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Delivery of Anxiety Disorder Treatment in Addictions Centers

Adaptation of CALM for Comorbid Anxiety and Substance Use Disorders

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01764698
Enrollment
98
Registered
2013-01-09
Start date
2013-11-15
Completion date
2016-11-15
Last updated
2017-10-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety Disorders, Substance Use Disorders

Keywords

anxiety disorders, substance use disorders, treatment effectiveness, cognitive behavioral therapy

Brief summary

Anxiety disorders are highly prevalent among those with substance use disorders, but the majority of addictions treatment centers provide little to no evidence-based treatment for anxiety disorders. Furthermore, tension reduction models suggest that treating anxiety should also improve substance use outcomes. This study is aimed at improving symptoms for people who have substance use and anxiety problems. The study is comparing regular Intensive Outpatient treatment for addiction to Intensive Outpatient treatment for addiction plus treatment for anxiety disorders. Clinicians at a community addictions clinic will participate by receiving training in delivering cognitive behavioral therapy for anxiety disorders and will deliver the treatment to the patient participants. They will also complete some questionnaires. Patient participants will be asked to complete a baseline assessment. Those who are eligible will be randomly assigned to one of the two treatment groups. Those who are assigned to addiction treatment as usual will continue their regular care at the Matrix Institute. Participants who are assigned to also receive the anxiety treatment will be asked to participate in 6, 90-min treatment sessions and an orientation session. All participants will be asked to complete post-treatment and follow-up assessments. The assessments should take approximately 1 hour, and the follow-up assessment will be completed 6 months after treatment is over. It is hypothesized that those who get the additional anxiety disorder treatment will show greater improvement in anxiety and substance use outcomes than those who get Intensive Outpatient Program without the anxiety disorder treatment.

Interventions

BEHAVIORALCALM-SUD

6-session group for anxiety disorders. Cognitive behavioral therapy including self-monitoring, relaxation, cognitive restructuring, exposure therapy, and relapse prevention. In addition, participants in this arm are also enrolled in an Intensive Outpatient Program for their substance use disorder. The program is run by an outpatient addictions facility and includes up to 16 weeks of groups that meet 3 to 4 times per week in addition to up to 10 individual sessions of therapy. The group model includes motivational interviewing, cognitive behavioral therapy, contingency management, and relapse prevention skills.

BEHAVIORALTreatment as usual

The program is run by an outpatient addictions facility and includes up to 16 weeks of groups that meet 3 to 4 times per week in addition to up to 10 individual sessions of therapy. The group model includes motivational interviewing, cognitive behavioral therapy, contingency management, and relapse prevention skills.

Sponsors

University of California, Los Angeles
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* 18-60 years old * speak English * meet diagnostic criteria for at least one anxiety disorder * score at least an 8 on the OASIS (see Assessments), indicating at least moderate but clinically significant anxiety symptoms * be enrolled in the Intensive Outpatient Program (IOP) at the Matrix Institute (community partner) * meet diagnostic criteria for substance abuse or dependence

Exclusion criteria

* have unstable medical conditions * marked cognitive impairment * active suicidal intent or plan * active psychosis * unstable Bipolar I disorder.

Design outcomes

Primary

MeasureTime frameDescription
Brief Symptom Inventorybaseline, 6 weeks, 6 monthsChange over time is being assessed.
Timeline Follow Backbaseline, 6 week, 6 monthChange over time is being assessed
Overall Anxiety Severity and Impairment Scalebaseline, 6 week, 6 monthChange over time is being assessed.

Secondary

MeasureTime frameDescription
Panic Disorder Severity Scalebaseline, 6 week, 6 monthChange over time is being assessed.
Social Phobia Inventorybaseline, 6 week, 6 monthChange over time is being assessed.
urine toxicology screenbaseline, 6 week, 6 monthChange over time is being assessed.
Posttraumatic Stress Disorder Checklistbaseline, 6 week, 6 monthChange over time is being assessed.
Penn State Worry Questionnairebaseline, 6 week, 6 monthChange over time is being assessed.
Patient Health Questionnaire-8baseline, 6 week, 6 monthbrief depression measure; Change over time is being assessed.
Anxiety Sensitivity Indexbaseline, 6 week, 6 monthChange over time is being assessed.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026