Web-based Education to Enhance Fibromyalgia Management
Fibromyalgia, Fibrositis
About this trial
This is an interventional treatment trial for Fibromyalgia focused on measuring Pain, Fibromyalgia, Internet
Eligibility Criteria
SUBJECTS WILL NEED TO COME TO SIOUX FALLS FOR THE STUDY VISITS.
The study sample will be drawn from a population of individuals diagnosed with fibromyalgia in a five state region consisting of North and South Dakota, Iowa, Minnesota, and Nebraska.
Subjects will be recruited into the study by practicing physicians either at the main hospital in Sioux Falls or in any of 15 affiliated rural clinic study sites. In order to be included in the study, potential subjects must meet the study inclusion and exclusion criteria.
Inclusion Criteria:
- Ability to travel to Sioux Falls, SD for study visits.
- All subjects must fulfill the diagnostic criteria for fibromyalgia as established by the American College of Rheumatology (ACR) in 1990 (Wolfe et al., 1990)
- Be 18 years of age
- All subjects must have been in standard medical care with a physician for at least 3 months.
Subjects must have a home computer or access to a computer with the following features:
- An Internet browser that is Internet Explorer version 5.0 or higher.
- Printer
- Speakers or headphones
- Ability to use e-mail and access to the Internet
Subjects must be able to perform the following screening test designed to assess computer ability:
- Go to a webpage Log in to a website
- Click on an icon
- Click on a radio button to answer a multiple choice question
- Fill a name into a text box
- Click on a submit button
- Print a document
Exclusion Criteria:
Subjects will be excluded from participation if they have any of the following:
- A severe physical impairment that precludes receiving/using the website or using the CBT skills contained on the website (e.g. complete blindness)
- Co-morbid medical illnesses capable of causing a worsening of physical functional status independent of fibromyalgia (e.g. morbid obesity, autoimmune diseases,) cardiopulmonary disorders (e.g. angina, congestive heart failure, COPD, chronic asthma), uncontrolled endocrine or allergic disorders (e.g. thyroid dysfunction, Type I diabetes), and malignancy within 2 years.
- Any present psychiatric disorder involving a history of psychosis (e.g. schizophrenia, schizoaffective disorder, schizophreniform disorder, delusional disorder etc.), current suicide risk or attempt within 2 years of the study, or substance abuse within 2 years. Note: Subjects with mood disorders will not be excluded.
- Prior face to face CBT for pain management.
- Receiving or applying for or considering seeking disability payments.
Sites / Locations
- Avera Research Institute
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Standard Care and Web
Standard Care
Standard care plus a web site based on cognitive behavioral principals.
Subject recieve standard care from their primary care provider.