Web-Based Survey of Pain, Stress and Complementary and Alternative Medicine

NCT ID: NCT00740233

Last Updated: 2014-03-27

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 2300 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2008-06-30
• Study Completion Date: 2010-10-31

Brief Summary

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

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.

Conditions

Gastrointestinal Diseases; Chronic Pain; Stress; Anxiety; Depression

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Eligibility 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.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

National Center for Complementary and Integrative Health (NCCIH)

NIH

Sponsor Role: collaborator

University of California, Los Angeles

OTHER

Sponsor Role: lead

Responsible Party

University of California, Los Angeles

Principal Investigators

Deborah Ackerman, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

UCLA School of Public Health

Other Identifiers

PROCAIM2008

Identifier Type: -

Identifier Source: org_study_id