OPERA Database - Crohn's Protocol
OPERA
IBD-OPERA Database IBD OPERA Database: Inflammatory Bowel Disease - Outcomes, Preferences, Education, Resource Utilization, Assessment Database - Crohn's Protocol
1 other identifier
observational
50
1 country
1
Brief Summary
The investigators believe that patients with Crohn's disease are able to report details of their own medical history accurately and record changes in clinical status effectively over time. Using an internet-based database the investigators will ask patients to report their own disease history, and the investigators will compare their reports to the medical record.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Oct 2012
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2012
CompletedFirst Submitted
Initial submission to the registry
October 31, 2012
CompletedFirst Posted
Study publicly available on registry
November 2, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2015
CompletedAugust 17, 2015
August 1, 2015
2.4 years
October 31, 2012
August 14, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Validity of patient self reporting
The validity of patient self report on details of their Crohn's disease compared to chart review. Validity is defined as a match between patient self report and medical records.
12 months
Study Arms (2)
1st Group of 50 patients
2nd Group of 50 patients
Eligibility Criteria
Men and women over 18 years of age with Crohn's disease
You may qualify if:
- Adults (over 18 years of age) with physician diagnosed Crohn's disease
- A current or past prescription of anti-TNF
- Access to medical record for validation of clinical information
You may not qualify if:
- Unwilling or unable to provide informed consent for study participation
- Unable to access or use the internet
- Ulcerative colitis or IBD-U
- Illiterate or does not possess minimum level of literacy required to complete questionnaire
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Dartmouth-Hitchcock Medical Centerlead
- Abbottcollaborator
Study Sites (1)
Dartmouth Hitchcock Medical Center
Lebanon, New Hampshire, 03756, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 31, 2012
First Posted
November 2, 2012
Study Start
October 1, 2012
Primary Completion
March 1, 2015
Study Completion
June 1, 2015
Last Updated
August 17, 2015
Record last verified: 2015-08