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Trial of a Novel Cognitive-Behavioral Treatment for Posttraumatic Stress and Substance Dependence

Primary Purpose

Posttraumatic Stress Disorder, Substance Dependence

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Treatment for Integrated Posttraumatic Stress and Substance Use (TIPSS)
Cognitive-Behavioral Therapy for Substance Dependence
Sponsored by
The University of Texas Health Science Center, Houston
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Posttraumatic Stress Disorder focused on measuring posttraumatic stress disorder, PTSD, substance dependence, substance use

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18-65
  • English language proficiency
  • Current (past month) substance dependence, noting exclusions as delineated below
  • History of trauma exposure, as per DSM-5 Criterion A1 definition
  • Current (past month) PTSD symptoms: score of at least 25 on PCL-5 and/or at least 4 symptoms of moderate severity (scored 2 or higher) endorsed on CAPS-5
  • Seeking treatment for trauma-related symptoms and substance dependence

Exclusion Criteria:

  • Exclusive [only] nicotine dependence
  • Alcohol dependence requiring detoxification
  • Opiate dependence requiring detoxification
  • Current or past bipolar I disorder
  • Current or past major psychotic disorder
  • Active (past 6 months) psychotic spectrum symptoms
  • Major unstable medical conditions
  • Current (past month) suicidal ideation with intent and/or plan
  • Current (past month) homicidal ideation with intent and/or plan
  • Inability to provide verbal/written consent

Sites / Locations

  • University of Texas Health Science Center at Houston - Center for Neurobehavioral Research on Addiction

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

CBT for Substance Dependence

Integrated CBT for PTSD and Substance Dependence

Arm Description

Standard CBT for substance use disorders

Integrated CBT for PTSD and substance use disorders, combining elements of cognitive processing therapy for PTSD with coping skills and relapse prevention for substance use disorders

Outcomes

Primary Outcome Measures

PTSD Symptoms
PCL-5 self-report measure: severity of symptoms
Substance Use
(1) rates of substance abstinence, as measured via urine toxicology testing, alcohol breath level analyses, and participants' self-reports of substance use; (2) longest sustained abstinence, defined as the maximum number of self-reported days of abstinence for each participant.
PTSD Diagnosis
CAPS interview measure: severity of symptoms

Secondary Outcome Measures

Full Information

First Posted
May 22, 2015
Last Updated
May 9, 2017
Sponsor
The University of Texas Health Science Center, Houston
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1. Study Identification

Unique Protocol Identification Number
NCT02461732
Brief Title
Trial of a Novel Cognitive-Behavioral Treatment for Posttraumatic Stress and Substance Dependence
Official Title
Randomized Controlled Trial of a Novel Cognitive-Behavioral Treatment for Posttraumatic Stress and Substance Dependence
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
August 2014 (undefined)
Primary Completion Date
November 2016 (Actual)
Study Completion Date
November 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Texas Health Science Center, Houston

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the study is to determine whether a novel integrated cognitive-behavioral treatment for posttraumatic stress disorder (PTSD) and substance dependence (i.e., Treatment for Integrated Posttraumatic Stress and Substance use; TIPSS) is more effective than cognitive-behavioral treatment for substance dependence alone with regard to PTSD symptoms and substance use quantity and frequency.
Detailed Description
The proposed study is a randomized controlled clinical trial, comparing the efficacy of two cognitive-behavioral therapy (CBT) interventions: standard CBT for substance dependence and a novel integrated CBT program for PTSD and substance dependence. The study will run for approximately 3 years. A total of 100 participants will be enrolled at a rate of 4 participants per month over 25 months to ensure that 80 participants complete the protocol (presuming 20% attrition). Each participant will attend 12 treatment sessions, meeting twice per week for 6 weeks. Treatment sessions will last 1-hour each. Primary study outcomes will include frequency and quantity of substance use and PTSD symptom severity. Substance use-related outcomes will include: rates of substance abstinence, as measured by (1) urine toxicology testing, (2) alcohol breath level analyses, and (3) participants' self-report of substance use. PTSD symptom outcomes will include symptom severity ratings as measured by clinical interview (i.e., Clinician-Administered PTSD Scale-5; CAPS-5) and self-report (Posttraumatic Checklist; PCL-5). Secondary study outcomes will include examination of mediational effects. Specifically, changes in distress tolerance, as indexed via self-report (Distress Tolerance Scale) and computer/behavioral tasks (i.e., Mirror-Tracing Task, Paced Auditory Serial Addition Task-Computerized Version, Breath-Holding Task), are expected during the course of the treatment. Changes in cue reactivity are also expected over the course of treatment, as indexed by decreased psychophysiological reactivity (heart rate, respiration rate) during script-driven imagery tasks (listening to trauma/drug related scripts vs. netural). A total of four sessions (baseline/screening and sessions 4, 8, 12) will be preceded by the laboratory sessions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Posttraumatic Stress Disorder, Substance Dependence
Keywords
posttraumatic stress disorder, PTSD, substance dependence, substance use

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CBT for Substance Dependence
Arm Type
Active Comparator
Arm Description
Standard CBT for substance use disorders
Arm Title
Integrated CBT for PTSD and Substance Dependence
Arm Type
Experimental
Arm Description
Integrated CBT for PTSD and substance use disorders, combining elements of cognitive processing therapy for PTSD with coping skills and relapse prevention for substance use disorders
Intervention Type
Behavioral
Intervention Name(s)
Treatment for Integrated Posttraumatic Stress and Substance Use (TIPSS)
Intervention Description
Topics covered include: drug triggers; antecedents/consequences of drug use; relapse prevention; coping skills; problem thinking; changing problem thinking; lifestyle balance; values; increasing non-drug activities; education on PTSD and trauma/PTSD/substance use associations; discussion and written statement of impact of trauma on beliefs about self, others, world; written account of trauma memory and in-session review and discussion; cognitive exercises and cognitive restructuring regarding trauma-related thoughts; review of any between-session trauma-relevant substance use and cravings
Intervention Type
Behavioral
Intervention Name(s)
Cognitive-Behavioral Therapy for Substance Dependence
Intervention Description
Topics covered include: drug triggers; antecedents/consequences of drug use; relapse prevention; coping skills; problem thinking; changing problem thinking; lifestyle balance; values; increasing non-drug activities
Primary Outcome Measure Information:
Title
PTSD Symptoms
Description
PCL-5 self-report measure: severity of symptoms
Time Frame
for the duration of the study / through the conclusion of treatment, up to 8 weeks
Title
Substance Use
Description
(1) rates of substance abstinence, as measured via urine toxicology testing, alcohol breath level analyses, and participants' self-reports of substance use; (2) longest sustained abstinence, defined as the maximum number of self-reported days of abstinence for each participant.
Time Frame
for the duration of the study / through the conclusion of treatment, up to 8 weeks
Title
PTSD Diagnosis
Description
CAPS interview measure: severity of symptoms
Time Frame
for the duration of the study / through the conclusion of treatment, up to 8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-65 English language proficiency Current (past month) substance dependence, noting exclusions as delineated below History of trauma exposure, as per DSM-5 Criterion A1 definition Current (past month) PTSD symptoms: score of at least 25 on PCL-5 and/or at least 4 symptoms of moderate severity (scored 2 or higher) endorsed on CAPS-5 Seeking treatment for trauma-related symptoms and substance dependence Exclusion Criteria: Exclusive [only] nicotine dependence Alcohol dependence requiring detoxification Opiate dependence requiring detoxification Current or past bipolar I disorder Current or past major psychotic disorder Active (past 6 months) psychotic spectrum symptoms Major unstable medical conditions Current (past month) suicidal ideation with intent and/or plan Current (past month) homicidal ideation with intent and/or plan Inability to provide verbal/written consent
Facility Information:
Facility Name
University of Texas Health Science Center at Houston - Center for Neurobehavioral Research on Addiction
City
Houston
State/Province
Texas
ZIP/Postal Code
77054
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Trial of a Novel Cognitive-Behavioral Treatment for Posttraumatic Stress and Substance Dependence

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