The Efficacy and Effectiveness of Online CBT - Jeroen Ruwaard
The Efficacy and Effectiveness of Online CBT - Jeroen Ruwaard The Efficacy and Effectiveness of Online CBT - Jeroen Ruwaard
66 Chapter 4. Online CBT of Panic Symptomsanalyses showed that approximately 70 participants (35 per group) were needed todetect a large, d = .8, between-group effect (with ANCOVA, an estimated pre-postcorrelation of .5 and Holm-Bonferroni corrections for comparisons on 10 outcomemeasures).Screening. Respondents were screened through web-administered self-report questionnairesand a semi-structured 15-minute telephonic interview. Participants firstcompleted the self-report questionnaires. Next, the results were used to prepare theclinical interview. In this interview, the presence of at least subsyndromal PD/A wasestablished, according to the guidelines as listed in Diagnostic and Statistical Manualof Mental Disorders (DSM-IV; American Psychiatric Association, 2000), i.e., respondentswere included only if they experienced at least one full or limited symptompanic attack in the previous month. Diagnoses were made by trained interviewers andchecked by supervising researchers.The following inclusion criteria applied: age 18 years or older; no heightened riskof dissociation, psychosis, or suicide; no history of serious mental illness; no otherprevailing mental illnesses; absence of a medical condition that might explain panicsymptoms; no drug abuse; no use of neuroleptic medication; no use of anxiolyticsor antidepressants for less than 3 months or use of unstable doses (i.e., clients tookmedications as prescribed and in the targeted dosage); and no concurrent othertreatment. Excluded respondents were referred to their general practitioner, toother mental health institutions or to other Web-CBT programs. Eligible respondentsdownloaded, signed and returned an Informed Consent form.Risk of dissociation was assessed using the Somatoform Dissociation Questionnaire(SDQ-5; citeNPNijenhuis1997). Respondents who scored above the cut-off (8),completed the more specific Dissociation Questionnaire (DIS-Q) (Vanderlinden, vanDyck, Vandereycken, & Vertommen, 1991; cut-off: 3.0). The Screening Device forPsychotic Disorder (SDPD; Lange, Schrieken, et al., 2000) was used to assess the riskof psychotic episodes, with a cut-off value of 5 on the Hallucination scale. Hypochondriasiswas assessed using the Whitely Index (Speckens, Spinhoven, Sloekers, Bolk, &van Hemert, 1996; cut-off: 15). The occurrence of a prevailing posttraumatic stressdisorder was assessed using the Dutch version of the Impact of Events Scale - Revised(IES-R; Weiss & Marmar, 1996; cut-off 36: Neal et al., 1994). Obsessive compulsive
4.2. Method 67disorder, social phobia and specific phobia, and bipolar disorder were signalled usingseven items from the Diagnostic Interview Schedule (DIS: Helzer & Robins, 1988).Therapists. The therapists were 7 graduate students in clinical psychology, 2 postgraduatestudents, and 2 psychologists. They were supervised by two senior specialistsin web-CBT. All therapists had followed advanced courses in CBT, and received additionaltraining in administering web-CBT. They were taught how to use the feedbacktemplates of the manual, to increase motivation by adopting a stimulating emphaticattitude, to avoid the pitfalls of electronic, text-based communication (e.g., Brennan& Ohaeri, 1999) and to profit from the asynchronous nature of the communication toenhance the quality of the feedback (i.e. by discussing cases with one another or withthe supervisor). Participants were assigned to therapists by the supervisor based onthe availability of the therapists.4.2.3 Outcome measuresPrimary outcome measures were the self-rate version of the Panic Disorder SeverityScale (PDSS-SR; Houck et al., 2002; Shear et al., 2001) and a one-week Panic Diary.Secondary measures were the Avoidance when ALone subscale of the Mobility Inventory(MI-AAL; Chambless, Caputo, Bright, & Gallager, 1984), the Agoraphobic CognitionsQuestionnaire and the Body Sensations Questionnaire (ACQ/BSQ; Chambless et al.,1984) and the Depression Anxiety Stress Scales (DASS-42; Lovibond & Lovibond, 1995).For all measures, higher scores indicate greater symptom severity.Panic diary. In the Panic Diary, participants monitored panic attacks occurring ina one-week period. Participants were instructed to report each distinct period thatwas characterized by a sudden onset of intense apprehension, fearfulness, or terror,possibly associated with feelings of impending doom (American Psychiatric Association,2000). They were asked to note the occurrence of each attack and to rate theattack severity (on a 1-10 scale) and the specific symptoms experienced during theattack. To this end, participants checked each of 13 key symptoms of panic disorderoccurring during the attack, e.g., “palpitations, pounding heart or accelerated heartrate”, “trembling or sweating”. Three outcome measures were derived from the
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66 Chapter 4. <strong>Online</strong> <strong>CBT</strong> <strong>of</strong> Panic Symptomsanalyses showed that approximately 70 participants (35 per group) were needed todetect a large, d = .8, between-group effect (with ANCOVA, an estimated pre-postcorrelation <strong>of</strong> .5 <strong>and</strong> Holm-Bonferroni corrections for comparisons on 10 outcomemeasures).Screening. Respondents were screened through web-administered self-report questionnaires<strong>and</strong> a semi-structured 15-minute telephonic interview. Participants firstcompleted the self-report questionnaires. Next, the results were used to prepare theclinical interview. In this interview, the presence <strong>of</strong> at least subsyndromal PD/A wasestablished, according to the guidelines as listed in Diagnostic <strong>and</strong> Statistical Manual<strong>of</strong> Mental Disorders (DSM-IV; American Psychiatric Association, 2000), i.e., respondentswere included only if they experienced at least one full or limited symptompanic attack in the previous month. Diagnoses were made by trained interviewers <strong>and</strong>checked by supervising researchers.<strong>The</strong> following inclusion criteria applied: age 18 years or older; no heightened risk<strong>of</strong> dissociation, psychosis, or suicide; no history <strong>of</strong> serious mental illness; no otherprevailing mental illnesses; absence <strong>of</strong> a medical condition that might explain panicsymptoms; no drug abuse; no use <strong>of</strong> neuroleptic medication; no use <strong>of</strong> anxiolyticsor antidepressants for less than 3 months or use <strong>of</strong> unstable doses (i.e., clients tookmedications as prescribed <strong>and</strong> in the targeted dosage); <strong>and</strong> no concurrent othertreatment. Excluded respondents were referred to their general practitioner, toother mental health institutions or to other Web-<strong>CBT</strong> programs. Eligible respondentsdownloaded, signed <strong>and</strong> returned an Informed Consent form.Risk <strong>of</strong> dissociation was assessed using the Somat<strong>of</strong>orm Dissociation Questionnaire(SDQ-5; citeNPNijenhuis1997). Respondents who scored above the cut-<strong>of</strong>f (8),completed the more specific Dissociation Questionnaire (DIS-Q) (V<strong>and</strong>erlinden, vanDyck, V<strong>and</strong>ereycken, & Vertommen, 1991; cut-<strong>of</strong>f: 3.0). <strong>The</strong> Screening Device forPsychotic Disorder (SDPD; Lange, Schrieken, et al., 2000) was used to assess the risk<strong>of</strong> psychotic episodes, with a cut-<strong>of</strong>f value <strong>of</strong> 5 on the Hallucination scale. Hypochondriasiswas assessed using the Whitely Index (Speckens, Spinhoven, Sloekers, Bolk, &van Hemert, 1996; cut-<strong>of</strong>f: 15). <strong>The</strong> occurrence <strong>of</strong> a prevailing posttraumatic stressdisorder was assessed using the Dutch version <strong>of</strong> the Impact <strong>of</strong> Events Scale - Revised(IES-R; Weiss & Marmar, 1996; cut-<strong>of</strong>f 36: Neal et al., 1994). Obsessive compulsive