Impact of Family-based Pulmonary Rehabilitation (PR) on Patients With Chronic Obstructive Pulmonary Disease (COPD) and Their Family Members
Primary Purpose
Chronic Obstructive Pulmonary Disease (COPD)
Status
Completed
Phase
Not Applicable
Locations
Portugal
Study Type
Interventional
Intervention
Family-based PR program
Conventional PR program
Sponsored by
About this trial
This is an interventional supportive care trial for Chronic Obstructive Pulmonary Disease (COPD) focused on measuring Chronic obstructive pulmonary disease (COPD), Pulmonary rehabilitation, Family, Integrated care, Mixed methods
Eligibility Criteria
Inclusion criteria for patients:
- clinical diagnosis of COPD according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria
- ≥ 18 years old
- clinically stable
- able to provide their own informed consent
Exclusion criteria for patients:
- presence of severe psychiatric conditions
- inability to understand and co-operate
- exacerbations or hospital admissions one month prior to the intervention
- presence of severe neurologic/ musculoskeletal conditions and/or unstable cardiovascular disease
Inclusion criteria for family members:
- caring for a relative with COPD on a regular basis
- ≥ 18 years old
- able to provide their own informed consent
Exclusion criteria for family members:
- presence of severe psychiatric conditions
- inability to understand and co-operate
Sites / Locations
- University of Aveiro
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Family-based PR group
Conventional PR group
Arm Description
Outcomes
Primary Outcome Measures
Change in family coping behaviors
Family Crisis Oriented Personal Scales (F-COPES) include 5 sub-scales which identify family coping patterns. Higher scores indicate more positive coping and problem solving strategies.
Secondary Outcome Measures
Change in psychosocial adjustment to the disease
Psychosocial adjustment to the disease will be measured using the Psychosocial Adjustment to Illness Scale-Self report (PAIS-SR), which is a 46-item scale with 7 domains. Two types of scores arise from the data: a score from each domain and a total PAIS-SR score, with higher scores indicating poorer adjustment.
Change in psychological well-being (depression, anxiety and stress)
Depression Anxiety Stress Scales are designed to measure the 3 related negative emotional states of depression, anxiety and stress. Higher scores indicate a worst psychological outcome.
Change in caregiving difficulties (for family members only)
Caregiving difficulties will be measured with the Carers Assessment of Difficulties Index (CADI), which comprises 7 sub-scales. Higher scores indicate greater subjective burden.
Patients and family members' perspectives of the Family-based PR program (for Family-based PR group only)
Semi-structured focus group interviews will be conducted with patients and family members to explore the impact of the Family-based PR program.
Full Information
NCT ID
NCT02048306
First Posted
January 24, 2014
Last Updated
January 28, 2014
Sponsor
Aveiro University
Collaborators
Fundação para a Ciência e a Tecnologia
1. Study Identification
Unique Protocol Identification Number
NCT02048306
Brief Title
Impact of Family-based Pulmonary Rehabilitation (PR) on Patients With Chronic Obstructive Pulmonary Disease (COPD) and Their Family Members
Official Title
Rehabilitation for Elderly Patients With COPD and Their Families: Promoting a Comprehensive, Integrated Intervention Based on the International Classification of Functioning, Disability and Health (ICF)
Study Type
Interventional
2. Study Status
Record Verification Date
January 2014
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aveiro University
Collaborators
Fundação para a Ciência e a Tecnologia
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to explore the impact of Family-based pulmonary rehabilitation (PR) on patients with chronic obstructive pulmonary disease (COPD) and their family members.
Dyads (patient and respective family member) will be randomly allocated to either a Family-based PR group or a Conventional PR group. PR programs will consist of exercise training and psychoeducation. In the Family-based PR program, both patients and family members will participate in psychoeducation sessions. In the Conventional PR group, only patients will be included. In both groups, exercise training sessions will be exclusively for patients.
It is expected that, by including patients with COPD and their family members in Family-based PR, they will become more competent and confident in the management of the disease, thus reducing the overall impact of COPD on patients and family members' well-being.
Detailed Description
Patients with COPD often need assistance from their significant others (family member) to cope with the impacts of the disease. Family members are, therefore, the primary source of support to patients and may be affected by patient's condition through role changes, impact on social activities, emotional stress and financial burden.
Although the impact of COPD on family members is an emergent area of research, there are few interventions directed at supporting both patients and families. The World Health Organization has recognized the importance of changing the focus of the interventions for patients with chronic diseases and has recommended family integration in rehabilitation programs. In COPD, the inclusion of family members in PR programs, a core component of the management of patients with COPD, may contribute to promote a better adjustment of the whole family to the disease and, thus, improve their well-being. However, this has not been investigated yet.
The purpose of this study is to explore the impacts of Family-based PR on patients with COPD and their family members.
This study will enroll patients with COPD and family members who are identified as their primary caregiver. Recruitment will take place at primary care centers via general practitioners.
A Family-based PR program will be designed according to a comprehensive literature review and the findings from a previous observational study exploring the expectations, needs and concerns of patients and family members about a Family-based PR program.
Then, dyads (patient and respective family member) who agree to participate will be randomly assigned to either the Family-based PR group or the Conventional PR group. The former group will participate in a Family-based PR program consisting of exercise training for patients and psychoeducation for dyads. In the Conventional PR group, only patients will participate in the exercise sessions and psychoeducation. Both programs will last 12 weeks and will be implemented in primary care centers by physiotherapists and gerontologists.
The impact of Family-based PR will be explored using a mixed-methods approach.
Assessments will be conducted in both groups at 4 time points: before, immediately after, 3 and 6 months after the interventions. Patients and family members' adjustment to the disease, family coping behaviors and psychological well-being will be evaluated in these time points. In addition, patients' clinical status will be assessed with a wide range of outcomes, such as activities limitation resulting from breathlessness, exercise tolerance and health-related quality of life. Difficulties associated with the caregiving experience will be assessed in family members.
Dyads participating in the Family-based PR program will also be invited to attend focus groups immediately after the intervention to assess their perspective about the intervention.
Descriptive statistics will be used to characterise the sample. To analyse changes in outcome measures, data from the two groups will be compared at each time point.
A sample size calculation using the primary outcome was performed based in a previous pilot study. It was found that statistically significant differences between groups would be detected with 21 dyads in each group. However, as PR programs usually have considerable dropouts (around 30%), 28 dyads will be recruited for each group.
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
Chronic obstructive pulmonary disease (COPD), Pulmonary rehabilitation, Family, Integrated care, Mixed methods
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
56 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Family-based PR group
Arm Type
Experimental
Arm Title
Conventional PR group
Arm Type
Active Comparator
Intervention Type
Behavioral
Intervention Name(s)
Family-based PR program
Intervention Description
The 12-week Family-based PR program will consist of psychoeducation for patients and family members (once a week) and exercise training for patients (3 times a week). The psychoeducation component aims to empower the family with strategies to facilitate a functional and healthy adjustment to the disease and includes educational and psychosocial support components.
Intervention Type
Behavioral
Intervention Name(s)
Conventional PR program
Intervention Description
The 12-week Conventional PR program will consist of psychoeducation (once a week) and exercise training (3 times a week) for patients only.
Primary Outcome Measure Information:
Title
Change in family coping behaviors
Description
Family Crisis Oriented Personal Scales (F-COPES) include 5 sub-scales which identify family coping patterns. Higher scores indicate more positive coping and problem solving strategies.
Time Frame
Before, immediately after, 3 and 6 months after the intervention
Secondary Outcome Measure Information:
Title
Change in psychosocial adjustment to the disease
Description
Psychosocial adjustment to the disease will be measured using the Psychosocial Adjustment to Illness Scale-Self report (PAIS-SR), which is a 46-item scale with 7 domains. Two types of scores arise from the data: a score from each domain and a total PAIS-SR score, with higher scores indicating poorer adjustment.
Time Frame
Before, immediately after, 3 and 6 months after the intervention
Title
Change in psychological well-being (depression, anxiety and stress)
Description
Depression Anxiety Stress Scales are designed to measure the 3 related negative emotional states of depression, anxiety and stress. Higher scores indicate a worst psychological outcome.
Time Frame
Before, immediately after, 3 and 6 months after the intervention
Title
Change in caregiving difficulties (for family members only)
Description
Caregiving difficulties will be measured with the Carers Assessment of Difficulties Index (CADI), which comprises 7 sub-scales. Higher scores indicate greater subjective burden.
Time Frame
Before, immediately after, 3 and 6 months after the intervention
Title
Patients and family members' perspectives of the Family-based PR program (for Family-based PR group only)
Description
Semi-structured focus group interviews will be conducted with patients and family members to explore the impact of the Family-based PR program.
Time Frame
Immediately after the intervention
Other Pre-specified Outcome Measures:
Title
Change in activities limitation resulting from breathlessness
Description
The Modified British Medical Research Council questionnaire comprises five grades (statements) in a scale from 0 to 4, with higher grades indicating greater perceived respiratory limitation.
Time Frame
Before, immediately after, 3 and 6 months after the intervention
Title
Change in Body Mass Index
Time Frame
Before, immediately after, 3 and 6 months after the intervention
Title
Change in exercise tolerance
Description
Patients' exercise tolerance will be assessed with the 6-minute walk test. The maximal distance walked during 6 minutes and the associated respiratory symptoms will be collected.
Time Frame
Before, immediately after, 3 and 6 months after the intervention
Title
Change in muscle strength (arm flexors and knee extensors)
Description
Isotonic muscle strength will be assessed with the 10 repetition maximum (10-RM), which is the maximum amount of weight that can be moved through the full range of motion 10 times with the proper technique and without compensatory movements. Isometric muscle strength of the knee extensors will be assessed with a hand-held dynamometer.
Time Frame
Before, immediately after, 3 and 6 months after the intervention
Title
Change in functional balance
Description
Functional balance will be measured with the Timed Up-and-Go test. The time needed to perform the test will be recorded.
Time Frame
Before, immediately after, 3 and 6 months after the intervention
Title
Change in health-related quality of life
Description
The St. George's Respiratory Questionnaire (SGRQ) is a disease-specific instrument designed to measure quality of life in patients with chronic lung disease. It has 3 domains: symptoms, activities and impact. Scores range from 0 to 100 and higher values indicate a poorer quality of life.
Time Frame
Before, immediately after, 3 and 6 months after the intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria for patients:
clinical diagnosis of COPD according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria
≥ 18 years old
clinically stable
able to provide their own informed consent
Exclusion criteria for patients:
presence of severe psychiatric conditions
inability to understand and co-operate
exacerbations or hospital admissions one month prior to the intervention
presence of severe neurologic/ musculoskeletal conditions and/or unstable cardiovascular disease
Inclusion criteria for family members:
caring for a relative with COPD on a regular basis
≥ 18 years old
able to provide their own informed consent
Exclusion criteria for family members:
presence of severe psychiatric conditions
inability to understand and co-operate
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alda S. Marques, PhD
Organizational Affiliation
School of Health Sciences of the University of Aveiro (ESSUA)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Daniela M. Figueiredo, PhD
Organizational Affiliation
School of Health Sciences of the University of Aveiro (ESSUA)
Official's Role
Study Chair
Facility Information:
Facility Name
University of Aveiro
City
Aveiro
ZIP/Postal Code
3810-193
Country
Portugal
12. IPD Sharing Statement
Citations:
PubMed Identifier
23343360
Citation
Marques A, Jacome C, Gabriel R, Figueiredo D. Comprehensive ICF core set for obstructive pulmonary diseases: validation of the activities and participation component through the patient's perspective. Disabil Rehabil. 2013 Sep;35(20):1686-91. doi: 10.3109/09638288.2012.750691. Epub 2013 Jan 24.
Results Reference
background
PubMed Identifier
23294436
Citation
Jacome C, Marques A, Gabriel R, Figueiredo D. Chronic obstructive pulmonary disease and functioning: implications for rehabilitation based on the ICF framework. Disabil Rehabil. 2013 Aug;35(18):1534-45. doi: 10.3109/09638288.2012.745625. Epub 2013 Jan 7.
Results Reference
background
PubMed Identifier
23909830
Citation
Figueiredo D, Gabriel R, Jacome C, Marques A. Caring for people with early and advanced chronic obstructive pulmonary disease: how do family carers cope? J Clin Nurs. 2014 Jan;23(1-2):211-20. doi: 10.1111/jocn.12363. Epub 2013 Aug 2.
Results Reference
background
PubMed Identifier
24053489
Citation
Figueiredo D, Gabriel R, Jacome C, Cruz J, Marques A. Caring for relatives with chronic obstructive pulmonary disease: how does the disease severity impact on family carers? Aging Ment Health. 2014;18(3):385-93. doi: 10.1080/13607863.2013.837146. Epub 2013 Sep 20.
Results Reference
background
PubMed Identifier
25340477
Citation
Marques A, Jacome C, Cruz J, Gabriel R, Brooks D, Figueiredo D. Family-based psychosocial support and education as part of pulmonary rehabilitation in COPD: a randomized controlled trial. Chest. 2015 Mar;147(3):662-672. doi: 10.1378/chest.14-1488.
Results Reference
derived
Learn more about this trial
Impact of Family-based Pulmonary Rehabilitation (PR) on Patients With Chronic Obstructive Pulmonary Disease (COPD) and Their Family Members
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