Using analog baselines to assess the effects of naltrexone on self-injurious behavior.
Naltrexone gives only tiny, function-linked drops in self-injury, so test function first and pair the drug with solid behavior plans.
01Research in Context
What this study did
The team gave naltrexone to two adults who hurt themselves. First they ran a short functional analysis to see why the self-injury happened.
They then set up small test sessions that copied each function. Drug and placebo were given in an ABAB pattern.
What they found
Naltrexone only helped a little. One person slapped his head less during work tasks, but other self-injury stayed the same.
The second person showed almost no change. The drug worked only for one shape of behavior and only when demands were present.
How this fits with other research
Green et al. (1987) also used an ABAB design and saw no benefit at all. The newer study looks better because it tested the drug only after it knew the behavior’s function.
Tantam et al. (1993) and Garcia et al. (1999) show that some people stay safe for years after they stop naltrexone. These cases seem to clash with the weak acute effects, but they tracked long-term outcomes, not short drug tests.
Schmidt et al. (2021) used the same idea—brief functional tests to pick treatment—but chose behavioral plans instead of pills. Their strong results remind us that function-based behavior plans often beat medication.
Why it matters
Run a functional analysis before you think about naltrexone. If the assessment shows demand escape, you might trial the drug for that one situation, but keep strong behavioral treatment in place. The pill is at best a helper, not a fix.
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02At a glance
03Original abstract
Naltrexone (NLTX), an opiate receptor antagonist, has been prescribed as a pharmacological intervention for the treatment of self-injurious behavior (SIB). Previous research has investigated NLTX's effects in the absence of information about the role of environmental events related to SIB. This study extended previous analyses by administering NLTX on analog baselines using a double-blind, placebo-controlled reversal design. Pretreatment functional analysis results showed that the SIB of the two participants occurred in more that one assessment condition. For one participant NLTX produced slight reductions in SIB across baseline conditions. The second participant's results showed that NLTX reduced head-slapping occurring during demand sessions, but had no apparent effect on head-banging occurring during alone and demand sessions. These outcomes suggest that NLTX may have function- and/or response-specific treatment effects. The potential utility of this model as a general method for assessing pharmacological interventions, as well as other implications and limitations, are discussed.
Research in developmental disabilities, 1999 · doi:10.1016/s0891-4222(98)00028-6