Implementing HearVA (I-HearVA)

Status: Recruiting
Location: See all (6) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

HearVA involves six VA facility emergency departments (ED) over a 3-year intervention period. The first part of this study will test whether providing personal amplifiers to Veteran ED patients who self-report hearing difficulty is acceptable to these patients, can improve their hearing, enhance understanding of discharge instructions, and can reduce the risk of coming back to the ED in a short period of time (3 days and 30 days). The second part of the study will then identify whether ED staff can implement this program and achieve similar results. The second part will give ED staff increasing levels of responsibility for screening Veterans for hearing difficulty and providing personal amplifiers when such difficulty is detected.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 60
Healthy Volunteers: f
View:

• English speaking

• Emergency severity index criterion of 3 (medium), 4, or 5 (low acuity)

• Hearing Handicap Inventory-Screen greater than or equal to 10 or positive answer to a single-item screening question

• Capacity to consent to participate in research

Locations
United States
Colorado
Rocky Mountain Regional VA Medical Center, Aurora, CO
RECRUITING
Aurora
North Carolina
Durham VA Medical Center, Durham, NC
RECRUITING
Durham
New York
VA NY Harbor Healthcare System, New York, NY
RECRUITING
New York
Syracuse VA Medical Center, Syracuse, NY
NOT_YET_RECRUITING
Syracuse
James J. Peters VA Medical Center, Bronx, NY
RECRUITING
The Bronx
Texas
VA North Texas Health Care System Dallas VA Medical Center, Dallas, TX
NOT_YET_RECRUITING
Dallas
Contact Information
Primary
Joshua Chodosh, MD MSHS
Joshua.Chodosh@va.gov
(310) 478-3711
Backup
Jarrett T Repasky, BS AA
jarrett.repasky@va.gov
(941) 387-5442
Time Frame
Start Date: 2021-12-08
Estimated Completion Date: 2025-09-30
Participants
Target number of participants: 1050
Treatments
Experimental: Intervention: Personal Amplifier
Consenting participants will be randomly assigned to the intervention group while receiving care in the emergency department
Other: Control: No Personal Amplifier
Consenting participants will be randomly assigned to the control group while receiving care in the emergency department
Related Therapeutic Areas
Sponsors
Collaborators: NYU Langone Health
Leads: VA Office of Research and Development

This content was sourced from clinicaltrials.gov