Introduction Only 30–40% of depressed patients treated with medication achieve full remission. Studies that change medication or augment it by psychotherapy achieve only limited benefits, in part because current treatments are not designed for chronic and complex patients. Previous trials have excluded high-risk patients and those with comorbid personality disorder. Radically Open Dialectical Behaviour Therapy (RO-DBT) is a novel, transdiagnostic treatment for disorders of emotional over-control. The REFRAMED trial aims to evaluate the effectiveness and cost-effectiveness of RO-DBT for patients with treatment-resistant depression.
Methods and analysis REFRAMED is a multicentre randomised controlled trial, comparing 7 months of individual and group RO-DBT treatment with treatment as usual (TAU). Our primary outcome measure is depressive symptoms 12 months after randomisation. We shall estimate the cost-effectiveness of RO-DBT by cost per quality-adjusted life year. Causal analyses will explore the mechanisms by which RO-DBT is effective.
Ethics and dissemination The National Research Ethics Service (NRES) Committee South Central – Southampton A first granted ethical approval on 20 June 2011, reference number 11/SC/0146.
Trial registration number ISRCTN85784627.
- Refractory Depression
- Radically Open Dialectical Behaviour Therapy
- Study Protocol
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Strengths and limitations of this study
This study tests a novel and promising psychotherapeutic intervention, specifically designed for patients with chronic depression that is hard to treat.
Radically Open Dialectical Behaviour Therapy (RO-DBT) is manualised, and is increasingly used for over-controlled patients.
Our inclusive sample will add general findings to the limited evidence base on interventions for refractory depression.
Our mechanistic analyses will estimate the role of mediators, including therapeutic alliance and adherence to treatment, by reducing bias inherent in conventional analyses of mediation.
Our comparator for the effectiveness of RO-DBT is usual clinical practice, including medication and other psychotherapies.
The WHO predicts that by 2020 depression will be the second most frequent cause of disability worldwide.1 In the UK, the estimated treatment cost of mood disorders was £25 billion in 2006, some 1.5% of gross domestic product (GDP).2 Although there are efficacious treatments for depression, only half of these individuals respond to psychological treatment and only 30–40% of individuals treated with antidepressants achieve full remission.3 Treatment resistance is a common outcome for individuals with depression,3 and those with chronic depression are least likely to respond to current available treatments.4 Treatment-resistant depression (TRD) is depression that does not respond to adequate intervention, whereas chronic depression is depression lasting more than 2 years. In practice, chronic depression and TRD overlap, with many patients meeting both definitions. The term refractory depression (RD) encapsulates both definitions.
Research on intervention for RD is sparse, and most have focused on pharmacological or somatic methods. A recent systematic review of trials of medication for TRD reported many conceptual and methodological problems relating to consensus on defining and assessing RD, or on adequate response to treatment.3 Another review identified only four trials of psychotherapeutic treatment for TRD, none of which recruited more than 25 participants.5 Most such trials also exclude the most severely disturbed individuals, for example, those with comorbid personality disorder (PD) who are known to respond less favourably to existing treatments for acute depression, notably cognitive behavioral therapy.4
Few psychotherapy trials focus on patients with RD because current treatments may not be designed to meet their needs. One exception is Cognitive Behavioral Analysis System of Psychotherapy (CBASP) which was developed specifically to respond to chronic depression.6 In one trial, depressed individuals who did not respond to nefazodone, an antidepressant and were randomised to receive CBASP had a better response rate than those who continued to receive nefazodone only.7 However, a recent large trial showed when an individualised regimen of antidepressants was augmented by either CBASP or brief supportive psychotherapy (BSP) in partial or non-responders, neither psychotherapy added significant benefit to medication; only 38% derived clinically significant improvement from further medication or psychotherapy.8 This study reflects earlier findings from the Sequenced Treatment Alternatives to Relieve Depression study (STAR*D) which found that, among patients who failed to respond to antidepressant medication (ADM), fewer than one-third benefited from adding or switching to, cognitive therapy.9 ,10 Finally, although the Re-ChORD trial showed that a package of group interpersonal psychotherapy, medication and occupational therapy achieved better remission rates than treatment as usual (TAU) at the end of the treatment trial, it lacked data to show that these gains were maintained.11
This protocol outlines a randomised controlled trial of Radically Open Dialectical Behaviour Therapy (RO-DBT), a novel psychotherapeutic treatment for RD.12 ,13 RO-DBT arises from neurobiosocial theory14 and the observation that current treatments neglect the role of emotional over-control in RD. It proposes that, although the ability to inhibit competing urges, impulses, behaviours and desires is valued by most societies,15 too much self-control can be problematic. Excessive self-control has been linked to social isolation, aloof interpersonal functioning, maladaptive perfectionism, disingenuous emotional expression and mental health problems like anorexia nervosa, obsessive-compulsive PD and chronic depression.16–20 Of the unipolar depressed patients, 40–60% meet criteria for comorbid PD;21–23 over-controlled PDs, notably paranoid, avoidant and obsessive-compulsive, are the most common and least likely to respond to treatment.4 ,21 ,24 Children exhibiting behavioural over-controlled traits like shyness, timidity, restrained emotional expression and risk aversion are more likely to develop internalising disorders and become socially isolated adults.16 ,17 ,25 ,26 Adults with chronic depression are characterised by over-controlled traits, including greater self-criticism, impaired autonomy, rigid internalised expectations, excessive control of spontaneous emotion and inordinate fears of making mistakes.23
The neurobiosocial theory underlying RO-DBT posits that individuals presenting with problems of over-control are biologically predisposed to exhibit heightened threat sensitivity, diminished reward sensitivity, strong tendencies towards constraint and preoccupation with details.14 Heightened biotemperamental threat sensitivity predisposes a person to prioritise the potential for harm over the potential for reward when entering new or unfamiliar situations, thereby activating sympathetic nervous system (SNS) defensive-arousal and fight–flight responses. These perceptual biases are strengthened by family or environmental histories reinforcing avoidance of risk and masking of emotions. Heightened SNS arousal also triggers withdrawal of social safety engagement responses mediated by the parasympathetic nervous system ventral vagal complex (PNS-VVC).27 Unfortunately, when the PNS-VVC is withdrawn and SNS-mediated flight–fight responses dominate, neuroregulatory responses linked with prosocial engagement are impaired, facial expressions become frozen and the ability to express oneself flexibly is lost.27 ,28 Inhibited or incongruent expressions of emotion are perceived as inauthentic or untrustworthy by others and thus increases social ostracism.29 ,30 Since these responses may create or maintain depressive symptoms, RO-DBT uniquely emphasises both communicative and facilitative functions of emotional expressions in the formation of close social bonds and empathic behaviours via micromimicry and the mirror neuron system.12 ,13 ,31 Therapy includes training patients to relax rigid inhibitory self-control efforts, to activate the VVC-mediated social-safety system, to use non-verbal social-signalling skills linked to the mirror neuron system and the establishment of trust to allow vulnerable self-disclosure, to practice self-enquiry to learn from new experiences and critical feedback, and to reduce maladaptive social comparisons related to envy and bitterness.
Earlier versions of RO-DBT showed promise in two trials of patients with refractory depression and comorbid PD.32 ,33 The manualised version of RO-DBT12 has also been effective in two open trials of adults with anorexia nervosa.34 ,35
Our primary aim is to estimate the effectiveness of RO-DBT in treating RD, compared with TAU. We shall also estimate the cost-effectiveness of RO-DBT relative to TAU alone. We also plan to study moderators of treatment effects and mechanisms of therapeutic change. As RO-DBT emphasises the therapist's role as a model of interpersonal skills, we predict that the development and maintenance of a strong therapeutic alliance will mediate reductions in depressive symptoms. Similarly, since the treatment is challenging, we regard adherence as an important potential mediator.
Design and setting
REFRAMED is a multicentre, randomised controlled trial conducted at three National Health Service (NHS) sites in the UK—Dorset, Hampshire and North Wales. These sites routinely offer outpatient psychological treatment. All trial participants receive TAU, but those allocated at random to the experimental arm also receive 7 months of RO-DBT. We also allocate participants at random between non-therapeutic alternatives designed to facilitate mediational analyses. We measure clinical outcomes at four time points—baseline, and 7, 12 and 18 months after randomisation, using assessors blind to participants’ allocated treatment.
Participants must be 18 years or older, and have a Hamilton-Depression Rating Scale (HAM-D)36 score of at least 15, a current diagnosis of major depressive disorder in the Structured Clinical Interview for DSM-IV Axis I (SCID-I),37 and either TRD defined as two or more previous episodes of depression or chronic depression. In their current episode, furthermore, participants must have taken an adequate dose of ADM for at least 6 weeks without relief.
We exclude those who meet criteria for dramatic–erratic PD (Cluster B), bipolar depression or psychosis, or have a primary diagnosis of substance dependence or substance abuse disorder. Patients must have an IQ of more than 70 and speak English well enough to participate in the research, including treatment.
Please see figure 1 for a CONSORT diagram of the REFRAMED study participant recruitment, assessment and follow-up timeline.
We recruit participants through mental health clinicians, general practitioners (GPs) and advertisements in clinics and community. Clinical study officers within local NHS organisations handle enquiries and screen potential participants for inclusion criteria and the absence of exclusion criteria by telephone, using a standardised checklist. If eligible and willing, participants attend a second assessment interview.
Our team of trained assessors establish whether these potential participants are indeed eligible. They also administer the baseline assessment of the outcome measures set out in table 1. After the interview, participants receive further questionnaires for home completion. Our assessment lead (HO) monitors interassessor reliability, in particular whether κ’s for SCID and HAM-D are consistently at least 0.70.
Once we receive all baseline questionnaires, we allocate each participant between treatments through an adaptive randomisation algorithm administered by Swansea Trials Unit. This maintains the balance across groups of three stratifying variables chosen as potential outcome moderators, but stochastically rather than deterministically to minimise risk of subversion:64
Early onset of depression, that is, before 21 years of age
Depression severe at baseline (HAM-D above 25)
Personality disorder (meets SCID-II criteria for cluster A or cluster C)
We also use adaptive randomisation to allocate patients between therapists so as to use as many feasible treatment slots at each centre. The allocation sequence was determined dynamically using a database independently administered at the study's Clinical Trials Unit; the database incorporated a study-specific version of a published dynamic randomisation allocation method,65 and the resulting allocations were then sent by email to the Trial Manager for further dissemination to study therapists.
Mediation and instrumental variables
To understand the mechanisms by which RO-DBT improves outcomes, we shall conduct mediation analyses to estimate the effects of postrandomisation measures on the pathway from randomisation to outcome. Conventional mediation analyses may be biased by unobserved confounding, that is confounding by unobserved variables related to both the mediators and the outcomes.66 ,67 Confounding arises because, following randomisation to treatment arm, patients choose the manner in which they adhere to treatment and the level of adherence; if one patient adheres in a certain way and coincidentally suffers worse depression, confounding ensues. To address unobserved confounding, we shall use ‘instrumental variables’ (IVs) which:
Predict the likelihood that a patient will adhere to treatment;
Are unrelated to the study outcome; and
Are unrelated to the unobserved confounding variables.
If we can find one or more IVs, we can use methods like two-stage least squares to estimate the unconfounded effect of the mediator. The biggest challenge is to find IVs. Some occur naturally; for example, genes can serve as IVs: one variant of the ALDH2 gene makes it unpleasant for individuals to drink alcohol, facilitating unbiased estimates of the effect of alcohol on health from observational data.68 Alternatively, researchers make additional random allocations between options that are not therapeutic in their own right, but may influence mediators;69 for example, enhancing the therapeutic environment may enhance alliance (the mediator), but have no direct effect on symptoms (the outcome).
REFRAMED has adopted both approaches to facilitate bias-corrected estimates of the effects of two hypothesised mediators: strength of therapeutic alliance and adherence to treatment. We randomly allocate all RO-DBT participants to one of eight combinations of contextual non-therapeutic features within a 2×2×2 factorial design:
They receive individual RO-DBT in either a standard therapy room or an enhanced therapy room, which potentially improves both strength of therapeutic alliance and attendance at treatment;
After every session they either have or do not have opportunity to provide written feedback to their therapist, which improves strength of therapeutic alliance;70 and
They receive compensation potentially for questionnaire completion either personally (via their therapists) or impersonally (via mail), again potentially increasing attendance at treatment.
While we recognise that these ploys may have limited influence on our adopted mediators,71 we include them both for their potential to reduce bias in our estimates, and to encourage the wider adoption and discussion of these methods in psychotherapy research.
Intervention phase (29 weeks)
Treatment as usual
This control intervention permits participants to receive any psychotherapy or prescribed (ADM) with the exception of standard DBT. We monitor type and amount of psychotherapy, and type of ADM and adherence to it. Reporting these data will better describe this generic intervention. In particular, we do not restrict access to appropriate mental healthcare during follow-up.
Radically open-dialectical behavior therapy
This experimental intervention comprises 29 weekly individual therapy sessions lasting 50–60 min, and 27 weekly skills training classes lasting 2.5 h, including a 15 min break (table 2). RO-DBT therapists meet weekly for 1.5–2.5 h, and by telephone when needed.12 ,13 While RO-DBT participants receive ADM as prescribed, we strongly discourage them from seeking additional psychotherapy during RO-DBT. The RO-DBT treatment developer and study chief investigator (TRL) does not contribute to the treatment.
Therapist training and supervision
All therapists had to complete a two-part, 10-day RO-DBT intensive training course over 6 months and additional training or supervision when needed to achieve adherence to the treatment manual. We videotape all treatment sessions and shall sample 10% of both therapy sessions and skills classes at random, stratified by therapist and participant, for adherence rating.
If participants are unable or unwilling to attend RO-DBT sessions, we consider them as treatment drop-outs but encourage them to provide outcome data. If they withdraw from data collection, we permit them to continue with RO-DBT. If they withdraw consent to participate in the study, however, we do not seek further data.
Table 1 summarises the schedule of outcome measures.
The primary outcome is depressive symptoms, measured on the 17-item Hamilton Rating Scale for Depression (HAM-D)36 at four points (baseline, and 7, 12 and 18 months after randomisation) by assessors who report their ‘blindness’ after each assessment. We replace them with unblinded assessors for subsequent assessments.
Secondary outcomes at the same four points include remission status, and suicidal ideation and behaviour. We define remission as the combination of a HAM-D score of less than 8 and minimal functional impairment on the Longitudinal Interval Follow-up Evaluation—Range of Impaired Functioning Tool (LIFE-RIFT);50 we measure suicidal thoughts and behaviours on the Modified Scale for Suicidal Ideation52 and the Suicidal Behaviors Questionnaire.57
Health economics data
We collect health economic data alongside our primary outcomes. For health costs we use the Adult Service Use Schedule (AD-SUS); and for health utility the European Quality of Life Questionnaire (EQ-5D-3 L).46 The AD-SUS measures medication and service use, and lost productivity due to illness, in mental health populations, including patients with depression.39 We also ask therapists about unscheduled time in treating RO-DBT patients, notably calls out of hours.
Mediators of outcome
We collect data on potential outcome mediators throughout the treatment and follow-up using questionnaires to measure interpersonal, emotional, and psychosocial functioning, strength of therapeutic alliance, use of skills taught in treatment and expectancy (table 1).
Between these questionnaires, we collect data on mood, emotional coping and the credibility of and expectancy attached to the intervention, once a month for the first 12 months and again at 18 months. We also use an automated telephone system to measure mood (PANAS Short-Form),72 coping skills (6 items from the DBT-WCCL)44 and self-compassion (Self-Compassion Scale)59 once a week over the first 6 months that participants are in the trial.
At baseline we collect data on potential moderating variables, including basic demographics and Axis I and Axis II disorders, childhood experiences and invalidation, and personality and markers of personality disorder (table 1). To control for social desirability, we ask participants to complete the Balanced Inventory of Desirable Responding-Short Form. (Hart CM, Ritchie T, Hepper EG, et al. The Balanced Inventory of Desirable Responding Short Form: Reliability, validity, and factor structure. submitted manuscript 2012).
Characteristics of therapists
To investigate whether therapist characteristics, and their relationship with patient characteristics influence outcome, we collect measures of perfectionism (Frost Multidimensional Perfectionism Scale),47 personal values (Schwartz Values Scale)61 and attachment experiences (Measure of Parenting Style).51 To provide an instrumental variable for strength of therapeutic alliance, we measured therapists’ capacity to generate strong alliances before the trial by asking several patients from the caseload of each therapist to complete the California Therapeutic Alliance Scale.41
Sample size estimation
Based on an average effect sizes close to one from two RO-DBT pilot trials for RD32 ,33 and one pilot trial of DBT for TRD,73 we judged it feasible and desirable to power REFRAMED to detect a standardised difference of 0.4 between-groups (RO-DBT and TAU)—likely to be considered clinically relevant by the UK National Institute of Health and Care Excellence (NICE).
In the absence of intraclass correlation, a sample of 200 analysable participants from the three centres would yield 80% power when using a significance level of 5% to detect a mean difference of two points on the HAM-D, equivalent to a standardised difference of 0.4. Since we expect to collect analysable data from 83% of participants, we increased our initial target to 240. To increase the power of our mechanistic analyses, we planned to randomise 144 of these to RO-DBT. As participants receiving RO-DBT are clustered by therapist, we increased the target RO-DBT sample size from 144 to 180 to allow for an intracluster correlation coefficient of 0.025 for HAM-D scores, and an average cluster size of 11. Thus we aim to randomise 276 patients—180 to RO-DBT and 96 to TAU (a final allocation ratio of 15:8).
For our primary measure of depression (HAM-D), we shall analyse by treatment allocated and use a mixed-effects model to estimate the effectiveness of RO-DBT. This will include random effects to account for clustering of outcomes by therapist, and fixed effects to account for treatment allocation, differences between sites and their interaction. In particular, this model does not assume that all therapists are equally effective.74 Covariates will include baseline HAM-D score, diagnosis of PD at baseline and age at first onset of depression. Repeated HAM-D measurements enable us to compare RO-DBT and TAU at 7, 12 and 18 months after randomisation. Secondary analyses will test for interaction between treatment allocation and covariates, and estimate the marginal effect of RO-DBT within strata. If data are missing at random (MAR), these models will be unbiased and efficient. We shall, therefore, analyse missing data thoroughly and qualify our conclusions accordingly.
Mechanisms, instrumental variables and causal analyses
Initially our causal analysis will consider each potential mediator in turn, estimating both the direct effect of treatment via exposure, and the indirect effect via the mediator. Following Baron and Kenny,75 we shall compare the resulting estimates with those from a naïve analysis that assumes no unobserved confounding, and state the assumptions under which the causal estimates are unbiased and consistent. Finally we shall extend these analyses to a joint model of all mediators and IVs. To explore patterns of temporal ordering from skill acquisition, through development of the therapeutic alliance, to changes in depressive symptoms, we shall use multivariate growth curve models including autoregressive and lagged terms.
We shall undertake cost-utility analysis to estimate the cost effectiveness of RO-DBT relative to TAU alone in terms of cost per Quality-Adjusted Life Year (QALY) derived from the EQ-5D-3L. We shall use cost-effectiveness analysis of depressive symptoms from the HAM-D as sensitivity analysis. Our primary perspective will be that of the NHS and personal social services, as preferred by the National Institute for Health and Care Excellence (NICE).76 Again we shall consider societal losses due to lost productivity, including both absence from work and reduced productivity during work, in the sensitivity analysis. We shall estimate cost-effectiveness through both approaches used to estimate clinical effectiveness: conventional analysis by treatment allocated, and IV analysis based on treatment received, that is adherence. We shall use non-parametric bootstrapping to generate the joint distribution of mean incremental costs and effects of RO-DBT relative to TAU and thus, explore the probability that one treatment is better, given NICE's ‘willingness-to-pay’ threshold of £20 000 to £30 000 per QALY. We shall summarise uncertainty around these estimates by cost-effectiveness acceptability curves.77
Data collection and management
To ensure accuracy, completeness and reliability, trained assessors collect outcome data during interviews in person or by phone by following standard operating procedures for data collection and transfer to the trial office in Southampton. Each month we post additional paper questionnaires direct to participants with a free return envelope, and send text or email reminders after 10 days.
Electronic data capture system
We enter all paper data twice onto Signalbox (http://www.thesignalbox.net), a validated electronic data capture system. This system also collects the data from automated phone calls and therapists’ treatment notes online, notably by issuing weekly electronic reminders.
The Trial Steering Committee (TSC) and Data Monitoring Committee (DMC) monitor the trial to ensure we comply with the rigorous standards defined in the Medical Research Council's (MRC) Guidelines for Good Clinical Practice. The TSC meets twice a year throughout the trial. The DMC met twice in the first year and annually since then. Both the TSC and DMEC are independent from the Funder and Sponsor.
Reporting of adverse events and study termination
Site principal investigators (PIs) monitor and assess serious adverse events (SAEs) and report them to the chief investigator immediately, and to the DMC regularly, or immediately when the SAE is a Suspected Unexpected Serious Adverse Reaction (SUSAR). Site PIs discuss SAEs with the relevant participants and their GPs with their permission. The trial will terminate if the TSC, on the recommendation of the DMC or the chief investigator, judges it necessary for the welfare of trial participants or for the scientific validity of the trial.
Ethical considerations and dissemination
We ask trial participants to give consent on three occasions:
Oral consent to the phone screen;
Signed consent for the baseline assessment, stating that they have read and understood the information sheet and giving permission for the interview to be audio recorded;
Eligible participants sign the reverse of their consent forms, stating that they understand the patient information sheet and are willing to participate in the trial.
Personal information will kept on secure databases (one for each site), only accessible to members of staff who need these details for making assessment appointments and sending letters. These are the only files that link personal information with the participant identification numbers.
We conduct REFRAMED in accordance with the Declaration of Helsinki. We have received approval from the Hampshire Research Ethics Committee (National Research Ethics Service (NRES) reference number 11/SC/0146) and the Ethics & Research Governance Department of the University of Southampton, the Sponsor. REFRAMED has insurance cover under the Sponsor's Professional Indemnity and Clinical Trials policy. All investigators comply with REFRAMED's policy on conflicts of interest, and will report conflicts of interest in all resulting publications.
We shall implement and report REFRAMED in accordance with all relevant CONSORT guidance. We plan to publish the findings in high-impact, peer-reviewed journals and disseminate them to service providers and users across the UK and beyond via public forums and websites. In accordance with Research Council guidelines, we shall store anonymised individual patient data from REFRAMED in a repository accessible by other researchers following publication.
REFRAMED is a randomised controlled trial of a promising treatment for refractory depression with implications for other diagnoses. It will contribute to the clinical literature in three ways:
Our broad selection criteria include patients routinely excluded from depression trials, namely those with comorbid personality disorder, suicidal behaviour, non-suicidal self-injury, prior psychotherapy, frequent relapse or older age. Hence the evidence base is weak for these patients in most need of effective treatment. Our inclusion criteria may mean that this trial will have a higher rate of reported suicide attempts than trials that exclude patients with PDs, comorbid disorders and suicidal ideation. However, our use of open criteria reflects the growing recognition that symptoms of many mental health conditions may share a common aetiology, and that to exclude patients with comorbidities significantly undermines the generalisability and utility of clinical trials.
RO-DBT offers a major change in approach to the treatment of refractory depression. Most important is a novel focus on behavioural over-control as a core aetiological factor. The treatment proposes a new mechanism of therapeutic change by linking neuoregulatory theory and the communicative functions of emotional expression to the formation of close social bonds. This translates into novel skills focused on social signalling and changing psychophysiological arousal—a key component differentiating RO-DBT from other treatments.
REFRAMED is the first mental health trial to use instrumental variables to analyse causes of mediation. In particular, we have randomised RO-DBT participants between eight combinations of three contextual features that are not intended to be therapeutic in their own right, but may affect mediating variables, including strength of therapeutic alliance and adherence to the treatment. This approach will yield estimates of the effects of mediating variables that are less biased by confounding than conventional estimates. Thus it has the potential to resolve a longstanding criticism of the literature that links strength of therapeutic alliance with outcome—that patients most likely to recover are those most able to form strong alliances.
Design implications and limitations
REFRAMED does not use an active comparator. Instead, patients in the control arm may access any type of treatment available through the NHS or private healthcare. NICE guidelines suggest combined approaches like ADM and CBT for moderate to severe depression or depression not responding to first-line treatments.76 However, ADM alone is more readily available and often preferred for those with unresponsive depression.8 Moreover, there is little evidence whether augmenting ADM with psychotherapy is more or less effective than switching between ADMs. Indeed NICE recommendations stem from one multisite study designed to compare switching and augmentation following poor response to acute ADM treatment, but whose findings do not justify firm recommendations.
REFRAMED has recruited participants from March 2012 until May 2015, and will complete data collection by June 2016. All trial therapists have achieved good adherence to the manual. During the pilot phase, the leading site in Dorset achieved three other critical targets by: recruiting 20 participants over 6 months; ensuring that 70% of these responded in full to the primary outcome; and showing that they were satisfied with treatment according to the Client Satisfaction Questionnaire–8.43 These achievements enabled the TSC to approve the trial in full.
The authors thank the participants, our NHS study sites, therapists and research staff (assessors and administrators) for their valued contributions and support. REFRAMED acknowledges the support of the National Institute of Health Research Clinical Research Network (NIHR CRN).
Contributors TRL, BW and ITR conceived and designed the study. TRL, BW, RJH, ITR and SB were responsible for writing and submitting the grant proposal. TRL, BW, BR and RJH drafted this protocol, and BR and HO provided detailed feedback. TRL, ITR and RJH organised and supervised study implementation. PC, ITR and BW provided methodological and statistical expertise. SB and JS provided health economics expertise. TRL provided RO-DBT expertise, and therapist training and supervision. HO provided assessment expertise and supervision. SC, DK and MSt, and MSW were the site principal investigators, and provided clinical expertise and site management. RJH managed the trial day to day, including monitoring recruitment and data collection. All authors critically reviewed and approved the final version of the manuscript.
Funding This project is funded by the Efficacy and Mechanism Evaluation (EME) Programme, an MRC and NIHR partnership, grant number EME 09/150/12. REFRAMED is sponsored by the University of Southampton. The views expressed in this publication are those of the author(s) and not necessarily those of the MRC, NHS, NIHR or the Department of Health.
Competing interests TL developed and wrote the manual for RO-DBT which will be published by Guilford Press, for which he will receive royalties. TRL and RJH are shareholders of Radically Open Ltd, the RO-DBT training and dissemination company.
Ethics approval Hampshire Research Ethics Committee, 20 June 2011, National Research Ethics Service (NRES) reference number 11/SC/0146. Protocol V.4, approved 08//08/2014.
Provenance and peer review Not commissioned; peer reviewed for ethical and funding approval prior to submission.