Substance Addiction Clinical Trial
Official title:
Combating Craving With Contingency Management: Neuroplasticity and Methamphetamine Abuse in South Africa
This study will correlate MA-abstinence outcomes from an 8-week contingency management (CM) program of voucher- based incentives using an escalating schedule that has been successfully implemented as an adjunct to MA treatment by the investigators collaborators in the United States. Pre- and post- treatment neuroimaging and neurocognitive assessments will assist in identifying structures and/or processes that may represent targets for development of novel behavioral and/or medication therapies.
Methamphetamine addiction (MA) is a global health problem with high prevalence and great
social and health costs in the United States and in the Republic of South Africa, and there
is a strong need for development and implementation of effective MA treatment approaches.
This study will correlate MA-abstinence outcomes from an 8-week contingency management (CM)
program of voucher- based incentives using an escalating schedule that has been successfully
implemented as an adjunct to MA treatment by the investigators collaborators in the United
States. Pre- and post- treatment neuroimaging and neurocognitive assessments will assist in
identifying structures and/or processes that may represent targets for development of novel
behavioral and/or medication therapies.
The study has 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; (2) to determine whether structural changes in frontostriatal circuitry over the
8-week CM intervention correspond with neurocognitive, psychological and MA abstinence
measures. Findings from this study will describe associations between: (1) functional and
structural indices of brain areas that support working memory, cognitive control/inhibition;
(2) performance on select neurocognitive and psychological assessments; and (3) associations
between these with MA abstinence outcomes. Study activities and the neuroscience data
generated will provide preliminary data for a larger, adequately powered study that will
test ways to optimize behavioral therapies for treating stimulant use disorder.
Furthermore, the public health relevance of this study is enhanced by its effort to develop
capacity for a productive and impactful neuroscience research agenda between groups of
strong clinical scientists in the U.S. and in the Republic of South Africa.
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Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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