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Motivation, Syringe Exchange, and COVID-19

University of Oregon logo

University of Oregon

Status

Completed

Conditions

COVID-19 Pandemic

Treatments

Behavioral: Connect2Test

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05534061
1U01DA055982-01 (U.S. NIH Grant/Contract)
11162020.013b

Details and patient eligibility

About

People who inject drugs (PWIDs) are highly vulnerable to SARS-CoV-2 infection and to the disease caused by SARS-CoV-2, coronavirus disease 2019 (COVID-19), however, rates of SARS-CoV-2 testing and vaccination uptake -vital to mitigating the spread of COVID-19 and achieving herd immunity - are lower among PWIDs compared to the general population. Building on our Phase I Rapid Acceleration of Diagnostics project, which found that contingency management (CM) increased testing utilization among PWIDs, the proposed project evaluates the comparative effectiveness of CM versus CM plus a brief motivational enhancement intervention on SARS-CoV-2 testing and vaccination uptake among PWIDs. This project has the potential to reduce COVID-19 health disparities among PWIDs and to decrease population level COVID-19 morbidity and mortality.

Full description

This study uses contingency management, specifically $10 financial incentives for participation in SARS-CoV-2 testing and $10 for participating in COVID-19 vaccination. It also uses a motivational enhancement intervention which is a brief conversation with clients to improve intrinsic motivation for testing and vaccination. Thus, the clinical trials portion of this study is a randomized control trial (N = 349) in which 177 participants will be assigned to contingency management plus the Connect2Test intervention and 172 will be assigned to the contingency management alone (i.e. services as usual). There will be a per site quota to ensure there are relatively equivalent numbers of participants per site to avoid site-specific biases. The data collection software (e.g., Qualtrics, PowerBI) will randomly assign individuals to condition in real time, after a participant consents to participate in the study.

Enrollment

349 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18 and older, understand English

Exclusion criteria

  • none

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

349 participants in 2 patient groups

Connect2Test Intervention + Contingency Management
Experimental group
Description:
$10 financial incentive for vaccination and $10 financial incentive for testing plus a brief feedback-based motivational enhancement intervention.
Treatment:
Behavioral: Connect2Test
Contingency Management Alone
Active Comparator group
Description:
$10 financial incentive for vaccination and $10 financial incentive for testing.
Treatment:
Behavioral: Connect2Test

Trial documents
3

Trial contacts and locations

1

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Central trial contact

Camille C Cioffi, PhD; Anne Marie Mauricio, PhD

Data sourced from clinicaltrials.gov

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