- Study protocol
- Open Access
Task sharing for the care of severe mental disorders in a low-income country (TaSCS): study protocol for a randomised, controlled, non-inferiority trial
Trials volume 17, Article number: 76 (2016)
Task sharing mental health care through integration into primary health care (PHC) is advocated as a means of narrowing the treatment gap for mental disorders in low-income countries. However, the effectiveness, acceptability, feasibility and sustainability of this service model for people with a severe mental disorder (SMD) have not been evaluated in a low-income country.
A randomised, controlled, non-inferiority trial will be carried out in a predominantly rural area of Ethiopia. A sample of 324 people with SMD (diagnoses of schizophrenia, schizoaffective disorder, bipolar disorder or major depressive disorder) with an ongoing need for mental health care will be recruited from 1) participants in a population-based cohort study and 2) people attending a psychiatric nurse-led out-patient clinic. The intervention is a task-sharing model of locally delivered mental health care for people with SMD integrated into PHC delivered over 18 months. Participants in the active control arm will receive the established and effective model of specialist mental health care delivered by psychiatric nurses at an out-patient clinic within a centrally located general hospital. The hypothesis is that people with SMD who receive mental health care integrated into PHC will have a non-inferior clinical outcome, defined as a mean symptom score on the Brief Psychiatric Rating Scale, expanded version, of no more than six points higher, compared to participants who receive the psychiatric nurse-led service, after 12 months. The primary outcome is change in symptom severity. Secondary outcomes are functional status, relapse, service use costs, service satisfaction, drop-out and medication adherence, nutritional status, physical health care, quality of care, medication side effects, stigma, adverse events and cost-effectiveness. Sustainability and cost-effectiveness will be further evaluated at 18 months. Randomisation will be stratified by health centre catchment area using random permuted blocks. The outcome assessors and investigators will be masked to allocation status.
Evidence about the effectiveness of task sharing mental health care for people with SMD in a rural, low-income African country will inform the World Health Organisation’s mental health Gap Action Programme to scale-up mental health care globally.
NCT02308956 (ClinicalTrials.gov). Date of registration: 3 December 2014.
Task-sharing care to alleviate the burden of severe mental disorders in Africa
The unmet need for mental health care is high in all countries of the world but is particularly acute in low-income countries . Ethiopia is typical of most low-income countries, with fewer than 10 % of people with severe mental disorders (SMD) receiving mental health care . SMDs are predominantly psychotic disorders that are chronic or recurrent, have a substantial impact on affected people and their families and rank highly in terms of disease burden [3, 4]. The lack of treatment or inadequate treatment for SMDs is associated with a high level of suffering and disability [5–7], family burden , stigma, discrimination and human rights abuses [9, 10], out-of-pocket costs and opportunity costs to affected individuals and their families , poor physical health and under-nutrition , and premature mortality [13, 14].
Centralised services, a critical shortage of specialist mental health workers and an absence of mental health care in general health care settings are the main causes of this large treatment gap for SMDs in the low-income countries of sub-Saharan Africa . In Ethiopia, outside of the capital city, Addis Ababa, mental health services are largely limited to regional cities, with most care provided within psychiatric nurse-led, hospital-based clinics [16, 17]. The majority of Ethiopia’s population, however, lives in rural areas . In order to improve access to mental health care, a ‘task sharing’ approach is required. The concept of task sharing is similar to that of task shifting, defined as delegating tasks to existing or new cadres with either less training or narrowly tailored training [19, 20] but also recognises the ongoing role of specialists. For mental health care, it is advocated that primary care and general health care workers be given brief training to deliver circumscribed aspects of care for prioritised mental, neurological and substance-use disorders, with the support of specialist mental health workers who provide supervision, consultation, refresher training and referral .
In a series of systematic reviews conducted by the World Health Organisation (WHO), packages of mental health interventions were identified (detailed in the Mental Health Gap Project Intervention Guide: mhGAP-IG) that can be delivered in the PHC setting and have demonstrated effectiveness for a range of mental, neurological and substance use disorders . The task sharing model of mental health care integrated into PHC, proposed by WHO in mhGAP, is expected to be more affordable and accessible for the majority of people with SMD in low-income countries. By locating mental health care in PHC, the potential exists for people with SMD to receive improved physical health care .
The need for trials of task-sharing interventions for mental health care
Despite the potential advantages of task-sharing mental health care, little is known about how different aspects of the care needed by people with SMDs can be safely and effectively transferred to the PHC setting in a rural, low-income country setting such as Ethiopia. In a recent review of task-sharing approaches to health care in LMICs, evidence was offered that task sharing can improve the productive efficiency of services (that is, the greatest amount of care at a given quality and a given cost), although challenges regarding quality, safety and sustainability were also identified . Most of the identified evaluations of task sharing were in the fields of surgery, obstetrics and HIV care, and few employed randomised, controlled trial designs. With respect to mental health care in particular, little is known about the acceptability of task sharing to service users or PHC workers  or the feasibility and sustainability of such a model [25, 26]. Uncertainty also exists as to whether stigma will be greater or lesser in a separate psychiatric clinic that is further from the place of residence compared to an integrated service that is in the person’s locality. The paucity of clinical trials of interventions for SMD in Africa has been highlighted, concluding that there is a pressing need for high-quality evidence from pragmatic trials with adequate follow-up periods . In a consensus exercise conducted to set priorities for global mental health, the integration of mental health care into primary care was within the top five issues to be addressed to improve scale-up and impact of mental health care . The TaSCS trial, therefore, addresses an important evidence gap and has the potential to inform policy initiatives to scale-up mental health care in the African region and beyond.
Context of the TaSCS trial
The Africa Focus on Intervention Research for Mental health (AFFIRM) programme was established in 2011 with the objective of investigating strategies for narrowing the treatment gap for mental disorders in sub-Saharan Africa . AFFIRM connects six countries of sub-Saharan Africa - Ethiopia, Ghana, Malawi, South Africa, Uganda and Zimbabwe - and is engaged in developing contextualised trial outcome measures , building capacity for intervention research, developing a collaborative network and conducting trials of task-sharing interventions in South Africa  and Ethiopia. Ethiopia was selected as the setting for a task-sharing trial for care of people with SMD for several reasons: 1) the Federal Ministry of Health of Ethiopia is just beginning to scale up mental health care through integration into PHC and has prioritised care for people with SMD ; 2) a well-described, population-based cohort of persons with standardised, clinician-defined diagnoses of SMD in Butajira, Ethiopia , provides a more relevant sample within which to nest a trial to inform scale-up than the usual facility-based samples; and 3) Ethiopia is a predominantly rural, low-income African country, which provides an important test case for WHO’s mhGAP.
Rationale for a non-inferiority trial
In this trial, we propose to investigate the non-inferiority of a task-sharing model of mental health care in PHC compared to the established alternative service model within Ethiopia: a less accessible (more centralised), but more specialist, psychiatric nurse-led model of care. The psychiatric nurse-led model of care has been demonstrated to be acceptable and associated with improved clinical outcomes for people with SMD engaged in the service in this sample in Butajira, Ethiopia, thus making this an appropriate comparison model . Task-sharing mental health care in PHC in Ethiopia is expected to allow more mental health care to be provided for the same cost compared to expanding specialist mental health care and is, therefore, of critical importance in addressing the high treatment gap. However, the important policy question for Ethiopia, and other low-income countries, is to establish whether or not the new task-sharing model for mental health care in PHC is good enough to meet the needs of people with SMD. At present, no evidence exists to inform this policy question. We will therefore conduct a non-inferiority trial in order to evaluate whether or not task sharing is at least no worse than specialist mental health care across a range of outcomes.
The overall objective of the TaSCS trial is to determine the acceptability, affordability, effectiveness and sustainability of mental health care for people with SMD, delivered by trained and supervised non-specialist PHC workers compared to an existing psychiatric nurse-led service.
The specific objectives are as follows:
To determine the effectiveness and cost-effectiveness of task-sharing mental health care for people with SMD with PHC, compared to psychiatric nurse-led mental health care, on the primary outcome measure of symptom severity and on a series of secondary outcome measures.
To examine factors influencing the implementation of the task sharing intervention and future scale-up, by examining the feasibility, sustainability, quality and safety, and by qualitative exploration of the experience of task sharing from the perspectives of service users, PHC workers and health service managers.
People with SMD who receive mental health care that is task shared with PHC will have a non-inferior clinical outcome, defined as a difference in the mean symptom score on the Brief Psychiatric Rating Scale, expanded version (BPRS-E) , of no more than six points higher, compared to people with SMD who receive a psychiatric nurse-led model of mental health care, after 12 months.
The study is an individual level, randomised, controlled non-inferiority trial.
The study will be conducted in the Meskan and Mareko districts of the Gurage Zone and the Silti Zone of the Southern Nations, Nationalities and People’s region, Ethiopia. The Meskan and Mareko districts have an estimated population of 159,884 and 63,436, respectively . The area is predominantly rural. Most inhabitants are farmers, growing maize for subsistence and chili pepper and khat (an amphetamine-like substance) as cash crops. The main town is Butajira, located around 130 km from the capital city, Addis Ababa. Road infrastructure has expanded in the last few years, but the majority of the population do not live close to all-weather roads. The population is prone to food insecurity and was affected by famine in 1974, 1985, 1999 and 2003. Mental health research activities have been carried out in the Butajira area for the last 18 years.
Within the study site, one government general hospital is present, located in the town of Butajira. The hospital is staffed by general physicians, a surgeon and obstetrician, as well as health officers (3 to 4 years of training at BSc level) and nursing staff (2 to 3 years training at BSc and Diploma level). There are 13 health centres in the rural areas surrounding the town of Butajira. Health centres provide PHC services comprising preventive health care, treatment of acute illness and delivery services, but no in-patient care. Health centres are staffed by health officers and general nurses. Each health centre is linked to five satellite health posts, staffed by two community health extension workers and located within walking distance of most residents (most with 5 to 10 km). Health extension workers are all women from the local area who have completed high school (grade 10) and a year of training in health promotion and illness prevention. The health extension workers form an interface between the PHC system and the community, dividing their time between house-to-house visits, community awareness-raising activities and a limited range of health post-based primary care services.
Study participants will be recruited from two sources: (1) the population-based Butajira SMD cohort study sample and (2) the Butajira psychiatric nurse-led out-patient clinic.
Butajira SMD cohort
The Butajira SMD population-based cohort was established between 1998 and 2001 . People with possible SMD were identified in two ways: (1) through a house-to-house survey covering 68,378 people using the Composite International Diagnostic Interview (CIDI)  as a screening tool, and (2) through community key informants, who had been trained using vignettes describing typical presentations of SMD . All potential cases were invited for a second phase clinician assessment conducted by an Ethiopian physician using the Schedule for Clinical Assessment in Neuropsychiatry (SCAN) . Of the 2285 SCAN assessments conducted, 844 people were diagnosed as having SMD and recruited into the cohort. Incident cases (n = 75) from the geographical catchment area over the next 2 years also underwent confirmatory diagnosis with SCAN and were recruited into the cohort, giving a total of 919 people with SMD: 359 with schizophrenia or schizoaffective disorder, 345 with bipolar disorder and 215 with severe major depressive disorder . After 10 years (2011/2012) of follow-up, a clinician assessment was carried out using the Longitudinal Interval Follow-up Evaluation (LIFE) chart . At that time, loss to follow-up from the cohort was as follows: 121 had died, 112 had refused to continue study assessments, 15 were vagrant and 70 had changed address and were not contactable. Study participants were more likely to be lost to follow-up if they were male, unmarried, had a diagnosis of schizophrenia and were more severely unwell at baseline, although the differences were small. However, loss to follow-up was not associated with age, literacy or employment status. The Butajira SMD cohort is one of the very few population-based studies of SMD from a LMIC. Even with the potential attrition bias, the Butajira SMD cohort offers a unique opportunity to obtain a sample that is free from the substantial selection bias associated with facility-based recruitment and is potentially more generalisable to people with SMD, who would access task-shared mental health care in PHC.
Butajira hospital psychiatric out-patient clinic
In Butajira, the general hospital has a psychiatric out-patient clinic run by psychiatric nurses. At present this clinic is the only mental health care available within the districts covered by the TaSCS trial, as is the case in most of Ethiopia . Since completion of the Butajira SMD cohort recruitment, additional people with SMD living in the Butajira SMD/TaSCS recruitment area have sought care from this clinic because they are (1) incident cases, (2) missed cases from the original recruitment, or (3) they have migrated into the area. If the TaSCS trial is unable to recruit a sufficient sample size from the Butajira SMD cohort, consecutive attendees at the Butajira hospital psychiatric clinic will be screened for eligibility.
Recruitment into the trial will be divided into two phases. In Phase 1, only people with SMD who are clinically stable will be recruited. Three months after beginning recruitment, the Data Safety and Monitoring Board (DSMB) will review adverse events, including non-engagement with the service, disengagement from care and evidence of potentially dangerous prescribing, before Phase 2 recruitment is permitted. In Phase 2, people with SMD who have more complex needs or who are clinically unstable will be recruited.
Eligibility criteria for both phases of recruitment
To be eligible, participants must meet the following criteria:
A Diagnostic and Statistical Manual of Disorders (version IV)  diagnosis of schizophrenia, schizoaffective disorder, bipolar disorder or major depressive disorder made using a standardised, semi-structured clinician-administered assessment.
Ongoing need for mental health care, defined as active prescription of psychotropic medication or prescription of psychotropic medication within the preceding 2 years, or the person being in partial or full relapse.... These severity criteria were developed to reflect realities of service provision in Ethiopia: a person with SMD who has been well off medication for at least 2 years is unlikely to engage actively with treatment services or be considered a priority by PHC workers .
Not treated with a mood-stabiliser, second generation antipsychotic medication or thioridazine (still used in clinical practice in Ethiopia), as these medications are not available routinely in the study area.
Living in the catchment area of one of the health centres in the trial study site, excluding Butajira health centre catchment area. Butajira health centre is excluded because formative work indicated a lower acceptability of randomization in those who live in close proximity to the psychiatric nurse-led unit in Butajira hospital .
Planning to continue living in the area for the duration of the trial (at least 18 months).
The age criterion for recruitment into the original Butajira SMD cohort was 18 years or older, but participants are now older than this in view of the length of time that the cohort has been running. Therefore, participants recruited from the Butajira hospital psychiatric clinic will be required to be 25 years or above in order to ensure comparability.
Participants recruited from the Butajira hospital psychiatric clinic will also be required to have been in contact with mental health services for at least 2 years to ensure comparability with the Butajira SMD cohort recruits.
Competent in the Amharic language. There is high ethnic and linguistic diversity within the study site, but the majority of people speak Amharic, the official language of Ethiopia, even if it is not their first language.
Not expressing active suicidal intent.
Not receiving treatment for a co-morbid medical condition at Butajira hospital.
Not pregnant while receiving depot medication.
Able to give informed consent or, if lacking capacity to consent and no evidence of refusal, guardian permission obtained.
Additional eligibility criteria for Phase 1
Not pregnant or breast-feeding.
No co-morbid complex or unstable medical condition interfering with management of SMD.
Not fulfilling criteria for a diagnosis of alcohol or khat use disorder in the past 12 months.
Not prescribed depot antipsychotic medication at the time of assessment.
Stable clinical condition: either in remission from SMD or with residual symptoms that have been stable over the preceding three months.
No suicide attempt in the past three months.
The eligibility criteria for the trial are designed to ensure that the findings can be generalised to people with SMD in Ethiopia who will be receiving mental health care integrated into PHC as part of the planned scale up of mental health care by the Federal Ministry of Health. The population will also be comparable to the Ethiopian studies that have shown the psychiatric nurse-led care (control arm) to be clinically effective [2, 41]. The operationalisation of eligibility criteria and their assessment is detailed in Additional file 1.
Recruitment and screening
See Fig. 1.
Phase 1 (Butajira SMD cohort only)
Because the last formal assessment of all cohort participants was in 2011/2012, a process of pre-screening will take place prior to starting recruitment into the trial. A pre-screen will be completed from the project clinical records and in consultation with project outreach workers. At this stage, people who are known to be prescribed psychotropic medications that are unavailable outside of Addis Ababa or who are taking depot medication, those who are documented to be pregnant or breast-feeding and those who are documented to have relapsed (within the previous three months) will be excluded. These criteria provide the sampling frame for Phase 1.
Each person with SMD included in the sampling frame for Phase 1 will be ordered randomly using computerized generation of random numbers. This random order will form the sequence in which potentially eligible patients will be invited for assessment by project outreach workers who are well known to the patients and their families. At the time of invitation, the project outreach workers will also identify the appropriate caregiver to accompany the patient to the baseline assessment. The recruitment and assessment will take place at the mental health research office in Butajira where there will be full access to the clinical notes. The target sample size for Phase 1 is 124.
For people with SMD who attend a trial assessment, a psychiatric nurse will conduct an assessment of capacity to consent to participate in the trial. After obtaining informed consent from the patient (if they have capacity) or permission from the guardian (if they lack capacity and are not refusing to participate), the initial baseline assessment measures will be administered by psychiatric nurses. On the basis of this initial assessment, eligibility for inclusion within Phase 1 of the trial will be determined. All patients who are eligible will then complete further assessments administered by non-clinical data collectors. The caregiver of the patient will also be invited to participate in the study, their consent obtained and measures administered by non-clinical data collectors. Once both patient and caregiver assessments are complete, randomization will take place.
Phase 2 (Butajira SMD cohort and Butajira hospital psychiatric clinic)
Phase 2 recruitment will be from the sampling frame of the Butajira SMD cohort in the first instance, only progressing to the Butajira hospital psychiatric clinic if the required sample size has not been reached.
Butajira SMD cohort
Phase 2 recruitment will proceed as for Phase 1. Pre-screening will only exclude women who are recorded as being pregnant at the same time as being prescribed depot and people who have already been recruited into the trial. The target sample size for Phase 2 is 200.
Butajira hospital psychiatric out-patient clinic
If it is not possible to obtain the sample size for Phase 2 from the Butajira SMD cohort alone, we will expand recruitment to the Butajira hospital out-patient clinic. Unlike participants recruited from the Butajira SMD cohort, these recruits will not have undergone diagnostic research assessments. This adds an additional step to the recruitment process. Consecutive attendees who have a clinical diagnosis of SMD (as defined previously) will be pre-screened by the Butajira hospital psychiatric nurses. If the person fulfils all of the pre-screening criteria, they and their accompanying caregiver will be invited to meet with the trial psychiatric nurse who will evaluate the capacity of the person to consent to participate in the trial. If the person has capacity and gives informed consent or the eligible caregiver gives permission, they will be undergo a standardised, semi-structured diagnostic evaluation by a mental health professional [35, 42]. If the person fulfils criteria for DSM-IV diagnoses of schizophrenia, schizoaffective disorder, bipolar disorder or depressive disorder, they will be invited to return to the Butajira mental health research office on a convenient date when they can undergo the full screening and baseline assessment accompanied by an eligible caregiver.
Randomisation and service allocation
Sequence generation and allocation concealment
A computerized system will be used to generate a randomization list. The randomization will be stratified by health centre catchment area. Within each health centre catchment area, randomization will be organized with permuted blocks of random size so that an equal number will be randomized to the new intervention arm and to the active control arm. From the randomization list, labelled and sealed envelopes will be prepared containing cards with intervention allocation. The sealed envelopes will be handed over to independent clinicians working in Butajira hospital and will be kept in a secure place.
Upon completion of the baseline assessment, participants will be accompanied to Butajira hospital. In a fully private location, the independent clinician will open the next sequential envelope for the health centre catchment area where the person resides and inform the participant of the service to which they have been allocated (that is, psychiatric nurse-led care or care from the health centre staff).
Outcome assessors and trial investigators will be masked to the intervention allocation of participants, but it is not possible for trial participants and clinicians involved in delivering the intervention service to be masked. To minimise the possibility of unmasking of outcome assessors, 1) outcome assessments will be carried out by project-employed mental health professionals and lay interviewers in a location that is independent of and geographically separated from the health service; 2) the outcome assessors will not work in the trial districts; 3) when patients and caregivers are registered for their follow-up assessments, they will be instructed not to tell the interviewer where they are receiving mental health care; 4) selected trial clinical assessments will be observed by non-project psychiatrists to ensure that ratings are being conducted without bias; and 5) at the end of each follow-up assessment, the assessor will be asked whether they have become unmasked to patient allocation group during the course of the assessment. This information will be used to conduct a sensitivity analysis to investigate any evidence of bias. Data analysis for the primary outcome will be carried out by an independent organization, and those involved in data analysis will be masked to the intervention status of the participant.
The intervention is a task sharing model of mental health care for people with SMD integrated into PHC, as recommended by the WHO in the mental health Gap Action Programme (mhGAP)  and endorsed by the Ethiopian Federal Ministry of Health . Adaptation of the task-sharing model for the study setting was informed by extensive formative work and community consultation in the study site  and from findings arising from a sister project implementing integrated mental health care in a neighbouring district [43, 44].
In the TaSCS intervention, PHC-based health centre nurses and health officers will be trained to deliver the mhGAP packages of mental health care, supported by community-based health extension workers. The training and supervision requirements are summarised in Table 1. As all trial participants have an existing care plan used by project psychiatric unit staff, this will be transferred to PHC when a patient has been randomised to a PHC site. A minimum of monthly, facility-based follow-ups will be stipulated during the initial phase, and thereafter, 3-monthly follow-ups, although contacts can be more frequent depending on patient need. The current outreach by project workers will be replaced by outreach by health extension workers, who are required to make house-to-house visits every 3 months, as part of their health promotion and illness prevention responsibilities. Psychiatric nurse-led mental health support will be provided to the PHC health officers and nurses through (1) supervision including case reviews, discussion of difficult cases, developing supportive relationships with the primary health care provider and trouble-shooting; (2) emergency consultation with project psychiatric nurses; and (3) referral for a second opinion or for a period of follow-up by the specialist team in Butajira psychiatric unit, as per mhGAP guidelines. Psychiatric nurses can in turn consult project psychiatrists. The roles of the PHC workers in the task shared model are summarised in Additional file 2.
Active comparison arm
The active comparison sample for the TaSCS trial is a psychiatric nurse-led, centralised model of out-patient specialist mental health care augmented by community outreach by lay workers as part of the Butajira SMD study. There are 57 psychiatric nurse-led units across Ethiopia providing the lion’s share of specialist mental health care in the country . Psychiatric nurse-led clinics constitute the only model of mental health care available in rural areas in Ethiopia. The comparison arm of the TaSCS trial can be considered to be an enhanced version of specialist mental health care, in that community outreach is provided. Evaluation of the longitudinal illness course of patients in the Butajira SMD study showed improved outcomes for those who engaged with the service compared to those who did not engage .
The Butajira hospital psychiatric nurses are able to prescribe psychotropic medication (including depot antipsychotic medication), monitor and intervene against side effects, diagnose co-morbid psychiatric conditions and provide simple psychosocial interventions. Follow up will be arranged on the basis of need, but at least a face-to-face assessment every three months. Consultation with project psychiatrists or referral for in-patient psychiatric care (in Addis Ababa) will be as indicated.
The psychiatric nurses will receive 2 days of refresher training in order to familiarise them with the WHO’s evidence-based guidelines for management of mental disorders (mhGAP-IG). They will also receive refresher training on the management of SMD in pregnant and breastfeeding women.
The competence of the PHC workers to deliver mental health care will be evaluated through pre- and post-training assessments of knowledge and attitudes  towards mental health, post-training evaluation of clinical skills  and structured supervision reports from the project psychiatric nurses. The fidelity of the task shared mental health care to the mhGAP intervention packages will be measured through structured evaluation of clinical follow-up forms by independent psychiatrists, including prescribing, risk assessment, psychoeducation and symptom review. Medication is being supplied by the trial, but a record will be kept of any interruptions to supply.
The fidelity of the active comparison specialist mental health care model to evidence-based mental health care will be measured through structured evaluation of clinical follow-up forms by independent psychiatrists, as for the intervention arm.
The trial outcomes are summarised in Table 2.
The primary outcome is non-inferior symptom level, defined as no more than a six-point higher mean score on the BPRS-E . The BPRS-E is a 24-item, clinician-rated scale that was originally developed for detection of symptom change in persons with persistent SMD . Each item is rated on a scale from 1 to 7 (1 = not present; 2 = very mild; 3 = mild; 4 = moderate; 5 = moderately severe; 6 = severe and 7 = extremely severe). The maximum total score is 168. The BRPS-E focuses on symptoms of psychosis but also has items covering the symptom domains of somatic concerns, anxiety, depression and mania. The total BPRS-E score is sensitive to change in treated in-patient populations of persons with persistent SMD, including those with diagnoses of schizophrenia, bipolar disorder and major depressive disorder . The BPRS-E has also been used in treatment trials with out-patient populations of persons with SMD [49, 50] and has been used in Ethiopia previously . The factor structure and sensitivity to change of the BPRS-E has been shown not to vary significantly across diagnostic groups . Inter-rater and test-retest reliability, as well as internal consistency, have been shown to be high .
The non-inferiority margin for the primary outcome needs to be defined in relation the minimal clinically important difference (MCID) . Previous studies have defined clinically significant change in score on the BPRS-E in different ways. Using a statistical approach, the ‘reliable change index’  for change in BPRS-E score from beginning to end of an in-patient admission in persons with SMD equated to 18 points . However, change in symptoms in a person with acute psychosis receiving in-patient care is likely to be larger than the MCID and not applicable to the out-patient sample of people with SMD to be included within this sample. In a study looking at change in symptoms in response to a psychological intervention for an out-patient sample of people with chronically symptomatic schizophrenia, a mean change of 7.9 points on the BPRS-E was considered clinically important . A mean change of 7.9 points equates to a standardised effect size of around 0.50, which we take to be the MCID. In line with recommendations for non-inferiority trials, the non-inferiority margin for this trial will be 75 % of the presumed MCID, that is, a six-point difference in mean BPRS-E scores between arms of the trial [53, 56]. A six-point difference on the BPRS-E equates to a standardised effect size of 0.4.
See Table 2.
A wide range of secondary outcomes are being assessed in view of the importance of exploring the full range of possible harms when conducting a non-inferiority trial. The secondary outcomes are functional impairment, relapse of SMD, service use costs, satisfaction with mental health care, nutritional status, service use for physical health conditions, disengagement from care, non-adherence with medication, experience of side effects, perceived stigma, experience of being restrained, quality of care and adverse events. Caregiver outcomes are perceived stigma, family burden, time burden and opportunity costs of care giving.
In order to be able to adjust for potential confounding in case of randomly unequal distribution of variables, baseline measurement of the following variables will be carried out: socio-demographic characteristics, socio-economic status, alcohol use disorder, khat use disorder and medical co-morbidity and physical disability. See Table 2.
Sample size calculation
The following formula was used to calculate the required sample size (n):
where delta = non-inferiority margin (mean BPRS-E scores of six points), sigma is the standard deviation of the BPRS-E score (estimated standard deviation of 15 ), Zalpha is the standardised mean difference for the probability of type 1 error (alpha = 0.05) and Zbeta is the standardised mean difference for the probability of type 2 error (beta =0.1 (that is, power of 0.9). Therefore, a sample size of 107 persons per arm of the trial (that is, a total of 214) is required . No published studies from Ethiopia are available to guide us in our estimation of the intra-cluster correlation (ICC) for study subjects receiving treatment from a specific health centre. We therefore estimate the ICC to be 0.01, which is the median ICC from a review of 31 cluster-based interventions in PHC . Given that there are 13 health centres within the three districts covered by the Ethiopia TaSCS trial, the design effect will be 1 + (n-1)*ICC (where n = number of subjects per cluster). Therefore, the design effect = 1 + (17–1)*0.01 = 1.16. Assuming a worst-case scenario of 30 % loss to follow-up, the required sample size = 214 * 1.30 * 1.16 = 323 participants. For equal numbers in each arm of the trial, the total sample size will be 324 (n = 162 in each arm).
Data management and analysis
A data management plan was developed to specify all procedures relating to the handling of trial data. Management of data for the masked outcome data will be handled by the Clinical Trials Unit at the Armauer Hanssen Research Institute (AHRI) with support from the trial statisticians. Data will be doubled entered from the Patient Report Forms into an electronic Case Report Form. Trial data with unmasking potential (process data and data pertaining to adverse events) will be handled by the Butajira mental health research office following the same standardised operating procedures as for the Clinical Trials Unit. Data cleaning based on frequency distributions and logic checks will follow standard procedures with reference to source documents as required.
Data analysis approach
Data analysis will follow a detailed statistical analysis plan that specifies all planned analyses. Data analysis will take place using Stata Version 13 (Stata Corporation, College Station, Texas, USA) under the direction of the trial statisticians. All analyses will be masked to study arm until the analysis is finalized and approved by all investigators. Descriptive analyses will include frequency distributions and measures of central tendency and dispersion, as appropriate, with 95 % confidence intervals. Bivariable comparisons will employ χ2, Fisher’s exact, Student’s t- or rank-sum tests, as appropriate. All statistical tests will be one-sided at α = 0.05, as we are testing a hypothesis of non-inferiority and not superiority or equivalence.
Analysis will be by intention-to-treat, that is, on the basis of the group to which the participant is allocated randomly at the beginning of the trial. Intention-to-treat has the potential to lead to false acceptance of the hypothesis of non-inferiority in the presence of a true difference if there is a large cross-over from the primary care to the psychiatric nurse service . Therefore, the intention-to-treat analysis will be presented together with the percentage of participants who deviate from the protocol in the following ways: (1) cross-over protocol deviation which is indicated by the percentage who attend for more than two consecutive visits at the service they were not randomised to receive, unless they were referred to that service, and (2) disengagement from care protocol deviation, which is the percentage who miss more than 50 % of their scheduled health facility appointments (not attending within 2 weeks of the appointment date). Per protocol analyses will also be conducted, and the findings presented as a sensitivity analysis. Account will be taken of clustering at the level of the health facility.
Analysis will be carried out on the complete data set at 12 and 18 months. For the primary outcome time-point of 12 months, it would not be appropriate to carry forward the last observation to replace missing data as this would have taken place at the baseline of the study and could, therefore, increase the chance of non-inferiority even in the presence of a difference between the allocated services.
If more than 15 % of the primary outcome scores are missing, we will conduct multiple imputation analysis (including age, sex, baseline symptom severity and substance use disorder) in the model and present this as an exploratory analysis alongside the analysis on the complete dataset.
An interim analysis will be conducted at 12 months. The DSMB will assess the primary outcome (BPRS-E score) and adverse events by arm of the trial and decide if there is evidence of inferiority of one arm, guided by the definition of clinical inferiority used for the primary hypothesis.
Analysis of primary outcome
The analysis for the primary outcome will be carried out by AHRI in order to ensure masking of the treatment group. The primary outcome measure (change in BPRS-E score) will be analysed using linear regression adjusting for baseline symptom severity. Statistical tests will be one-sided, reflecting our interest in testing the hypothesis that task-shared care is non-inferior. The validity of regression assumptions will be checked using residual plots. For the purpose of safety monitoring, the Phase 1 primary outcome at 12 months will be analysed as an interim analysis. For the purpose of hypothesis-testing for the main trial, Phase 1 and Phase 2 primary outcomes at 12 months will be combined. Both crude and adjusted (for baseline symptom severity, age and sex) effect sizes will be presented for the primary analysis. Exploratory analysis of the non-inferiority of the new intervention in the Phase 1 and Phase 2 participants will be carried out separately.
Analysis of secondary outcomes
These analyses will be carried out by the trial statisticians. The planned approach for data analysis of secondary outcomes is outlined in Additional file 3. Multivariable analysis will be used to adjust for the following potential confounding variables measured at baseline: age, sex, socioeconomic status, substance use and symptom severity.
The economic analysis will measure both the costs associated with a task-sharing model of care, as well as the consequential impact on service use. Local unit costs will be applied to resources used so as to estimate changes in services costs in both intervention and comparator groups. Time lost from work by people with SMD and their caregivers will be valued using appropriate wage rates, adjusted to take account of patterns of employment in an agrarian economy. Costs will be analysed using multiple regression analysis so that the effect of the intervention on costs can be estimated whilst adjusting for differences in participant characteristics. Non-parametric bootstrap methods will be used if the residuals of the regression model are non-normally distributed. Further regression models will include the main clinical measures so that the relationship between costs and outcomes can be assessed. A cost-effectiveness analysis will be carried out. Differences in cost and primary outcome measure (BPRS-E) that take into account the uncertainty around point estimates will be plotted and subsequently presented as a cost-effectiveness acceptability curve.
Ethical approval for the trial has been obtained from the Institutional Review Board of the College of Health Sciences, Addis Ababa University (Reference Number 030/12/Psy), the AHRI-ALERT Ethics Review Committee (Reference Number P037/13), the National Research Ethics Review Committee of Ethiopia (Reference Number 3.10/758/07), the Food, Medicine and Health Care Administration and Control Authority (Reference Number 02/6/22/13), the University of Cape Town Human Research Ethics Committee (Reference Number 226/2011) and the National Institute of Mental Health Data Safety and Monitoring Board (DSMB).
The trial will include people with SMD who lack capacity to consent to participate in the trial as long as they are not actively refusing and they have a guardian who gives permission. Given the lack of knowledge on task-sharing care for people with SMD, and the intention of the Ethiopian Ministry of Health to implement this new model of service provision, it is crucial that people with SMD who are representative of those who will receive the task sharing model in the future have the opportunity to participate in the study. In participants who lack capacity at baseline, the capacity to consent will be reviewed at follow-up assessment time-points. If the participant regains capacity, they will be informed about the trial and will only continue in the trial if they give informed consent. No out-patient treatment from non-specialist mental health workers will be provided to people with any mental disorder against their will, except for management of acute behavioural disturbance where the person poses an imminent risk to themselves or others.
There is genuine uncertainty as to whether or not a task-sharing model of mental health care for SMD can be as effective as mental health care delivered by mental health specialists, but also no evidence that it is any worse, supporting a position of clinical equipoise. In the absence of any difference in effectiveness of care, a task-sharing model of care may be preferred through being locally available, even if the practitioners delivering the care are not specialists.
During the trial period participants will directly benefit from free treatment for both mental and physical health problems. Participants will be compensated for transport and their time when attending for trial-related assessments. Transport costs for attending Butajira hospital will also be covered.
We anticipate that the main risks for those allocated to the task-sharing model of mental health care in PHC will be modest: 1) moving from a familiar arrangement to a new treatment setting may be unsettling at the beginning, and therefore, monthly reviews will be scheduled at the beginning of the trial in order to facilitate engagement; and 2) there is a risk of receiving inferior care, which will be detected through monitoring of clinical records, supervision and the 12 month interim analysis. It is not anticipated that either arm of the trial will be associated with an increase in serious or other adverse events; however, procedures are in place for minimising the risk of adverse events and ensuring monitoring, reporting and management of adverse events to the DSMB and other regulatory bodies. The risk of suicide will be minimised by excluding people who express active suicidal intent at the time of recruitment and requiring clinicians to use structured clinical follow-up forms that prompt for screening for suicide risk. The phased nature of recruitment is also designed to reduce risk of adverse events by ensuring that PHC workers have gained competence in managing care of people with stable or uncomplicated SMD before they take on the care of people with more complex illness. The occurrence of serious or other adverse events will be formally reviewed at 12 months as part of the interim analysis.
All trial-related assessments will take place in a location that respects the participant’s privacy. The confidentiality of the participants will be respected, and the names of the patients will not be quoted or published.
The trial will be subjected to rigorous on-site monitoring of safety and quality at study initiation and thereafter twice per year by an independent external monitor reporting to the NIMH DSMB, in addition to routine reporting to the NIMH DSMB twice per year.
A pressing need exists to scale up evidence-based packages of mental health care in LMICs and thereby improve the clinical, functional and social outcomes of people with mental disorders. Alongside this imperative runs a critical need to evaluate the success of the task-sharing models of mental health care, which are proposed as solutions to the treatment gap for mental disorders. Human resource and health system constraints mean that interventions that are demonstrated to be efficacious when evaluated individually cannot be assumed to be effective when delivered as part of a service in more real-world conditions. The dearth of high-quality mental health service trials from LMICs generally, and from low-income countries in particular, is a serious impediment to the successful scale-up of mental health care. The TaSCS trial seeks to provide high-quality evidence that will be timely for informing mental health care scale-up in other rural, low-income countries, as well as contributing to the international discourse on task sharing as an acceptable model of care for people with SMD.
Recruitment started on 13 March 2015 and is ongoing.
mental health Gap Action Programme
Mental Health Service Satisfaction Scale
severe mental disorder
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The authors would like to express their heartfelt appreciation for the dedicated work of Mrs Aynalem Tesfaye, an invaluable asset to our team, who sadly passed away during the formative period of the trial.
This research was conducted as part of the Africa Focus on Intervention Research for Mental Health (AFFIRM). Research reported in this publication was funded by the National Institute of Mental Health (NIMH) of the National Institutes of Health (NIH) under Award Number U19MH095699. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. We wish to acknowledge the regulatory expertise provided by Dr Adam Haim (Clinical Trials and Biostatistics Branch, NIMH) and Dr LeShawndra Price (NIMH) in the process of developing this protocol.
None of the authors have competing interests.
CH designed the study, coordinated the formative work and drafted the manuscript. AA participated in the design of the study and the coordination and interpretation of the formative work. GM participated in the design of the study and contributed to the statistical analysis plan. TS participated in the design of the study. DE participated in the development of safety and regulatory procedures for the trial. HN contributed to the development of the data management and safety monitoring procedures. MD was involved in the design of the trial and development of the statistical analysis plan. LW, MP, ES and CL were involved in the design of the trial and interpretation of the formative work. AF conceived the study, participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.
Operationalisation and assessment of eligibility criteria. Description: Specifies the eligibility criteria, together with the measures for assessing eligibility. (DOCX 14 kb)
Roles of primary care workers in the task sharing intervention service. Description: Describes the roles that the primary care workers are being trained to do within the new task-shared service. (DOCX 12 kb)
Planned data analyses for secondary outcomes. Description: Gives details of the analysis plan for secondary trial outcomes. (DOCX 12 kb)
CONSORT Statement 2006 - Checklist for Non-inferiority and Equivalence Trials. Description: Gives detail about where the required CONSORT information is located within the manuscript. (DOC 67 kb)
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Hanlon, C., Alem, A., Medhin, G. et al. Task sharing for the care of severe mental disorders in a low-income country (TaSCS): study protocol for a randomised, controlled, non-inferiority trial. Trials 17, 76 (2016). https://doi.org/10.1186/s13063-016-1191-x
- Mental disorder
- community mental health care
- primary healthcare
- sub-Saharan Africa
- developing countries