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N/A N=117 Randomized Health Services Research

SUPER Study (Substance Use and PTSD Treatment Effectiveness Research Study)

Substance Use Disorders · Posttraumatic Stress Disorder

Enrolled (actual)
117
Serious AEs
0.0%
Results posted
Sep 2020
Primary outcome: Primary: Severity of Alcohol Use (ASI Alcohol Composite Scores) — .259; .225; .169; .152 units on a scale — p=> .05

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Modified Seeking Safety integrated into std outpatient SUD care (Behavioral); Standard outpatient SUD care (Behavioral)
Age
Adult, Older Adult · 18+ yrs
Sex
Male
Sponsor
VA Office of Research and Development
Primary completion
Apr 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Severity of Alcohol Use (ASI Alcohol Composite Scores)
.259; .225; .169; .152; .138; .141 > .05
PRIMARY
ASI Drug Composite Score
.089; .106; .057; .095; .051; .088 <.05 sig
SECONDARY
PTSD Symptoms (IES Total Score)
46.76; 47.66; 40.80; 42.40; 38.90; 36.47 >.05

Summary

This study proposes a prospective program of research that will identify feasible and inexpensive methods to detect and treat comorbid PTSD among VA SUD patients, thereby improving substance abuse treatment outcomes.

Eligibility Criteria

Inclusion Criteria

  • veteran status and VA healthcare eligibility,
  • a diagnosis of any alcohol or drug use disorder,
  • having completed an intake for outpatient SUD treatment at the VA Oakland outpatient mental health clinic, and
  • meeting criteria for a PTSD diagnosis based on a preliminary screen with the PC-PTSD and subsequent full clinical evaluation using the CAPS

Exclusion Criteria

  • current participation in any day or inpatient mental health treatment,
  • any contraindications communicated by that patient's primary clinician,
  • acute psychosis, mania, dementia, or suicidal intent
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00265564). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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