Objectives To evaluate the effectiveness of individual counselling on functioning of clients participating in a mental health intervention in a humanitarian setting.
Design Randomised controlled trial.
Setting Mental health programme implemented by Médecins Sans Frontières in Grozny, Republic of Chechnya.
Participants 168 eligible clients were randomly assigned to the intervention and waitlisted (2 months) arms between November 2014 and February 2015.
Intervention Individual counselling sessions.
Main outcome measures Change in functioning was measured using the Short Form 6 (SF6) and gender-specific locally adapted Chechen functioning instruments in the intervention group at the end of counselling and the waitlisted group after their waitlisted period. Unadjusted differences in gain scores (DGSs) between intervention and waitlisted groups were calculated with effect size (Cohen’s d) for both tools. Linear regression compared the mean DGS in both groups.
Results The intervention group (n=78) improved compared with waitlisted controls (n=80) on the SF6 measures with moderate to large effect sizes: general health (DGS 12.14, d=0.52), body pain (DGS 10.26, d=0.35), social support (DGS 16.07, d=0.69) and emotional functioning (DGS 16.87, d=0.91). Similar improvement was seen using the Chechen functioning instrument score (female DGS −0.33, d=0.55; male DGS −0.40, d=0.99). Adjusted analysis showed significant improvement (p<0.05) in the intervention group for all SF6 measures and for the Chechen functioning instrument score in women but not men (p=0.07).
Conclusions Individual counselling significantly improved participants’ ability to function in the intervention group compared with the waitlisted group. Further research is needed to determine whether similar positive results can be shown in other settings and further exploring the impact in male clients’ population.
Trial registration number NTR4689.
- mental health
- anxiety and depression
- individual counselling
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Strengths and limitations of this study
Randomised controlled trial conducted in a humanitarian setting in a scientifically rigorous way.
Very low rate of loss to follow-up in the intervention and waitlisted group throughout the study period.
Intervention impact evaluated using different psychological measurement instruments.
Participant recruitment occurred at hospitals, thus the study population might not be fully representative of the general population in Grozny.
Blinding of study counsellors to the intervention and waitlisted group could not be ensured in all cases.
Mental health (MH) needs of people affected by emergencies are undisputed. Recognition of the need for scale-up of MH programming in lower income countries and humanitarian contexts was solidified by the WHO mhGAP 2010 Intervention Guide, updated in 2016.1 WHO recently issued Problem Management Plus (PM+) guidance to support implementation of individual psychological support for adults in communities affected by adversity.2 The guidelines recommend the implementation of brief MH interventions during humanitarian emergencies as often these contexts limit the ability to implement longer term counselling strategies. Furthermore, the guidelines recognise that fully trained MH workers in emergency-affected areas are often limited and thus MH interventions often rely on non-specialised MH staff.
MH interventions involving non-specialised counselling for adults conducted in emergency settings have shown to have a beneficial effect on post-traumatic stress disorder (PTSD) in meta-analysis conducted on seven studies in 2011.3 Several randomised controlled trials (RCTs) looking at different MH interventions in humanitarian settings have since been published.4 However, the interventions vary in their approach, target groups, duration of intervention and types of MH staff used. Cognitive–behavioural therapy (CBT) and cognitive processing therapy have been shown to have positive outcomes on depression, anxiety and PTSD in RCTs in Iraq and Iraqi Kurdistan in war-traumatised adults and survivors of violence, torture and militant attacks.5–7 Several other RCTs have addressed other methods of psychosocial support including transdiagnostic approaches, Common Elements Treatment Approach (CETA), behavioural interventions and psychosocial counselling in individual and group interventions in various countries.8–14
The main MH intervention implemented by Médecins Sans Frontières – Operational Centre Amsterdam (MSF-OCA) is the provision of individual counselling.15 It aims to enhance clients’ functionality, reduce symptoms of mental distress and identify new coping strategies.15 The intervention does not address severe MH disorders such as severe depression, bipolar disorder or psychosis. The counselling approach is based on principles derived from brief trauma-focused therapy and CBT’s techniques integrated into the cultural context.16 A review of 18 MSF-OCA individual-focused non-specialised counselling programmes comprising 15 000 clients showed positive outcomes among those returning for follow-up.15 However, no evaluation using a control group to determine the impact of this form of individual counselling was conducted before this study.
Grozny, the capital of the Republic of Chechnya, has been exposed to different waves of violence and humanitarian strife since 2001. Between 2001 and 2003, MSF provided MH services to internally displaced people with trauma-related symptoms resulting from heavy shelling and massive explosions. Since 2008, the situation in Chechnya has improved, but there continued to be ongoing violence and insecurity. Between 2008 and 2017, MSF provided individual counselling and psychosocial services support to the population through three hospitals in Grozny, one hospital in Shatoy district and one hospital in Vedeno district.
The primary objective of our study was to estimate the effectiveness of the individual counselling intervention in Grozny on the daily functioning of clients enrolled using an individual level stepped-wedge RCT. Functioning was chosen as the main outcome of the study as this is the primary goal in the MSF individual counselling approach. Our hypothesis was that the individual counselling would lead to improved functioning in daily life for intervention clients compared with waitlisted clients.
Study location and design
The study was conducted in Grozny, capital of the Republic of Chechnya, and implemented in three Ministry of Health hospitals where MSF’s MH programme functions. The design was an RCT using a stepped-wedge design at the individual level.17 Stepped-wedge randomised trial designs involve sequential roll-out of an intervention to participants (individuals or clusters) over a number of time periods.17 Study participants were randomly assigned to intervention or waitlisted control arms, based on order of arrival for counselling (figure 1), and thus by the end of the random allocation, all individuals enrolled in the study would have received the individual counselling intervention. The intervention group received individual counselling immediately after enrolment. The waitlisted group had their counselling deferred for 2 months. The 2-month waiting period was based on the average length of treatment for clients enrolled in the programme in Grozny before the study and on a community consultation exercise implemented prior to the study.18 The intervention group completed measurements at enrolment/preintervention (B/T0), postintervention (T1) and 3 and 6 months postintervention (T2 and T3). The waitlisted group completed measurements at enrolment (baseline/B), preintervention immediately before the start of counselling (T0), following the end of counselling (T1) and 3 months later (T2) (figure 1). The waitlisted group was not followed up at 6 months postintervention due to practical considerations around the duration of the trial.
All clients seeking care at the MSF-OCA MH programme in Grozny between November 2014 and February 2015 were considered for eligibility. Clients were self-referred or referred by staff and volunteers at the three hospitals. Clients included outpatients but could also include those admitted to the hospitals in question. Clients were eligible for inclusion if they were aged 18 years or older, able to provide informed consent and willing and able to return for follow-up. Clients were not eligible if they had cognitive, visual or other impairments that would limit their ability to participate, were considered at acute risk of suicide, had a severe MH disorder requiring medications or had been enrolled in MSF counselling services in the previous 6 months. Inclusion and exclusion criteria were established at presentation by a study interviewer/counsellor using a pre-established checklist.
All eligible clients were asked if they would consent to undergoing screening using the Hopkins Symptom Checklist-25 (HSCL-25). All those scoring 1.75 or greater on this questionnaire were asked to undergo the informed consent process to participate in the study. This included a detailed explanation of the study, the process of randomisation, the possibility of being waitlisted for 2 months, and the required follow-up periods. They received the same explanation in writing, after which they could ask further questions, and were then invited to sign the informed consent.
The counselling approach was based on principles derived from brief trauma-focused therapy, with an ‘individual development oriented’ approach.19 The first task of the counsellor is to make a personal and meaningful contact with the client.20 After identifying the main complaint, the counsellor explores any specific precipitating events to gain a clear picture from the client’s point of view about the history of the complaint. During subsequent sessions, the counsellor works with the client according to the goals set during the first consultation and an individualised treatment plan. No intervention other than individual counselling was offered. Sessions aimed to finish within 50 min, and the number of sessions held was dependent on the needs of the individual, thus there was no formal limit.
The counselling approach was standardised through training modules delivered by trainers from the Netherlands Institute of Psychology. Follow-up supervision and quality control used the MSF-OCA MH guideline,19 clinical supervision by international MH experts based in Grozny and oversight from headquarters-based MH advisors. The training for the counselling approach included: theory of psychosocial counselling, the five categories of problems that are covered in sessions (lack of practical and social skills, practical problems, inner conflict, overwhelming feelings and trauma-related symptoms), general problems that counsellors might encounter with the clients they see, knowledge/attitudes/skills of the counsellor, intervention options, counselling processes and reporting and referral procedures. Clinical supervision was done on-site by the international MH experts and through weekly discussions and case reviews. The MH advisor from headquarters would also undertake annual visits in which all aspects of supervision were reviewed. The MH advisor would also have regular telephone/Skype contact with the MH expert in Grozny to discuss arising questions, issues and progress.
During the study period, there were eight full-time counsellors providing the individual counselling intervention. Most counsellors had an academic background in psychology and had been working for MSF for more than 10 years. Of the eight counsellors, five specialised in pedagogy and psychology, one specialised in clinical psychology and two had completed medical school. Six of the eight full-time counsellors were involved in counselling study participants as they were based at the three hospitals, which were the study locations. The remaining two counsellors worked in other locations not included in the study.
The primary outcome was change in functioning, measured using the Short Form 6 (SF6; an adapted version of the SF36) and locally adapted gender-specific Chechen functioning instruments.21 22 The SF6 selected six questions from the SF-36 to assess self-perceived general health, bodily pain, social functioning and role emotional functioning. The SF6 has been used successfully in similar work conducted in war-affected adults in Afghanistan.23 The raw scores of each of the four individual items from the SF6 are transformed to fit a 0–100 scale, with high scores representing better functioning.21 We also developed and piloted two daily functioning scales for men and women in Chechnya, using an extensive qualitative study before the start of this study.22 These gender-specific instruments use a scale from 1 to 4, including a ‘not applicable’ score, to rate the participant’s abilities to participate in activities considered to be part of daily life for people in Chechnya. The female instrument included 27 items, and the male instrument included 28 items. A reduction in score suggested improvement in functioning.
Secondary outcomes included changes in symptoms of anxiety and depression, coping strategies and perceived social support as measured by the HSCL-25, the Coping Strategy Indicator (CSI) and the Social Provisions Scale (SPS), respectively.24–26 We also aimed to measure whether any changes were sustained at 3 and 6 months postintervention. The HSCL-25 evaluates anxiety-related and depression-related symptoms and is rated on a scale from 1 to 4, where 1 means that the client does not associate with the symptom and 4 means they associate with it ‘extremely’. Three scores are calculated: an anxiety score, a depression score and an overall score measuring psychological distress.24 The scale was validated in the Russian language in Chechen refugees living in Austria.27 Mean overall symptom scores of more than 1.75 for each subcategory have been found to predict clinical diagnosis of anxiety and affective disorders.28 We used this cut-off as an indication of symptoms of mental distress in clients eligible for enrolment in the study. The CSI25 includes three subscales of coping strategies: problem solving, avoidance and social support seeking. A reduction in scores indicates an improvement in coping strategies. The 12-item SPS measures perceived social support,26 29 using a 5-point Likert scale allowing for an unsure response. Participants rated their level of agreement from 1 (strongly disagree) to 5 (strongly agree) with statements regarding respect from others, offering support to others, common interests, feeling supported by others and feeling close to others. An increase in score indicated an improved perception of social support.
Finally, the proportion of study participants with PTSD before and after the intervention was measured using the Harvard Trauma Questionnaire (HTQ-16).30 This instrument evaluates the 16 commonly reported symptoms of PTSD on a scale of 1–4, as described in the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV).31 It has been used as a screening tool for PTSD in numerous war-affected populations and has been validated in Chechen refugees in Austria.32 This definition of PTSD requires a score of 3 or 4 on at least one of four re-experiencing symptoms, at least three of seven avoidance and numbing symptoms and at least two of five arousal symptoms.30 Thus, any person that met the aforementioned criteria was considered to be screened positive PTSD. The prevalence of PTSD in the intervention and waitlisted group was calculated by dividing the number of PTSD-screened positive participants by the total number of participants in their study group.
As Chechen is mostly an oral language but the majority of Chechens speak, read and write Russian, we chose to translate the instruments into Russian. All Russian translations were back translated into English to ensure consistency of language. The Russian terminology used in each instrument was carefully double checked in the piloting process of all instruments. Together with the study interviewers, we created verbal Chechen translations for specific Russian phrases or words that were not well understood by individuals who participated in the pilot of the instruments. As such, study interviewers used the closest term that conveyed the same meaning in Chechen and Russian language for all administered instruments.
A case reporting form (CRF) was created for each participant for each relevant visit. The visits were defined as baseline (B; at enrolment for both groups), T0 (just before the counselling intervention in both groups), T1 (after the intervention for both groups), T2 (3 months after the intervention for both groups) and T3 (6 months after the intervention for the intervention group). This CRF included all study instruments and allowed the study interviewer to collect information on important life events that occurred between visits. Study interviewers were trained for 2 weeks to ensure consistency in language and style of administering the instruments.
Routine data on the counselling intervention was collected separately according to the MSF-OCA MH programme specifications, using a unique patient ID number and no other identifying data. Linkage between the participant’s number and their patient ID number could only be done by the study coordinator through a password-protected database.
A sample size of 46 in both the waitlisted and intervention arms was calculated for an estimated effect size (estimated difference in means between intervention and waitlisted divided by common SD) of 0.40, 80% power and an alpha of 0.05. We conservatively assumed a 45% loss to follow-up in our total sample, and thus aimed to include 84 participants in each arm for a total sample size of 168.
Randomisation and masking
Randomisation to the intervention and waitlisted groups used a computer-generated sequence for each hospital. This sequence was only accessible to the study coordinator and study assistant in a password-protected file. The statistician generated the random allocation sequences before the study started, using the Proc Plan procedure in SAS V.9.4.
After participants had provided written informed consent and officially been enrolled, the study interviewers called the study coordinator for information on the allocated study arm of that participant. Participants were informed of their allocated study arm, and a follow-up visit for the counselling intervention or for the follow-up visit after the waitlist period was established. At the next visit (T1 for the intervention group and T0 for the waitlisted group), the study interviewer was switched to maintain blinding of the allocation arm. Participants were instructed not to reveal their allocation at this visit. Although the study team did their best to ensure blinding up to T1 for the intervention group and T0 for the waitlisted group, maintaining this at all times was difficult, as normal conversation between interviewers and participants might have elicited this information. After the postintervention visit, no further blinding was maintained.
Descriptive analysis on demographic indicators (sex, age, marital status and so on) for both groups involved calculating means (and SD) for continuous variables and proportions for categorical variables. Differences between the groups were determined using the t-test to compare means and χ2 to test differences between proportions.
For each participant, we calculated individual scores for the SF6, HSCL-25, CSI and SPS at each visit. For the intervention group, we calculated mean changes in individual gain scores between the B/T0 and T1 visits and the mean gain score for this period. For the waitlisted group, we calculated the individual gain scores between enrolment at baseline and T0 after their waitlisted period and the mean gain score for the whole group for the same period. We then compared the difference between the mean gain scores (DmGS) of the groups using mixed regression models accounting for individual change. A multivariable regression model was constructed to estimate the adjusted DmGS between the groups, incorporating the following covariates to adjust for potential confounding: hospital, age, sex, education level, marital status and employment status at enrolment. We also adjusted for the total number of counselling sessions for each participant.
We analysed the data in the intention-to-treat model to test the intervention effects, including all participants enrolled in the study even if they dropped out between the two time points. For participants lost to follow-up, we imputed the last known value from the previous visit.
Cohen’s d effect sizes were calculated for the unadjusted differences in gain scores between the groups. We defined an effect size of <0.15 as negligible, 0.15–0.40 as small, 0.41–0.75 as medium and >0.75 as large.33 The difference between the mean adjusted difference in gains scores for the two groups were compared using the F-statistic and corresponding p values (equations of the analysis are available in the online supplementary information).
To determine whether the change in scores after the intervention was maintained in both groups, we combined all data for mean scores at T1 and T2 (3 months after finishing counselling). This analysis did not use the intention-to-treat model. We also looked at maintenance of the score in the intervention group 6 months after counselling finished (T3). Mixed regression models were used to measure the difference in the mean of the pooled scores between T1 and T2 (both groups combined) and between T2 and T3 (intervention group only). The analysis was only performed on those participants for whom we had outcome measures at these time points.
For the HTQ-16 (PTSD), we calculated prevalence of PTSD in the two groups at all visits by identifying participants meeting DSM-IV criteria. We compared the change in prevalence in the intervention group between B/T0 and T1 with the change in prevalence in the waitlisted group between B and T0, using logistic regression estimated by generalised estimating equations to account for the repeated measures of PTSD. The model included an interaction term for group and time to account for the change in the PTSD status of participants in each group between the two time points and adjusted for sex, hospital of recruitment and age. Measures of association were calculated as ORs with 95% CIs and p values. This analysis was not using the intention-to-treat model.
All analysis was done in STATA V.13.0 and SAS V.9.4.
In February 2013, a community consultation about this study was conducted in Grozny with six groups of participants including nurses, social workers, pharmacy staff and patients in the hospital.18 The outcomes were used to inform the final study design (notably reducing the waitlist period from 3 months to 2 months). The study protocol was also reviewed at Centers for Disease Control and Prevention (CDC) and determined to meet the criteria for non-engagement of CDC staff in human subjects’ research.
Informed consent forms were translated into Russian and verbal Chechen, back-translated into English and piloted in the area of the study. We explained to clients that participation in the study was voluntary, that they could discontinue from the study at any time without explanation and that they would receive the same standard of treatment whether they agreed to participate. Participants were reimbursed approximately US$10 to cover transport costs for each study-related follow-up visit.
Patient and public involvement
Prior to the implementation of this RCT, two community-based studies were carried out in Grozny in preparation for this study. The first was a community consultation that discussed the stepped-wedge design of the RCT and the acceptability around the waitlist group and the length of the waitlisted period.18 As mentioned before, the waitlisted period for this RCT was reduced from the proposed 3 months to 2 months following this community consultation. The second study involved the design of culturally adapted instruments to measure mental distress in the current RCT.22 We assumed that the communities involved in these two prior studies were the same as those from which the participants of the RCT arose. Also, at the end of the study, all participants were offered an appointment (and transport costs) to review their own results.
Participant recruitment and follow-up
Between 17 November 2014 and 9 February 2015, we assessed 203 patients presenting for care at the MSF MH programme for eligibility. Thirty-five people were not eligible (n=12) or declined to participate (n=23). Those who declined to participate in the study cited the following reasons: personal reasons (n=11, 47.8%), unwilling to wait for counselling (n=6, 26.1%), distance too far for counselling (n=3, 13.0%), no permission from family to attend counselling (n=1), lack of time to attend counselling (n=1) and for one individual this information was missing. We randomised 168 participants: 84 to each group.
One participant’s MH condition deteriorated immediately following enrolment into the study (intervention group); the participant was referred for psychiatric care before starting the intervention and was no longer followed in the study. We lost another 19 participants to follow-up (11.30%): 6 (7.14%) in the intervention group (five during the intervention and one between 3 months and 6 months postintervention) and 13 (15.48%) in the waitlisted group (four during the waitlisted period, seven during the intervention and two between the end of counselling and 3-month follow-up). The total proportion lost to follow-up did not differ between the groups (p=0.082) (figure 1).
Demographic characteristics of the intervention and waitlisted group participants were similar; most were female, married and employed, had completed high school and were not hospitalised at the time of enrolment (table 1). Out of the 14 hospitalised participants, it should be noted that they were all hospitalised for non-MH-related reasons. There was no evidence of differences in characteristics of the two groups (p≥0.26).
For the 78 intervention group participants who completed counselling, information was available for 76 participants on the number of counselling sessions completed and the duration of those sessions (mean sessions: 3.8 (SD=0.7); duration: 29.7 days (SD=9.7)). Seventy-one waitlisted participants for whom this information was available (of the 73 participants who completed counselling) had a higher mean number of counselling sessions (4.1 (SD=0.6); t-value=2.1, p=0.04) and mean duration of counselling (33.6 days (SD=12.0); t-value=2.2; p=0.03). The presenting complaint for counselling as assessed by the counsellor was similar between the groups (χ2=5.5, p=0.6); most sought counselling for anxiety-related (n=54, 36.7%), mood-related (n=34, 23.1%), family-related (n=22, 15.0%) and behaviour-related complaints (n=20, 13.6%). The precipitating event leading to seeking counselling was also similar between groups (χ2=10.3, p=0.2), with similar proportions seeking care due to psychological violence (n=43, 39.3%), domestic discord or domestic violence (n=41, 27.9%) or non-violence-related events (n=41, 27.9%). During the intervention, the counselling focus was similar in the two groups (χ2=1.62, p=0.8). The counselling focus was on practical problems (n=58, 39.5%), overwhelming feelings (n=32, 21.8%), trauma-related symptoms (n=29, 19.7%), inner problems (n=17, 11.6%) and lack of essential practical or social skills (n=11, 7.5%). (Please note that this data is collected in our routine MH programme data. For further details on how this information is collected, please contact the corresponding author).
For the primary outcome and secondary outcomes looking at differences in mean gain scores between the groups from T0 and T1 for the intervention group and baseline and T0 for the waitlisted group, we included 84 participants in both groups with imputed data on scores from the last known follow-up visit. For PTSD analysis, we compared the difference in PTSD prevalence in the intervention group between B/T0 (84 participants) and T1 (80 participants) to that in the waitlisted participants between B (84 participants) and T0 (80 participants). For the maintenance of scores after the intervention, we included 78 people in the intervention group and 71 from the waitlisted group.
Using the SF6, the counselling intervention had moderate to large effect sizes in the intervention group compared with the waitlisted group (general health DmGS=12.14, effect size=0.52; bodily pain DmGS=10.26, effect size=0.35; social functioning DmGS=16.07, effect size=0.69; and role emotional DmGS=16.87, effect size=0.91) (table 2). The Chechen functioning instruments showed a DmGS of −0.33 (effect size=0.54) for females and a DmGS of −0.40 (effect size=0.99) for males. In the adjusted analysis, the intervention group also showed improved functioning by SF6 and the Chechen female functioning scale (all p<0.05) (table 3). For the male score, the adjusted analysis showed less strong evidence of an improvement in functioning in the intervention group compared with the waitlisted group (F=3.52, p=0.0691).
Anxiety and depression
The unadjusted DmGS between the intervention and waitlisted groups using the HSCL-25 was −0.55 for anxiety symptoms, −0.50 for depression symptoms and −0.52 for overall psychological distress (table 4). The effect sizes calculated in the unadjusted analysis for all three measurements were large (all d>1.0 and p<0.0001). This positive impact of counselling in the intervention group compared with the waitlisted group was maintained in the adjusted analysis, with p<0.0001 for all three measurements (table 5).
Coping and perceived social support
Using the CSI, the unadjusted DmGS related to problem solving and social support were very small with small effect sizes (problem solving DmGS=0.11, d=0.25, p=0.103; social support DmGS=-0.01, d=0.02, p=0.871) (table 4). In the adjusted analysis, problem solving and social support showed no significant evidence of difference between the groups (p=0.08 and p=0.86, respectively) (table 5). The coping scale for avoidance showed a significant worsening, with a moderate effect size (DmGS=0.31, d=0.72, p<0.0001). In the adjusted analysis, the worsening in avoidance coping skills remained (F=20.16, Pp<0.001). Perceived social support improved in the intervention group compared with the waitlisted group, with a moderate effect size (DmGS=1.89, d=0.43, p=0.006), and this remained relevant in the adjusted analysis (F=8.83, p=0.0034) (table 5).
Maintenance of scores after counselling
A continued improvement was observed using the scales for SF6 social functioning, SF6 role emotional and the Chechen female and male functioning scales at T2 compared with T1 (all p<0.05). The effect was maintained at T3 with no further improvement for SF6 social functioning (p=0.60), SF6 role emotional (p=0.25) or the Chechen male functioning scale (p=0.17). Further significant improvement was observed at T3 compared with T2 in female participants from the intervention group (p=0.02). The effect of counselling was sustained (but not further improved) at T2 compared with T1 when measured on the SF6 general health (p=0.38) and body pain (p=0.10) scales. Similar trends were observed for these two scales at T3 compared with T2 (p=0.94 and p=0.95, respectively) (table 6).
Symptoms of anxiety, depression and psychological distress, measured by the HSCL-25, improved further at T2 compared with T1 (p=0.03, p=0.003 and p=0.005, respectively). This improvement continued in the intervention group at T3 compared with T2 (p=0.0009, p=0.001 and p=0.0005, respectively). Results for all aspects of the CSI showed either no change or a slight deterioration at T2 and T3. For perceived social support, a small improvement was observed at T2 (p=0.002) compared with T1, which was sustained but not further improved at T3 in the intervention group (table 7).
Post-traumatic stress disorder
At baseline, 32 (n=84, 38.10%) participants in the intervention group and 39 (n=84, 46.43%) in the waitlisted group were classified as meeting DSM-IV criteria for PTSD using HTQ-16 (χ2=1.20, p=0.274). At T1, the prevalence in the intervention group had reduced (n=5/78, 6.41%). The prevalence of PTSD in the waitlisted group was 38.75% after the waitlisted period at T0 and had also reduced at T1 (n=8/73, 10.96%). The adjusted reduction in PTSD prevalence in the intervention group between baseline/T0 and T1 was significantly lower than that in the waitlisted group between baseline and T0 (OR 0.11; 95% CI 0.04 to 0.28, p<0.001) (table 8).
We have shown that individual counselling in conflict-affected adults in Chechnya improved their daily functioning. Both study instruments used to test functioning, including one that was specifically designed for use in Chechen adults, showed an improvement in the intervention group compared with the waitlisted group. The unadjusted and adjusted analyses for the functioning instruments showed very similar results, suggesting that the improvement in the intervention group compared with the waitlisted group was not importantly influenced by age, sex, marital and employment status, number of counselling sessions or hospital of recruitment. The absence of statistical evidence for a true difference in the Chechen male functioning scale is likely due to the study being underpowered to detect differences among subgroups.
The results are especially encouraging as different instruments to measure functioning recorded similar positive outcomes, strongly suggesting that the counselling is effective in improving this aspect of clients’ lives. Such positive outcomes have also been shown in a retrospective review of programmatic data from 18 MSF projects with MH programmes in conflict and postconflict settings.15 As this study was a stepped-wedge RCT using validated outcome measures, we provide further evidence that the brief counselling intervention used among people affected by conflict can have a positive impact on their ability to function.
Different counselling strategies in other studies have also shown positive effects on functioning, PTSD, depression and anxiety. Moderate to high improvements in the intervention group compared with the waitlisted group on these outcomes were measured using CETA in Burmese refugees in Thailand and in Iraqi Kurdistan.12 14 In contrast, mixed results from group problem-solving counselling in terms of functioning were observed in war-affected adults in Aceh, Indonesia.13 A recent RCT in adults with psychological distress in a conflict area in Pakistan identified a large improvement in functioning and symptoms of PTSD, depression and anxiety following 5 weekly sessions of individual counselling delivered by trained lay workers using the WHO PM+ approach.10 This study mirrors the intervention described in our study in that it limited the number of counselling sessions to five and did not rely on clinically trained MH professionals. It slightly differs from our approach in that the PM+ is a manualised intervention, whereas the MSF one is a semistructured approach allowing for individual adaptation by the counsellor.
The coping scale did not show evidence for improvement with the intervention, and avoidance appeared to worsen. This suggests that the improvement in functioning and symptoms was not achieved through improvement in the three coping skills measured by the CSI. Alternately, the CSI may not be well adapted to measure coping strategies in this population. The study by our colleagues in Aceh13 also observed a small decline in the use of coping strategies among women in the intervention group.
The SPS showed a significant increase in perceived social support in the intervention group compared with the waitlisted group, which was sustained after completion of counselling. The MSF-OCA MH programme in Grozny includes encouragement to establish positive coping mechanisms (including social support). Social support has been shown to have a positive effect on mental and physical health34 and is associated with lower post-traumatic stress scores.35 It is also notable that social functioning improved with the intervention.
We were able to determine that there was longer term efficacy of the individual counselling on functioning and symptoms of depression and anxiety in both the intervention and waitlisted groups. Scores on the instruments that tested these items either maintained the improvement or continued to improve at 3 and 6 months after completion of counselling. Studies on Rwandan and Somali refugees in Uganda showed that Narrative Exposure Therapy counselling sustained the reduction in PTSD in all participants at 6 and 12 months’ follow-up, although the dropout rates were high.36 Very few studies have measured the maintenance of these scores, and thus the current study provides much needed evidence in this regard.
The expression of MH difficulties as physical symptoms, called somatisation, is common in many cultures.37 In our study, the functioning scales addressing general health and body pain were not sustained or further improved after completion of counselling. Whether this is due to continuing physical complaints in the study population or because of ongoing psychosomatic complaints, we cannot say. However, we believe the latter is unlikely as the counselling intervention is addressing medically unexplained physical symptoms but did not change or address any physical illness. Neither coping mechanisms nor social support showed any further changes following the end of counselling.
The study has some limitations. Although few of the participants were hospitalised at enrolment, the MSF MH programme is located in hospital settings, which might have biased care-seeking behaviour. The study population therefore might not be entirely representative of those seeking help for MH concerns in Grozny. We worked hard to ensure that study interviewers remained blinded to the group allocation up to T1 of the intervention group, but this could not be ensured in all cases. We do not think that this potential bias would have changed our findings substantially, as all instruments had a fixed script for questions to be asked by interviewers and answers provided by participants, not allowing much space for interviewers to influence participants’ answers. Grozny represents a specific and long-term unstable situation, so we cannot be certain that similar outcomes would be found in other acute emergencies. The counsellors delivering the intervention, while non-specialised, all had academic training and many years of experience delivering the intervention, which is not the case in many humanitarian settings. However, we have shown previously that although lay counsellors used more sessions than academically trained counsellors, the outcomes in clients were similar.15 Also, we conducted a sensitivity analysis that included the counsellor as a covariate in the multivariate regression models, and the results did not change the interpretation of the study findings. This suggests that the positive outcomes measured were not linked to individual counsellors. Finally, we employed widely used instruments to measure MH distress and functioning in this study and thus have equated numerical improvements in the scores of study participants with clinical improvements. This is supported by the knowledge that individual counselling in Grozny was only finalised when the client and counsellor agreed that the main complaint for attending counselling had been resolved (thus improved).
Despite its limitations, this study represents a scientifically rigorous evaluation of an individual counselling intervention in a humanitarian setting, in that it includes a randomised waitlisted group to avoid overestimating improvements due to the effect of time alone. We were also able to show that the improvements due to the intervention were maintained and continued to improve at 3 and 6 months after completion of the intervention. This approach both improved functioning in daily life and reduced symptoms of mental distress including anxiety and depression, while decreasing the prevalence of PTSD in adults in Chechnya with similar effect sizes to other interventions. In parallel with the PM+ guidelines, we have shown that low-intensity MH interventions in humanitarian settings play an important role in improving functioning and reducing psychosocial distress. Further research is needed to determine whether similar results can be shown in acute conflict settings and where less experienced/trained counsellors deliver the intervention. Additionally, further exploration on the impact of individual counselling in men specifically would be important as they are frequently under-represented in studies in this area.
The study was registered with the Netherlands Trial Register (http://www.trialregister.nl/trialreg/index.asp), which is recognised by the WHO and the International Committee of Medical Journal Editors (ICJME) under registration number NTR4689 (http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=4689). The protocol is available from http://fieldresearch.msf.org/msf/bitstream/10144/618741/1/1326_MSFH+MH+Chechnya+outcomes+evaluation+protocol_amendment+November+2016_clean_final.pdf.
We would like to extend our thanks to all the counsellors of the MSF Mental Health Programme in Grozny for their continued dedication and support to the population of Chechnya in confronting and alleviating mental health problems. We would like to thank the Directors of Hospital 7, Hospital 9 and the Regional Hospital in Grozny for allowing this study to take place in these locations. We would like to thank Marise Denault for critical review of the manuscript. Clare Griffith provided editorial assistance to this manuscript. Finally, we would like to thank all study participants for their contribution to this study.
Contributors BL-C, LS, CB, KI, PAB and GP designed the study. CF, ZT, GP and AL acquired the data. CF, CB and AL analysed the data. All authors contributed to the interpretation of data. AL, BL-C and GP wrote the manuscript, and all authors critically reviewed the manuscript.
Funding All research was carried out by MSF staff as part of their roles.
Disclaimer The findings and conclusions in this report are those of the authors and do not represent the official position of the Centers for Disease Control and Prevention. The corresponding author had full access to all the data in the study and is the final responsible.
Competing interests None declared.
Patient consent Not required.
Ethics approval The study protocol was reviewed and approved by the MSF Ethical Review Board and the Ethical Review Board in Chechnya State University. The study protocol was also reviewed at CDC and determined to meet the criteria for non-engagement of CDC staff inhuman subjects’ research.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement MSF has a managed access system for data sharing. Data are available on request in accordance with MSF’s data sharing policy. Requests for access to data should be made to firstname.lastname@example.org.
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