Internet-delivered eye movement desensitization and reprocessing ( iEMDR ) : an open trial

Recent research indicates internet-delivered cognitive behavioural therapy (iCBT) can reduce symptoms of post traumatic stress disorder (PTSD). This study examined the efficacy of an internet-delivered treatment protocol that combined iCBT and internet-delivered eye movement desensitization and reprocessing (iEMDR), in an uncontrolled trial. Eleven of the 15 participants completed post-treatment questionnaires. Large effect sizes were found from pre-treatment to 3-month follow-up ( = 1.03 – 1.61) on clinician-assessed and d self-reported measures of PTSD, anxiety and distress, with moderate effect sizes ( = 0.59 – 0.70) found on measures of depression and disability. At d post-treatment, 55% of the participants no longer met criteria for PTSD and this was sustained at follow-up. Symptom worsening occurred in 3 of 15 (20%) of the sample from preto post-treatment; however, these participants reported overall symptom improvement by follow-up. Future research directions for iEMDR are discussed. Jay Spence ( ) Corresponding author: jay@jayspence.com.au Spence J, Titov N, Johnston L How to cite this article: et al. Internet-delivered eye movement desensitization and reprocessing (iEMDR): 2013, :79 (doi: ) an open trial [v2; ref status: indexed, ] http://f1000r.es/zr F1000Research 2 10.12688/f1000research.2-79.v2 © 2013 Spence J . This is an open access article distributed under the terms of the , which Copyright: et al Creative Commons Attribution Licence permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Data associated with the article are available under the terms of the (CC0 1.0 Public domain dedication). Creative Commons Zero "No rights reserved" data waiver The author(s) declared that no grants were involved in supporting this work. Grant information: Competing interests: There are no competing interests for any author. 06 Mar 2013, :79 (doi: ) First published: 2 10.12688/f1000research.2-79.v1 21 Mar 2013, :79 (doi: ) First indexed: 2 10.12688/f1000research.2-79.v1 Referee Status:


Introduction
Results of meta-analyses indicate that both trauma-focused cognitive behavioural therapy (TF-CBT) and eye movement desensitization and reprocessing (EMDR) 1 are effective in reducing PTSD symptoms. However, barriers to accessing these treatments include stigma, cost, distance, low mental health literacy, and long waiting lists 2,3 .
Internet-delivered psychological treatments may increase access to psychological therapy 4 . TF-CBT has been delivered via the internet and has shown promise in significantly reducing PTSD symptoms in military personnel 5,6 , university students 7,8 , and community samples in the U.S. 7 , Holland 9 , Iraq 10 , Australia 11,12 and German-speakers in Europe 13 . For example, in a previous study 12 we evaluated an internet-delivered TF-CBT (iCBT) protocol with Australian adults with a primary diagnosis of PTSD. We found large within-group effect sizes (ESs) and small-to-moderate between-group ESs on measures of PTSD symptoms, depression, anxiety and disability, in a treatment group relative to a control condition.
Time burdens on participants could hinder effective dissemination of internet treatments for PTSD. This study investigated the efficacy of internet-delivered EMDR (iEMDR) on the basis of metaanalytic findings showing that outcomes from face-to-face EMDR are equivalent to TF-CBT with the important distinction that TF-CBT required approximately 23 hours (SD = 11) of homework while EMDR required only 3 hours (SD = 4) 14 . iEMDR may offer an alternative model of remote treatment for PTSD to iCBT. The present study aimed to explore the acceptability and efficacy of iEMDR when used in conjunction with an iCBT protocol (iCBT/ iEMDR course), and evaluated using an open trial design. To increase generalizability of results, inclusion criteria were consistent with those of outpatient services. The primary hypothesis was that the iCBT/iEMDR course would be associated with significant improvements in PTSD symptoms, depression, anxiety, distress, and disability.
Secondary hypotheses were that the treatment would be rated as acceptable to participants and would not be associated with adverse events.

Methods
The study was approved by the Macquarie University Human Research Ethics Committee (HREC#: 5201100382). Participants provided informed consent. The trial is registered with the Australian and New Zealand Clinical Trials registry as ACTRN12611000151932.

Participants and recruitment
Participant flow is shown in Figure 1. Participants were recruited from visitors to a research website that evaluates internet-elivered treatments (www.ecentreclinic.org). During the recruitment period, which ran over 2 weeks during June 2011, 32 individuals applied and 15 met the following inclusion criteria: (i) self-identified as having a principal complaint of PTSD as indicated by total scores above a clinical cut-off recommended to indicate probable diagnosis of PTSD 15 (defined as > 44 on the PTSD Checklist (PCL-C) 16 ) as well as a confirmed primary diagnosis of PTSD determined by clinician-administered interview using the PTSD Symptom Scale-Interview (PSS-I) 17 ; (ii) at least one month had elapsed since the primary trauma; (iii) no psychotherapy for PTSD during the treatment period (however, supportive group and individual counselling that did not specifically target PTSD symptoms was permitted); (iv) if using psychotropic medication, no change in dosage or type of medication 1 month prior to or during treatment; (v) a resident of Australia, (vi) at least 18 years of age, (vii) had computer and internet access, (viii) not currently experiencing a psychotic mental illness, extreme current symptoms of depression (defined as a total score > 22 or responding > 2 to Question 9 (suicidal ideation) on the Patient Health Questionnaire -9 Item (PHQ-9) 18 , current suicidal intent and plan, or highly dissociative (defined as a total score above 22) on the Dissociative Experiences Scale -Brief Version (DES-B)) 19 .

Measures
The primary outcome measures were severity of symptoms of PTSD, measured by the PSS-I and the PCL-C. The PSS-I 17 is a 17-item semi-structured clinician-administered interview based on the DSM-IV criteria for PTSD. The PCL-C 16 is also a 17-item, selfreport scale of PTSD symptoms based on the DSM-IV criteria for PTSD.
Secondary outcomes measures included the Generalized Anxiety Disorder 7-Item Scale (GAD-7, which measures anxiety) 20 , the PHQ-9 (which measures depression) 18 , the Mini International Neuropsychiatric Interview (MINI; which was used to determine the presence of a major depressive episode, panic, agoraphobia, social phobia, obsessive compulsive disorder, and generalized anxiety disorder) 21 , the Kessler 10 Item 22 (K10; which measures general distress), and the Sheehan Disability Scale 23 (SDS, which measures impairment in psychosocial functioning). Traumatic experiences were assessed using the Life Events Checklist (LEC) 24 , which provides a list of traumatic events and assesses the occurrence rates of common Criterion A1 (life-threatening) traumas according to the DSM-IV. Additional outcomes included completion rates (percentage of participants who read the six online lessons of the iCBT/iEMDR course within the six weeks of the course), and treatment satisfaction (percentage who reported feeling satisfied with the program or who would recommend it to a friend).

Changes from Version 1
We would like to thank the reviewers for their comments on this manuscript, which has been edited to address their feedback concerning following points: (i) the rationale for the development of iEMDR has been clarified; (ii) the participant flow process has been clarified; (iii) the process of anchoring the positive belief followed a standardized procedure, which has now been referenced more clearly; (iv) the section comparing findings to the face-to-face literature has been edited to highlight the differences between mixed trauma and single incident trauma samples; (v) symptom worsening has been clarified; (vi) references have been updated; (vii) telephone support with a specialist PTSD therapist has been emphasized to highlight that this was not a purely internet-based treatment; (viii) the basis of the findings (completer analyses) has been clarified; and, (ix) significance indicators have been added to the tables.

Intervention
The iCBT/iEMDR course is a six lesson online intervention utilising evidence-based principles of TF-CBT 25 and EMDR 26 . The TF-CBT components were similar to those used in a previous internet-based CBT program for PTSD 12 . The course comprises text-based information and instructions and educational case stories.
Lesson 1 of the iCBT/iEMDR course includes information about the causes, symptomatology and neurobiology of PTSD, how cognitive, behavioural, and physical symptoms maintain PTSD, and provides instructions for physiological de-arousal strategies.
Lesson 2 provides the rationale for using EMDR and detailed instructions about a self-guided iEMDR process. Lesson 3 describes cognitive restructuring strategies. Lesson 4 provides more detail on how to use cognitive restructuring for common trauma-related cognitions. Lesson 5 describes avoidance and safety behaviours and the principles of graded exposure. Lesson 6 describes the principles of relapse prevention.

iEMDR intervention:
The EMDR intervention follows the standard EMDR treatment protocol by Shapiro 26 with the following adaptations for self-directed use via the internet: the protocol was divided into a desensitisation phase (weeks 2-4) followed by a phase aimed at anchoring the positive belief (weeks 5-6). The desensitization phase followed Shapiro's protocol for reducing the Subjective Units of Distress (SUDS) rating to less than 2. Anchoring the positive belief also followed Shapiro's protocol 26 until the Validity of Cognition (VoC) rating was above 5. Participants were instructed to anchor the positive belief in week 5 of the course only for trauma memories that were no longer distressing (SUDS < 2).
iEMDR was conducted using a web-based EMDR tool (http:// www.rapidtables.com/tool/EMDR.htm). The initial session of EMDR was conducted with the support of the therapist (JS) who guided participants by telephone through the procedure while they accessed the web-based EMDR tool. Further therapist-guided EMDR was provided as requested. Participants who reported not having used self-guided EMDR by mid-treatment were contacted and offered a second guided EMDR session. Instructions for working with blockages to processing were provided in an additional resource one week after giving the iEMDR instructions.

Therapist
One Clinical Psychologist (JS) provided all clinical contact with participants, which occurred via weekly telephone calls or secure email. The clinician had received Level I and II training in EMDR by a certified EMDR instructor, and had two years experience in administering iCBT and in facilitating EMDR in face-to-face treatment. The clinician was supervised by NT.

Statistical analysis
Primary analyses were conducted using data only from questionnaire completers, defined as those who completed treatment, posttreatment or follow-up questionnaires. A secondary set of analyses was performed using an intention-to-treat (ITT) model where missing data were addressed by carrying forward the first available data (i.e. baseline-observation-carried-forward model; BOCF).
Pre-to post-treatment and pre-treatment to follow-up changes in questionnaire scores were analysed using paired-sample t-tests. Effect sizes (Cohen's d) 27 were calculated based on the pooled standard deviation. All analyses were performed in PASW version 18.0 (SPSS, Inc., Chicago, IL).
Changes in prevalence of PTSD and comorbid disorders were calculated based on the results of telephone administered diagnostic interviews administered at pre-treatment, post-treatment and follow-up.
To measure adverse events we used Tarrier's 28 definitions of treatment worsening, defined as any increase in symptom scores greater than zero from pre-to post-treatment or follow up, and defined serious adverse events as self-reported hospitalizations, suicide attempts, or onset of substance abuse due to treatment.

Baseline data
The mean age of participants was 47 years (SD = 10.4), and 10/15 (66%) were women. Ten of 15 participants (67%) reported being either married or in a de facto relationship, 4/15 (27%) reported being separated or widowed and 1/15 (7%) reported being single or never married. Four of fifteen (27%) had a tertiary education, 9/15 (60%) reported having a post-high school certificate and 2/15 (13%) reported as having year 10 high school level education. One participant (7%) was in full-time employment, eight (53%) were employed part-time or studying and six (40%) reported being unemployed, retired, or disabled. Fourteen of fifteen participants (93%) reported having had previous mental health treatment and 10/15 (67%) reported taking medication related to their symptoms of anxiety or depression. One half (5/10) of the participants who completed post-treatment questionnaires reported that they were receiving individual or group supportive counselling during the treatment period that was not specifically directed at the treatment of PTSD symptoms (mean sessions = 3; SD = 2.1). Between post-treatment and follow-up, 25% (2/8) of respondents reported receiving ongoing supportive therapy (not specifically for PTSD) and 13% (1/8) commenced treatment with a psychologist specifically for PTSD (mean sessions = 4; SD = 3.5). There were no reported medication changes during the course. One quarter (2/8) of respondents reported changing their medication posttreatment. Five participants (33%) who reported not having used self-guided EMDR by mid-treatment were contacted and offered a second EMDR session guided by the therapist via telephone. None elected to participate in further EMDR, citing that EMDR had led to an increase in re-experiencing symptoms.

Attrition
The flow is shown in Figure 1. Eleven participants (73%) completed all six lessons. One participant completed a single lesson and did not complete further assessments. Three participants completed two lessons, one of whom completed post-treatment and follow up assessments and one who completed post-treatment assessments only. One participant completed six lessons, but not the post-treatment or follow-up assessments. Twelve participants completed clinicianassessed post-treatment interviews although one of these participants did not complete the self-report questionnaires. Nine participants completed follow-up questionnaires, including the abovementioned participant who had only completed two lessons. There were no pretreatment differences between completers and non-completers on the PSS-I, PCL-C or the GAD-7 at pre-treatment.
Completer analysis Primary outcome measures. Primary outcome scores for completers improved from pre-to post-treatment as shown in Table 1.

Primary outcome measures. A paired-sample t-test comparing
pre-and post-treatment scores for the ITT sample revealed significant reductions on the PSS-I (t 14 = 3.50, p = 0.004), and this was maintained at follow up (t 14 = 4.59, p < 0.0001). Scores on the PCL-C did not significantly improve from pre-to post-treatment (t 14 = 2.12, p = 0.053). However, at follow-up, scores on the PCL-C had significantly improved from pre-treatment (t 14 = 17.76, p < 0.0001).

Effect sizes
Using the completer analysis, large effect sizes were reported on the PSS-I, PCL-C, GAD-7, and K10 at post-treatment and a moderate effect size was reported on the PHQ-9 and SDS (Table 1). Large effect sizes were reported on all measures between pre-treatment and follow-up.
Using the ITT analysis, from pre-treatment to post-treatment a large within-group effect size was found on the PSS-I. Moderate withingroup effects were found on the GAD-7, PHQ-9, and K10. A small effect size was reported on the SDS. From pre-treatment to followup, large effect sizes were found on the PSS-I, PCL-C, and GAD-7, and moderate effect sizes for the PHQ-9, and SDS.

Clinical significance
Based on the results of the clinician and telephone-administered PSS-I, 6/11 (55%) participants no longer met criteria for PTSD at post-treatment and 5/9 (56%) no longer had PTSD at follow-up. Based on an ITT approach with the BOCF, 5/15 (33%) no longer met criteria for PTSD at post-treatment and follow-up.
With regard to co-morbid diagnoses for completers as measured by clinician-administered MINI, the average number of co-morbid diagnoses reduced from 2.5 (SD = 2.0) at intake to 1.2 (SD = 1.0) at post-treatment, and further reduced to 0.6 (SD = 1.6) at followup. According to an ITT analysis the average number of co-morbid diagnoses reduced from 2.5 (SD = 1.7) at intake to 1.4 (SD = 0.9) at post-treatment, and 1.1 (SD = 1.1) at follow-up.

Adverse events
Three participants reported symptom worsening as defined by Tarrier 28 and no participants reported serious adverse events. Of the participants who completed post-treatment questionnaires, three participants showed symptom worsening between pre-and post-treatment on the PCL-C, and one of these had dropped out of treatment after the third lesson. All three improved between post-treatment and follow-up such that no participants worsened between pre-treatment and follow-up. No participants worsened on the PSS-I between any time points.

Acceptability
At post-treatment, 6/11 (55%) reported that they were very satisfied with the course, one participant (9%) was mostly satisfied, and 4/11 were neutral or somewhat satisfied. None of the participants reported being dissatisfied with the course. Nine of 11 (82%) reported they would recommend this course to a friend with PTSD.

Discussion
This study explored the feasibility of a combined iCBT/iEMDR course for treating PTSD in adults using an open-trial design. The results indicated significantly reduced symptoms of PTSD, depression, anxiety, distress, and disability between pre-treatment and three-month follow-up according to an analysis of completers. By post-treatment, 55% of the participants no longer met criteria for PTSD, and the number of comorbid diagnoses had halved.
These reductions indicate that PTSD can be treated via the internet using a combination of CBT and EMDR techniques when telephone support from a specialist therapist is also included. With respect to acceptability, this protocol was moderately tolerated, indicating that improvements would be required for further use of this intervention.
Compared with ITT data from our previous trial 12 , the within-group effect size (ES) on the PCL-C was lower at post-treatment and follow-up. These differences may be due to changes to the protocol, the use of a patient sample composed primarily of childhood sexual abuse survivors, or due to the influence of attrition on the ITT analysis as a result of using a small sample. According to outcomes from the PCL-C, these results compare favourably to other studies that used the same measure with mixed trauma samples in both face to face 29,30 and online interventions 11,31 . However, results compared less favourably with face to face TF-CBT treatment of motor vehicle accident survivors 32 indicating that outcomes could potentially be improved if future iCBT treatments are tailored and delivered to a specific trauma population.
In our trial, 3/15 (20%) reported symptom worsening according to the PCL-C score between pre-and post-treatment, although all three reported treatment gains by follow-up. Although no serious adverse events (e.g., hospitalizations, suicide attempts, relapse to substance use) occurred during the program, an increase in re-experiencing symptoms (such as intrusive thoughts and increased emotional/ physiological reactivity when reminded about the event) following iEDMR lead three participants (20%) to discontinue and five (33%) to cease using iEMDR. This potentially contributed to the higher attrition, moderate acceptability, and limited course and questionnaire completion rates, relative to our earlier study. Although this may have been due to exposure-based components such as iEMDR and in vivo exposure, it is important to note that investigations of symptom deterioration and adverse events from the face-to-face literature have failed to indicate differences between exposure-and nonexposurebased treatments 33 . Furthermore, symptom exacerbation is no higher than reported in waiting lists nor is it greater than the error rates of the instruments used to detect adverse events 34,35 .

Limitations
The absence of a waitlist control condition means that the improvements could have been the results of time, repeated measurement or other non-specific effects. The design did not allow determination of whether the effects were due to the iCBT or iEMDR components. The small sample size composed of a high number of multiply traumatized, childhood sexual abuse survivors may not apply to other PTSD populations.

Conclusions
The results of this small feasibility study indicate that the combined iCBT/iEMDR protocol is potentially efficacious. The magnitude of gains did not appear to be as large as our previous study, although these may have been attenuated by differences in the sample and iCBT protocol. These results indicate that future research of the relative benefits of iCBT/iEMDR is warranted. The authors' changes have made have made the paper stronger. I have provided a few minor points of feedback but think the paper acceptable as it is overall, a good feasible evaluation of an innovative online intervention.

Open Peer Review
The rationale for testing iEMDR is very clear but the rationale for combining iEMDR and i-TF-CBT could be stronger. In the 3 paragraph of the introduction the authors cite evidence that iEMDR is as effective as TF-CBT and can be delivered in a shorter period of time. So this provides a rationale for testing iEMDR but the addition of CBT components does not clearly follow as a rationale.
As I suggested previously the paper that includes follow-up assessment data is more Klein . 2010 et al relevant to cite than the (reference number 11) paper that reports only pre-and Klein 2009 et al. post-assessment data for the same trial. There is one sentence under "Adverse events" in the "Results"section that doesn't seem to clearly follow from the previous sentence: "All three improved between post-treatment and follow-up such that no participants worsened between pre-treatment and follow-up". However, the changes made to the "Discussion" section about symptoms worsening has made the findings on worsening symptoms much clearer.
I have read this submission. I believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard.
No competing interests were disclosed. Competing Interests: rd