Veterans Experiences Using Secure Messaging

This study is currently recruiting participants.
Verified February 2013 by Department of Veterans Affairs
Sponsor:
Information provided by (Responsible Party):
Department of Veterans Affairs
ClinicalTrials.gov Identifier:
NCT01382186
First received: June 15, 2011
Last updated: February 12, 2013
Last verified: February 2013
  Purpose

Deployment of Secure Messaging (SM) in primary care and women's clinics throughout the Veteran Health System by 2011 is an implementation priority for the Secretary and Under Secretary for Health for FY11 under the VHA T21 initiative. Secure Messaging is in early phases of implementation, this eHealth tool requires thoughtful evaluation to promote the successful implementation and dissemination of this tool. The primary aim of this project is to describe Veterans' experiences when using the SM feature on MyHealtheVet (MHV). This project will have local, VISN, and national impact on the implementation and sustainability of the SM feature on MHV through its qualitative examination of users' experiences. Findings from this research will explore why Veterans choose to, or not to, use the SM feature on MHV, identify facilitators and barriers, and examine if experiences differ by health literacy or computer literacy. In addition to the interview data, findings from the usability testing will build knowledge about Veterans' experiences using the SM feature on MyHealtheVet. These data will inform systems improvements, educational approaches, and marketing strategies to increase adoption and long-term utilization among Veterans.


Condition
Focus of Study- Veteran Computer Interface User

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Veterans' Experiences Using Secure Messaging on MyHealtheVet

Further study details as provided by Department of Veterans Affairs:

Primary Outcome Measures:
  • Usability of Secure Messaging [ Time Frame: November 2011 - April 2012 ] [ Designated as safety issue: No ]
    To determine user ability of secure messaging at baseline (ex. Navigate to Secure Messaging Log-in site; Secure Messaging Log-in; Set user preferences; Check Inbox; Open Secure Message; Open and read attachment; Send Secure Message)


Secondary Outcome Measures:
  • Secure Messaging use and content patterns [ Time Frame: November 2011 - August 2012 ] [ Designated as safety issue: No ]
    To longitudinally examine the quantity and quality of content, exchange patterns, and timing of inbound and outbound SM between participants and their healthcare teams.

  • User experiences with Secure Messaging [ Time Frame: January - August 2012 ] [ Designated as safety issue: No ]
    These interviews will assess usability, barriers, facilitators and satisfaction of Secure Messaging at 3 months post-testing.


Estimated Enrollment: 40
Study Start Date: April 2012
Estimated Study Completion Date: March 2013
Estimated Primary Completion Date: February 2013 (Final data collection date for primary outcome measure)
Groups/Cohorts
Group 1
Purposive sampling will be used to identify a sample of 30 Veterans who have been Personally Authenticated for the SM feature on MHV. Fifteen participants will be recruited from each site (Tampa, Boston). Women will be purposively recruited to ensure females are represented in data findings.

Detailed Description:

The primary aim of this project is to describe Veterans' experiences when using the SM feature on MyHealtheVet (MHV):

Objective 1: Describe Veterans' beliefs, attitudes, and perceptions toward using SM.

RQ1.1: Are there differences in beliefs, attitudes, and perceptions for adopters of SM (high volume, active users); and non-adopters of SM (low volume, not active users, or opted out)? RQ1.2: How do beliefs, attitudes, and perceptions toward using SM differ based on Veteran characteristics, including socio-demographic factors, health literacy, and computer literacy? Objective 2: Describe the user patterns and trends of Veterans when using SM. RQ2.1: How do user patterns and trends differ for adopters of SM and non-adopters of SM? RQ2.2: How do user patterns and trends differ based on Veteran characteristics, including socio-demographic factors, health literacy, and computer literacy? Objective 3: Identify the barriers to and facilitators for using SM. RQ3.1: How do barriers and facilitators differ for adopters of SM and non-adopters of SM? RQ3.2: How do barriers and facilitators differ based on Veteran characteristics, including socio-demographic factors, health literacy, and computer literacy? Objective 4: Identify strategies for overcoming barriers to using the Secure Messaging feature on My HealtheVet? RESEARCH DESIGN: This mixed-methods descriptive study will utilize in-person qualitative interviews, usability testing of the SM feature on MHV; SM secondary data analysis and 3-month follow-up interviews. Purposive sampling will be used to identify a sample of 30-40 Veterans who have been Personally Authenticated for the SM feature on MHV. Fifteen participants will be recruited from each site (Tampa, Boston). Two types of participants will be recruited at each site: (1) high volume users; and (2) low volume- or non- users. High volume user is defined by the quantity of SM use since opting in the SM program. Low volume user is defined by minimal or no use of SM since opting in the SM program. Data Collection Procedures: (1) In-person interviews; (2) usability testing; (3) SM secondary data collection; and (4) three-month follow-up telephone interviews will be conducted to complete study objectives.

ANALYSIS: Content analysis methods will be used to manage transcript data to identify domains and taxonomies related to Veteran experiences using SM. Data will be categorized and interpreted, and barriers and facilitators will be identified. Quantitative data will be summarized with descriptive statistics to describe sample characteristics. We will examine frequency counts and proportions to provide a descriptive picture of the usability. Using Morae software, a usability analysis will be conducted to analyze and interpret the patterns and trends of veteran testing data. Descriptive statistics will be used to examine group differences and effect sizes will be calculated to provide data for planning future studies. These data sources will be triangulated to increase the knowledge base of Veteran experiences when using SM.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

Veterans in Tampa and Boston who have been Personally Authenticated for the SM feature on MHV.

Criteria

Inclusion Criteria:

Individuals who have been Personally Authenticated for the SM feature on MHV and who use SM independent of other caregivers, and cognitive impairment that prevents use of a personal computer.

Exclusion Criteria:

Unable or unwilling to provide informed consent.

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01382186

Contacts
Contact: Jolie N Haun, PhD MS BS (813) 558-7622 jolie.haun@va.gov
Contact: Stephen L Luther, PhD MA (813) 558-3966 Steve.Luther@va.gov

Locations
United States, Florida
James A. Haley Veterans Hospital Recruiting
Tampa, Florida, United States, 33637-1022
Contact: Mary E Reeder, BIS     (813) 558-3933     mary.reeder@va.gov    
Sub-Investigator: Gail M. Powell-Cope, PhD MSN BSN            
Sub-Investigator: Jason D. Lind, PhD MPH BA            
Principal Investigator: Jolie N. Haun, PhD MS BS            
Sub-Investigator: Stephen Lee Luther, PhD MA            
United States, Massachusetts
VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA Recruiting
Boston, Massachusetts, United States, 02130
Contact: Steve Simon, MD     857-203-5111     steven.simon2@va.gov    
Sponsors and Collaborators
Investigators
Principal Investigator: Jolie N. Haun, PhD MS BS James A. Haley Veterans Hospital