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Open Access Study protocol

The effectiveness and cost-effectiveness of lay counsellor-delivered psychological treatments for harmful and dependent drinking and moderate to severe depression in primary care in India: PREMIUM study protocol for randomized controlled trials

Vikram Patel12*, Benedict Weobong23, Abhijit Nadkarni12, Helen A Weiss2, Arpita Anand1, Smita Naik1, Bhargav Bhat1, Jesina Pereira1, Ricardo Araya2, Sona Dimidjian4, Steven D Hollon5, Michael King6, Jim McCambridge2, David McDaid7, Pratima Murthy8, Richard Velleman9, Christopher G Fairburn10 and Betty Kirkwood2

Author Affiliations

1 Sangath Centre, Alto-Porvorim, 403521 Goa, India

2 Faculty of Epidemiology and Population Health, London School of Hygiene and Tropical Medicine, London, UK

3 Kintampo Health Research Centre, Ghana Health Service, Kintampo, Ghana

4 Department of Psychology and Neuroscience, University of Colorado, Boulder, CO, USA

5 Department of Psychology and Human Development, Vanderbilt University, Nashville TN, USA

6 Department of Mental Health Sciences, University College, London, UK

7 Personal Social Services Research Unit, London School of Economics and Political Science, London, UK

8 National Institute of Mental Health and Neurosciences, Bangalore, India

9 Department of Psychology, University of Bath, Bath, UK

10 Department of Psychiatry, University of Oxford, Oxford, UK

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Trials 2014, 15:101  doi:10.1186/1745-6215-15-101

The electronic version of this article is the complete one and can be found online at: http://www.trialsjournal.com/content/15/1/101


Received:30 November 2013
Accepted:19 March 2014
Published:2 April 2014

© 2014 Patel et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Abstract

Background

The leading mental health causes of the global burden of disease are depression in women and alcohol use disorders in men. A major hurdle to the implementation of evidence-based psychological treatments in primary care in developing countries is the non-availability of skilled human resources. The aim of these trials is to evaluate the effectiveness and cost-effectiveness of two psychological treatments developed for the treatment of depression and alcohol use disorders in primary care in India.

Methods/design

This study protocol is for parallel group, randomized controlled trials (Healthy Activity Program for moderate to severe depression, Counselling for Alcohol Problems for harmful and dependent drinking) in eight primary health centres in Goa, India. Adult primary care attendees will be screened with the Patient Health Questionnaire for depression and, in men only, the Alcohol Use Disorders Identification Test for drinking problems. Screen-positive attendees will be invited to participate; men who screen positive for both disorders will be invited to participate in the Counselling for Alcohol Problems trial. Those who consent will be allocated in a 1:1 ratio to receive either the respective psychological treatment plus enhanced usual care or enhanced usual care only using a computer generated allocation sequence, stratified by primary health centre and, for depression, by sex. The enhanced usual care comprises providing primary health centre doctors with contextualized World Health Organization guidelines and screening results. Psychological treatments will be delivered by lay counsellors, over a maximum period of three months. Primary outcomes are severity of disorder and remission rates at three months post-enrolment and, for the Counselling for Alcohol Problems trial, drinking and the impact of drinking on daily lives. Secondary outcomes include severity of disorder and remission rates at 12 months, disability scores, suicidal behaviour and economic impact, and cost-effectiveness at three and 12 months. 500 participants with depression and 400 participants with harmful drinking will be recruited. Primary analyses will be intention-to-treat.

Discussion

These trials may offer a new approach for the treatment of moderate-severe depression and drinking problems in primary care that is potentially scalable as it relies on delivery by a single pool of lay counsellors.

Trial registration

Both trials are registered with the International Society for the Registration of Clinical Trials (Healthy Activity Programme registration number ISRCTN95149997; Counselling for Alcohol Problems registration number ISRCTN76465238).

Keywords:
Alcohol use disorders; Depression; Low- and middle-income countries; Non-specialist health workers; Psychological treatments

Background

Psychological treatments (PTs) are ‘talking’ treatments in which a therapist aims to modify ways of thinking, feeling, behaving and relating with others with the goal of facilitating recovery from distressing mental phenomena. The vast majority of people with mental disorders who live in low- and middle-income countries (LMICs) do not have access to any form of treatment, particularly PTs. Two major barriers to making treatments accessible are the lack of skilled human resources for delivering treatments and concerns regarding the context and generalizability of treatments developed in ‘western’ cultural settings. The goal of PREMIUM, a Program for Effective Mental Health Interventions in Under-resourced Health Systems, is to implement a PT development and evaluation methodology that will lead to effective PTs for mental disorders that are culturally appropriate, feasible, acceptable and affordable in under-resourced settings. A core element of this methodology is a long-term vision of ultimate scalability of treatments by emphasizing their delivery by the same pool of lay counsellors working in routine primary health care settings.

This methodology is being applied for the treatment of two mental disorders affecting adults: depression and alcohol use disorder (AUD). These two disorders have been chosen for the following reasons. First, they are the two leading causes of the global burden of mental disorders; depression is the leading mental disorder affecting women, AUD is the leading mental disorder affecting men [1]. Both disorders are associated with profound adverse social impacts on the persons affected and their families. Second, although effective pharmacological treatments exist for the severe forms of both disorders, PTs are recommended as first-line treatments in LMICs [2,3]. The primary target groups will be moderate to severe depression and harmful drinking (HD). This is because the World Health Organization (WHO) treatment guidelines for primary care advocate the use of brief structured PTs for moderate to severe depression and HD [4]. Antidepressants are also advocated for moderate to severe depression but these benefit only a third to half of patients with depression [5] and a recent trial of collaborative care for common mental disorders in primary care in India observed low adherence [6]. Furthermore, PTs are associated with lower relapse rates when compared with antidepressant medication [7] and a recent UK trial demonstrated that adding PT to routine primary care for treatment-resistant depression greatly enhanced recovery rates [5]. ‘Brief interventions’ are the cornerstone for the management of HD [8]; they are as effective as more extended interventions, can be effectively delivered in primary care and are twice as likely to reduce drinking compared with no intervention [9-12]. Limited evidence exists in support of brief interventions for reducing drinking in patients with more severe forms of AUD, namely alcohol dependence (AD). However, there is some evidence that shows that brief interventions lead to reduced drinking in patients with AD [13,14] and it is well established that rates of engagement with addictions treatment services can be enhanced [9,13,15-17].

The vast majority of trials of PT for depression and AUD are from specialist settings in high-income countries. The generalizability of these findings to LMICs is compromised by several major contextual factors, such as variations in the explanatory models of these disorders, ways of coping and dealing with them, marked variability in access to specialist services, and distinct socio-economic determinants (such as literacy) [18,19]. There is a growing evidence base testifying to the effectiveness of approaches that address these challenges, notably the systematic adaptation of PTs to suit the local context and task-sharing their delivery to appropriately trained and supervised lay and community health workers in primary care and community settings [20]. There is emerging evidence testifying to the cost-effectiveness of task-sharing of PTs to non-specialist health workers (NSHW) compared with enhanced usual care [21]. However, a recent systematic review observed that task-sharing is associated with a number of barriers, primarily a lack of resources [22], and generating further evidence on its cost-effectiveness is a key strategy to address this barrier. Identifying effective PTs delivered by NSHWs was ranked amongst the leading research priorities for global mental health in a recent systematic priority-setting exercise [23].

PREMIUM is a Wellcome Trust-funded programme that seeks to develop and evaluate PTs for priority mental disorders for delivery by NSHWs in routine health care settings in India. The programme has systematically developed PTs for moderate to severe depression and HD and AD (Chowdhary et al., in preparation; Nadkarni et al., in preparation). PREMIUM will now implement two concurrent randomized controlled trials to evaluate each of these treatments, delivered by the same NSHWs (referred to as lay counsellors).

Objectives and hypotheses

The objectives of the two trials are to evaluate the effectiveness and cost-effectiveness of the Healthy Activity Program (HAP), for adults with moderate to severe depression, and the Counselling for Alcohol Problems (CAP), for adults with HD or AD, delivered by the same pool of lay counsellors in primary care in Goa, India. The primary analysis group for the CAP trial are participants with HD. The primary hypotheses are that the PT intervention in addition to enhanced usual care (EUC) will be superior to EUC alone in reducing the severity of symptoms and in increasing remission rates in participants with depression and HD at three months post-enrolment. In addition, we hypothesize that the CAP will reduce the physical, social, intrapersonal, impulsive and interpersonal consequences of alcohol use at three months in participants with HD. Secondary hypotheses are that the PT intervention in addition to EUC will be superior to EUC alone in reducing disability, suicidal behaviour and intimate partner violence, and that it will be cost-effective from a health systems perspective. That is, it would have a gain in quality-adjusted life years of no more than the annual per capita gross domestic product in India. Further to this, from a societal perspective, the intervention will be dominant over EUC, with both a reduction in costs and superior outcomes.

We further hypothesize that the PT intervention will increase activation (HAP trial) and uptake of detoxification services (CAP trial). Table 1 provides a summary of the trials outcomes.

Table 1. Primary and secondary outcomes of the PREMIUM trials

Methods/design

Setting

The trials will be conducted in eight primary health centres (PHC) in the district of North Goa, a state on the west coast of India. The publicly funded PHC is the first port of call in India for people who wish to seek health care in the public system.

Design

We will carry out a parallel arm randomised controlled trial with equal allocation of participants between arms.

Participants and procedures

The flow chart (Figure 1) shows the process of recruitment and follow-up of participants in the trials. The HAP trial will include participants of both genders, and the CAP trial will only include male participants because HD and AD are rare in women in India [24]. Eligible patients will be invited to participate in either the HAP or CAP trial as appropriate by the health assistant after the patient’s consultation session with the PHC doctor. After provision of written and verbal information, consent will be sought. A record of the age, educational attainment, marital status, gender, screening questionnaire score and reason for refusal will be maintained for those who do not consent. Eligible patients who are willing to participate in the trial but are unable to complete the informed consent procedure due to time constraints will be invited to return on another occasion, or followed-up by the health assistant at their homes or a convenient location to complete the procedure. Such patients will be allowed a period of two weeks to confirm their participation in the trials. Recruitment will be censored to a maximum of the first two to three eligible participants per day (irrespective of the type of disorder) to ensure uniform staggering across all PHCs (which vary in size of patient attendance) and to avoid over-loading of counsellors.

thumbnailFigure 1. PREMIUM trials flow chart. AUDIT, Alcohol Use Disorders Identification Test; Counselling for Alcohol Problems; HAP, Healthy Activity Program; PHQ-9, Patient Health Questionnaire-9; PHC, Primary Health Clinic; FU, Follow Up.

Inclusion criteria

Eligible participants will be PHC attendees aged 18 to 65 years who are intending to reside at the same address in the catchment area of the PHC for at least 12 months. This age range was chosen because persons younger than 18 years require parental consent for participation in research and our pilot study showed that those over the age of 65 had particular difficulties in engaging with the PT. Participants will be included if they screen positive on the Patient Health Questionnaire-9 (PHQ-9) and/or the Alcohol Use Disorders Identification Test (AUDIT), and if they give informed consent.

Exclusion criteria

Pregnant women, patients who need urgent medical attention (defined as needing emergency treatment or in-patient admission), patients who are unable to communicate clearly (for example, due to a speech or hearing disability or inability to comprehend one of the programme’s four languages: Konkani, Hindi, Marathi or English), and patients who are intoxicated at the point of assessing inclusion and exclusion criteria will not be eligible. These criteria will be determined by trained health assistants at the PHC.

Identification of the target mental health conditions

Trained health assistants will interview consecutive PHC attendees at the out-patient department who meet the inclusion criteria. To detect depression they will use the PHQ-9, a nine-item questionnaire that has previously been validated for use in the study setting [25]; the cut-point of 14 selected is the most accurate for detection of moderate to severe depression [26] and has a high positive predictive value for depressive disorder defined by the International Classification of Diseases revision 10 [27]. To detect HD or AD, they will use the AUDIT, a 10-item screening questionnaire for AUD, developed by the WHO [28]. The AUDIT has been validated and used in cross-national studies, including in India [29], and has been field-tested in the study setting [30]. The AUDIT allows for varying the cut-off score depending on the country’s drinking patterns, the alcohol content of standard drinks, and the nature of the screening program. For the purpose of this study the threshold score will be 12. The AUDIT has been adapted to cover a three-month period to be consistent with the three-month outcome assessment, as in other studies [31].

The order of assessments for male patients will be the AUDIT first, followed by the PHQ-9; those who screen positive for both disorders will be invited to participate in the CAP trial, following the guidelines for the treatment of co-morbid depression and HD and AD [32]. Patients who screen negative and re-enter the PHC will not be offered the opportunity for re-screening until three months after their initial screening.

Baseline assessments

After consent has been obtained, the health assistant will collect the following data on potential moderators of treatment effect: age group, gender, marital status, employment status [33], duration of the illness [33] (for HAP), readiness to change drinking behaviour [34] (for CAP), severity of depression or drinking [35], and the patient’s expectations in the effectiveness of PTs for their health problem [36]. All assessments will be audio-taped (with permission), and the tapes randomly selected for review by the supervisor for quality assurance.

Randomization

Randomization will be carried out after completion of the baseline assessments. The randomization list will be generated by a statistician independent of the trial. The list will be stratified by PHC and sex (for the HAP trial) using randomly sized blocks of four to six (two to four for men in the HAP trial). The randomization code will be concealed using sequentially numbered opaque sealed envelopes to maximise allocation concealment [37]. The envelopes will be prepared at the London School of Hygiene and Tropical Medicine (LSHTM) by personnel independent of the trial and shipped to the data manager at the trial site. We will ensure fidelity of treatment allocation is not compromised by using differently coloured envelopes for the two trials, each of which will have a sticker with clinic number, gender (for HAP) and trial ID number. The envelopes will be taped down for extra security. Inside will be a plain piece of card folded in two, and inside the card will be a sticker with the ID number and allocation. A daily check by the data manager will be performed to evaluate if allocations done are consistent with the allocation code.

Sample size estimation

The sample size estimations are made on the following assumptions: patients are randomized within each of the eight clinics; one counsellor per PHC; an intra-cluster correlation of 0.04 (this is based on the MANAS trial [6] and may be conservative, as the CoBalT trial found within-therapist clustering of only 0.0027 [5]); a loss to follow-up of 15% over three months (conservative, based on the MANAS trial in Goa, which was 13% over six months [6]); and equally sized groups (1:1 allocation ratio).

Based on these assumptions, we aim to recruit 500 participants with depression for the HAP trial and 600 participants with HD or AD for the CAP trial, to yield the required sample size of 400 patients with HD (AUDIT scores of 12 to 19; those who score > 19 are categorized as AD). The power we will have to detect effect sizes for the outcomes for analyses of primary and secondary analysis groups are specified in Tables 2, 3 and 4.

Table 2. Power calculations for the Healthy Activity Program trial

Table 3. Power calculations for the Counselling for Alcohol Problems trial

Table 4. Power calculations for the Counselling for Alcohol Problems trial on available sample sizes for sub-group analyses

The PREMIUM interventions

The psychological treatments

The PTs were developed in a systematic process that built upon the experiences of the investigators in adapting mental health interventions for use in under-resourced and socio-culturally diverse contexts [43-50]. The key principles of this approach were to dismantle evidence-based PTs and combine them with strategies identified as being useful in the local context. Evidence-based PTs were identified based on the WHO Mental Health Gap Action Programme (mhGAP) guidelines for use in primary care [4]. Contextually appropriate strategies were identified through a review of explanatory models, PT studies and qualitative studies with persons with the target disorders, their care-givers and health care providers (including alternative and religious healers) about key outcomes and coping strategies. The strategies were collated and the list reduced by merging those that were similar. Strategies that were rated by local mental health providers and NSHWs as being acceptable, safe and feasible for delivery by NSHWs in primary care were taken to the next stage of synthesis into a formal PT in intervention development workshops. This process led to the identification of behavioural activation and motivational enhancement therapy as the theoretical framework for the emerging PTs for depression and HD or AD respectively. The next phase of treatment development involved the development and adaptation of PT manuals based on the source behavioural activation manual [51] and motivational enhancement therapy manual [52], and by testing the delivery of the PTs to patients with the target disorders both by specialists and lay counsellors. The PTs were finally subjected to a pilot study in which lay counsellors delivered them to patients in PHCs; modifications were made at this stage to enhance acceptability, feasibility and scalability, notably through the inclusion of home-based delivery, use of pictorial patient resource materials, strategies to encourage the involvement of a significant other in the treatment, and task-sharing the supervision of lay counsellors to peer-groups. In addition, a generic counselling skills manual was used to train counsellors in core skills required for the delivery of both PTs. These manuals of the treatments are available on a database on the Sangath website [53].

The resulting PT for depression is the HAP. HAP comprises up to eight sessions delivered in three flexible phases over two to three months with each session lasting between 30 and 45 minutes. The optimal number of sessions for HAP are five or six, at which point the pilot study showed the largest reduction in depression scores; however, a few patients needed up to eight sessions to achieve this outcome. Patients are encouraged to complete the first session on the day of recruitment; those unable to complete a full session are offered an abbreviated session. The core strategies of HAP are behavioural assessment and self-monitoring, psychoeducation about the relationship between activity and mood, activity structuring and scheduling, and problem-solving. The CAP uses content derived from motivational interviewing along with other behavioural and cognitive components. CAP has three phases, and is delivered flexibly over one to four sessions (30 to 45 minutes each) over six to eight weeks. The optimal number of sessions is two, with a maximum of four sessions for the small proportion of patients who are either at the more severe end of the spectrum or do not achieve treatment goals. The core strategies of CAP are detailed assessment, personalised feedback, evoking commitment to change and development of a change plan, drink refusal skills, managing drinking urges, management of emotions, problem-solving skills, and relapse prevention. In addition, patients with AD will receive a structured referral to detoxification services.

Both PTs will be delivered on an individual basis either at the PHC, the patient’s home or a convenient place suggested by the patient, or on the telephone. Any participant receiving the maximum number of stipulated sessions of the PT or completing treatment goals in fewer sessions will be discharged. Participants receiving HAP who do not respond to the PT at the end of eight sessions will receive a referral to psychiatric services. Any participants missing three consecutive scheduled sessions will be considered as a treatment drop-out. However, participants who re-engage at any point during the trial will be offered the opportunity to continue from the last session.

Counsellors

The PTs will be delivered by lay counsellors who are members of the local community, are above 18 years of age, have completed at least high school education, do not have professional mental health training, and have an expressed desire to help people with mental health problems. Trainee counsellors were recruited by placing advertisements in newspapers and through word of mouth, and selected based on their performance in a structured interview and role play. Post selection, the trainees underwent a three-week participatory workshop covering both PTs. Trainees who met competency standards (based on role play and multiple choice questions) progressed to the pilot study. Training was conducted by five local specialists who were previously trained by international experts and continued to receive once monthly supervision via Skype. In the pilot study the trainee counsellors delivered the PT to eligible patients in PHCs. Supervision was carried out both in individual and weekly group format by the local specialists. Therapy quality was assessed mainly through rating of audio-taped sessions using a specially developed scale, the Quality of HAP and Quality of CAP adapted from the Counselling Skills Scale [54], the Quality of Behavioural Activation Scale (Dimidjian S, Hubley A, Martell CR, Herman-Dunn R, Dobson KS: Quality of behavioral activation scale (Q-BAS): Unpublished) and the Motivational Interviewing Target Scheme [55]. As the trainee counsellors gained experience in delivering the intervention, the supervision format evolved from expert led (that is, local mental health professionals skilled in the delivery of the PT) to peer-led group supervision. Only trainees who achieved competence, as assessed by standardised role plays and therapy quality assessments, were selected to deliver the PTs in the trials. Each PHC will have one counsellor, with a pool of back-up counsellors in the event of counsellors leaving or if weekly load of patients exceeds counsellor limit.

Supervision

Supervision during the trial will be primarily in a peer-led group format with supervision groups held once a week in the field office or a PHC. Supervision will comprise two types of activities: first, assessment of the quality of sessions (using the quality rating scales) based on selected audio-recordings of sessions and, provision of peer feedback; and second, discussion of any difficult cases. If treatment-related issues cannot be resolved in the peer group they will be discussed with experts. In addition, individual supervision will take place twice a month on-site (that is, at the respective PHC) by an expert who will review individual patient progress and quality of documentation, assess any patient safety issues, and address any site- or counsellor-specific practical difficulties or concerns.

Enhanced usual care

Usual care in primary care for depression and HD or AD in India is, in effect, no care at all. This has been confirmed in the study setting during the pilot study. This is primarily because most cases are not diagnosed and, amongst those who are, most do not receive either antidepressants or PT. In the PREMIUM trials, usual care will be enhanced by providing the screening results to the primary care physician; providing a contextualized version of the mhGAP guidelines [4] for the target disorders to the primary care physician, including guidelines on when and where to refer patients for psychiatric care.

This EUC is the most intensive model of primary care for both target disorders that may be envisaged in the foreseeable future in India or other LMICs, and is the one that is currently recommended by the WHO’s mhGAP [56].

Minimization of contamination

Contamination of the EUC arm will be minimized by masking the PHC doctor to the allocation status of the patient and not offering formal training in the PTs to any of the PHC staff. If there are any clinical issues arising from the counselling that need PHC doctor involvement, the counsellor will advise the patient to speak to the doctor about this, or will consult the expert supervisor for guidance.

Outcome evaluation

Outcome data will be collected at three months and 12 months post-enrolment. The three-month outcome is the primary end-point for both trials as the PTs delivery will be completed and we would expect the optimal effect of the treatment. The 12-month end-point is included to evaluate the sustainability of the effect of the intervention. The outcome assessment measures with the specific outcomes for each trial are summarized in Table 5. The primary outcome measures for the HAP trial are the Beck’s Depression Inventory and the PHQ-9, and for the CAP trial, the Time Line Follow Back, the Short Inventory of Problems and the AUDIT. The additional costs of delivering PTs and EUC, impacts on the use of health care services, lost time from everyday usual activities including paid work, as well as time and monetary costs to families will be assessed using data collected with a tailored version of the Client Service Receipt Inventory.

Table 5. PREMIUM outcome assessments

Masking of outcome assessments

Baseline assessments will be carried out by the health assistants in the PHC before randomization. The three- and 12-month outcome assessments will be carried out by an independent team of field workers who have no contact with the PHCs and who will be entirely community based (that is, assessments will be done at home, to minimize the risk of unmasking). The intervention and outcome evaluation teams will not have any interactions during the trial and will maintain separate physical location and administrative management. The evaluators and participants will be told that we are evaluating two different interventions and that there is clinical equipoise about whether one is better than the other. Primary outcome measures will be completed at the first contact, reducing the likelihood of it being affected by unmasking during the assessment.

Fidelity assessments

Two types of indicators will be collated to evaluate the fidelity of the delivery of the PTs, namely, their quantity and quality. Quantity indicators collated through counsellor case records will measure the number, mode of delivery (that is, home, PHC, telephone), and duration of PT sessions. Quality indicators will be assessed through ratings of 10% of audio-recording transcripts of all sessions by independent experts blind to outcome data using the respective PT quality assessment scales.

Nested qualitative study

The aim of the qualitative study is to explore patient perceptions of the quality of the care received and any beneficial or adverse effects, satisfaction with care, and the impact of their health problems on their daily lives, economic productivity and lives of family members. Participants will be purposively recruited after completing the 12-month outcome assessments by the independent statistician (to maintain blinding) to ensure balance of arms, recovery status and PHCs. We expect to carry out in-depth interviews with up to 40 participants from each trial, within one to two weeks of completion of the secondary end-point quantitative assessments. In-depth interviews will be conducted until data saturation is reached. All interviews will be audio-taped. Subsequently, the memos (reflective notes about the interviews) and field notes written by the interviewers will be attached to the main text of the interviews. The qualitative researchers will be separate from the quantitative outcome assessment team.

Data management

Three types of quantitative data will be collected: baseline, intervention process and outcome assessment. All baseline and outcome data (with the exception of a part of the Client Service Receipt Inventory) will be captured electronically using tablet computers, as will process data from lay counsellors. The data will be remotely uploaded as comma separated values (CSV) files on the main data server running online using the customized STAR software program [70], which is compliant with Good Clinical Practice (including a date- and time-stamp for original data entry, and an audit trail documenting any subsequent changes). PT process data and therapy quality data will be collected in paper form; these will be manually entered and stored as CSV files using the same data collection platform used for the electronic data. Range and consistency checks will be performed at weekly intervals separately for each data source. Queries identified will be resolved promptly by the trial management team, and the database updated, maintaining the audit trail. All data will be kept in separate databases and only merged into a master database after data collection is completed and each individual database is locked. All data is backed-up on external hard disks on a daily basis. Access to pre-locked data will be password-protected at multiple levels and no member of the trial team apart from the data manager and independent statistician will have access to these passwords. After the dataset is locked, it will remain password-protected and trial investigators will have access to the datasets. Qualitative data will be collected using digital recorders together with written field notes and memos. The former will be transcribed in the language of the interview, anonymized but linked with the trial ID and then translated for analysis. A similar procedure will be followed for the written data. Digital recordings will be stored in a secure, password-protected folder. For all data, a separate file linking names and trial IDs will be kept and password-protected.

Analysis

Quantitative analyses will be carried out using Stata (version 13). Below is a summary of our approach to the analysis. A detailed analysis plan will be agreed with the Data Safety and Monitoring Committee towards the end of the trial and before any analysis is undertaken.

Descriptive analyses

Initial analyses will compare baseline characteristics of individuals who consented and did not consent, and participants who did and did not complete outcome assessments respectively. Baseline characteristics of enrolled participants will be compared between treatment arms. Findings will be reported as per the CONSORT guidelines [71], including a trial flow chart. This will include total adult PHC attendees within period of screening, total assessed for inclusion and exclusion criteria, number of patients meeting inclusion or exclusion criteria, number screened for eligibility, number consenting to enter the trials, and number refusing or excluded (with reasons). The number continuing through the trials, actively withdrawing, and passively lost to follow-up will be shown by arm. The outcome measures will be summarised at recruitment, at three-month and 12-month follow-up by intervention arm, and overall. These will be summarised by means (standard deviation), medians (interquartile range), or numbers and proportions as appropriate by key relevant subgroups (such as age, gender and baseline outcome score). For continuous outcomes, histograms will also be plotted within each arm to assess normality and whether any transformation is required.

Outcome analyses

The primary analyses will be intention-to-treat at the three-month end-points adjusted for baseline values (where assessed), regardless of adherence to the PT. The size of the trial and the randomization design should ensure balance between arms. However, this will be checked and adjustments included for any a priori defined potential confounding variables for which randomization did not achieve reasonable balance between the two arms at baseline. PHC will be adjusted for as a fixed effect in the analysis to allow for within-PHC clustering. There will usually be only one counsellor per PHC so we will not additionally adjust for counsellor variation. Analyses of outcome will be conducted using logistic regression for binary outcomes (for example, percentage with depression, percentage with HD), and linear regression for continuous outcomes (for example, depression scores). Effect sizes will be reported as crude and adjusted relative risks estimated using the marginal standardization technique with 95% confidence intervals for the ratios estimated via the delta method [72] for binary outcomes; and mean differences and standardised mean differences with 95% confidence intervals for continuous outcomes. Missing outcome data will be imputed using multiple imputation, implemented in Stata [73]. Given that we have only two follow-up time points (three and 12 months), the analyses will be conducted and interpreted separately for each of these time points. No interim analyses of outcomes are planned.

Moderator analyses

A moderator analysis will be conducted to help clarify for whom and under what circumstances (moderators) each of the PT treatments work. We will assess modification of treatment effect by a priori defined modifiers (age group, gender, marital status, employment status, chronicity of illness (for depression), readiness to change drinking (for HD or AD) severity of depression or drinking, and patient expectations), by fitting relevant interaction terms and testing for heterogeneity of treatment effects in regression models.

Compliance analysis

As we expect a proportion of our participants to have poor compliance to the PTs, we will undertake Complier’s Average Causal Effect analyses, which estimates the effect of the PT on the participants who received it in full as intended by the original randomization [74].

Economic evaluation

Cost-effectiveness analysis and cost utility analysis will be conducted assessing the incremental cost-effectiveness of PT versus EUC in both trials. The cost-effectiveness analysis will make use of the primary clinical outcome data collected in the trials, while quality of life impacts estimated by transforming data collected using the WHO Disability Assessment Schedule will be used for cost utility analysis. The economic analysis will be conducted from both a health system perspective and a wider perspective incorporating societal impacts that include costs to families and impacts on economic productivity. The costs of the PTs will be estimated by deriving a monetary value for each component of the treatment based on actual time and resources required for delivery and costs incurred, and applying these to each individual based on the process indicators that reflect the actual uptake of the treatment. Other health care, patient- or family-borne resource use and costs, including any informal caregiver time costs, and productivity losses will be computed and compared at three and 12 months, and subsequently related to changes in health outcome. In the event that dominance is not shown, that is, the PT is more effective but the costs are also more than the EUC group, incremental cost-effectiveness ratios will be computed, together with their confidence intervals (using bootstrapping techniques to overcome expected skewness of cost data). Cost-effectiveness acceptability curves will also be derived in order to show the probability of any cost-effective advantages for the PTs at a range of 'willingness to pay' threshold levels, for both the health system and the broader societal perspectives.

Qualitative study analysis

Thematic analysis will be carried out using appropriate software. Two researchers will first read and familiarize themselves with the data. Then they will select 10 interviews and inductively generate initial codes through reading the interview transcript. Based on the coded data and the original research questions, the codes will be defined and collated into potential themes, and the code book refined. Inter-rater reliability will be tested by double-coding 10 randomly selected interview transcripts and the code book finalized. The researchers will then code the entire dataset. Vivid and compelling examples of narrative extracts will be selected, analysed and related to the research questions. Deviant case analysis will be done to examine narratives that are not consistent with the themes.

Ethical considerations

The trial protocol has been granted ethical approval from the Sangath and LSHTM Institutional Review Boards. The LSHTM is the trial sponsor. Written (or witnessed, if the participant is illiterate) informed consent will be mandatory for enrolment. All consent procedures will be audio-taped, with the patient’s approval, for quality assurance. Separate consent will be taken for participation in the qualitative study. All participants will be able to access EUC, which represents a higher quality of care than what is currently available and is consistent with the type of care currently envisaged in India's District Mental Health Program. We will protect the confidentiality of personal data principally through procedures to separate study data and participant identifiable data. Quantitative data gathered in the tablets for each participant at baseline will retain personal identification items to minimize errors in transcribing identities, but these will be removed before transferring the data to Stata for analysis. We will monitor the occurrence of three specific serious adverse events (SAEs) - death, suicide attempt, and unplanned hospitalization from any cause, will be recorded at three- and 12-month outcome assessments. Their reporting and appropriate responses will be governed by the standard operating procedure approved by the Data Safety and Monitoring Committee, which sets out the a priori criteria for unblinding of adverse events (that is, a statistically significant difference in prevalence between the two arms at P <0.01). SAEs will be compiled by the data manager at the end of the week during outcome follow-ups, and the report shared with the principal investigator and a psychiatrist independent of the trials. The independent psychiatrist will make contact with the respondent within 24 hours of receiving the SAE report, to arrange a convenient time and place to complete a detailed interview either on phone or face to face and offer any necessary intervention. A blinded summary of SAEs will be sent to the Data Safety Monitoring Committee and Institutional Review Boards on a quarterly frequency. Patients in the HAP trial who remain symptomatic at the end of the trial will be offered free specialist care services from the independent psychiatrist.

Trial management

Three committees will monitor the progress of the trial (Table 6). Trial monitoring will comprise the collation and reporting of routine trial process indicators and adverse events. Summary statistics and graphs showing trends over time will be compiled for the process indicators, and reported on a weekly basis to the Trial Management Committee and monthly to all members of the Trial Steering Committee. The Data Safety and Monitoring Committee will receive three-monthly reports of SAEs, the trial flow charts, and tables showing baseline comparability of patient characteristics between arms.

Table 6. Trial management committees

Discussion

The PREMIUM trials will extend evidence on the effectiveness of PTs when delivered by NSHWs in LMIC contexts [20]. The trials, which address two leading causes of the mental health-related global burden of disease, are designed to be used in routine primary health care settings, employing minimum exclusion criteria for participation, using the same pool of affordable and available human resources, and include a comprehensive economic assessment. These factors all point to the potential scalability of the findings. The main limitation of our trial design is that we are not using diagnostic interviews to characterize our participants or the outcomes; however, these are not practical in the context of the trial and not generalizable in the real-world of primary health care. The delivery agent of the PTs is not a routine health care worker but a counsellor specifically employed by the programme, and thus the trial findings will need to be interpreted cautiously in terms of their scalability. Finally, while we have argued for the rationale of using the same pool of counsellors to deliver both PTs, there is an obvious risk that this design may reduce their effectiveness in delivering each PT with optimal quality and fidelity. Ultimately, we anticipate that the long-term impact of the evidence generated by PREMIUM will be to contribute to closing the treatment gap for mental disorders in low-resourced settings through scaling-up effective PTs for delivery by NSHWs by offering a range of practical tools (such as treatment manuals, patient resource materials and quality assessment tools) to complement the WHO’s mhGAP guidelines. In doing so, new treatments will be developed with potential applicability not only in LMICs but in well-resourced contexts as well, as the human resource costs of mental health care spiral in all countries.

Trials status

Enrolment for the trials begun on 28 October 2013. Based on our experiences with the pilot study, we expect approximately 4% prevalence of depression and HD (based on screening over 14,000 adult PHC attendees) and a 50% participation rate. Thus, with eight PHCs, each enrolling three participants per week for either trial, we expect to complete recruitment of our target samples in 12 months (that is, by the end of October 2014) and complete the primary end-point three-month outcome evaluation by the end of January 2015. The final 12-month outcome evaluation will be completed by the end of October 2015. In the event that one trial attains the expected sample size ahead of the other, recruitment will still continue till the other trial achieves its target. This is to ensure consistency in trial design and that counsellors are able to see similar groups of patients so that they do not behave differently.

Abbreviations

AD: alcohol dependence; AUD: alcohol use disorders; AUDIT: Alcohol Use Disorders Identification Test; CAP: Counselling for Alcohol Problems; EUC: enhanced usual care; HAP: Healthy Activity Programme; HD: harmful drinking; LSHTM: London School of Hygiene and Tropical Medicine; LMICs: low- and middle-income countries; mhGAP: Mental Health Gap Action Programme; NSHWs: non-specialist health workers; PHC: primary health centre; PHQ-9: patient health questionnaire; PREMIUM: Program for Effective Mental Health Interventions in Under-resourced Health Systems; PTs: psychological treatments; SAE: serious adverse events; WHO: World Health Organization; WHO DAS: WHO Disability Assessment Schedule.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

VP: conception, design, analysis of pilot data and manuscript writing. BW and AN: pilot data collection, analysis of pilot data and critical revision of the manuscript. HAW: design, analysis of pilot data and critical revision of the manuscript. AA, SN, BB, JP, SD, SH: pilot data collection and critical revision of the manuscript. RA, RV: design and critical revision of the manuscript. MK, JM: design and critical revision of the manuscript. DM, PM: pilot data analysis and critical revision of the manuscript. CF, BRK: conception, design and critical revision of the manuscript. All authors read and approved the final manuscript.

Acknowledgements

This trial has been entirely funded by a Wellcome Trust Senior Research Fellowship to VP. The trial is conducted through a partnership of the London School of Hygiene & Tropical Medicine, UK (the trial sponsor), Sangath, Goa and the Directorate of Health Services, Government of Goa, India.

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