alexa Brief Cognitive-Behavioural Therapy for Methamphetamine Use among Methadone-Maintained Women: A Multicentre Randomised Controlled Trial | Open Access Journals
ISSN: 2155-6105
Journal of Addiction Research & Therapy
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Brief Cognitive-Behavioural Therapy for Methamphetamine Use among Methadone-Maintained Women: A Multicentre Randomised Controlled Trial

Zahra Alammehrjerdi1*, Nadine Ezard2,3, Philip Clare4, Atena Shakeri5, Nima Babhadiashar5, Azarakhsh Mokri5and Kate Dolan1

1Program of International Research and Training, National Drug and Alcohol Research Centre, School of Public Health and Community Medicine, University of New South Wales, Sydney, Australia

2Alcohol and Drug Service, St Vincent’s Hospital, Sydney, Australia

3St Vincent’s Clinical School, University of New South Wales, Sydney, Australia

4National Drug and Alcohol Research Centre, School of Public Health and Community Medicine, University of New South Wales, Sydney, Australia

5Iranian National Centre for Addiction Studies, Iranian Institute for Reduction of High-Risk Behaviours, Tehran University of Medical Sciences, Tehran, Iran

*Corresponding Author:
Zahra Alammehrjerdi
National Drug and Alcohol Research Centre
University of New South Wales
Sydney 2052, Australia
Tel: +61(2) 93850333
Fax: +61(2) 93850222
E-mail: [email protected]

Received date: August 04, 2016; Accepted date: August 24, 2016; Published date: August 31, 2016

Citation: Alammehrjerdi Z, Ezard N, Clare P, Shakeri A, Babhadiashar N, et al. (2016) Brief Cognitive-Behavioural Therapy for Methamphetamine Use among Methadone-Maintained Women: A Multicentre Randomised Controlled Trial. J Addict Res Ther 7:294. doi:10.4172/2155-6105.1000294

Copyright: ©2016 Alammehrjerdi Z, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.


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Objective: Addressing co-existing methamphetamine (MA) use disorder in methadone treatment services can improve treatment adherence and outcomes. This study aimed to assess the feasibility and efficacy of brief cognitive-behavioural therapy (BCBT) on MA use disorder among a group of methadone-maintained women.
Methods: In this multicentre randomised controlled trial, women who had been stabilised on at least three months of methadone treatment and reported at least weekly MA use were enrolled from four methadone treatment centres in Iran and randomly assigned (1:1) to receive either BCBT or standard drug information for four weeks. The primary outcome was self-reported number of days of MA use over the treatment period. Outcomes were assessed at weeks 0, 4 and 12. Urinalysis was used to confirm self-reported abstinence from MA at weeks 4 and 12.
Results: Overall, 120 women were enrolled and randomised; 60 were assigned to the BCBT group and 60 to the control group. Only 16 women were lost to 12 week follow-up. The BCBT group had significant reductions in number of days of MA use, quantity/frequency of MA use and severity of MA dependence at week four. MA use reduction was accompanied with significant improvements in readiness to change MA use, psychological well-being and social functioning following intention-to-treat analysis. All results remained significant at 12 week follow-up.
The study results supported the feasibility and efficacy of BCBT in reducing MA use disorder and improving the health and social contexts of the participants. The findings of this study may assist methadone treatment providers to better understand the role of BCBT for co-existing MA use disorder among women in methadone treatment services.


Cognitive-behavioural therapy; Iran; Methamphetamine; Methadone; RCT; Women


Co-existing methamphetamine (MA) use disorder among methadone clients is a global health concern [1,2]. Amphetamine-Type Stimulants (ATS) including MA are the major illicit drugs used by over 20% of those in drug treatment in Asian countries, 12% in North American region and nine percent in the European region [1]. These statistics are concerning in light of poor treatment outcomes and high treatment costs [3,4].

MA use disorder is common as an important health problem among methadone-maintained women in Iran [5,6]. Among female methadone-maintained clients, MA use is associated with greater depression and dependence and lower treatment retention than men [1,2]. Therefore, it is critical to deliver MA treatment for this group before poor treatment outcomes occur.

To date, there is no any approved pharmacotherapy for MA use disorder [7]. Long-term psychosocial treatments such as the Matrix Model and contingency management are the main interventions [8,9]. These treatments are resource intensive and expensive [10]. Existing literature shows that such treatments have produced moderate effects in terms of either reducing or ceasing MA use. Furthermore, attrition rates are high [10].

In recent years, brief cognitive-behavioural therapy (BCBT) has been suggested as a new treatment for ATS use disorder. This is because BCBT has a strong potential to overcome operational barriers to implementation and suggests numerous advantages over existing psychosocial treatments [11]. BCBT aims to reduce or cease substance use and harms by enhancing client skills, motivation and commitment to change substance use behaviour [11]. BCBT offers increased feasibility compared with existing psychosocial treatments, requiring shorter training and less staff time for delivery. Second, BCBT consists of practical skills that can be implemented with high fidelity in drug treatment settings. Finally, the ability of BCBT to incorporate motivational enhancement therapy and CBT elements creates an interactive environment which can foster high client engagement [11,12].

BCBT was first devised for amphetamine use in Australia in 2001 [11]. In two randomised controlled trials in Australia, BCBT was found to be more effective than drug education in reducing regular amphetamine use, sustained at six-month follow-up [12,13]. Although these preliminary results are promising, an important next step is to evaluate the feasibility and efficacy of BCBT in the treatment of MA use disorder. Evaluation can also help determine the generalizability of BCBT to methadone treatment services [12,13]. As female methadonemaintained clients are more likely to suffer from the side effects of MA use disorder than men [14], the current study aimed to evaluate the effects of BCBT on a group of these women.



A multicentre, randomised, controlled trial (RCT) was conducted in Tehran, Iran in 2014-2015. The study design included baseline assessments, four weeks of BCBT and standard drug information, and a 12 week follow-up. The study settings included four central methadone treatment clinics which were under the supervision of the Ministry of Health (MoH) and reported high rates of MA use among their clients to MoH. The study was approved by the University of New South Wales (HC13310) in Australia, Tehran University of Medical Sciences (92-04-49-25491) and the Iranian National Centre for Addiction Studies (25491). The study was registered with Iranian Clinical Trial Registry (2015-0914-24012-N1).

Participants and recruitment

Participants were women enrolled in methadone treatment at the study sites who were at least 18 years of age and reported regular MA use. Regular MA use was defined as at least weekly use (a score of 0.14 or more on the MA items of the Opiate Treatment Index (OT) [15]. Participants were also required to provide urine specimens and report a stable methadone dose for at least three months prior to recruitment. Additional concomitant substance use was not a reason for exclusion. Participants were excluded if they reported severe medical and/or psychiatric conditions or engagement with CBT within the past 12 months.

Potential participants were identified by the centre managers and were referred for screening. Participation was confidential and voluntary. Participant screening and enrolment were completed by a research coordinator (a graduate psychologist). Recruitment was completed between July 28-12 Oct 2014 and 14 Jan-15 May 2015. All recruited participants provided informed consent.

Randomisation and allocation concealment

Randomisation and allocation concealment were done based on a standard guide [16]. To account for randomisation and to detect a standardised between-group mean difference of 0.20 with 80% power (p=0.05) [17], 120 participants were required. This was done to detect the between group differences in outcome measures. Participants were randomly assigned (1:1) into one BCBT group (n=60) and one control group (n=60) using STATA-9 [18]. Blocked randomisation was used for group allocation by a research coordinator.

Research team

Two trained clinicians (doctoral-level psychologists) with at least eight years of experience in providing CBT provided the treatment and control sessions. Two research assessors (masters-level clinical psychologists) completed assessments at weeks 0, 4 and 12. One nurse took urine specimens at weeks 0 and 4 and one nurse took urine specimens at week 12.


The research team was masked to the participants’ group allocation and had no connections to the study sites. The study clinicians informed participants about group allocation and the importance of concealment. Other precautionary strategies included the clinicians and research assessors considering booking arrangements and room use and participants being reminded not to talk with other participants about treatment allocation or questionnaires. There was no case of an allocation being revealed to the research team.

Treatment and control guides

The BCBT guide of Baker and colleagues in Australia [11] was used to conduct the treatment sessions. The interactive role play sessions consisted of weekly individual one-hour motivational enhancement therapy and CBT for four weeks as well as daily homework assignments [19]. The control sessions consisted of weekly individual one hour standard drug information [20].

Outcome measures

There were one primary outcome and eight secondary outcomes. For each outcome measure, it was hypothesised that the betweengroup difference was significant at week four and the results would remain significant at week 12. All of the outcome measures were assessed over the last four weeks.

Primary outcome

The primary outcome included number of days of MA use assessed by the Timeline Follow Back (TLFB).The TLFB is an internationallyused calendar that measures days of drug use. The TLFB has high reliability and validity [21]. The reliability of the TLFB has been evaluated for illicit drug users in Iran and has been found to be high (a=0.86) [22].

Secondary outcomes

The OTI was used to assess the quantity/frequency of MA use. Higher scores on the MA items indicate more frequent and higher dose MA use. A score of at least 0.14 is consistent with at least weekly use. The OTI has high reliability and validity [15]. The reliability of the OTI has been evaluated among illicit drug users in Iran and has been found to be high (a=0.85) [23].

Severity of MA dependence was assessed using the Severity of Dependence Scale (SDS). The SDS is a 5-item questionnaire and scores are in the range of 0-15. Higher scores indicate higher severity of MA use [24]. Because of no Persian version, the SDS was assessed for testretest reliability on 30 women in two-weeks which was found to be high (a=90).

Readiness to change MA use was assessed using the Contemplation Ladder (CL). The CL has a score range of 0-10. Higher scores on the CL indicate greater readiness to reduce MA use [25]. The reliability of the CL has been evaluated in a study of illicit drug users in Iran and has been found to be high (a=92) [26].

Psychological well-being was assessed using the General Health Questionnaire (GHQ-28). Scores are in the range of 0-28. Higher scores indicate greater psychiatric distress. The questionnaire has high reliability and validity [27]. The reliability of the GHQ-28 has been evaluated for illicit drug users in Iran and has been found to be high (a=0.85) [28].

Other secondary outcomes included quantity/frequency of heroin use, quantity/frequency of benzodiazepine use, social functioning, HIV risk behaviours and criminality which were assessed using the OTI. Social functioning scores range between 0 and 48. Higher scores indicate better social functioning. The sub-scale of HIV risk behaviours measures drug injecting and sexual behaviours. In this study, only the subscale of sexual behaviours was used because of no reported drug injection; the score is between 0 and 25. The criminality score ranges between 0 and 16. Higher scores in these two subscales indicate greater risk behaviours and criminality [15].


All study procedures were conducted at the study sites between 28 July 2014 and 15 September 2015. Following the completion of baseline assessments, four weeks of treatment and control sessions were conducted. The BCBT group was also given pamphlets to practice new learnt skills for two hours every day between sessions. If a homework assignment was left incomplete, it was completed in the next session.

The clinicians called participants by telephone between sessions to maintain treatment momentum. The chief investigator (Z. AM) supervised the research team weekly to monitor adherence to the study protocol. All participants received small gifts after completing the assessments. Furthermore, participants were asked to provide feedback about the sessions and homework assignments following the completion of the sessions. Those participants who were abstinent from MA at weeks 4 and 12 were also asked to provide feedback about the sessions and homework assignments at week 12.

Urine specimens were taken from all participants to detect MA use at week 0 and from those participants who reported no MA use at weeks 4 and 12. The specimens were stored in plastic urine cups and were sent immediately for laboratory analysis. This was done to double-check the likelihood of self-reported abstinence from MA at weeks 4 and 12. Urine specimens were analysed in a laboratory using Gas Chromatography/Mass Spectrometry (GC/MS).

Treatment sessions were audio-recorded and rated with participant agreement for adherence to the BCBT guide by two clinical psychologists. Control sessions were individually supervised by the same psychologists to assess adherence to the drug information materials. The rating of all sessions was based on a 0-6 Likert Scale which 0 indicated appropriate performance and six indicated high performance [29]. Psychologists were also asked to provide feedback about the fidelity assessment following the completion of rating.

Statistical analyses

Data analyses were done using the statistical software of Stata (version 13.1). Baseline equivalence between the groups was examined using Chi-square test for categorical variables, independent samples t-test and one-way analysis of variance (ANOVA) for continuous variables. To assess treatment effects on each outcome measure over time, Intention-To-Treat analysis and logistic Generalised Estimating Equations Regression Model were performed. These methods were selected for data analyses because they include all data in analysis and do not have the common limitations of Repeated Measures Analysis of Variance [30].

All analyses were adjusted for baseline scores on the outcomes. For continuous data, independent samples t-test was performed. For other variables, Wilcoxon Rank-Sum tests were performed. Each variable was tested for normality using Shapiro-Wilk tests. Variables that were non-normal were analysed using Rank-Sum tests while normally distributed variables were analysed using t-test.

To account for the treatment effects, Cohen’s effect size was calculated. An effect size of 0.3 indicates a small statistical effect while an effect size of 0.5 indicates a moderate statistical effect and an effect size of 0.8 or higher indicates a large statistical effect. A series of sensitivity analyses and multiple imputation models are recommended methods for handling missing data related to attrition in RCTs [31]. In this study, multiple imputation models were not feasible because of a low rate of attrition. Therefore, Little’s MCAR test was performed. Furthermore, sensitivity analyses were performed to examine the impacts of attrition on the outcome measures.


The flowchart related to the participants through each stage of the study is presented in Figure 1. All of the enrolled participants consented into the study and completed either the BCBT or the control sessions.


Figure 1: CONSORT flow chart of recruitment and trial completion.

Baseline equivalence

The baseline characteristics were similar between the two groups. No participant had a history of MA injection. All participants smoked MA. However, participants in the BCBT group were more likely to be separated (p<0.05) and report lifetime imprisonment (p<0.05) than the control group (Table 1).

Characteristics BCBT group, n=60 Control group, n=60 p value
Mean age, years 39.1 (SD 9.9) (range: 21-70) 38.5 (SD 7.9) (range: 20-60)  
<12 years 50 (83.3%) 50 (83.3%)  
12 years 7 (11.7%) 8 (13.3%)  
13-16 years 3 (5%) 2 (3.3%)  
Partner status      
Living with partner 16 (26.7%) 15 (25.0%)  
Never partnered 5 (8.3%) 14 (23.3%)  
Separated 11 (18.3%) 3 (5.0%) 0.05*
Divorced 28 (46.7%) 28 (46.7%)  
Employment status      
Home duties 22 (36.7%) 16 (22.7%)  
Jobless 36 (6.0%) 35 (85.3%)  
Paid employment 2 (3.3%) 9 (15.0%)  
Lifetime imprisonment 16 (26.6%) 9 (15.0%) 0.05*
Duration of MA dependence (years) 5.3 (SD 2.6) 5.5 (SD 1.5)  
Heroin smoking 14 (23.3%) 17 (28.3%)  
Benzodiazepine ingestion 9 (15.0%) 11 (18.3%)  
Mean methadone dose (mg)1 70.7 (SD 28.1) 61.1 (SD 24.9)  
Mean range of methadone dose (mg)1 10-165 15-115  
Duration of methadone treatment, month 26 (SD 19.5) 24 (SD 13.4)  

Table 1: Baseline characteristics of the participants, 1 Last three months.

Treatment effects

Primary outcome

As presented in Table 2, the two groups were almost similar at week 0. There were significant reductions in the mean number of days of MA use per week in the BCBT group (z=8.10, d=0.74, p<0.001) while the control group showed no significant reduction. This result remained significant at week 12 (z=8.49, d=0.78, p<0.001) (Table 2).

Characteristics OR (95% CI) group time*, mean (SD) or n (%) test results P value Effect (d)
  BCBT group Control group      
Days of MAË¡ use per week*          
Baseline 3·88 (3·50, 4·25) 3·75 (3·50, 4·25) - - -
Treatment 1·50 (0·00, 2·00) 3·00 (2·50, 3·50) z=8·10 0·001 0.74
Follow-up 1·25 (0·00, 1·75) 4·00 (3·75, 4·50) z=8·49 0·001 0.78
Quantity/frequency of MA use*          
 Baseline 1·00 (0·33, 2·00) 0·94 (0·66, 1·27) - - -
 Treatment 0·12 (0·00, 0·25) 1·00 (0·64, 1·25) z=7·79 0·001 0.71
 Follow-up 0·11 (0·00, 0·25) 1·00 (0·66, 1·33) z=7·27 0·001 0.66
Severity of MA dependence†          
 Baseline 9.98 (9.43,10.54) 10.23 (9.65-10.82) - - -
 Treatment 5.40 (4.62, 6.18) 10.97 (10.28, 11.66) t (118)=10.71 0.001 1.96
 Follow-up 5.25 (4.47, 6.03) 10.58 (10.30, 11.40) t (118)=11.73 0.001 2.14
Readiness to changeMA use *          
 Baseline 5·00 (4·00, 5·00) 4·00 (3·00, 4·50) - - -
 Treatment 8·00 (7·50, 10·00) 4·00 (3·00, 5·00) z=-9·31 0.001 0.85
 Follow-up 8·00 (7·00, 10·00) 4·00 (3·00, 4·00) z=-8·96 0.001 0.82
Psychological well-being†          
 Baseline 16.72 (15.66,17.77) 16.28 (15.32,17.25) - - -
 Treatment 8.52 (7.66,9.38) 15.60 (14.82,16.38) t(118)=12.20 0.001 2.23
 Follow-up 10.27 (9.57,10.96) 17.20 (16.44,17.96) t(118)=13.50 0.001 2.47
Social functioning*          
 Baseline 25.50 (21.50, 28.00) 20.00 (18.00, 22.00) - - -
 Treatment 25.00 (21.00, 28.50) 19.50 (17.00, 21.00) z=-5.87 0.001 -0.54
 Follow-up 25.50 (21.50, 28.00) 20.00 (18.00, 21.00) z=-6.30 0.001 -0.58
High risk sexual behaviours*          
 Baseline 4.00 (2.00,10.00) 5.50 (4.00,10.00) - - -
 Treatment 4.00 (2.00,9.00) 5.00 (3.00,9,00) z=1.36 0.173 0.12
 Follow-up 5.00 (3.00,9.00) 5.00 (3.50, 9.00) z=0.78 0.433 0.07
 Baseline 0.00 (0.00,2.00) 1.00 (0.00,2.00) - - -
 Treatment 0.50 (0.00, 2.50) 1.00 (0.00,2.00) z=0.53 0.595 0.05
 Follow-up 1.00 (0.00, 2.00) 0.00 (0.00, 1.00) z=-1.43 0.153 -0.13

Table 2: Treatment outcomes, Ë¡ MA:Methamphetamine; * Data not normally distributed: median and interquartile range presented and difference tested with Wilcoxon rank-sum test; † Data normally distributed: mean and 95% confidence interval are presented and difference tested with independent samples t-test.

Secondary outcomes

There was a significant reduction in the mean score of MA use on the OTI in the BCBT group at week 4 (z=7.79, d=0.71, p<0.001) which remained significant at week 12 (Table 2). Furthermore, the severity of MA dependence significantly declined in the BCBT group at week 4 (t (118)=10.71, d=1.96, p<0.001). There were also significant improvements in readiness to change MA use (z=-9.31, d=0.85, p<0.001), psychological well-being (t (118) =12.20, d=2.23, p<0.001) and social functioning in the BCBT group at week 4 (z=-5.87, d=-0.54, p<0.001). These results remained significant in the BCBT group at week 12. However, the control group showed no significant changes over the same time (Table 2).

No significant score differences in high risk sexual behaviours and criminality were detected between the two groups due to the small number of participants reporting these problems (Table 2). Furthermore, 31 participants reported heroin use at week 0. Overall, 24 and 21 participants in the two groups reported heroin use at weeks 4 and 12 respectively. Additionally, 20 participants reported benzodiazepine use at week 0. Overall, 16 and 12 participants reported benzodiazepine use at weeks 4 and 12 respectively. Due to the small numbers of heroin and benzodiazepine users, the score differences between the groups were zero in the statistical model which indicated no significant changes at weeks 0, 4 and 12. Therefore, data have not been shown in Table 2.


Urine specimens were taken from those participants who reported no MA use (n=20) at weeks 4 and 12. All twenty participants reporting no MA use were in the BCBT group and nineteen of them (31.6% of the BCBT group) provided urine specimens at week 4 which were negative for MA. No participant in the control group reported abstinence from MA. Therefore, no urine specimen was collected. These results remained stable at week 12.

Attrition analyses

The overall attrition rate was low (i.e., 13.3%). All participants completed the treatment and week four assessments; and only seven participants (11.6%) in the BCBT group and nine participants (15%) in the control group were lost to follow-up. Attrition analyses were performed to determine whether participants that were lost to followup were different from others. The result of Little’s MCAR test was not significant (χ2 (23)=14.941, p=0.897). There were no significant associations between attrition and the study outcomes.

Participant and psychologist feedback of the sessions

All participants in the BCBT group evaluated the treatment favourably, with over 71% indicating that the treatment was a feasible method to reduce MA craving and relapse and they planned to use the learnt skills in their own lives. Participants in the control group (n=60) evaluated the sessions favourably, with over 83% indicating that the sessions were enjoyable to them. The psychologists who did the fidelity assessments reported that all sessions were satisfactory (100%). They reported that 82% of the sessions were conducted with high quality and the remaining sessions (18%) were held at an acceptable level.

Participant evaluation of homework assignments

Overall, 39 participants (62%) completed homework assignments at home. They reported that homework assignments were needed to maintain the treatment effects. Twenty one participants (51%) completed homework assignments in sessions and they reported the same. Those participants who ceased MA use reported completing all homework assignments. All of them rated homework assignments as effective methods to maintain the treatment effects.


To the best of our knowledge, this RCT is among the few studies that has specifically evaluated the effects of BCBT in reducing MA use disorder in methadone treatment services. While MA use disorder is a current global health concern, there are few RCTs of effective psychological treatments for this problem [10]. Therefore, the present study makes a significant contribution to the literature by addressing recommendations to invest in MA use treatment [10,32].

Results of this RCT revealed that BCBT had significant treatment effects on some primary and secondary outcomes. In terms of MA use, BCBT had moderate treatment effects on reducing days and quantity/ frequency of MA use as well as significant treatment effects on readiness to change MA use. Furthermore, there were a substantial treatment effect with a considerable effect size on social functioning and strong treatment effects with large effect sizes on reducing severity of MA dependence and improving psychological well-being. These results reinforce the conclusion that the trial was sufficiently powered to detect treatment effects at reliable statistical levels. These findings are also consistent with the results of other similar RCTs in terms of both significance and magnitude of effects [12,13,32]. Importantly, the link between reduced psychostimulant use and improved measures in other domains such as psychiatric distress and social functioning has been recently supported by research studies [33]. It will be important to replicate this study to assess the magnitude and sustainability of these treatment effects over longer follow-up periods.

Part of the positive treatment effects can be related to the combination of BCBT with homework assignments. Participants reported that homework assignments as part of treatment were reliable methods to reduce MA use and relapse. In fact, participants in the BCBT group were engaged in learning the techniques related to MA refusal skills, relapse prevention and craving management on a daily basis. Therefore, homework assignments were likely to create great opportunities to generalise the learnt CBT skills in the treatment sessions to real-world situations. We found no similar study to compare this study result with. In particular, it will be important to assess whether the effects of homework assignments can be translated into behavioural changes in methadone treatment settings at later time points.

The link between reduced psychostimulant use and improved measures in concurrent heroin and benzodiazepine use, high risk behaviours and criminality has been supported by research evidence [12]. In these domains, numbers were too small to assess apart from sexual risk behaviour and criminality which showed no significant changes. This issue has been reported elsewhere [34], and may be related to the retention of participants on a stable methadone dose and the effectiveness of methadone treatment in reducing these problems.

Although the study aimed to assess the effects of BCBT on reducing MA use disorder, 19 participants became completely abstinent from MA. This may be related to high motivations to change among successful participants, their enhanced engagement in the treatment procedure and their success in generalising the learnt CBT skills to real-world situations. This is particularly important given previous findings from a large RCT of 871 MA-dependents indicated that high client engagement in CBT was associated with sustained abstinence from MA and providing negative urine specimens for MA use at 12 and 36 month follow-ups [35].

Strengths of the study include the rigorous design and the strong follow-up rates. The study not only provides important information about the efficacy of BCBT in reducing MA use disorder but also adds to the treatment science field, in which there is a current paucity of RCTs. The attrition rates were low in the two groups which primarily imply the internal validity of the study. A low attrition rate indicates high client engagement in the study procedure, reduced bias and increased generalizability of the results [32]. High retention in studies of psychostimulant users in methadone treatment and CBT has been demonstrated elsewhere [36]. This finding may suggest the high clinical utility of BCBT delivered through the methadone programme.

A further strength is fidelity data which indicate that the sessions were conducted well, primarily due to their feasible nature which ensured that core study components were retained within methadone treatment centres. This is important given the strong link between high quality implementation and study outcomes [37] and lends support to the feasibility of BCBT to deliver treatment. Furthermore, participant feedback confirmed their positive perceptions of the trial.

Results must be interpreted in the context of several limitations which warrant discussion. The study was limited to methadonemaintained women. Therefore, the findings may not necessarily be generalizable to other clinical populations and settings. Furthermore, the study was limited to one follow-up. This was related to no enough fund. Because of the high potential risk of MA relapse, 24 week and 36 week follow-ups are required to investigate the sustainability of the BCBT effects on participants. The other limitation is the use of self-report data which are subject to recall and social desirability bias. Nonetheless, self-report is a valid method for measuring illicit drug use [38]. In this study, assurances of confidentiality were provided and women voluntarily participated in the study, factors both of which have been indicated to enhance the accuracy of self-report [38].


In summary, we found that BCBT was feasible and efficacious for addressing co-existing MA use disorder and the associated harms among our participants. Importantly, reduced severity of MA dependence and psychological health appeared to be more influenced by BCBT compared with other domains in this study. These findings may have important clinical implications for the treatment of MA use disorder among this group. The treatment of MA use disorder among methadone-maintained women may be facilitated by integrating BCBT into methadone treatment services. This issue should be investigated by conducting more studies.


The authors would like to thank National Drug and Alcohol Research Centre (NDARC) in Australia.

Competing Interests

All authors have no competing interests.


The study was supported by a fund (HC13310) from NDARC through a postgraduate research scholarship to Z. AM in Australia.


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