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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03022669
Other study ID # NRI 15-455
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 2016
Est. completion date September 30, 2022

Study information

Verified date September 2021
Source San Francisco Veterans Affairs Medical Center
Contact Linda Park, PhD, MS, FNP
Email Linda.Park@ucsf.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether text messages/messaging (TM) or a mobile application (app), compared with an educational website-control provided to all Veterans, can improve adherence to antiplatelet therapy among patients following acute coronary syndrome or percutaneous coronary intervention (ACS/PCI).


Description:

Adherence to antiplatelet medications is critical to prevent life threatening complications (i.e., stent thrombosis); yet rates of non-adherence range from 21-57% by 12 months. Mobile technology through TM or mobile apps is a practical and inexpensive strategy to promote behavior change and enhance medication adherence. The three specific aims of this proposal are to: 1) determine preferences for content and frequency of TM to promote medication adherence through focus groups; 2) determine the most patient-centered app to promote adherence through a content analysis of all commercially available apps for medication adherence and focus groups centered on usability; and 3) compare adherence to antiplatelet medications in 225 Veterans post ACS/PCI through a randomized controlled trial. Participants will be randomized to either TM, mobile app, or website-control group. The focus groups will be stratified by low/high mobile phone use and sex.


Recruitment information / eligibility

Status Recruiting
Enrollment 225
Est. completion date September 30, 2022
Est. primary completion date September 30, 2022
Accepts healthy volunteers No
Gender All
Age group 21 Years and older
Eligibility Inclusion Criteria: - = 21 years of age, - recent ACS or PCI within 1 week - new antiplatelet (thienopyridine) prescription - owns a smartphone Exclusion Criteria: - cognitive impairment - lack of English proficiency/literacy

Study Design


Intervention

Behavioral:
Text Message
Annie (VA text messaging program) or mobile Health manager (private text messaging program for non-VA female participants recruited at non-VA facility)
Mobile Application

Other:
Website
American Heart Association patient education website

Locations

Country Name City State
United States John Muir Medical Center Concord California
United States VA North Texas Health Care System Dallas Texas
United States North Florida/South Georgia Veterans Health System Gainesville Florida
United States VA Palo Alto Health Care System Palo Alto California
United States San Francisco Veterans Affairs Medical Center San Francisco California

Sponsors (5)

Lead Sponsor Collaborator
San Francisco Veterans Affairs Medical Center John Muir Medical Center, North Florida/South Georgia Veterans Health System, North Texas Veterans Healthcare System, VA Palo Alto Health Care System

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in medication adherence over 12 months Medication Event Monitoring System (MEMS) which is an electronic pill bottle cap that captures medication taking patterns 12 months
Primary Change in medication adherence over 12 months Adherence to Refills and Medications Scale (ARMS)- There are two subscale scores for medication taking and medication refills. The total score is found by adding both subscales. Scores can range from 12 to 48 with 12 being completely medication adherent and 48 being completely non-adherent. 12 months
Primary Change in medication adherence at 12 months Medication recall questionnaire that will assess how many missed doses there were. 12 months
Primary Change in medication adherence at 12 months VA Corporate Data Warehouse refill data (Veteran participants) 12 months
Primary Change in medication adherence at 12 months Peoplechart Meds Incontext refill data (non-Veteran participants) 12 months
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