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Health Information for Infected Veterans (HI-FIV Trial)

Bedford, MA
N/A
Waitlist Available
Led By Amanda M. Midboe, PhD
Research Sponsored by VA Office of Research and Development
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
* HIV diagnosis (determined by the presence of two outpatient HIV diagnoses or one inpatient HIV diagnosis from 10/2007 to 10/2018)
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights
No Placebo-Only Group

Summary

This is a study of My HealtheVet (MHV) use by Veterans diagnosed with Human Immunodeficiency Virus (HIV) and VA providers/staff who care for them. The investigators hope to learn and understand how MHV can improve the self-management of chronic conditions like HIV. First, the investigators will review Veteran medical records to look at the relationship between use of MHV and whether it has a positive or negative impact on the Veteran's management of HIV. Next, the investigators will interview participants to find out how MHV for self-management is used by Veterans and to find out why Veterans and providers choose to use (or not use) specific MHV tools. Lastly, the investigators will use the information found from the first two steps and create an intervention that will encourage non-MHV users to use the MHV tools that can help achieve health-related goals. Once the intervention has been developed, Veterans and providers will participate in a "cognitive walkthrough" to help the researchers test the intervention to see if it is usable, possible, and acceptable.

See full description
Eligible Conditions
  • HIV/AIDS

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
* HIV diagnosis (determined by the presence of two outpatient HIV diagnoses or one inpatient HIV diagnosis from 10/2007 to 10/2018)

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Intervention
Interviews
Medical Record Review

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

3Treatment groups
Experimental Treatment
Group I: Providers and staff of HIV-infected veteranExperimental Treatment1 Intervention
This groups represents the population of providers and staff who utilize the MHV portal to deliver care for HIV-infected veterans.
Group II: HIV-infected Veterans who use MHVExperimental Treatment1 Intervention
This group represents the population of HIV-infected Veterans active in care at a VA health system, who have been diagnosed with HIV and use MHV.
Group III: HIV-infected Veterans who do not use MHVExperimental Treatment1 Intervention
This group represents the population of HIV-infected Veterans active in care at a VA health system, who have been diagnosed with HIV and do not use MHV.

Find a Location

Closest Location:Richard L. Roudebush VA Medical Center, Indianapolis, IN· Indianapolis, IN· 168 miles

Who is running the clinical trial?

VA Palo Alto Health Care SystemFED
96 Previous Clinical Trials
58,344 Total Patients Enrolled
VA Office of Research and DevelopmentLead Sponsor
1,686 Previous Clinical Trials
3,758,595 Total Patients Enrolled
Edith Nourse Rogers Memorial Veterans HospitalFED
7 Previous Clinical Trials
361,683 Total Patients Enrolled
Amanda M. Midboe, PhDPrincipal InvestigatorVA Palo Alto Health Care System, Palo Alto, CA
~0 spots leftby Mar 2025