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Randomized Controlled Trial
. 2016 Apr:79:7-14.
doi: 10.1016/j.brat.2016.02.001. Epub 2016 Feb 15.

The impact of treatment condition and the lagged effects of PTSD symptom severity and alcohol use on changes in alcohol craving

Affiliations
Randomized Controlled Trial

The impact of treatment condition and the lagged effects of PTSD symptom severity and alcohol use on changes in alcohol craving

Antonia N Kaczkurkin et al. Behav Res Ther. 2016 Apr.

Abstract

Given the high rates of comorbidity between posttraumatic stress disorder (PTSD) and substance use disorder (SUD), we investigated an integrated treatment for these disorders. Individuals with comorbid PTSD and alcohol dependence were randomized to receive naltrexone or placebo, with or without prolonged exposure (PE). All participants also received BRENDA (supportive counseling). The naltrexone plus PE group showed a greater decline in alcohol craving symptoms than those in the placebo with no PE group. The PE plus placebo and the naltrexone without PE groups did not differ significantly from the placebo with no PE group in terms of alcohol craving. No treatment group differences were found for percentage of drinking days. Alcohol craving was moderated by PTSD severity, with those with higher PTSD symptoms showing faster decreases in alcohol craving. Both PTSD and alcohol use had a lagged effect on alcohol craving, with changes in PTSD symptoms and percentage of days drinking being associated with subsequent changes in craving. These results support the relationship between greater PTSD symptoms leading to greater alcohol craving and suggest that reducing PTSD symptoms may be beneficial to reducing craving in those with co-occurring PTSD/SUD.

Trial registration: ClinicalTrials.gov NCT00006489.

Keywords: Alcohol dependence; Naltrexone; PTSD; Prolonged exposure; Substance use disorder.

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Figures

Figure 1
Figure 1
Raw mean PSS-I (PTSD Symptom Severity Interview) scores during treatment (weeks 1-24) and follow-up (weeks 38 and 52). Treatment conditions: naltrexone with PE (NAL+PE), placebo with PE (PLA+PE), naltrexone with no PE (NAL+NoPE), and placebo with no PE (PLA+NoPE). All participants also received BRENDA (supportive counseling).
Figure 2
Figure 2
Raw mean percentage of days drinking during treatment (weeks 1-24) and follow-up (weeks 38 and 52). Treatment conditions: naltrexone with PE (NAL+PE), placebo with PE (PLA+PE), naltrexone with no PE (NAL+NoPE), and placebo with no PE (PLA+NoPE). All participants also received BRENDA (supportive counseling).
Figure 3
Figure 3
Raw mean alcohol craving scores during treatment (weeks 1-24) and follow-up (weeks 38 and 52). Treatment conditions: naltrexone with PE (NAL+PE), placebo with PE (PLA+PE), naltrexone with no PE (NAL+NoPE), and placebo with no PE (PLA+NoPE). All participants also received BRENDA (supportive counseling).
Figure 4
Figure 4
Interaction between PSS-I scores (high, mid, and low) and time (log transformed) for alcohol craving. High and low values represent +1 and−1 standard deviations from the raw mean PSS-I score (mid).

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