Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Interventions to improve medication adherence in tuberculosis patients: a systematic review of randomized controlled studies


Non-adherence to anti-tuberculosis (anti-TB) medication is a major risk factor for poor treatment outcomes. We therefore assessed the effectiveness of medication adherence enhancing interventions in TB patients. We report a systematic review of randomized controlled trials that included either latent tuberculosis infection (LTBI) or active TB patients. Outcomes of interest included adherence rate, completed treatment, defaulted treatment and treatment outcomes. We identified four LTBI and ten active TB studies. In active TB patients, directly observed treatment (DOT) by trained community workers, short messaging service combined with education, counselling, monthly TB vouchers, drug box reminders and combinations of those were found effective. In LTBI patients, shorter regimens and DOT effectively improved treatment completion. Interestingly, DOT showed variable effectiveness, highlighting that implementation, population and setting may play important roles. Since non-adherence factors are patient-specific, personalized interventions are required to enhance the impact of a programme to improve medication adherence in TB patients.


Tuberculosis (TB) remains an important worldwide health issue. World Health Organization (WHO) reported that TB is the cause of illness for around 10 million people every year and has been ranked among the top ten causes of death globally1. TB, caused by Mycobacterium tuberculosis, can be spread easily from patients suffering from pulmonary TB to healthy people by air transmission1. Consequently, anti-TB drug treatment is required for TB patients to cure the disease and prevent disease transmission.

Comparable to other complex diseases, TB patients have to be treated with several drugs for a long period. According to the WHO guideline, active pulmonary TB patients should take drugs for at least 6 months2, while latent tuberculosis infection (LTBI) patients should take drugs for at least 3 months3. The treatment duration can be extended if TB patients are diagnosed as multi-drug resistant tuberculosis (MDR-TB), a resistance of the pathogen to the most potent anti-TB medicines (isoniazid and rifampicin). MDR-TB treatment can be up to 24 months using multiple drugs4.

Poor adherence to medication is widely known as a causal factor for increased risk of morbidity, mortality and cost burden5,6,7. A global meta-analysis revealed that non-adherence to treatment is a risk factor for MDR-TB8. Furthermore, MDR-TB patients, as compared to drug-susceptible patients, have more frequently poor treatment outcomes9,10. Treatment adherence is affected by multiple factors. These factors are divided into five different interacting dimensions, including socio-economic, health care system, condition, therapy and patient factors11. Although studies on adherence in other diseases than TB showed that interventions targeting these factors can significantly improve adherence rates12,13,14, a better understanding of the effects of possible interventions in TB is required. We therefore systematically reviewed the effectiveness of various interventions to improve medication adherence in LTBI and active TB patients.


Study selection

During the search, we found 200 records from the Medline/PubMed database and 186 records from the Cochrane database. We identified 72 duplicate records using the Refwork® software. A total of 314 articles were screened for the title and abstract. This initial screening excluded 268 irrelevant records, then the full-text screening process was continued for 46 records. In the full-text screening, 32 articles were excluded owing to different populations (3 articles), different study outcomes (12 articles) and non-randomized study design (17 articles). We finally analysed 14 studies for qualitative synthesis. The flow diagram, literature search and screening process are presented in Fig. 1.

Fig. 1: Flow diagram of the included articles.

The PRISMA flowchart reporting the number of papers identified, screened, excluded and included.

Study characteristics and interventions

In total, 15,507 subjects were included in the analysis. In all, 1991 LTBI patients and 13,516 active TB patients participated. The minimum number of subjects in the included studies was 89, while the maximum number was 4154 subjects. The included studies were conducted in both low- and high-burden TB countries, i.e. Pakistan15,16, Australia17, Iraq18, China19,20, Senegal21, South Africa22,23,24, Timor Leste25, Canada26, United States24,27, Spain24, Hong Kong24 and Mexico28.

The 14 randomized controlled trials (RCTs) assessed a broad range of adherence management interventions. These included Short Message Service (SMS) intervention15,16,18,19,20,24, directly observed treatment (DOT) administered by health care workers24, family members17 and non-health care worker communities18,22, a reinforced counselling method21, a trained lay health workers intervention to manage TB case22, monthly TB vouchers23, a drug box reminder20, a combination text messaging and drug box reminder20, a nutritious intervention25, shorter regimen26, a peer-based intervention27 and a behavioural intervention28. The characteristics of the included studies are shown in Table 1.

Table 1 Characteristics of the included articles.

Study outcomes

In the active TB patients, the primary outcomes were treatment completion15,16,17,19,22,23, interrupted rate15,16,18,21,23 and adherence rate20,25, while the other outcomes were negative sputum conversion18,19, cured18,21 and poor treatment outcomes20. In the LTBI studies, we observed that treatment completion was the only outcome. Regarding the intervention effect, not all interventions significantly improved drug adherence and treatment outcomes. Several interventions were found effective in improving medication adherence and outcomes of active TB patients, i.e. DOT by trained community members, SMS combined with TB education, a reinforced counselling method, monthly TB voucher, drug box reminder and a combination drug box reminder and text messaging. However, only two studies reported adherence rate as the study outcome20,25. We identified that a drug box reminder (mean ratio (MR) 0.58; 95% confidence interval (CI) 0.42 to 0.79) and its combination with text messaging (MR 0.49; 95% CI 0.27 to 0.88) significantly reduced missing a drug dose among active TB patients20, while food incentives were not significantly different from the comparator for the intensive (MR −4.7; 95% CI −0.8 to −8.6) and continuation phase (MR 0; 95%CI −1.7 to 1.7) in the active TB patients25, see Table 2.

Table 2 Effect of the intervention on the study outcomes in active tuberculosis patients.

In the LTBI patients, shorter regimens and DOT interventions significantly improved treatment completion. We identified that 4 months of daily rifampicin 10 mg/kg was more effective to improve treatment completion than 9 months of daily isoniazid 5 mg/kg (relative risk (RR) 1.2; 95% CI 1.02–1.4)26, while DOT intervention was more effective to improve treatment completion than self-administration therapy (SAT) with monthly monitoring (RR 1.18; 95% CI 1.09–1.27)24. In contrast, several interventions such as SAT with weekly text message reminders plus monthly monitoring (RR 1.03; 95% CI 0.95–1.13)24, a peer-based intervention (RR 1.06; 95% CI 0.86–1.31)27, adherence coaching intervention (RR 1.36; 95% CI 0.98–1.88)28 and self-esteem counselling (RR 1.12; 95% CI 0.78–1.58)28 did not significantly improve treatment completion in LTBI patients, see Table 3.

Table 3 Effect of the interventions on the study outcomes in latent tuberculosis infection (LTBI) patients.

Quality assessment of the included studies

A double-blinding method was either not possible or not applied for most of the included studies. This is due to the fact that intervention activities were impossible to blind, such as SMS reminders, DOT, counselling, monthly vouchers, drug box reminders, food incentive and peer-based intervention. Often, an open-label design was applied. Therefore, none of the included had a maximum JADAD score (five points). Three points of the JADAD score was the maximum score among the included studies because none of the studies applied the blinding method. Five of the 14 studies had the lowest JADAD score (2 points) due to the absence of a description of randomization procedure17,18,19,27,28. The other studies had a higher score (three points) given they appropriately described the randomization method and clearly illustrated the withdrawals of participants15,16,20,21,22,23,24,25,26. The risk of bias assessment is presented in Table 4.

Table 4 Risk of bias assessment for randomized studies using the JADAD score.


We observed various interventions that were successful in improving medication adherence and outcomes in TB patients. The interventions targeted several factors of adherence, such as socio-economic, patient, health care and treatment aspects. The effective interventions to improve treatment completion in active TB patients were DOT with daily home visits by community-trained members, SMS reminders combined with TB education, a reinforced counselling method and a monthly voucher intervention. In LTBI patients, DOT and a shorter regimen significantly improved treatment completion. We identified that the drug box reminder or its combination with text messaging reminders significantly improved medication adherence rates among active TB patients, while no studies were found showing an effective intervention to improve medication adherence rate in LTBI patients. In contrast, we found that some interventions, such as SMS reminders or its combination with motivational messages, family DOT, involving trained lay health workers in TB management, and food incentives were not significantly different compared with the comparator groups regarding improving treatment completion and outcomes in active TB patients. Similarly, we identified SMS reminders combined with monthly monitoring, peer-based intervention, coaching adherence and self-esteem counselling were not effective in improving treatment completion in LTBI patients.

Interestingly, interventions using DOT showed variable effects on the study outcomes. Family DOT17 were not superior in the improvement of treatment outcomes among active TB patients, while institutional DOT significantly improved treatment completion in LTBI patients. Unfortunately, a meta-analysis of the crude data was impossible, because heterogeneities were identified across the included studies with regard to population, intervention and study outcomes. However, a previous meta-analysis stated that the understanding of resources and situations in which DOT can be beneficial is an essential part of successful implementation of DOT29. Furthermore, the interaction between DOT providers and TB patients may also influence the effect on medication adherence and outcome. Therefore, the differences of resources, situation and interaction between DOT providers and TB patients may indicate that the effects of interventions can vary across studies and settings.

Generally, the differences in observed effect sizes of the interventions in this review can be explained by several aspects: (1) characteristics of the subjects, (2) measurement method of the adherence (outcome), (3) characteristics of the comparator group, and (4) the quality of the study design and intervention. According to WHO11, adherence is a multidimensional phenomenon that can be determined by the interaction of the five essential factors, i.e., socio-economic, provider–patient/health care system, condition related, therapy related and patient related. Since the essential causal factors for poor adherence can be individual, assessing the individual non-adherence factors is a critical approach to have effective personalized interventions to increase medication adherence. The most optimal intervention to improve medication adherence should not be “one-size-fits-all”. As an example, an intervention using SMS reminders for taking medicine may not be effective if the individual problem of medication adherence is mainly caused by inaccessibility of the patient to have a qualified medicine.

In terms of outcome measurement, heterogeneity was shown in the included studies. Most of the studies used a treatment completion parameter measured by temporary patient visits or self-reported/medical documentation as the outcome parameter for medication adherence. An implication of this is the possibility of misclassification of medication adherence. The measurement did not represent the daily consumption of the medicines during the treatment phase. Hence, potential information bias is high in the studies that used temporary patient visits or self-reported/medical documentation to assess medication adherence. The accuracy of adherence measurement in TB patients was reported in a systematic review30. Methods to measure adherence can be categorized as direct (e.g. DOT, ingestible sensors, drug or metabolites measurements) and indirect (e.g. patient self-report, pill counts, health information system, electronic pill bottles and SMS). Currently, digital adherence technologies have been developed that offer large potential to measure and improve medication adherence in TB patients31. The technology potentially facilitates monitoring of adherence that provides a more patient-centric approach than the existing DOT32. The digital technology for monitoring medication adherence of TB patients was reported in the form of video observed therapy and electronic medication monitoring33. Measurement of medication adherence was also reported using pharmaceutical databases33. However, considering the accuracy and validity, direct measurement should be preferably used for measuring medication adherence in an interventional study.

There were some variations in the comparator group in the included studies, which may also have affected the validity of the findings. We noted that self-administration of treatment without supervision and DOT were the comparator groups in the included studies. Theoretically, the effect of the studied intervention will be higher in the studies that used self-administration without supervision as the comparator group instead of DOT. A previous study showed that DOT was more effective than SAT in the improvement of treatment adherence34 and DOT was also recommended by WHO for improving treatment adherence in TB patients34. It is possible, therefore, that using different comparators to compare two or more intervention studies will lead to an under- or over-estimation.

Another aspect, which may explain the variations in the results of studied interventions, is the quality of the included studies. Among the randomized studies, the randomization method was unclear in five studies17,18,19,27,28. The investigators did not describe how the random allocation was conducted. In most of the included studies, blinding was impossible. Since the intervention involved direct activities with the research subjects such as reminders, counselling, education and incentives, performing a blinding procedure was impossible. In addition, the quality of implementation of the intervention is also essential. For instance, in DOT studies, the ability of the treatment observer to improve medication adherence of TB patients will affect the success of the intervention. As previously described, the interaction between treatment observer and TB patients should therefore be considered in order to understand potential changes in medication adherence.

Several limitations to our review should be acknowledged. First, the review was based on the two databases with restriction to English publications and searching period, hence not all the intervention studies may be covered in this study. However, to the best of our knowledge, the vast majority of relevant studies are published in the English language and recent trials incorporated knowledge from the potential trials before 2003. Second, only a few studies used adherence rate as the study outcome. Most of the studies mentioned treatment outcomes (i.e. sputum conversion, cured and poor treatment outcome) but did not include sufficient detail on medication adherence as the study outcome. Since treatment outcomes were associated with medication adherence in previous studies5,6,8, we included treatment outcomes as the secondary outcomes in this review. Therefore, the effectiveness of the interventions to improve medication adherence, as reported in the studies, should be carefully interpreted, and clearly high-quality intervention studies should be developed in the future. Lastly, in order to assess intervention effects in a homogeneous population regarding patient characteristics, this review excluded interventions in more complex or high-risk TB patients, such as those with comorbid human immunodeficiency virus (HIV), drug-resistant TB, alcoholism and illicit drug use. We acknowledge that these are, however, important subgroups regarding non-adherence, for which we recommend separate, focussed studies and reviews.

Our review highlighted various potential interventions to improve medication adherence among LTBI and active TB patients. Characteristics of the research subjects, accurate measurement of the adherence, type of the comparator group, the robustness of study design and implementation of the intervention should be considered to observe an effective and unbiased intervention for medication adherence in TB patients. Since non-adherence factors can be individual, interventions that takes into account individual patient barriers are required to have an effective medication adherence programme. Therefore, future intervention studies should use objective adherence measures and focus on the effectiveness of TB medication adherence programmes that use a more personalized approach.


Literature review

We performed a systematic review of articles that were published between January 1, 2003 and April 24, 2018 and reported in the English language. According to the study protocol, the search period was restricted to articles published from 2003 onwards because in that year the influential WHO Adherence report was published and created wide-scale awareness on the issue of non-adherence ever since11. This systematic review was reported according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidance35. The PICOS items, i.e. population, intervention, comparator, outcomes and study design, are specified in the following sections.


To be able to better distinguish between the potential impact of experienced symptoms on extent of adherence, the study population was divided into two different groups, i.e. patients with LTBI and active TB. The status of TB disease should be confirmed by clinical or laboratory examination (e.g. TB symptoms, Mantoux, IGRA, chest radiograph or other TB examination) and/or microbiological verification (e.g. smear sputum test, phenotyping drug susceptibility test or polymerase chain reaction). In order to draw conclusions based on a population as homogeneous as possible, we excluded studies restricted to specific high-risk treatment non-adherence groups, such as TB patients with HIV, drug-resistant TB, alcoholism and illicit drug use.

Interventions and comparator

Studies that analysed interventions related to improving medication adherence and treatment outcomes were included in this review. The intervention was allowed to target one or multiple factors of adherence, such as socio-economic, health care team and system, health condition, therapy or patient factors. The intervention should have a comparison group to analyse the effect of the intervention.


In terms of the study outcomes, we followed the global definition published by WHO in 201436. We defined medication adherence as the primary outcome. Of note, medication adherence consists of three phases: initiation, implementation, and persistence37. In our assessment, persistence was deemed a synonym for “completed treatment” and non-persistence was a synonym for “defaulted treatment”. Implementation was deemed similar to “adherence rate”. Moreover, we defined “cured treatment”, “negative sputum conversion” and “poor treatment” outcomes as the secondary outcome in this study.

According to the global definition, “completed treatment” was defined as a TB patient who completed treatment without evidence of failure but with no record showing that sputum smear or culture results were positive in the last month of treatment, while “defaulted treatment” was defined as an interruption of TB treatment for two or more consecutive months. “Adherence rate” was identified by the proportion of anti-TB drug dose taken during the treatment period. As the other outcomes, “cured treatment” was defined as smear or culture negative in the last month of treatment and on at least one previous occasion, while “negative sputum conversion” was defined as the conversion sputum to a negative result. Furthermore, “poor treatment outcome” is a combination of defaulted, failed treatment and death outcome. Failed treatment was defined as a positive sputum smear or culture at the fifth month after treatment initiation.

Study design

We only included RCTs. Given their increased risk for bias, quasi-experimental, cohort, cross-sectional, case–control, case reports, case series, review articles and abstract conference were not eligible for inclusion.

Data collection

The relevant articles were obtained from the Medline/PubMed and Cochrane databases with specific key terms. To effectively obtain the relevant articles, we used restriction to the following filters in the Medline/PubMed database, such as clinical trial, comparative study, controlled clinical trial, observational study, RCT and humans. Applying observational study in the Medline/PubMed filter was intended to anticipate potential RCTs in the group labelled as observational studies. Key terms for obtaining the articles can be found in Supplementary Information.

Data extraction and quality assessment

Title and abstract of the articles were screened by I.S.P. and D.H., then the full-text of the articles were assessed for the eligibility and quality by I.S.P. Duplicated articles from two databases were removed using the Refwork® software. The eligible articles were then reviewed for relevant information. Information related to year of publication, population, type of intervention, comparator group and study outcome was extracted by I.S.P. Any disagreements between the reviewers during the screening phase were solved by discussion until consensus was reached.

Regarding the quality assessment, we used the JADAD score for assessing the quality of the RCTs38. Three main domains were appraised in the JADAD score system, i.e. randomization, blinding method and subject withdrawal. The domains were assessed by five questions. For each question, a study could earn one point, with a total score of five points. The five questions are described as follows: Was the study described as randomized?; Was the method used to generate sequence of randomization described and appropriate?; Was the study described as double blind?; Was the method of double-blinding appropriately described?; and Was there a description of withdrawals and dropouts?

Summary measures and synthesis of results

The total number and group of patients with any specific outcome for both primary and secondary outcomes were extracted by I.S.P. and summarized in tables. For the point estimate of the intervention, we used RR for dichotomous outcome data and MR for continuous outcome data with a 95% CI.

Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.

Data availability

The data that support the findings of this study are publicly available through the following electronic biomedical literature databases: Medline/PubMed and Cochrane.

Code availability

No special code was described in this report.


  1. 1.

    World Health Organization. Global tuberculosis Report WHO 2018. WHO Report, Vol. 69 (WHO, 2018).

  2. 2.

    World Health Organization. Guidelines for Treatment of Drug-Susceptible Tuberculosis and Patient Care 2017 Update (World health Organization, 2017).

  3. 3.

    Jasmer, R. M., Nahid, P. & Hopewell, P. C. Clinical practice latent tuberculosis infection. N. Engl. J. Med 347, 1860–1866 (2002).

    Article  Google Scholar 

  4. 4.

    World Health Organization (WHO). Consolidated Guidelines on Drug-Resistant Tuberculosis Treatment (World health Organization, 2019).

  5. 5.

    Munro, S. A. et al. Patient adherence to tuberculosis treatment: a systematic review of qualitative research. PLoS Med. 4, 1230–1245 (2007).

    Article  Google Scholar 

  6. 6.

    Patel, A. R. et al. Burden of non-adherence to latent tuberculosis infection drug therapy and the potential cost-effectiveness of adherence interventions in Canada: a simulation study. BMJ Open 7, 1–10 (2017).

    Google Scholar 

  7. 7.

    Abolhassani, R. et al. Clinical and economic impact of medication non-adherence in drug-susceptible tuberculosis: systematic review. Int. J. Tuberc. Lung Dis. 24, 8 (2020).

    Article  Google Scholar 

  8. 8.

    Pradipta, I. S., Forsman, L. D., Bruchfeld, J., Hak, E. & Alffenaar, J. W. Risk factors of multidrug-resistant tuberculosis: a global systematic review and meta-analysis. J. Infect. 77, 469–478 (2018).

    Article  Google Scholar 

  9. 9.

    Pradipta, I. S., Van’T Boveneind-Vrubleuskaya, N., Akkerman, O. W., Alffenaar, J. W. C. & Hak, E. Treatment outcomes of drug-resistant tuberculosis in the Netherlands, 2005-2015. Antimicrob. Resist. Infect. Control 8, 1–12 (2019).

    Article  Google Scholar 

  10. 10.

    Pradipta, I. S., van’t Boveneind-Vrubleuskaya, N., Akkerman, O. W., Alffenaar, J. W. C. & Hak, E. Predictors for treatment outcomes among patients with drug-susceptible tuberculosis in the Netherlands: a retrospective cohort study. Clin. Microbiol. Infect. 25, 761.e1–761.e7 (2019).

    CAS  Article  Google Scholar 

  11. 11.

    World Health Organization. Adherence to Long-Term Therapies (World Health Organization, 2003).

  12. 12.

    Norris, S. L., Grothaus, L. C., Buchner, D. M. & Pratt, M. Effectiveness of physician-based assessment and counseling for exercise in a staff model HMO. Prev. Med. 30, 513–523 (2000).

    CAS  Article  Google Scholar 

  13. 13.

    Tutty, S., Simon, G. & Ludman, E. Telephone counseling as an adjunct to antidepressant treatment in the primary care system. A pilot study. Eff. Clin. Pract. 3, 170–178 (2000).

    CAS  PubMed  Google Scholar 

  14. 14.

    Ostrop, N. J., Hallett, K. A. & Gill, M. J. Long-term patient adherence to antiretroviral therapy. Ann. Pharmacother. 34, 703–709 (2000).

    CAS  Article  Google Scholar 

  15. 15.

    Mohammed, S., Glennerster, R. & Khan, A. J. Impact of a daily SMS medication reminder system on tuberculosis treatment outcomes: a randomized controlled trial. PLoS ONE 11, 1–13 (2016).

    Google Scholar 

  16. 16.

    Farooqi, R. J., Ashraf, S. & Zaman, M. The role of mobile SMS-reminders in improving drugs compliance in patients receiving anti-TB treatment from DOTS program. J. Postgrad. Med. Inst. 31, 156–162 (2017).

    Google Scholar 

  17. 17.

    MacIntyre, C. R. et al. A randomised controlled clinical trial of the efficacy of family-based direct observation of anti-tuberculosis treatment in an urban, developed-country setting. Int. J. Tuberc. Lung Dis. 7, 848–854 (2003).

    CAS  PubMed  Google Scholar 

  18. 18.

    Mohan, A., Nassir, H. & Niazi, A. Does routine home visiting improve the return rate and outcome of DOTS patients who delay treatment? East. Mediterr. Health J. 9, 702–708 (2003).

    CAS  PubMed  Google Scholar 

  19. 19.

    Fang, X. H. et al. Effect of short message service on management of pulmonary tuberculosis patients in Anhui Province, China: a prospective, randomized, controlled study. Med. Sci. Monit. 23, 2465–2469 (2017).

    Article  Google Scholar 

  20. 20.

    Liu, X. et al. Effectiveness of electronic reminders to improve medication adherence in tuberculosis patients: a cluster-randomised trial. PLoS Med. 12, 1–18 (2015).

    Article  Google Scholar 

  21. 21.

    Thiam, S. et al. Effectiveness of a strategy to improve adherence to tuberculosis treatment in a resource-poor setting: a cluster randomized controlled trial. J. Am. Med. Assoc. 297, 380–386 (2007).

    CAS  Article  Google Scholar 

  22. 22.

    Clarke, M., Dick, J., Zwarenstein, M., Lombard, C. J. & Diwan, V. K. Lay health worker intervention with choice of DOT superior to standard TB care for farm dwellers in South Africa: a cluster randomised control trial. Int. J. Tuberc. Lung Dis. 13, 921 (2009).

    Google Scholar 

  23. 23.

    Lutge, E., Lewin, S., Volmink, J., Friedman, I. & Lombard, C. Economic support to improve tuberculosis treatment outcomes in South Africa: a pragmatic cluster-randomized controlled trial. Trials 14, 1–13 (2013).

    Article  Google Scholar 

  24. 24.

    Belknap, R. et al. Self-administered versus directly observed once-weekly isoniazid and rifapentine treatment of latent tuberculosis infection. Ann. Intern. Med. 167, 689–697 (2017).

    Article  Google Scholar 

  25. 25.

    Martins, N., Morris, P. & Kelly, P. M. Food incentives to improve completion of tuberculosis treatment: randomised controlled trial in Dili, Timor-Leste. BMJ 339, 1131 (2009).

    Article  Google Scholar 

  26. 26.

    Menzies, D. et al. Treatment completion and costs of a randomized trial of rifampin for 4 months versus isoniazid for 9 months. Am. J. Respir. Crit. Care Med. 170, 445–449 (2004).

    Article  Google Scholar 

  27. 27.

    Hirsch-Moverman, Y., Colson, P. W., Bethel, J., Franks, J. & El-Sadr, W. M. Can a peer-based intervention impact adherence to the treatment of latent tuberculous infection?. Int. J. Tuberc. Lung Dis. 17, 1178–1185 (2013).

    CAS  Article  Google Scholar 

  28. 28.

    Hovell, M. F. et al. Increasing Latino adolescents’ adherence to treatment for latent tuberculosis infection: a controlled trial. Am. J. Public Health 93, 1871–1877 (2003).

    Article  Google Scholar 

  29. 29.

    Karumbi, J. & Garner, P. Directly observed therapy for treating tuberculosis. Cochrane Database Syst. Rev. 29, 1–45 (2015).

    Google Scholar 

  30. 30.

    Valencia, S. et al. How do we measure adherence to anti-tuberculosis treatment? Expert Rev. Anti Infect. Ther. 15, 157–165 (2017).

    CAS  Article  Google Scholar 

  31. 31.

    Zijp, T. R., Mol, P. G. M., Touw, D. J. & van Boven, J. F. M. Smart medication adherence monitoring in clinical drug trials: a prerequisite for personalised medicine? EClinicalMedicine (2019).

  32. 32.

    Subbaraman, R. et al. Digital adherence technologies for the management of tuberculosis therapy: mapping the landscape and research priorities. BMJ Glob. Health 3, e001018 (2018).

    Article  Google Scholar 

  33. 33.

    Alfian, S. D., Pradipta, I. S., Hak, E. & Denig, P. A systematic review of measures estimates adherence and persistence to multiple medications. J. Clin. Epidemiol. 108, 44–53 (2019).

    Article  Google Scholar 

  34. 34.

    Friedena, T. R. & Sbarbarob, J. A. Promoting adherence to treatment for tuberculosis: the importance of direct observation. Bull. World Health Organ. 85, 407–409 (2007).

    Article  Google Scholar 

  35. 35.

    Moher, D., Liberati, A., Tetzlaff, J. & Altman, D. G. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. J. Clin. Epidemiol. 62, 1006–1012 (2009).

    Article  Google Scholar 

  36. 36.

    World Health Organization. Definitions and Reporting Framework for Tuberculosis – 2013 Revision (Updated December 2014) (World health Organization, 2013).

  37. 37.

    Vrijens, B. et al. What we mean when we talk about adherence in respiratory medicine. J. Allergy Clin. Immunol. Pract. (2016).

  38. 38.

    Clark, H. D. et al. Assessing the quality of randomized trials: reliability of the Jadad scale. Control. Clin. Trials 20, 448–452 (1999).

    CAS  Article  Google Scholar 

Download references


This work was supported by the Indonesia Endowment Fund for Education or LPDP in the form of a Ph.D. scholarship to I.S.P.; this funding source had no role in the concept development, study design, data analysis or article preparation.

Author information




Conceptualization (all authors), methodology (all authors), data curation (I.S.P., D.H.), formal analysis (I.S.P., D.H.), visualization (I.S.P.), writing—original draft (I.S.P., D.H.), writing—review and editing (all authors). All authors read and approved the final manuscript.

Corresponding author

Correspondence to Ivan S. Pradipta.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Pradipta, I.S., Houtsma, D., van Boven, J.F.M. et al. Interventions to improve medication adherence in tuberculosis patients: a systematic review of randomized controlled studies. npj Prim. Care Respir. Med. 30, 21 (2020).

Download citation

Further reading


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing