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Web-Based Survey of Pain, Stress and Complementary and Alternative Medicine (PROCAIM)
This study is currently recruiting participants.
Verified by University of California, Los Angeles, August 2008
Sponsors and Collaborators: University of California, Los Angeles
National Center for Complementary and Alternative Medicine (NCCAM)
Information provided by: University of California, Los Angeles
ClinicalTrials.gov Identifier: NCT00740233
  Purpose

The investigators are inviting people with fibromyalgia, IBS, interstitial cystitis, chronic pain, and other chronic and recurring conditions to sign up and participate in a year-long Internet-based survey to study the effectiveness of alternative medicine and the interactions among stress and coping, pain, and treatment outcomes.

The survey is called PROCAIM, which stands for Patient-Reported Outcomes from Complementary, Alternative, and Integrative Medicine. PROCAIM was developed under a grant to UCLA researchers from the National Center for Complementary and Alternative Medicine.

This is a web-based study composed of surveys that will recur at intervals over 1 year!

TO ENROLL

  • Log in to our web site: http://www.procaim.org/
  • Register as a New User.
  • Select clinic name: ClinicalTrials.gov.
  • Read and sign the Consent Form.

After participants"sign" the form with their email address, participants can begin to answer the first in a series of questionnaires. The system will send participants email reminders at the time of each scheduled follow-up for one year.

For further information about PROCAIM, please contact:

  • Deborah Ackerman, Ph.D.
  • Department of Epidemiology
  • UCLA School of Public Health
  • Box 951772
  • Los Angeles, CA 90095-1772
  • deborah.ackerman@ucla.edu

Condition
Gastrointestinal Diseases
Chronic Pain
Stress
Anxiety
Depression

MedlinePlus related topics: Depression Fibromyalgia
U.S. FDA Resources
Study Type: Observational
Study Design: Cohort, Prospective

Further study details as provided by University of California, Los Angeles:

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 1000
Study Start Date: June 2008
Estimated Study Completion Date: December 2010
Estimated Primary Completion Date: December 2010 (Final data collection date for primary outcome measure)
Detailed Description:

PROCAIM, which stands for Patient-Reported Outcomes from Complementary, Alternative, and Integrative Medicine, was developed to collect and manage longitudinal patient data and implement patient-based outcomes assessment protocols at clinical sites around the country that offer various forms of CAM as well as clinics that provide the combination of conventional medicine with complementary and alternative therapies. PROCAIM is currently being used for a 12 month longitudinal survey to evaluate interactions among stress, symptoms, severity, and general well-being among people with fibromyalgia, IBS, chronic fatigue, and other chronic pain conditions, and the frequency and impact of co-morbid conditions among users of complementary and alternative medicines.

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

In general, participants will be: at least 18 years of age; ambulatory (i.e., not depending upon a wheelchair for mobility); and meet general criteria for psychosomatic or functional disorders including irritable bowel syndrome, other functional disorders, fibromyalgia, chronic pain, or related mood and anxiety disorders.

Criteria

Inclusion Criteria:

  • Everyone who has a computer and is fluent in English will be eligible.

Exclusion Criteria:

  • Only people with access to personal computers and the Internet and fluency in English will be able to participate. These exclusions are not based on age, gender, pregnancy, racial, or ethnic origin.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00740233

Contacts
Contact: Deborah Ackerman, Ph.D. 310-398-8108 dackerma@ucla.edu

Locations
United States, California
UCLA School of Public Health Recruiting
Los Angeles, California, United States, 90095
Principal Investigator: Deborah Ackerman, Ph.D.            
Sponsors and Collaborators
University of California, Los Angeles
Investigators
Principal Investigator: Deborah Ackerman, Ph.D. UCLA School of Public Health
  More Information

Patient-Reported Outcomes from Complementary, Alternative, and Integrative Medicine  This link exits the ClinicalTrials.gov site

Responsible Party: University of California, Los Angeles ( Deborah Ackerman )
Study ID Numbers: PROCAIM2008
Study First Received: August 20, 2008
Last Updated: August 20, 2008
ClinicalTrials.gov Identifier: NCT00740233  
Health Authority: United States: Institutional Review Board

Keywords provided by University of California, Los Angeles:
fibromyalgia
irritable bowel syndrome
interstitial cystitis
chronic fatigue syndrome
vulvodynia
chronic stress
chronic pain
stress-related conditions
functional GI disorders

Study placed in the following topic categories:
Fatigue
Depression
Myalgic encephalomyelitis
Fibromyalgia
Myofascial Pain Syndromes
Gastrointestinal Diseases
Cystitis
Stress
Pain
Fatigue Syndrome, Chronic
Depressive Disorder
Behavioral Symptoms
Cystitis, Interstitial
Digestive System Diseases
Irritable Bowel Syndrome

Additional relevant MeSH terms:
Pathologic Processes

ClinicalTrials.gov processed this record on January 16, 2009