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Dyspnea Self-Management: Internet or Face-to-Face

Primary Purpose

Chronic Obstructive Pulmonary Disease (COPD)

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Internet DSMP
Face-to-Face Dyspnea Self-management
Attention Control
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease (COPD)

Eligibility Criteria

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

Inclusion Criteria:

  • Participants will have:

    1. a diagnosis of COPD which is clinically stable (including medications) for at least one month;
    2. spirometry results showing at least mild obstructive disease defined as post bronchodilator forced expiratory volume in one second (FEV1)/forced vital capacity (FVC) ratio <0.70 with FEV1<80% predicted or post-bronchodilator FEV1/FVC ratio <0.60 with FEV1>80% predicted;
    3. ADL limited by dyspnea;
    4. a designated primary care physician;
    5. ability to speak English and sign consent form;
    6. actively using a computer and the Internet;
    7. no formal pulmonary rehabilitation training for at least 12 months;
    8. patients receiving supplemental oxygen will be acceptable if their O2 saturation can be maintained at >80% on <6L/min of nasal oxygen;
    9. understands how to and is able to rate their shortness of breath during exercise;
    10. age > 40 years.

Exclusion Criteria:

  • Subjects will be excluded if they have active symptomatic illness (e.g., cancer, left heart failure, ischemic heart disease with known coronary artery or valvular heart disease, psychiatric illness, and neuromuscular disease).

Sites / Locations

  • Dyspnea Research Group, Dept. of Physiological Nursing, University of California, San Francisco
  • University of Washington, Seattle - Dept. of Biobehavioral Nursing and Health Systems

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

1: i-DSMP

2: f-DSMP

3: AC

Arm Description

Internet Dyspnea Self-management Program (i-DSMP)

Face-to-Face Dyspnea Self-management Program (f-DSMP)

Attention Control (AC)

Outcomes

Primary Outcome Measures

Dyspnea with ADL
Exercise and functional performance
Exercise adherence
Acute COPD exacerbations

Secondary Outcome Measures

Perception of social support
Self-efficacy for exercise and managing dyspnea
Health resource utilization

Full Information

First Posted
April 13, 2007
Last Updated
August 14, 2014
Sponsor
University of California, San Francisco
Collaborators
National Institute of Nursing Research (NINR)
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1. Study Identification

Unique Protocol Identification Number
NCT00461162
Brief Title
Dyspnea Self-Management: Internet or Face-to-Face
Official Title
Dyspnea Self-Management: Internet or Face-to-Face
Study Type
Interventional

2. Study Status

Record Verification Date
August 2014
Overall Recruitment Status
Completed
Study Start Date
January 2007 (undefined)
Primary Completion Date
August 2011 (Actual)
Study Completion Date
August 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
National Institute of Nursing Research (NINR)

4. Oversight

5. Study Description

Brief Summary
Chronic obstructive pulmonary disease, including emphysema and chronic bronchitis, is the fourth most common cause of death and the second leading cause of disability in the United States. COPD is estimated to be responsible for more than 13.4 million physician visits and 13% of hospitalizations nationally. These hospitalizations are usually caused by acute exacerbations characterized by an increase in symptoms including dyspnea or shortness of breath (SOB), cough, wheezing, and sputum production. The significant disability for people with COPD is primarily due to the symptom of dyspnea (shortness of breath) that affects an individual's quality of life more than does the physiological impairment. Despite optimal medical and pharmacological therapy, most people with COPD continue to suffer from chronic and progressive dyspnea and other symptoms of cough and fatigue. We have previously shown that an individualized face-to-face dyspnea self-management program was effective in improving dyspnea with activities of daily living (ADL), physical functioning, and self-efficacy for managing dyspnea. Using an experimental longitudinal design, the i-DSMP will be compared to the Face-to-Face Dyspnea Self-Management Program (f-DSMP) and to an Attention Control (AC) intervention
Detailed Description
At the present time, education about symptom management for patients and treatments, including exercise, are primarily provided within structured and episodic pulmonary rehabilitation (PR) programs. These PR programs are of short duration, are available for only a small percentage of people because they are expensive and not covered by all third party payers, and often require travel by patients who are disabled. Given estimates of 10 to 24 million U.S. adults with COPD,most of who would benefit from PR, only less than 0.1% can be accommodated at any given time. In the US the maintenance or exercise programs following PR are not reimbursed and, therefore, not available for most patients. A number of self-management programs have been tested in multiple chronic diseases,but there has been less study of self-management programs for patients with COPD. The few self-management programs for COPD that include only education and limited skills training have not significantly improved symptoms. Home-based PR and self-management programs with nurse home visits have been studied and provide a less costly and accessible alternative. Clearly there is a growing need for more accessible and alternative avenues for providing ongoing support and therapy for COPD patients. The Internet provides a new exciting delivery channel that offers patients with disabilities an opportunity for greater involvement in health care decision-making and unparalleled opportunities to learn, inform, and communicate with one another and for health care providers to support patients' self-management efforts. Several Internet-based studies for other chronic illnesses have increased self-efficacy for symptom management, perception of available support, and patients' involvement in health care decision making, while reducing symptoms and health care costs. The only published study evaluating the use of the internet to support self-management in COPD patients was our pilot study for this proposal. Our study demonstrated an improvement in both self-efficacy and dyspnea with daily activities measures. This study will expand on the findings of our pilot study.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
125 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1: i-DSMP
Arm Type
Experimental
Arm Description
Internet Dyspnea Self-management Program (i-DSMP)
Arm Title
2: f-DSMP
Arm Type
Experimental
Arm Description
Face-to-Face Dyspnea Self-management Program (f-DSMP)
Arm Title
3: AC
Arm Type
Active Comparator
Arm Description
Attention Control (AC)
Intervention Type
Behavioral
Intervention Name(s)
Internet DSMP
Intervention Description
Internet Dyspnea Self-management Program (i-DSMP): Education and skills training for dyspnea management; an individualized tailored exercise plan; self-monitoring of exacerbation symptoms and exercise; and reinforcement/personalized feedback for self management. I-DSMP participants will receive their accessing the modules through the website and participating in weekly online group chat sessions with the research nurse and other participants.
Intervention Type
Behavioral
Intervention Name(s)
Face-to-Face Dyspnea Self-management
Intervention Description
Face-to-Face Dyspnea Self-management Program (f-DSMP): Education and skills training for dyspnea management; an individualized tailored exercise plan; self-monitoring of exacerbation symptoms and exercise; and reinforcement/personalized feedback for self management. F-DMSP participants will attend face-to-face group education sessions. The f-DSMP participants will be provide with a hard copy of the education modules and will participate in six 1-hour group sessions for a period of 6 weeks.
Intervention Type
Behavioral
Intervention Name(s)
Attention Control
Intervention Description
6 Monthly general health education classes and biweekly telephone calls from a health educator.
Primary Outcome Measure Information:
Title
Dyspnea with ADL
Time Frame
3, 6, and 12 months
Title
Exercise and functional performance
Time Frame
3, 6, and 12 months
Title
Exercise adherence
Time Frame
3, 6, and 12 months
Title
Acute COPD exacerbations
Time Frame
3, 6, and 12 months
Secondary Outcome Measure Information:
Title
Perception of social support
Time Frame
3, 6, and 12 months
Title
Self-efficacy for exercise and managing dyspnea
Time Frame
3, 6, and 12 months
Title
Health resource utilization
Time Frame
3, 6, and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Participants will have: a diagnosis of COPD which is clinically stable (including medications) for at least one month; spirometry results showing at least mild obstructive disease defined as post bronchodilator forced expiratory volume in one second (FEV1)/forced vital capacity (FVC) ratio <0.70 with FEV1<80% predicted or post-bronchodilator FEV1/FVC ratio <0.60 with FEV1>80% predicted; ADL limited by dyspnea; a designated primary care physician; ability to speak English and sign consent form; actively using a computer and the Internet; no formal pulmonary rehabilitation training for at least 12 months; patients receiving supplemental oxygen will be acceptable if their O2 saturation can be maintained at >80% on <6L/min of nasal oxygen; understands how to and is able to rate their shortness of breath during exercise; age > 40 years. Exclusion Criteria: Subjects will be excluded if they have active symptomatic illness (e.g., cancer, left heart failure, ischemic heart disease with known coronary artery or valvular heart disease, psychiatric illness, and neuromuscular disease).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Virginia Carrieri-Kohlman, RN, DNSc
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dyspnea Research Group, Dept. of Physiological Nursing, University of California, San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Facility Name
University of Washington, Seattle - Dept. of Biobehavioral Nursing and Health Systems
City
Seattle
State/Province
Washington
ZIP/Postal Code
98195
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
23073395
Citation
Nguyen HQ, Donesky D, Reinke LF, Wolpin S, Chyall L, Benditt JO, Paul SM, Carrieri-Kohlman V. Internet-based dyspnea self-management support for patients with chronic obstructive pulmonary disease. J Pain Symptom Manage. 2013 Jul;46(1):43-55. doi: 10.1016/j.jpainsymman.2012.06.015. Epub 2012 Oct 13.
Results Reference
derived

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Dyspnea Self-Management: Internet or Face-to-Face

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