Rural Community Peer Partnerships for Improving Methamphetamine-Associated Heart Failure Screening and Engagement

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorOregon Health and Science University

About this trial

The goal of PEER-Heart is to implement and assess feasibility and preliminary effectiveness of a community peer-facilitated screening for methamphetamine-associated heart failure (MAHF) and linkage to evidence-based cardiology care for people who use methamphetamine in rural areas.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patient-defined regular use of methamphetamine in the last year

Any methamphetamine use in the past 30 days

Age 18 years or older

No client-reported diagnosis of heart failure

Disqualifiers

Self-reported engagement in medical care for heart failure in past 6 months.

Actively taking medications for heart failure.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Treatment as Usual

    Other intervention

    Peer-facilitated referral to a local primary care provider to follow-up their screening results.

  • Telehealth-Cardiology

    Other intervention

    Peer-facilitated virtual consultation with cardiovascular specialist, for follow-up of their screening results. Activities may include: referral for a locally performed testing including echocardiogram and additional blood work, and transitional care management facilitated by a remote nurse care manager and the peer Referral for a locally performed testing including echocardiogram Transitional care management facilitated by a remote nurse care manager and the peer

Treatment groups

200 Participants
are divided into 2 treatment groups
Group A: Peer-supported Treatment as UsualActive comparator 1 intervention
Group B: Peer-Supported Telehealth CardiologyExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Linkage to cardiology care

Proportion of participants who are engaged in cardiac care at 2 months after screening.

Time frame
2 months

Secondary outcomes

1

Linkage to diagnostic echocardiogram

Proportion of participants who complete a diagnostic echocardiogram within 2 months after randomization.

Time frame
2 months
2

Goal Directed Medical Therapy (GDMT) prescribed

Proportion of eligible patients who are on any GDMT at 6 months after randomization

Time frame
6 months

Other outcomes

Sponsors and contacts

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Oregon Health and Science University

Lead sponsor

University of Washington

Collaborator

Bay Area First Step

Collaborator