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Contingency Management for Stimulant Use Disorders

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University of Virginia

Status

Unknown

Conditions

Stimulant Use
Contingency Management

Treatments

Behavioral: Contingency Management

Study type

Interventional

Funder types

Other

Identifiers

NCT05097547
HSR210335
17803

Details and patient eligibility

About

The invetigators' objective is to implement Medication Assisted Treatment (MAT) and contingency management in patients affected by co-occurring opioid use disorder and stimulant use disorder. Participants will continue to receive standard of care for their opioid use disorder via MAT at our Outpatient Based Opioid Treatment (OBOT) Clinic. Participants' stimulant use disorder will be targeted through contingency management, with twice weekly urine drug screens and monetary prizes in exchange for negative urine drug screens. Through regular clinic visits and the use of incentives, the investigators hope to increase treatment adherence and increase the number of negative urine drug screens in subjects struggling with co-morbid opioid use disorder and stimulant use disorder. The investigators will determine whether or not this treatment is effective in this population, versus conventional treatment (baseline therapy patients were getting through OBOT). The investigators' primary outcome measure will be stimulant abstinence duration during the twelve week study.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18 and older
  • Patients treated for opioid use disorder in the Outpatient Based Opioid Treatment (OBOT) Clinic and who also struggle with stimulant use disorder but failed conventional treatment (positive urine drug screen for substances other than THC and buprenorphine)
  • Ideal candidates will test positive for 3 out of 4 weeks or more prior to starting contingency management

Exclusion criteria

  • Persons under the age of 18
  • Persons not able to attend follow-up clinic visits
  • Persons not able to consent

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Contingency management
Experimental group
Description:
This arm will include data from participants who received CM
Treatment:
Behavioral: Contingency Management

Trial contacts and locations

0

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Central trial contact

Nassima Ait-Daoud Tiouririne, MD

Data sourced from clinicaltrials.gov

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