Intervention Summary
Traumatic Incident Reduction
         Traumatic Incident Reduction (TIR) is a brief, memory-based, therapeutic intervention for children, adolescents, and adults who have experienced crime-related and/or interpersonal violence, war, disasters, torture, childhood abuse, neglect, emotional abuse, traumatic bereavement, or other severe or shocking events. The program is designed to resolve symptoms of posttraumatic stress disorder (PTSD), depression, anxiety, and low expectancy of success (i.e., low self-efficacy) by integrating dissociated cognitive and emotional aspects of traumatic memory. Through sessions that usually run between 90 and 120 minutes, the practitioner facilitates the client's examination and resolution of a past trauma. Depending on the incident and the symptoms experienced by the client, resolution may be achieved in one or two sessions, or it may take repeated sessions for clients who experience residual distress related to the incident. Each TIR session begins with an assessment step, in which the client identifies the most significant item to be addressed during the session. This item can be a descriptive item, which describes a particular traumatic incident, or a thematic item, which describes a particular negative feeling, attitude, or thought; if a thematic item is selected, the negative feeling, attitude, or thought is used to identify specific incidents for resolution. This step is followed by a viewing step, in which the client examines the incident, including aspects such as the time and duration of an incident, awareness of and connectedness to each incident, and a verbal report of the incident. At the completion of the session, it is expected that the client will be able to talk calmly about the traumatic incident with a sense of autonomy and without a return of the symptoms caused by the incident. Before administering TIR, a practitioner must complete training, which consists of a short, intensive workshop led by a certified trainer, followed by ongoing supervision. Further ongoing supervision and professional development training are highly recommended. A practitioner is not required to have an advanced degree to learn the approach. In one study reviewed for this summary, adult participants received one 3- to 4-hour session of TIR, and in the other study, adolescent and adult participants received a total of ten 2-hour sessions, which occurred two times per week. The population of one reviewed study was composed of female participants, and the population of the other study was largely composed of female participants; however, TIR was developed for, and is used with, both female and male clients. 
                            The documents below were reviewed for Quality of Research. The research point of
                            contact can provide information regarding the studies reviewed and the availability
                            of additional materials, including those from more recent studies that may have been conducted. Valentine, P. V., & Smith, T. E. Evaluating Traumatic Incident Reduction (TIR) therapy with female inmates: A randomized controlled clinical trial. Research on Social Work Practice, 11(1), 40-52. Bisbey, L. B. No longer a victim: A treatment outcome study for crime victims with post-traumatic stress disorder (Doctoral dissertation). Available from ProQuest Dissertations and Theses database. (UMI No. 9522269) 
                            The following populations were identified in the studies reviewed for Quality of
                            Research. 
                            External reviewers independently evaluate the Quality of Research for an intervention's
                            reported results using six criteria: 
                            For more information about these criteria and the meaning of the ratings, see Quality of Research.
                         One study used the PSS and BDI, which are gold standard instruments used widely with psychiatric patient populations; all other measures had good to excellent psychometric properties. In addition, the measures in both studies reflect multiple dimensions of PTSD. Both studies used a randomized design. Secondary analyses accounted for pretreatment differences between intervention and control group participants. TIR sessions are tailored on the basis of client needs; however, it is unclear how the tailored sessions were documented, monitored, and considered in terms of intervention fidelity, the ability of researchers to systematically collect data, and potentially unmeasured confounding variables. Although it was noted in one study that some participants did not complete a number of the questions, there was no indication of the extent of the missing data or whether missing data were addressed methodologically or statistically. In both studies, small sample sizes reduced the statistical power to control for confounding variables, to detect differences between groups, and to control for type I errors (i.e., identifying a significant relationship when one does not exist), given the large number of statistical tests conducted. 
                                The materials below were reviewed for Readiness for Dissemination. The implementation
                                point of contact can provide information regarding implementation of the intervention
                                and the availability of additional, updated, or new materials. Basic T.I.R. hitch hiking [DVD] Descilo, T. Training checklist for clinical staff, interns, and volunteers. Miami, FL: Trauma Resolution Center.  Volkman, M. K. (Ed.). Children and Traumatic Incident Reduction: Creative and cognitive approaches. Ann Arbor, MI: Loving Healing Press. Volkman, V. R. (Ed.). Beyond trauma: Conversations on Traumatic Incident Reduction (2nd ed.). Ann Arbor, MI: Loving Healing Press.  
                                    External reviewers independently evaluate the intervention's Readiness for Dissemination
                                    using three criteria: For more information about these criteria and the meaning of the ratings, see Readiness for Dissemination.
                                 The materials provide an overview of the program model, address a variety of implementation contexts, and provide a detailed implementation protocol for conducting sessions. The program Web site also contains articles about the program and case studies, which provide helpful information and insight for new implementers. The detailed materials describe the progression of the training process and supplemental workshops available. The training section of the program Web site lists available trainings and allows the user to search for certified trainers in different locations. Posttraining support is available, and its use is encouraged. The model uses standardized measures for trauma and anxiety, which contribute to program fidelity. Additionally, trainers are required to complete checklists, ensuring fidelity; trainees are also required to complete certification quizzes and evaluations at the end of the training, which supports fidelity and quality assurance. The program Web site, which is where many implementation materials are located, is difficult to navigate. Guidance for the ongoing monitoring of intervention fidelity is limited to that which is included in the apprenticeship each trainer completes as part of the trainer certification process. 
                The cost information below was provided by the developer. Although this cost information
                may have been updated by the developer since the time of review, it may not reflect
                the current costs or availability of items (including newly developed or discontinued
                items). The implementation point of contact can provide current information and
                discuss implementation requirements. Training is conducted by trainers certified by Applied Metapsychology International. Descriptive Information
        
    
             
        
                Areas of Interest
             
            
                Mental health treatment
             
        
             
        
                Outcomes
             
            
                  
        
1: PTSD symptoms
2: Depression
3: Anxiety
4: Expectancy of success
            
             
        
                Outcome Categories
             
            
                Mental health
             
        
             
        
                Ages
             
            
                13-17 (Adolescent) 
        
18-25 (Young adult)
26-55 (Adult)
55+ (Older adult)
            
             
        
                Genders
             
            
                Male 
        
Female
            
             
        
                Races/Ethnicities
             
            
                Black or African American 
        
Hispanic or Latino
White
Non-U.S. population
            
             
        
                Settings
             
            
                Outpatient 
        
Correctional
            
             
        
                Geographic Locations
             
            
                Urban
             
        
             
        
                Implementation History
             
            
                Traumatic Incident Reduction was first implemented. Since then, TIR has been implemented in all 50 States and in Puerto Rico. It also has been used in every Province of Canada, as well as in Argentina, Australia, Belgium, Bermuda, England, Germany, India, Ireland, Israel, Italy, Japan, Palestine, Portugal, Scotland, South Africa, Switzerland, Tobago, Trinidad, and Ukraine.
             
        
             
        
                NIH Funding/CER Studies
             
            
                Partially/fully funded by National Institutes of Health: No 
        
Evaluated in comparative effectiveness research studies: Yes
            
             
        
                Adaptations
             
            
                TIR implementation materials have been translated into Spanish, and TIR training materials have been translated into Arabic, French, German, Italian, Japanese, Portuguese, and Spanish.
             
        
             
        
                Adverse Effects
             
            
                No adverse effects, concerns, or unintended consequences were identified by the developer.
             
        
             
    
                IOM Prevention Categories
             
            
                IOM prevention categories are not applicable.
             
        
    
    
     
    
     
    
              
        
                 
              
                  
                   
                      Documents Reviewed
                        Study 1
Study 2
Outcomes
                       
                                    
                                
                                         
                                    Outcome 1: PTSD symptoms 
                                    
                                         
                                    
                                            Description of Measures
                                         
                                        
                                            PTSD symptoms were assessed with at least one of the following measures in each study: 
                                    
                                        
                                         
                                    
                                            Key Findings
                                         
                                        
                                            In one study, participants were randomly assigned to the TIR group or the wait-list control group. The PSS was administered to both groups at baseline and at 1-week and 3-month postintervention follow-ups. 
                                    
At the 3-month postintervention follow-up, participants in the TIR group had mean PSS scores that were lower than those of participants in the control group (8.5 vs. 15.8; p < .01), even after controlling for pretest differences (p < .05).
In another study, participants were randomly assigned to the TIR group, the Direct Therapeutic Exposure (DTE) group, or the wait-list control group. The Penn Inventory for PTSD, the Crime-related PTSD Symptom subscale of the SCL-90-R, and the IES were administered to all three groups at baseline and 5 weeks later, after the final intervention session.
At the completion of treatment, results included the following:
                                        
                                         
                                    
                                            Studies Measuring Outcome
                                         
                                        
                                            Study 1, Study 2
                                         
                                    
                                         
                                    
                                            Study Designs
                                         
                                        
                                            Experimental
                                         
                                    
                                         
                                
                                            Quality of Research Rating
                                         
                                        
                                            2.8
                                            (0.0-4.0 scale)
                                         
                                    
                                    
                                
                                         
                                    Outcome 2: Depression 
                                    
                                         
                                    
                                            Description of Measures
                                         
                                        
                                            Depression was assessed with the Beck Depression Inventory (BDI), a 21-question self-report instrument. Scores range from 0 to 63, with higher scores indicating greater severity of depression.
                                         
                                    
                                         
                                    
                                            Key Findings
                                         
                                        
                                            Participants were randomly assigned to the TIR group or the wait-list control group. The BDI was administered to both groups at baseline and at 1-week and 3-month postintervention follow-ups. 
                                    
At the 3-month postintervention follow-up, participants in the TIR group had mean BDI scores that were lower than those of participants in the control group (9.7 vs. 17.5; p < .01), even after controlling for pretest differences (p < .05).
                                        
                                         
                                    
                                            Studies Measuring Outcome
                                         
                                        
                                            Study 1
                                         
                                    
                                         
                                    
                                            Study Designs
                                         
                                        
                                            Experimental
                                         
                                    
                                         
                                
                                            Quality of Research Rating
                                         
                                        
                                            2.6
                                            (0.0-4.0 scale)
                                         
                                    
                                    
                                
                                         
                                    Outcome 3: Anxiety 
                                    
                                         
                                    
                                            Description of Measures
                                         
                                        
                                            Anxiety was assessed with the Clinical Anxiety Scale (CAS), a 25-item self-report instrument. Higher scores indicate greater anxiety.
                                         
                                    
                                         
                                    
                                            Key Findings
                                         
                                        
                                            Participants were randomly assigned to the TIR group or the wait-list control group. The CAS was administered at baseline and at 1-week and 3-month postintervention follow-ups. 
                                    
At the 3-month postintervention follow-up, participants in the TIR group had mean anxiety scores that were lower than those of participants in the control group (46.3 vs. 55.0; p < .01), even after controlling for pretest differences (p < .05).
                                        
                                         
                                    
                                            Studies Measuring Outcome
                                         
                                        
                                            Study 1
                                         
                                    
                                         
                                    
                                            Study Designs
                                         
                                        
                                            Experimental
                                         
                                    
                                         
                                
                                            Quality of Research Rating
                                         
                                        
                                            2.6
                                            (0.0-4.0 scale)
                                         
                                    
                                    
                        
                                         
                                    Outcome 4: Expectancy of success 
                                    
                                         
                                    
                                            Description of Measures
                                         
                                        
                                            Expectancy of success (i.e., self-efficacy) was assessed with the Generalized Expectancy for Success Scale (GESS), a self-report instrument with 30 items that measure the respondent's perceptions of whether his or her personal goals can be attained. Higher scores indicate a greater expectancy of success.
                                         
                                    
                                         
                                    
                                            Key Findings
                                         
                                        
                                            Participants were randomly assigned to the TIR group or the wait-list control group. The GESS was administered at baseline and at 1-week and 3-month postintervention follow-ups. 
                                    
At the 3-month postintervention follow-up, participants in the TIR group had mean GESS scores that were higher than those of participants in the control group (122.0 vs. 106.1; p < .01), even after controlling for pretest differences (p < .05).
                                        
                                         
                                    
                                            Studies Measuring Outcome
                                         
                                        
                                            Study 1
                                         
                                    
                                         
                                    
                                            Study Designs
                                         
                                        
                                            Experimental
                                         
                                    
                                         
                                
                                            Quality of Research Rating
                                         
                                        
                                            2.6
                                            (0.0-4.0 scale)
                                         
                                    Study Populations
                        
                                
                        
                                     
                                        
                                        Study
                                     
                                    
                                        Age
                                     
                                    
                                        Gender
                                     
                                    
                                        Race/Ethnicity
                                     
                                
                                             
                                        
                                                
                                                    Study 1
                                                
                                             
                                            
                                                18-25 (Young adult) 
                                            
26-55 (Adult)
                                            
                                                100% Female
                                             
                                            
                                                50% Black or African American 
                                        
38.5% White
24% Hispanic or Latino
                                            
                                             
                            
                                                
                                                    Study 2
                                                
                                             
                                            
                                                13-17 (Adolescent) 
                                            
18-25 (Young adult)
26-55 (Adult)
55+ (Older adult)
                                            
                                                80.7% Female 
                                            
19.3% Male
                                            
                                                100% Non-U.S. population
                                             
                                        
                            Quality of Research Ratings by Criteria (0.0-4.0 scale)
                        
                                    
                            
                            
                        
                                 
                                    
                                    Outcome
                                 
                                
                                    Reliability 
                                
                                    of Measures
                                
                                    Validity 
                                
                                    of Measures
                                
                                    Fidelity
                                 
                                
                                    Missing 
                                
                                    Data/Attrition
                                
                                    Confounding 
                                
                                    Variables
                                
                                    Data 
                                
                                    Analysis
                                
                                    Overall 
                            
                                    Rating
                                
                                         
                                    
                                            1: PTSD symptoms
                                         
                                        
                                            4.0
                                         
                                        
                                            3.5
                                         
                                        
                                            2.3
                                         
                                        
                                            2.3
                                         
                                        
                                            2.0
                                         
                                        
                                            2.5
                                         
                                        
                                            
                                                2.8
                                         
                                    
                                         
                                    
                                            2: Depression
                                         
                                        
                                            4.0
                                         
                                        
                                            3.5
                                         
                                        
                                            2.5
                                         
                                        
                                            1.0
                                         
                                        
                                            2.0
                                         
                                        
                                            2.5
                                         
                                        
                                            
                                                2.6
                                         
                                    
                                         
                                    
                                            3: Anxiety
                                         
                                        
                                            4.0
                                         
                                        
                                            3.5
                                         
                                        
                                            2.5
                                         
                                        
                                            1.0
                                         
                                        
                                            2.0
                                         
                                        
                                            2.5
                                         
                                        
                                            
                                                2.6
                                         
                                    
                                         
                        
                                            4: Expectancy of success
                                         
                                        
                                            4.0
                                         
                                        
                                            3.5
                                         
                                        
                                            2.5
                                         
                                        
                                            1.0
                                         
                                        
                                            2.0
                                         
                                        
                                            2.5
                                         
                                        
                                            
                                                2.6
                                         
                                    Study Strengths 
Study Weaknesses 
     
                     
        
                 
            
                   
                    
                     
                                Materials Reviewed
                            
                                    Readiness for Dissemination Ratings by Criteria (0.0-4.0 scale)
                                
                                    
                                    
                                    
                            
                                         
                                            
                                            Implementation
                                             
                                        
                                            Materials
                                        
                                            Training and Support
                                             
                                        
                                            Resources
                                        
                                            Quality Assurance
                                             
                                        
                                            Procedures
                                        
                                            Overall
                                             
                                    
                                            Rating
                                        
                                                 
                                
                                                    3.8
                                                 
                                                
                                                    4.0
                                                 
                                                
                                                    3.3
                                                 
                                                
                                                
                                                    3.7
                                                 
                                            Dissemination Strengths 
 Dissemination Weaknesses 
 
     
                
            
                     
                        
                        Item Description
                     
                    
                        Cost
                     
                    
                        Required by Developer
                     
                
                             
                        
                                Licensing fee (includes implementation manuals)
                             
                            
                                $40 per participant
                             
                            
                                Yes
                             
                        
                             
                        
                                Traumatic Incident Reduction Training
                             
                            
                                $350-$750 per participant, depending on location and trainer
                             
                            
                                Yes
                             
                        
                             
                        
                                Traumatic Incident Reduction Expanded Applications Workshop
                             
                            
                                $350-$650 per participant, depending on site needs
                             
                            
                                No
                             
                        
                             
                        
                                Supervision for Train-the-Trainer Certification
                             
                            
                                Varies by provider
                             
                            
                                Yes, for trainers
                             
                        
                             
            
                                Ongoing support from a certified trainer
                             
                            
                                Varies by provider
                             
                            
                                No
                             
                        Additional Information