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OpenTrials
Completed

NCT Number: NCT02907853

Contingency Management for Meth in South Africa Methamphetamine Abuse in South Africa

This study will link findings from neuroscience with clinical outcomes using contingency management (CM) to identify changes in brain structure and function that emerge during purely behavioral therapy for methamphetamine (MA) use.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Department of Psychiatry at Groote Schuur Hospital

Cape Town, 7925, South Africa

About this study

This study will correlate MA-abstinence outcomes from an 8-week program of voucher-based incentives using an escalating schedule for 30 treatment-seeking, MA-dependent individuals with scores on tasks of working memory and assessments of neuropsychological and demographic status. At the beginning and end of the CM program, participants will participate in MRI scans while performing a working memory task and will complete a battery of select neurocognitive and psychological assays to address two specific aims: (1) to determine whether changes in neural function within frontostriatal circuitry from baseline to end of the 8-week CM program are associated with parallel changes in measures of cognitive control and impulsivity and with MA abstinence outcomes and (2) to determine whether structural changes in frontostriatal circuitry over the 8-week CM intervention correspond with neurocognitive, psychological and MA abstinence measures.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • provide voluntary informed consent
  • meet DSM-5 criteria for MA or amphetamine use disorder
  • provide at least one urine sample positive for MA/amphetamine metabolites during screening (i.e. prior to the commencement of the study).
  • aged 18-45
  • right-handed
  • English-speaking

Exclusion criteria

  • currently receiving treatment for stimulant addiction or needing more intensive treatment than outpatient care
  • meet DSM-5 criteria for substance use disorder other than nicotine
  • unable to attend 4+ visits during the 2-week screening period or to complete measures
  • Physical or mental illness that would require intervention that would alter imaging or that would interfere with safe study participation
  • pregnant, claustrophobic, or have metal prostheses, cardiac pacemakers, or metal clips that are incompatible with the scanner
  • HIV positive status
  • unable to comprehend written or spoken English
  • currently taking psychiatric medication

Treatment and study plan

Contingency Management

Behavioral

as described above

Primary outcomes

  1. Responses to Contingency Management

    Time frame: 8 weeks

    urine samples documenting methamphetamine abstinence

  2. fMRI Measures

    Time frame: Change b/w baseline and 8 Weeks

    measures of resting state connectivity

Secondary outcomes

  1. Stop Signal Task

    Time frame: Change b/w baseline and 8 Weeks

    measure of inhibitory control

  2. Continuous Performance Task

    Time frame: Change b/w baseline and 8 Weeks

    test of sustained attention

  3. Stroop

    Time frame: Change b/w baseline and 8 Weeks

    test of inhibitory control

  4. Balloon Analog Risk Task

    Time frame: Change b/w baseline and 8 Weeks

    measure of risk taking and decision making

Sponsors and collaborators

Lead sponsor

University of California, Los Angeles

Other

Collaborators

  • University of Cape Town

Registry information

Official study title

Combating Craving With Contingency Management: Neuroplasticity and Methamphetamine Abuse in South Africa

Important dates

Study start
2015
Primary completion
2018
Study completion
2018
First posted
Sep 20, 2016
Registry last updated
May 10, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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