Viewing Study NCT00368771



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Last Modification Date: 2024-10-26 @ 9:27 AM
Study NCT ID: NCT00368771
Status: COMPLETED
Last Update Posted: 2016-11-28
First Post: 2006-08-24

Brief Title: A Six-month Study to Compare Outcome Differences and Visceral Response Irritable Bowel Syndrome
Sponsor: University of California Los Angeles
Organization: University of California Los Angeles

Study Overview

Official Title: A Six-Month Study to Compare Outcome Differences and Visceral Response in Subjects Randomized to a Psychological Intervention for Irritable Bowel Syndrome
Status: COMPLETED
Status Verified Date: 2016-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to assess the effect of participation in one of the following interventions 1 IBS Stress Management 2 IBS Symptom Management or 3 IBS Educational Training on improving IBS associated symptoms It is anticipated that this research will provide information on the usefulness of psychological approaches in treating IBS and will help scientists better understand the disorder
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
DK-NR07768 US NIH GrantContract None httpsreporternihgovquickSearchR01NR007768
R01NR007768 NIH None None