Viewing Study NCT00576160



Ignite Creation Date: 2024-05-05 @ 6:57 PM
Last Modification Date: 2024-10-26 @ 9:38 AM
Study NCT ID: NCT00576160
Status: TERMINATED
Last Update Posted: 2015-05-15
First Post: 2007-12-14

Brief Title: Improving Medication Adherence in Post-ACS Patients
Sponsor: Columbia University
Organization: Columbia University

Study Overview

Official Title: Improving Med Adherence in Post-ACS Patients Phase 1B Dose-Finding RCT
Status: TERMINATED
Status Verified Date: 2015-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: This was a dosing study to determine acceptability Participants found protocol burdensome and so we terminated
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Many post Acute Coronary SyndromeACS patients do not take their medications including aspirin as prescribed leading to an increase in mortality Patients enrolled in this study will be enrolled into one of two groups Patients in the first group will have their medication adherence measured but will receive all other care as usual Patients in the second group will also have their medication adherence measured but they will receive telephone-delivered problem solving therapy PST in addition to their usual care The two groups will be combined to determine the Minimally Effective Dose MED and the Maximally Tolerated Dose MTD for adherence to aspirin The medication adherence of the PST group will improve by 20 55 to 75
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
K24HL084034 NIH None httpsreporternihgovquickSearchK24HL084034