. 2013 Nov;107(11):1740-7. doi: 10.1016/j.rmed.2013.06.002. Epub 2013 Jun 28.
Results Reference
derived

Learn more about this trial

A Structured Lifestyle Intervention on Daily Physical Activity Level in COPD

We'll reach out to this number within 24 hrs