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CPT-SMART for Treatment of PTSD and Cigarette Smoking (CPT-SMART)

Primary Purpose

Smoking, Stress Disorders, Post-Traumatic

Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Smoking Cessation Cognitive Behavioral Therapy (CBT)
Bupropion
Cognitive Processing Therapy
Smoking Abstinence Reinforcement Therapy
Yoked Contingency Management
Sponsored by
VA Office of Research and Development
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Smoking focused on measuring Stress Disorders, Post-Traumatic, Smoking

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Is Veteran
  • Is between the ages of 18 and 80
  • Smokes ten or more cigarettes per day for the past year
  • Has been smoking for at least the past year
  • Meets criteria for current PTSD
  • Speaks and writes English
  • Is willing to attempt smoking cessation and trauma-focused psychotherapy

Exclusion Criteria:

  • Has had myocardial infarction in the past 6 months
  • Uses other forms of nicotine that he/she is unwilling to stop
  • Is pregnant
  • Has a primary psychotic disorder
  • Has a current substance use disorder other than tobacco use disorder
  • Has a contraindication to bupropion use with no medical clearance to use it
  • Is unwilling to use bupropion
  • Is receiving other behavioral smoking counseling or trauma-focused therapy or plans to do so during the study period
  • Is currently imprisoned or in psychiatric hospitalization

Sites / Locations

  • Durham VA Medical Center, Durham, NCRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

CPT-SMART

Combined Contact Yoked Control

Arm Description

COGNITIVE PROCESSING THERAPY with SMOKING ABSTINENCE REINFORCEMENT THERAPY (CPT-SMART) - an intervention that combines evidence-based PTSD treatment with guideline-concordant cognitive-behavioral smoking cessation counseling, bupropion, and intensive behavioral therapy through CM.

COMBINED CONTACT YOKED CONTROL (CCYC) - an intervention that is identical to CPT-SMART for PTSD and smoking treatment, except for using non-contingent payment (i.e., yoked CM) to control for compensation and monitoring.

Outcomes

Primary Outcome Measures

Number of participants whose self-report of 7 day point prevalence abstinence from smoking is bioverified
7-day point prevalence abstinence is defined as no smoking in the prior 7 days.

Secondary Outcome Measures

Number of participants whose self-report of 30 day point prevalence abstinence from smoking is bioverified
30-day point prevalence abstinence is defined as no smoking in the prior 30 days.
Number of participants whose self-report of 7 day point prevalence abstinence from smoking is bioverified
7-day point prevalence abstinence is defined as no smoking in the prior 7 days.
Number of participants whose self-report of 30 day point prevalence abstinence from smoking is bioverified
30-day point prevalence abstinence is defined as no smoking in the prior 30 days.
Number of participants who self-report prolonged abstinence
Prolonged abstinence is defined as 30 days abstinent.
Number of participants who self-report prolonged abstinence
Prolonged abstinence is defined as 30 days abstinent.
Number of participants who self-report early abstinence
Early abstinence is defined as 2 consecutive sessions abstinent in first month of quit attempt.
Number of participants who attended eight or more sessions of combined CPT and CBT for smoking
Those who complete eight or more treatment sessions will be considered to have had an adequate treatment dose.
Number of sessions attended by participants
The average number of treatment sessions attended by participants in each group will be considered a measure of treatment engagement.

Full Information

First Posted
June 5, 2019
Last Updated
July 28, 2023
Sponsor
VA Office of Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT03978442
Brief Title
CPT-SMART for Treatment of PTSD and Cigarette Smoking
Acronym
CPT-SMART
Official Title
CPT-SMART for Treatment of PTSD and Cigarette Smoking
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 7, 2019 (Actual)
Primary Completion Date
April 1, 2024 (Anticipated)
Study Completion Date
April 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
VA Office of Research and Development

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Smoking is the leading cause of preventable illness, disability, and death in the United States. The rate of smoking is disproportionately higher among Veterans with posttraumatic stress disorder (PTSD). Unfortunately, smoking cessation efforts that are effective in the general population have shown limited effectiveness in smokers with PTSD. The high smoking rate and difficulty with achieving abstinence indicate a critical need to develop effective interventions for Veterans who smoke and have PTSD. The investigators' data indicate that negative emotions and trauma reminders are associated with relapse for smokers with PTSD. In this context, an ideal strategy may be to combine evidence-based PTSD treatment with intensive smoking cessation treatment to maximize quit rates. Cognitive processing therapy (CPT) is a well-established evidence-based treatment for PTSD. The investigators have successfully developed a treatment manual that combines CPT with cognitive-behavioral counseling for smoking cessation. Contingency management (CM) is another intensive behavioral treatment that has been shown to help with reducing smoking. CM provides positive reinforcers such as money to individuals misusing substances contingent upon abstinence from use. The primary goal of this study is to evaluate the efficacy of a treatment that combines CM with cognitive-behavioral smoking cessation counseling, smoking cessation medication, and CPT. Proposed is a randomized, two-arm clinical trial in which 120 Veteran smokers with PTSD will be randomized to either: 1) COGNITIVE PROCESSING THERAPY with SMOKING ABSTINENCE REINFORCEMENT THERAPY (CPT-SMART) or 2) COMBINED CONTACT CONTROL, an intervention identical to CPT-SMART in PTSD and smoking treatment, except for using payment that is not contingent on abstinence. Specific aims include: AIM 1) To evaluate the efficacy of CPT-SMART on rates of short- and long-term abstinence from cigarettes; AIM 2) To evaluate the impact of CPT-SMART on treatment engagement and utilization; and an EXPLORATORY AIM) To explore mechanisms of CPT-SMART on long-term smoking abstinence. The positive public health impact of reducing smoking among Veterans with PTSD could be enormous as it would prevent significant smoking-related morbidity and mortality.
Detailed Description
Smoking is the leading cause of preventable illness, disability, and death in the United States. The rate of smoking is disproportionately higher among Veterans with posttraumatic stress disorder (PTSD). Unfortunately, smoking cessation efforts that are effective in the general population have shown limited effectiveness in smokers with PTSD. The high smoking rate and difficulty with achieving abstinence indicate a critical need to develop effective interventions for PTSD smokers. The investigators' data indicate that negative affect and trauma reminders are a significant antecedent of relapse for PTSD smokers. Further, despite evidence that nicotine may exacerbate PTSD symptoms, many smokers with PTSD expect that smoking helps manage their symptoms. In this context, an ideal strategy may be to combine evidence-based PTSD treatment with intensive smoking cessation treatment to maximize quit rates in this at-risk population. Cognitive processing therapy (CPT) is a well-established evidence-based treatment for PTSD. The investigators have successfully developed a treatment manual that integrates CPT with guideline-concordant cognitive-behavioral counseling for smoking cessation. Contingency management (CM) is an intensive behavioral treatment that has demonstrated efficacy for reducing smoking in a range of difficult-to-treat populations, including individuals with psychiatric disorders. CM provides positive reinforcers (e.g., vouchers, money) to individuals misusing substances contingent upon bioverified abstinence from drug use. The primary goal of the current study is to evaluate the efficacy of an intervention that combines clinic-based CM using twice weekly monitoring with salivary cotinine test strips, cognitive-behavioral smoking cessation counseling, smoking cessation medication, and evidence-based PTSD treatment. Proposed is a randomized, two-arm clinical trial in which 120 Veteran smokers with PTSD will be randomized to either: 1) COGNITIVE PROCESSING THERAPY with SMOKING ABSTINENCE REINFORCEMENT THERAPY (CPT-SMART) - an intervention that combines evidenced-based PTSD treatment with guideline-concordant cognitive-behavioral smoking cessation counseling, bupropion, and intensive behavioral therapy through CM; or 2) COMBINED CONTACT CONTROL: an intervention identical to CPT-SMART in PTSD and smoking treatment, except for using non-contingent payment (i.e., yoked CM) to control for compensation and monitoring. Specific aims include: AIM 1) To evaluate the efficacy of CPT-SMART on rates of short- and long-term abstinence from cigarettes (assessed with multiple measures including bioverified abstinence) measured at 1-week post-treatment, 4-months, and 6 months; AIM 2) To evaluate the impact of CPT-SMART on treatment engagement and utilization; and an EXPLORATORY AIM) To explore mechanisms of CPT-SMART on long-term smoking abstinence, including self-efficacy, salience of smoking, and psychiatric symptom reduction. The VA has already implemented CM for treatment of substance abuse. If shown efficacious, a combined PTSD treatment plus incentive-based approaches for smoking could be implemented into specialty PTSD programs. The positive public health impact of reducing smoking among Veterans with PTSD could be enormous as it would prevent significant smoking-related morbidity and mortality.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Smoking, Stress Disorders, Post-Traumatic
Keywords
Stress Disorders, Post-Traumatic, Smoking

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Randomized, two-arm clinical trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CPT-SMART
Arm Type
Experimental
Arm Description
COGNITIVE PROCESSING THERAPY with SMOKING ABSTINENCE REINFORCEMENT THERAPY (CPT-SMART) - an intervention that combines evidence-based PTSD treatment with guideline-concordant cognitive-behavioral smoking cessation counseling, bupropion, and intensive behavioral therapy through CM.
Arm Title
Combined Contact Yoked Control
Arm Type
Active Comparator
Arm Description
COMBINED CONTACT YOKED CONTROL (CCYC) - an intervention that is identical to CPT-SMART for PTSD and smoking treatment, except for using non-contingent payment (i.e., yoked CM) to control for compensation and monitoring.
Intervention Type
Behavioral
Intervention Name(s)
Smoking Cessation Cognitive Behavioral Therapy (CBT)
Other Intervention Name(s)
CBT
Intervention Description
12 sessions of cognitive behavioral therapy for smoking cessation, designed to help participants prepare for quitting smoking, make a quit attempt, and stay quit from smoking.
Intervention Type
Drug
Intervention Name(s)
Bupropion
Other Intervention Name(s)
Zyban
Intervention Description
All medically eligible participants will be prescribed bupropion to begin 7 days before the quit date and continued through 12 weeks post-quit. Participants will be scheduled to begin at 150mg/day of bupropion for at least 3 days before titrating up to 300mg/day dose of bupropion.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive Processing Therapy
Other Intervention Name(s)
CPT
Intervention Description
12 sessions of CPT, which is a well-established trauma-focused psychotherapy for PTSD that has demonstrated efficacy and effectiveness in Veterans.
Intervention Type
Behavioral
Intervention Name(s)
Smoking Abstinence Reinforcement Therapy
Other Intervention Name(s)
SMART
Intervention Description
Monetary reinforcement for smoking abstinence that is bioverified by breath carbon monoxide and saliva samples.
Intervention Type
Behavioral
Intervention Name(s)
Yoked Contingency Management
Other Intervention Name(s)
Control CM
Intervention Description
Participants in the yoked control will receive the monetary reinforcement of their yoked participant regardless of smoking abstinence or session attendance.
Primary Outcome Measure Information:
Title
Number of participants whose self-report of 7 day point prevalence abstinence from smoking is bioverified
Description
7-day point prevalence abstinence is defined as no smoking in the prior 7 days.
Time Frame
6 month follow-up
Secondary Outcome Measure Information:
Title
Number of participants whose self-report of 30 day point prevalence abstinence from smoking is bioverified
Description
30-day point prevalence abstinence is defined as no smoking in the prior 30 days.
Time Frame
6 month follow-up
Title
Number of participants whose self-report of 7 day point prevalence abstinence from smoking is bioverified
Description
7-day point prevalence abstinence is defined as no smoking in the prior 7 days.
Time Frame
4 month follow-up
Title
Number of participants whose self-report of 30 day point prevalence abstinence from smoking is bioverified
Description
30-day point prevalence abstinence is defined as no smoking in the prior 30 days.
Time Frame
4 month follow-up
Title
Number of participants who self-report prolonged abstinence
Description
Prolonged abstinence is defined as 30 days abstinent.
Time Frame
4 month follow-up
Title
Number of participants who self-report prolonged abstinence
Description
Prolonged abstinence is defined as 30 days abstinent.
Time Frame
6 month follow-up
Title
Number of participants who self-report early abstinence
Description
Early abstinence is defined as 2 consecutive sessions abstinent in first month of quit attempt.
Time Frame
Measured at the post-treatment visit (2 weeks after treatment completed)
Title
Number of participants who attended eight or more sessions of combined CPT and CBT for smoking
Description
Those who complete eight or more treatment sessions will be considered to have had an adequate treatment dose.
Time Frame
Measured at the post-treatment visit (2 weeks after treatment completed)
Title
Number of sessions attended by participants
Description
The average number of treatment sessions attended by participants in each group will be considered a measure of treatment engagement.
Time Frame
Measured at the post-treatment visit (2 weeks after treatment completed)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Is Veteran Is between the ages of 18 and 80 Smokes ten or more cigarettes per day for the past year Has been smoking for at least the past year Meets criteria for current PTSD Speaks and writes English Is willing to attempt smoking cessation and trauma-focused psychotherapy Exclusion Criteria: Has had myocardial infarction in the past 6 months Uses other forms of nicotine that he/she is unwilling to stop Is pregnant Has a primary psychotic disorder Has a current substance use disorder other than tobacco use disorder Has a contraindication to bupropion use with no medical clearance to use it Is unwilling to use bupropion Is receiving other behavioral smoking counseling or trauma-focused therapy or plans to do so during the study period Is currently imprisoned or in psychiatric hospitalization
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Eric A Dedert, PhD
Phone
(919) 286-0411
Ext
175526
Email
Eric.Dedert@va.gov
First Name & Middle Initial & Last Name or Official Title & Degree
Angela C Kirby, MS
Phone
(919) 286-0411
Ext
7456
Email
angela.kirby@va.gov
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eric A Dedert, PhD
Organizational Affiliation
Durham VA Medical Center, Durham, NC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Durham VA Medical Center, Durham, NC
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27705-3875
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eric A Dedert, PhD
Phone
919-286-0411
Ext
175526
Email
Eric.Dedert@va.gov
First Name & Middle Initial & Last Name & Degree
Angela C Kirby, MS
Phone
(919) 286-0411
Ext
7456
Email
angela.kirby@va.gov
First Name & Middle Initial & Last Name & Degree
Eric A Dedert, PhD

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
We do not plan to attend individual participant data.

Learn more about this trial

CPT-SMART for Treatment of PTSD and Cigarette Smoking

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