Introduction
Low- and middle-income countries (LMICs) have fragmented mental health systems which cannot cope with the high level of mental health needs (Jordans and Tol, Reference Jordans and Tol2013). LMICs have limited availability to provide adequate mental health treatment (Luitel et al., Reference Luitel, Jordans, Adhikari, Upadhaya, Hanlon, Lund and Komproe2015; Thornicroft et al., Reference Thornicroft, Chatterji, Evans-Lacko, Gruber, Sampson, Aguilar-Gaxiola, Al-Hamzawi, Alonso, Andrade, Borges, Bruffaerts, Bunting, de Almeida, Florescu, de Girolamo, Gureje, Haro, He, Hinkov, Karam, Kawakami, Lee, Navarro-Mateu, Piazza, Posada-Villa, de Galvis and Kessler2017). Innovative psychological treatments that utilise task-sharing are necessary to increase the availability of quality care in LMICs (Patel et al., Reference Patel, Saxena, Lund, Thornicroft, Baingana, Bolton, Chisholm, Collins, Cooper, Eaton, Herrman, Herzallah, Huang, Jordans, Kleinman, Medina-Mora, Morgan, Niaz, Omigbodun, Prince, Rahman, Saraceno, Sarkar, De Silva, Singh, Stein, Sunkel and UnUtzer2018). Problem Management Plus (PM+) is a five-session intervention developed by the World Health Organization (WHO) suitable for low-resource settings for clients impaired by psychological distress (Dawson et al., Reference Dawson, Bryant, Harper, Kuowei Tay, Rahman, Schafer and van Ommeren2015). Randomised controlled trials (RCTs) in Pakistan and Kenya found that PM+ delivered individually is effective for managing practical or psychological problems (Dawson et al., Reference Dawson, Schafer, Anjuri, Ndogoni, Musyoki, Sijbrandij, van Ommeren and Bryant2016; Bryant et al., Reference Bryant, Schafer, Dawson, Anjuri, Mulili, Ndogoni, Koyiet, Sijbrandij, Ulate, Harper Shehadeh, Hadzi-Pavlovic and van Ommeren2017; Khan et al., Reference Khan, Hamdani, Chiumento, Dawson, Bryant, Sijbrandij, Nazir, Akhtar, Masood, Wang, Wang, Uddin, van Ommeren and Rahman2019).
A group version of PM+ has been developed with the potential to reach a higher number of people and therefore is more cost-effective for low-resource settings. Group PM+ was shown to be effective in reducing anxiety and depression symptoms in women in a conflict-affected region of Pakistan (Rahman et al., Reference Rahman, Khan, Hamdani, Chiumento, Akhtar, Nazir, Nisar, Masood, Din, Khan, Bryant, Dawson, Sijbrandij, Wang and van Ommeren2019). Group PM+ has not yet been evaluated for feasibility and acceptability when delivered in both males and females, nor has it been evaluated following a natural disaster. The aim of this paper is to evaluate the feasibility and acceptability of the Group PM+ intervention in Nepal (Sangraula et al., Reference Sangraula, Van't Hof, Luitel, Turner, Marahatta, Nakao, van Ommeren, Jordans and Kohrt2018), in order to subsequently conduct a fully powered effectiveness trial of Group PM+.
Methods
Setting
Nepal is a low-income country with a history of conflict, political instability and natural disasters. In April 2015, Nepal was hit with two earthquakes resulting in 8000 deaths, 20 000 people injured, damaged homes and livelihood, and substantial internal displacement (Kane et al., Reference Kane, Luitel, Jordans, Kohrt, Weissbecker and Tol2018). Various studies suggest high rates of disabling distress after the earthquakes (Kohrt et al., Reference Kohrt, Hruschka, Worthman, Kunz, Baldwin, Upadhaya, Acharya, Koirala, Thapa, Tol, Jordans, Robkin, Sharma and Nepal2012; Luitel et al., Reference Luitel, Jordans, Sapkota, Tol, Kohrt, Thapa, Komproe and Sharma2013). An epidemiological study in three districts affected by the earthquake found that one in three adults were experiencing high levels of depression and anxiety symptoms, one in five adults engaged in harmful alcohol use, and one in ten adults had current suicidality (Kane et al., Reference Kane, Luitel, Jordans, Kohrt, Weissbecker and Tol2018).
This Group PM+ feasibility study took place in Sindhuli district, which was impacted by the earthquakes (Sangraula et al., Reference Sangraula, Van't Hof, Luitel, Turner, Marahatta, Nakao, van Ommeren, Jordans and Kohrt2018). Within Sindhuli district, we selected two Village Development Committees (VDCs) for the intervention and control arms.
Design
The feasibility study design and a priori aims are outlined in a separate pilot and feasibility protocol publication (Sangraula et al., Reference Sangraula, Van't Hof, Luitel, Turner, Marahatta, Nakao, van Ommeren, Jordans and Kohrt2018), and this study was registered on ClinicalTrials.gov (NCT03359486). The study was designed as a two-arm cluster randomised controlled trial (cRCT), comparing Group PM+ v. enhanced usual care (EUC).
Randomisation
Please see online Supplementary Material for detail.
Intervention: Group PM+
Participants in the intervention arm received five sessions of Group PM+, with each session lasting 2.5–3 hours. Sessions included: (1) Managing Stress, (2) Behavioural Activation, (3) Managing Problems, (4) Strengthening Social Support and (5) Review of Techniques (Dawson et al., Reference Dawson, Bryant, Harper, Kuowei Tay, Rahman, Schafer and van Ommeren2015). Please see online Supplementary Material for further detail on techniques used in Group PM+.
There were ten groups in the Group PM+ arm. Participants were allocated to groups based on their location of residence. The group consisted of six to eight people separated by gender and with gender-matched facilitators. Volunteer local helpers supported facilitators by organising logistics and reminding participants about the sessions. Community-based psychosocial workers (CPSW) were the service providers for the groups and are a cadre of psychosocial workers in Nepal that are trained through and work for NGOs, such as Transcultural Psychosocial Organization (TPO) Nepal.
Control: EUC
CPSWs delivered family meetings to participants in both arms. This consisted of: (a) consent to take part in the study and follow-up assessments, (b) psychoeducation on adversity, (c) benefits from support, (d) information on the availability of mental health services by a mental health Gap Action Programme Intervention Guide (mhGAP)-trained health worker in the nearby clinic. After the 2015 earthquakes, the mhGAP Humanitarian Intervention Guide was adapted and contextualised for Nepal (mhGAP HIG). Nepali psychiatrists were taught to train primary care workers using mhGAP (Jordans et al., Reference Jordans, Luitel, Pokhrel and Patel2016). One health worker from each study VDC received a 10-day mhGAP training to identify, assess and treat common mental disorders (CMDs).
Main outcomes
The main objective was to determine the acceptability and feasibility of Group PM+ in Nepal, using quantitative and qualitative data. These results will inform changes to the methodology for the fully-powered RCT. The quantitative indicators in Table 1 determined progression to the main trial.
Table 1. Feasibility and acceptability criteria and outcomes
Community detection and case identification
The research assistants (RAs) were briefed on the Community Informant Detection Tool (CIDT), a tool that incorporates vignettes, illustrations and local idioms of distress for lay workers to identify those with CMDs (PPV = 0.68 and NPV = 0.91 for adults) (Jordans et al., Reference Jordans, Kohrt, Luitel, Komproe and Lund2015; Subba et al., Reference Subba, Luitel, Kohrt and Jordans2017). While a general distress version was designed to recruit participants for the study, the RAs were trained on the psychosis CIDT so they could identify those that would not qualify for the study. Programme staff used the CIDT to train local leaders, such as female community health volunteers, to identify participants for screening. RAs were informed of potential participants, who were subsequently screened. Please see online Supplementary Material for further information on recruitment and training of non-specialists and RAs.
Blinding
Please see online Supplementary Material for detail.
Screening
Please see online Supplementary Material for detail.
Quantitative assessments
The primary clinical outcome measure was the Patient Health Questionnaire (PHQ-9), which measures symptoms of depression. It has been clinically validated in Nepal with a cut-off score of ⩾10 (sensitivity = 0.94, specificity = 0.80, PPV = 0.42 and NPV = 0.99) (Kohrt et al., Reference Kohrt, Luitel, Acharya and Jordans2016).
The WHODAS (>16) and the GHQ-12 (>2) were included in the screening as part of the inclusion criteria and as secondary outcome measures (Minhas and Mubbashar, Reference Minhas and Mubbashar1996; Tol et al., Reference Tol, Komproe, Jordans, Thapa, Sharma and De Jong2009; Tol et al., Reference Tol, Kohrt, Jordans, Thapa, Pettigrew, Upadhaya and de Jong2010; Thapa and Hauff, Reference Thapa and Hauff2012). The heart–mind screener, a locally developed tool, was used to determine if participants identified with a local idiom of distress and if they experienced impairment due to these problems (sensitivity = 0.94, specificity = 0.27, PPV = 0.17, NPV = 0.97) (Kohrt et al., Reference Kohrt, Luitel, Acharya and Jordans2016).
There were two other secondary clinical outcomes that included Post-traumatic Stress Disorder Checklist DSM-5 (PCL-5) and the Psychosocial Mental Health Problems (PMHP). The PCL-5, an eight-item scale, was shown to have comparable diagnostic utility to the 20-item PCL-5 in a recent study (Price et al., Reference Price, Szafranski, van Stolk-Cooke and Gros2016), and was used to reduce the burden on participants from using the full Nepali version of the PCL (Kohrt et al., Reference Kohrt, Hruschka, Worthman, Kunz, Baldwin, Upadhaya, Acharya, Koirala, Thapa, Tol, Jordans, Robkin, Sharma and Nepal2012; Luitel et al., Reference Luitel, Jordans, Sapkota, Tol, Kohrt, Thapa, Komproe and Sharma2013). The PMHP scale is a locally developed five-item assessment of common psychosocial problems in Nepal (Luitel et al., Reference Luitel, Jordans, Sapkota, Tol, Kohrt, Thapa, Komproe and Sharma2013).
Additionally, The Multidimensional Scale of Perceived Social Support (MSPSS) self-assesses participants' connectedness with family and friends (Zimet et al., Reference Zimet, Powell, Farley, Werkman and Berkoff1990) and has been locally adapted (Hendrickson et al., Reference Hendrickson, Kim, Tol, Shrestha, Kafle, Luitel, Thapa and Surkan2018) and validated to use with Nepali populations (Tonsing et al., Reference Tonsing, Zimet and Tse2012). The three subscales within the MSPSS were found to be significantly correlated (Family with Friends, r = 0.530, p < 0.01; Family with Significant Others, r = 0.540, p < 0.01; and Significant Others with Friends, r = 0.575, p < 0.01) (Tonsing et al., Reference Tonsing, Zimet and Tse2012).
The Reducing Tension Checklist (RTC) was developed for this study to evaluate the use of coping strategies of Group PM+ and was developed based on a coping checklist (Neacsiu et al., Reference Neacsiu, Rizvi, Vitaliano, Lynch and Linehan2010). The items are worded such that participants in the control arm could also endorse these strategies (e.g. questions on helping others, practising slow breathing and tackling everyday problems).
Demographic characteristics were assessed at baseline. Traumatic events were assessed using the Traumatic Events Inventory (TEI) (Schwartz et al., Reference Schwartz, Bradley, Sexton, Sherry and Ressler2005), which has been previously used in Nepal (Kohrt et al., Reference Kohrt, Worthman, Ressler, Mercer, Upadhaya, Koirala, Nepal, Sharma and Binder2015c). An earthquake questionnaire was also developed for this trial to determine the severity in which participants were affected by the earthquake. The Psychological Outcomes Profiles (PSYCHLOPS) (Ashworth et al., Reference Ashworth, Shepherd, Christey, Matthews, Wright, Parmentier, Robinson and Godfrey2004) was administered pre- and post-intervention and from sessions two to five for the intervention arm to assess the main problems that participants faced. Though the PSYCHLOPS was intended for analysis as a secondary outcome, it was used in the study as a clinical tool for facilitators and clinical supervisors to track the weekly progress of participants. Please see online Supplementary Material for further detail on the timeline of quantitative outcome measures.
Qualitative evaluation
Qualitative interviews followed a semi-structured interview guide. Key informants included Group PM+ participants (n = 7), family members of participants (n = 8), Group PM+ facilitators (n = 4), CPSWs in the control arm (n = 4), control arm participants (n = 5) and mhGAP trained health workers (n = 2). Both males and females with different rates of retention in the PM+ sessions were interviewed. Focus group discussions were conducted with PM+ participants and programme staff at different time points within the trial. The qualitative interviews explored questions on the acceptability, utility of the intervention, challenges faced and suggestions for trial procedures.
Data analyses
Quantitative analyses were predominantly descriptive. The main outcomes of interest for this pilot trial were generated using data collected on fidelity, outcome data availability and drop-out. Baseline participant characteristics were summarised by arm. Likewise, continuous clinical outcome measures and changes in these measures were summarised by arm at baseline and at endline as means and standard deviations. Because of the pilot nature of the trial, we did not generate estimates of intervention effect but instead descriptively compare between arms the mean change within the arm of each continuous outcome measure to obtain an indication of the potential for an intervention effect. To help inform a future fully-powered cRCT, we generated preliminary estimates of clustering measured by intracluster correlation coefficients (ICC) of five key outcomes (PHQ-9, WHODAS, GHQ, PCL-5 and RTC). Although in a future trial, we expect that randomisation will occur at the VDC level, it is not possible to obtain ICC estimates for clustering by VDC as only two VDCs are enrolled in this pilot. Instead, we sought to generate estimates of clustering at a smaller unit, namely that of the ward (at baseline) and of the group at endline for participants in the Group PM+ VDC. Such ICC estimates were generated using an intercept-only linear mixed model estimated using restricted maximum likelihood estimation with random intercepts for ward (for baseline data) or for group (for endline data).
The qualitative data were analysed using a thematic content analysis approach. Interviews were first recorded, transcribed verbatim and translated for subsequent analysis. Researchers first familiarised themselves with the transcripts, coded interviews based on previously identified themes and subthemes, added further themes if necessary and finalised coding. Data were then reviewed by code to further draw out key information and quotes were identified that illustrated significant themes.
Ethics
Ethical approval was obtained from the National Health Research Council (NHRC, reg #371/2016) and the WHO Ethical Review Committee (ERC.0002817). Participants were enrolled only after voluntary written consent (verbal consent only if the participant was illiterate). Participants with suicidal planning were reported immediately to the counsellor for follow-up and all changes in treatment resulting from adverse events or serious adverse events were reported to the Data Safety Management Committee (DSMC). TPO Nepal was responsible for the data collection, storage and making data available to the DSMC, funders and IRBs for audit when necessary.
Results
Study population and baseline descriptives
A total of 130 (25.8%) of the 503 screen individuals were screened positive, of which 66 and 64 were in the Group PM+ VDC and EUC VDC, respectively (Fig. 1). Of these 130 individuals, five were excluded due to an AUDIT score of 16 or more. Of the remaining 125 eligible individuals, all initially consented but there were four further exclusions before baseline. Three participants declined consent to conduct the family meeting and one participant moved away before the family meeting could be conducted. As a result, 121 (24.1%) individuals were eligible and did not withdraw before baseline, of which all (100%) completed the baseline survey. There were ten males in each arm.
Fig. 1. Group PM+ study flow chart.
Feasibility and acceptability
This study showed good feasibility with high retention (97.5%) of the 121 participants from baseline to endline. There were no missing items among the five multi-item variables, for the five quantitative outcome measures, for all the 121 participants at baseline. The 118 participants at endline, all of whom had all five key multi-item variables available, had no missing items. Moreover, a majority of (52.5%) participants attended all five group sessions with only five participants (8%) attending fewer than three of the five group sessions (Table 2).
Table 2. Quantitative acceptability and feasibility measures
a Unless otherwise noted.
b Of five key measures: PHQ-9, WHODAS, GHQ, PCL-5 and RTC. Note, at baseline, WHODAS and GHQ were measured at screening and the remaining three measures at the baseline interview. Additionally, there were no missing items for any of the five measures at either time point.
c Of those who were not lost to follow-up (n = 58 in intervention and n = 60 in control).
d All six were suicidal thoughts.
e Death unrelated to the study.
Ten of the 61 participants of Group PM+ were male, and six of the ten male participants attended all five sessions. Likewise, the fidelity of PM+ facilitators was adequate with all four Group PM+ facilitators adhering to 75% or more items in each of the group sessions they conducted. Regarding competency in common therapeutic factors, ENACT scores for Group PM+ and EUC groups were above 70%; two CPSWs who scored below 70% were dropped after the initial 20-day psychosocial skills training (as described above) (Table 3).
Table 3. Demographic characteristics of 121 enrolled participants by study arm
a Unless otherwise stated.
b If more than one was reported, the primary type was selected and the secondary reported in ‘Other’. In these data, each person reported at most one.
Clinical outcomes
At baseline, outcomes were broadly comparable between the participants of the Group PM+ and EUC arms with mean (s.d.) PHQ-9 scores of 9.8 (4.9) and 10.7 (4.4) in the Group PM+ and EUC arms, respectively (Table 4). Across the 121 participants, the PHQ-9 had a mean (s.d.) of 10.3 (4.6). The WHODAS had a mean (s.d.) of 21.3 (4.8), the GHQ-12 had a mean (s.d.) of 22.8 (5.0), the PMHP had a mean (s.d.) of 10.7 (3.0), and the PCL-5 had a mean (s.d.) of 19.5 (6.8). Baseline outcomes for the 118 participants who also had data at endline were comparable to those of the overall study population of 121 participants. For the 118 participants with endline data, nearly all outcomes improved on average over time in both arms, decreases in PHQ-9, GHQ-10, WHODAS, PMPH and PCL in both study arms and an increase in MSPSS in both study arms. For all five key outcomes, the estimated mean improvement was larger in the Group PM+ arm than the EUC arm, with larger mean decreases in scores observed for all five outcomes. No formal between-group comparisons were made given that the pilot trial was not powered to detect meaningful differences. For the other outcomes of RTC and MSPSS, as hypothesised, both increased on average in the Group PM+ arm, whereas very small decreases were observed in the EUC group; of 5.0 (s.d. = 5.8) in Group PM+ compared to an average decrease in EUC of −0.7 (4.6). Estimates of clustering by ward at baseline were large ranging from 0.10 (95% CI 0.03–0.41) for WHODAS to 0.21 (0.08–0.45) for PCL-5 when clustering was by ward at enrolment.
Table 4. Outcomes at baseline and endline of n = 121 enrolled participants by study arm – mean (s.d.) reported
MH, mental health.
a Estimated using linear mixed-effects regression with a fixed intercept and random intercepts for the unit of clustering, with estimation by restricted maximum likelihood estimation to account for the small number of clusters.
b Unit of clustering is ward at baseline, of which there are 17.
c Unit of clustering is PM+ group, of which there are 10.
d Not estimable.
Estimates of clustering by group at endline were smaller ranging from 0.03 (95% CI 0–0.97) to 0.09 (0.01–0.62), though were not estimable for PHQ-9 and PCL-5. As expected, confidence intervals were wide in all cases due to the small sample size.
Qualitative outcomes
As captured by responses from CPSWs and RAs, the study was initially met with hesitancy from community members due to prior notions that only those with severe mental illnesses need support. Referring to mental health issues as ‘man ko samasya’ (heart–mind problems) (Kohrt and Harper, Reference Kohrt and Harper2008) or ‘tension’ (an English term used commonly in Nepal for distress) (Clarke et al., Reference Clarke, Saville, Bhandari, Giri, Ghising, Jha, Jha, Magar, Roy, Shrestha, Thakur, Tiwari, Costello, Manandhar, King, Osrin and Prost2014b; Rai et al., Reference Rai, Gurung, Kaiser, Sikkema, Dhakal, Bhardwaj, Tergesen and Kohrt2018), non-stigmatising idioms of distress made the study more acceptable to community members. CPSWs reported that community sensitisation events helped clarify to the community that this programme was for people with general distress rather than severe mental illness. Group PM+ participants found the Nepali programme name, ‘Khulla Man’ meaning ‘an open and light heart–mind’ as a cultural concept of catharsis, to be acceptable. Both male and female participants also referred to their own heart–mind as being lighter after completion of the programme.
Male and female Group PM+ participants responded positively to the programme. Participants reported enjoying the group format of the programme and spending time outside the home with others. Both male and female participants reported that the group format helped them realise that others experience similar problems and that problems should be shared. They noted improvements in their somatic symptoms, such as restlessness and feelings of weakness, and social functioning. Though session materials such as calendars for reminders seemed to be effective as reported by the facilitators, some participants noted that they were too busy to practise techniques at home but enjoyed the sessions and requested additional weeks. Participants' expectations of monetary incentives, rather than the content of the programme, seemed to have attributed to drop-outs. Facilitators noted that after several rounds of conducting PM+ group sessions, other community members also showed interest in participating in Group PM+.
This was the first Group PM+ study that included males and demonstrated a high retention rate amongst their groups. Male participants also reported enjoying the session activities and case stories, and practised techniques at home. Programme staff reported that barriers to recruiting men included their initial hesitance in discussing personal problems and emotions with others, busy work schedule and lack of men in the villages due to labour migration.
Participants in both arms preferred to conduct assessments with gender-matched RAs due to fear of perceptions from family and community members. Some EUC participants noted that assessments helped them feel lighter and thought of them as the treatment. Others were disappointed by the lack of treatment especially because accessing referral services was a noted challenge. Participants that visited the health post for treatment and were dissuaded when it was closed or did not have the necessary medications. Health workers trained in mhGAP suggested additional refresher trainings to better support referrals (Table 5).
Table 5. Qualitative interview results
Discussion
The RCT met all pre-defined feasibility and acceptability criteria (Table 1). The high rates of participation in the sessions indicate that participants found the intervention to be acceptable, which was supported by the qualitative findings. Additionally, only three participants were lost to follow-up which indicates the feasibility of trial procedures. The feasibility of assessments, procedures and the intervention indicates that a fully-powered Group PM+ trial is achievable in the Nepal context.
The descriptive study results, if also supported by the fully-powered trial, suggest better improvements in the Group PM+ arm, especially in daily functioning and general distress, and indicate that Group PM+ delivered by non-specialists has the potential to reduce psychological distress relative to EUC. Though this study is not powered, findings are in line with current evidence that effective psychological interventions can be delivered by non-specialised workers (Singla et al., Reference Singla, Kohrt, Murray, Anand, Chorpita and Patel2017). This was supported by the qualitative analysis in which Group PM+ participants mentioned overall changes in somatic symptoms and an increased understanding of how to manage their problems.
The study was initially met with hesitancy amongst community members due to their understanding that only those with severe mental illnesses need support. This highlights the importance of using de-stigmatising local idioms and language during the initial planning phase with local stakeholders, the recruitment process, assessments and the intervention itself (Kohrt and Harper, Reference Kohrt and Harper2008; Kohrt and Hruschka, Reference Kohrt and Hruschka2010). As experienced by the CPSWs in both arms, sensitisation events worked to normalise experiencing adversity and distress, and to differentiate to the community that this programme was for those with general distress.
Based on the qualitative evaluations, the group format also had some inherent benefits, such as reducing self-stigma since participants felt that many others in their community were also seeking support. Perhaps because most of the Group PM+ participants were housewives, they noted enjoying the company of a group and taking time away from daily household chores. Furthermore, the pervasiveness of community groups (mother's groups, youth groups, etc.) in rural Nepal and other LMICs adds to the acceptability of a group intervention in the Nepal context (Clarke et al., Reference Clarke, Azad, Kuddus, Shaha, Nahar, Aumon, Hossen, Beard, Costello, Houweling, Prost and Fottrell2014a).
A strength of this study is the addition of the combined competency and fidelity checklist to measure facilitator competency in common factors and adherence to the manual during intervention delivery. Another strength was the use of the RTC to measure the participant's use of skills learned in Group PM+ sessions. The outcomes evaluation indicates an increase in RTC scores at follow-up in the intervention arm as compared to the control arm, suggesting that the delivery and uptake of intervention strategies appears feasible. However, participants indicated practising some techniques more than others. A recommendation for the definitive trial is to develop and strengthen tools that reinforce the techniques learned in the sessions.
Because the limited number of trained mental health workers is a larger barrier to care in LMICs (Kakuma et al., Reference Kakuma, Minas, van Ginneken, Dal Poz, Desiraju, Morris, Saxena and Scheffler2011), the referral system was a noted challenge. Though health posts with mhGAP trained health workers were near-by and an improvement from the standard of care in rural Nepal, participants faced barriers such as absence of trained health workers, lack of medication and closed facilities due to the rural nature of the study area. More efforts should be made in the next trial to refer all participants to better-resourced health facilities to ensure follow through, especially for the EUC arm.
This was the first Group PM+ study that included males and demonstrated a high retention rate amongst male groups. Recruiting men was a noted challenge because of labour migration, work outside of the home and their hesitancy in discussing personal problems. The overall feasibility and acceptability of conducting the intervention and EUC procedures amongst men indicates that it is possible to include both genders in a larger trial in the Nepal context, with some potential barriers in recruitment.
Limitations of the study design include the risk of contamination and the inability to maintain complete blinding. The CPSWs and RAs from the two arms were initially trained together. Study sites were close in distance, which may have increased the likelihood of participants, CPSWs or research staff communicating with each other. However, all local staff were assigned to work in their VDC only, which decreased the likelihood of un-blinding. Stricter blinding procedures are recommended for the fully-powered trial.
The initial planning phase with stakeholders, recruitment process, assessments and the Group PM+ intervention itself showed feasibility and acceptability among both male and female participants. The estimated mean improvement was larger, for all key outcome measures, in the intervention compared to the EUC arm. A larger fully-powered trial will seek to establish intervention effectiveness in the Nepal context.
Supplementary material
The supplementary material for this article can be found at https://doi.org/10.1017/S2045796020000414.
Data
Raw data are available as additional supporting files.
Acknowledgements
We are grateful to the study participants, CPSWs, RAs and the PM+ study team including Jananee Magar and Ashish Sapkota. We thank the TPO Nepal leadership including Suraj Koirala. We would like to thank Katie Dawson and Parveen Akhtar. We are indebted to the ethical oversight and approval provided by the Nepal Health Research Council (NHRC) and the WHO Ethics Research Committee. The authors alone are responsible for the views expressed in this article. They do not necessarily represent the views, decisions or policies of the institutions with which they are affiliated.
Author contributions
The study was designed by MJDJ, BAK, NPL, EvO, MS, RB and MvO. The manuscript was drafted by MS and ELT. Quantitative statistical analyses were conducted by ELT. Qualitative analyses were conducted by MS and RG. The manuscript was significantly revised by MJDJ and BAK. All authors have reviewed and approved the final manuscript for submission.
Financial support
This study was funded by USAID/OFDA. The trial sponsors had no role in the collection, management, analysis and interpretation of data; nor the decision to submit the report for publication. The authors alone are responsible for the views expressed in this article and they do not necessarily represent the views, decisions or policies of the institutions with which they are affiliated.
Conflict of interest
None.
Ethical standards
Ethical approval has been received from the NHRC and the World Health Organization. Informed consent was obtained from all study participants. The authors assert that all procedures contributing to this work comply with the ethical standards of the relevant national and institutional committees on human experimentation and with the Helsinki Declaration of 1975, as revised in 2008.
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