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Creating a Virtual Village for People Aging With HIV During COVID-19

U

University of California (UC), Riverside

Status

Unknown

Conditions

Aging
Depression in Old Age
Isolation, Social
Hiv

Treatments

Other: Virtual Village

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

In a PCORI-funded project on HIV and aging engagement that was co-led by the study team, the topics of isolation and depressions were identified as priority areas of deep concern among older PLWH. The COVID-19 pandemic has enhanced the urgency to test interventions to mitigate depression and isolation among older PLWH. However, there is scant evidence on effective interventions that help mitigate depression and isolation among older PLWH. While physical distancing and stay at home orders are a necessary strategy to flatten the curve, ease pressure on the healthcare system, and protect the most vulnerable, the order further increases the isolation faced by people aging with HIV, and creates barriers to accessing medications, health services, and other resources. This project will include 6 virtual focus groups and 12 individual interviews with adults ages 50 or older in California (Palm Spring, Los Angeles) and the Tampa-Bay region, Florida to (1): further characterize issues related to depression, isolation, and basic needs of people aging with HIV during the COVID-19 pandemic (2) utilizing results from Aim 1, co-develop ideas for what to include in a virtual village, and (3) create and pilot the virtual village in a group of people aging with HIV. The overall goal of this study is to execute an innovative solution to address issues related to isolation for older PLWH which have been exacerbated during the COVID-19 pandemic.

Enrollment

80 estimated patients

Sex

All

Ages

50+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • English or Spanish speaking adults
  • Living with HIV
  • residing in Palm Springs, Los Angeles, or Tampa Bay Florida
  • age 50 or older

Exclusion criteria

  • not able to read English or Spanish

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

80 participants in 1 patient group

Study participants
Other group
Description:
No participants will be randomized. All participants will have an opportunity to participate in the study procedures.
Treatment:
Other: Virtual Village

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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