Coping Skills for Patients With Chronic Obstructive Pulmonary Disease (COPD) and Their Caregivers
Primary Purpose
Chronic Obstructive Pulmonary Disease
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Telephone-based Enhanced Coping Skills Training (CST)
Usual Medical Care and COPD education and symptom monitoring (UMC)
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease focused on measuring Lung Disease, Chronic Bronchitis, Emphysema, Caregiver stress, COPD, Chronic Obstructive Pulmonary Disease
Eligibility Criteria
Inclusion Criteria:
- male or female outpatients 21 years of age or older
- a diagnosis of COPD
- FEV1 25%-80% of predicted value
- FEV1/FVC <70%
- capacity to give informed consent and follow study procedures
Exclusion Criteria:
- dementia
- psychotic features including delusions or hallucinations
- acute suicide or homicide risk
- other illness (e.g., cancer) that is likely to cause death within 3 years
- unstable angina
- congestive heart failure stage III - IV by NYHA classification
- active involvement in pulmonary rehabilitation or a formal exercise program
Sites / Locations
- Duke University Medical Center
- Ohio State University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
CST
UMC
Arm Description
Telephone-based Enhanced Coping Skills Training (CST)
Usual Medical Care and COPD education and symptom monitoring (UMC)
Outcomes
Primary Outcome Measures
Composite measure of psychological quality of life, composite index of all cause mortality and COPD-related hospitalization.
Secondary Outcome Measures
Composite measure of somatic quality of life
Full Information
NCT ID
NCT00736268
First Posted
August 13, 2008
Last Updated
August 6, 2014
Sponsor
Duke University
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
1. Study Identification
Unique Protocol Identification Number
NCT00736268
Brief Title
Coping Skills for Patients With Chronic Obstructive Pulmonary Disease (COPD) and Their Caregivers
Official Title
Telephone-based Intervention for Patients With COPD and Their Caregivers
Study Type
Interventional
2. Study Status
Record Verification Date
August 2014
Overall Recruitment Status
Completed
Study Start Date
August 2008 (undefined)
Primary Completion Date
May 2013 (Actual)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke University
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study is an NIH-funded clinical trial conducted at Duke University Medical Center and Ohio State University. The purpose of this study is to examine the effects of a telephone-based, care-giver assisted, coping skills training (CST) program in patients with Chronic Obstructive Pulmonary Disease (COPD) and their caregivers. This may help COPD patients and their caregivers to deal better with the stress of lung disease. This study will test 3 primary hypotheses: 1) That enhanced CST will be more effective in improving quality of life compared to a Usual Medical Care plus COPD education and symptom management control group; 2) That enhanced CST will be associated with better medical outcomes (i.e., greater survival and fewer COPD-related physician visits or hospitalizations) compared to Controls over a follow-up period of up to 4 years; and 3) That improvements in quality of life and survival will be mediated by increased functional capacity and better coping.
This proposed study builds upon our prior research by: a) adapting and refining our CST protocol, which was effective in improving psychosocial adjustment in patients awaiting lung transplantation, to a broader population of patients with COPD who are not immediate candidates for lung transplantation; b) enhancing our intervention to improve functional capacity, reduce somatic symptoms, and improve survival; c) examining the impact of CST on medical expenditures; and d) including caregivers in an enhanced CST intervention.
Detailed Description
Overall, 746 participants (patients and caregivers) were consented for participation into this study from both Duke University Medical Center and Ohio State University. Of these, 326 patients were randomized and participated in the study intervention along with 252 consented participants who acted as a caregiver; in total 578 participants (patients and caregivers) were involved with the study intervention.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease
Keywords
Lung Disease, Chronic Bronchitis, Emphysema, Caregiver stress, COPD, Chronic Obstructive Pulmonary Disease
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
746 (Actual)
8. Arms, Groups, and Interventions
Arm Title
CST
Arm Type
Experimental
Arm Description
Telephone-based Enhanced Coping Skills Training (CST)
Arm Title
UMC
Arm Type
Other
Arm Description
Usual Medical Care and COPD education and symptom monitoring (UMC)
Intervention Type
Behavioral
Intervention Name(s)
Telephone-based Enhanced Coping Skills Training (CST)
Intervention Description
Telephone-based Enhanced Coping Skills Training (CST) intervention will systematically train participants (and caregivers) in the use of coping skills for symptom management (i.e. activity pacing, pleasant activity scheduling, communications, relaxation, goal setting, imagery, calming self-statements, problem solving, and preventing and dealing with setbacks). Participants in the CST condition will receive 12 weekly 30 minute telephone sessions followed by 2 bi-weekly booster sessions for training in symptom management strategies. Participants and caregivers will be evaluated at baseline, at the conclusion of 4 months of treatment, and at annual follow-up intervals for up to 4 years.
Intervention Type
Other
Intervention Name(s)
Usual Medical Care and COPD education and symptom monitoring (UMC)
Intervention Description
COPD usual care plus education and symptom monitoring control condition will participate in a weekly 15 minute phone call followed by 2 bi-weekly phone calls, assessing their health status and providing them with support and COPD education. COPD Education topics include types of lung disease, oxygen use, medication management, preventing infection, managing daily activities, and nutrition. Participants and caregivers will be evaluated at baseline, at the conclusion of 4 months of treatment, and at annual follow-up intervals for up to 4 years.
Primary Outcome Measure Information:
Title
Composite measure of psychological quality of life, composite index of all cause mortality and COPD-related hospitalization.
Time Frame
4 years
Secondary Outcome Measure Information:
Title
Composite measure of somatic quality of life
Time Frame
4 months and up to 4 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
male or female outpatients 21 years of age or older
a diagnosis of COPD
FEV1 25%-80% of predicted value
FEV1/FVC <70%
capacity to give informed consent and follow study procedures
Exclusion Criteria:
dementia
psychotic features including delusions or hallucinations
acute suicide or homicide risk
other illness (e.g., cancer) that is likely to cause death within 3 years
unstable angina
congestive heart failure stage III - IV by NYHA classification
active involvement in pulmonary rehabilitation or a formal exercise program
Facility Information:
Facility Name
Duke University Medical Center
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
Facility Name
Ohio State University
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
16822110
Citation
Blumenthal JA, Babyak MA, Keefe FJ, Davis RD, Lacaille RA, Carney RM, Freedland KE, Trulock E, Palmer SM. Telephone-based coping skills training for patients awaiting lung transplantation. J Consult Clin Psychol. 2006 Jun;74(3):535-44. doi: 10.1037/0022-006X.74.3.535.
Results Reference
background
PubMed Identifier
18510641
Citation
Martinu T, Babyak MA, O'Connell CF, Carney RM, Trulock EP, Davis RD, Blumenthal JA, Palmer SM; INSPIRE Investigators. Baseline 6-min walk distance predicts survival in lung transplant candidates. Am J Transplant. 2008 Jul;8(7):1498-505. doi: 10.1111/j.1600-6143.2008.02264.x.
Results Reference
background
PubMed Identifier
1889242
Citation
Emery CF, Leatherman NE, Burker EJ, MacIntyre NR. Psychological outcomes of a pulmonary rehabilitation program. Chest. 1991 Sep;100(3):613-7. doi: 10.1378/chest.100.3.613.
Results Reference
background
PubMed Identifier
25251888
Citation
Blumenthal JA, Emery CF, Smith PJ, Keefe FJ, Welty-Wolf K, Mabe S, Martinu T, Johnson JJ, Babyak MA, O'Hayer VF, Diaz PT, Durheim M, Baucom D, Palmer SM. The effects of a telehealth coping skills intervention on outcomes in chronic obstructive pulmonary disease: primary results from the INSPIRE-II study. Psychosom Med. 2014 Oct;76(8):581-92. doi: 10.1097/PSY.0000000000000101.
Results Reference
derived
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Coping Skills for Patients With Chronic Obstructive Pulmonary Disease (COPD) and Their Caregivers
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