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| Name | Class |
|---|---|
| Mahidol Oxford Tropical Medicine Research Unit | OTHER |
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The overall aim of this study is to compare the proportion of antimicrobial prescriptions adherent with prescribing guidelines delivered by mobile phone application (app) versus paper-based prescribing guidelines in both in- and outpatients in six hospitals in Laos.
This is an open cohort stepped-wedge cluster randomized controlled trial 3-step trial (4-month intervals at each step) with a 4-month pre-intervention period). The study conducts in six hospitals across Laos. This is 16 months-study. The intervention is a MicroGuide antimicrobial prescribing guideline mobile phone application and antimicrobial stewardship (AMS) training; whilst the reference is paper-based antimicrobial prescribing guidelines. The main outcome of interest is the proportion of antimicrobial prescriptions adherent with prescribing guidelines delivered by app-based versus paper-based prescribing guidelines at month 16 (12 months' exposure in each group). Outcome measurements are Point prevalence surveys (PPS) of hospital antimicrobial use, prescriber questionnaires and AMS knowledge survey of the prescribers. Simple random sampling will be used to select the order (step) of interventions implementation for a group of hospitals (two hospitals per group and one group per step). Neither hospitals nor investigators are blinded to the timing of intervention. Open Data Kit (ODK) system will be used as data collection instrument. All data will be kept securely, protected by password access with automatic daily backup. A logistic mixed-effects regression model will be used to compare the proportion of antimicrobial prescription adherence measured cross-sectionally at month 0, 4, 8, 12 and month 16 after introduction of prescribing guidelines delivered by mobile phone application versus paper-based. This study was approved by University of Health Sciences, Vientiane, Lao PDR and Oxford Tropical Ethics Committee (OxTREC), University of Oxford, United Kingdom.
Background Antimicrobial prescribing applications are a promising tool to improve prescribing. However, there has been no evidence from trials to support whether the antimicrobial prescribing guidelines in the format of a mobile phone application are superior to conventional means (i.e. paper-based) in low- and middle-income countries (LMIC). This trial could have a significant impact in Laos and in other LMICs, and inform policy globally, by improving prescribing and hence reducing AMR.
Objectives Primary objective To compare the proportion of antimicrobial prescriptions adherent with prescribing guidelines delivered by mobile phone application (app-based) versus paper-based prescribing guidelines in both in- and outpatients in six general hospitals in Laos
Secondary objectives are to compare:
Study intervention and reference
1. Reference phase
Study duration is divided into two parts (reference and intervention phases). The order of activities at the start of the project are listed below:
2. Intervention phase
Intervention delivery
The intervention starts at month 4 after introducing the paper-based guidelines. This intervention is introduced in one pair of hospitals at a time and repeated every 4 months. The order of the activities during intervention phase of each step are listed below:
Note:
During the intervention period, prescribers in participating hospitals still have access to paper-based prescribing guidelines distributed at the start of the study.
Contamination prevention
There is a possibility of contamination of the app to the reference group by doctors from the intervention group:
• move to the reference group (training or changing workplace)
• give smart phones to other doctors in the reference group (unlikely)
• lose smart phones that are subsequently found and used by doctors in a reference group (unlikely) To avoid or reduce the problem of contamination, all participating hospitals are requested not to share the mobile app guidelines to others while hospitals are still under evaluation. The app guidelines will be installed by the PI. This app cannot be accessed without the approval from the PI (entering passcode). The security system is controlled by the MicroGuide team and PI of the project.
Endpoints Primary endpoint: The proportion of antimicrobial prescriptions adherent with prescribing guidelines delivered by app-based versus paper-based guidelines of 12 months' exposure in each group Secondary endpoints
1. Total antimicrobial DDDs prescribed in app-based versus paper-based groups of 12 months' exposure in each group 2. Proportion of patients prescribed antimicrobials by the intravenous route in app-based versus paper-based groups of 12 months' exposure in each group 3. AMS knowledge level of prescribers prescribed in app-based versus paper-based groups of 12 months' exposure in each group 4. Prescriber satisfaction/acceptability of the guidelines in app-based versus paper-based groups of 4 months' exposure in each group 5. Total costs of antimicrobial prescribed in app-based versus paper-based groups of 12 months' exposure in each group 6. Proportion of patients admitted to hospital receiving an antimicrobial prescription before and after introduction of the paper-based; and the app-based guidelines + AMS training of 12 months' exposure in each group Definitions of adherence to the guidelines
Outcome measurement
IPD and OPD PPS data will be collected in Open Data Kit (ODK) system on patients' characteristics and treatment status. Data on the frequency of use of the mobile app can also be downloaded from the MicroGuide App. Prescribing behaviors are collected via survey forms. All data will be entered to MACRO system. Only antibiotic cost data is collected. All complete survey forms are kept securely in a locked filling cabinet. Only PI of the project and project data management team have access to the raw data. Data checking and cleaning are done by PI. Data inconsistency will be discussed with the research team immediately.
Statistical analysis A logistic mixed effects regression model will be used to compare the proportion of antimicrobial prescriptions adherence measured cross-sectionally at month 0, 4, 8, 12 until month 16 after introduction of prescribing guidelines by mobile phone application versus paper-based. The model will compare all wedges in the intervention from month 4 to month 16 with all wedges in the reference arm from month 0 to month 12. Likert scale analysis will be used to evaluate prescriber satisfaction/acceptability of paper-based compared to mobile phone app delivered antimicrobial prescribing guidelines. Mann-Whitney test will be used to assess the differences between paper-based population and mobile phone app population. The overall proportion of correct answers from AMS survey in each time point will be compared. Cost of antibiotic therapy will be calculated from the start date of treatment to the survey day. DDD will be calculated using data from PPS in both IPD and OPD.
Safety considerations/Adverse Events No adverse event monitoring is planned Ethics Ethical approvals were received from the University of Health Sciences Ethics Committee, Ministry of Health, Lao PDR and the Oxford Tropical Research Ethics Committee (OxTREC), University of Oxford, United Kingdom to conduct this project.
Benefits This first therapeutic and prophylactic antimicrobial prescribing guidelines will encourage the rational use of antimicrobials. The mobile phone application version will allow clinicians to access guidelines easier. This will help to improve clinical decision of doctors and consistency of care. This will give the potential to improve health outcomes of patients, reduce morbidity and mortality and give value for money.
Risks There might be some risk that MoH would like to introduce the guidelines and the app before the study finishes if the results are very positive. In addition, it could be challenging to manage and control the travel of Lao doctors from one hospital to another as trainings, workshops or conferences (not related to this project) are conducted across the country. Moreover, another AMR program is also conducted in three participating hospitals (Salavan, Xiengkhang and Luang Namtha) to improve the quality of infectious diagnosis in these three hospitals. This program plans to start at the same time as this project.
Patient and doctor confidentiality There will not be any record of patients' personal details to be able to identify any individual. There will not be any direct interaction between the research team and patients.
Trial insurance The University of Oxford would operate in the event of any participant suffering harm as a result of their involvement in the research.
Data sharing and dissemination Survey data from this study will be shares using AMU-Laos app (computer dashboard). Preliminary results will be shared with the Lao Ministry of Health and the Wellcome Trust. Paper reports will be shared with participating hospitals, local public health offices, and the MoH. Oral presentation and posters will be used as tools to deliver progress updates and the results of the study in national, regional and international conferences. Results will also be published in open access peer reviewed medical journals.
Finance This research is supported by the Wellcome Trust of Great Britain, UK. No funding sources have any role in study design, data collection, or preparation of the protocol.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Reference phase | No Intervention | At the start (month 0), a point prevalence surveys (PPS) on hospital antimicrobial use are performed (more details on conduct of PPS are given in following section) to collect baseline data before introducing paper-based guidelines. All medical doctors of each participating hospital are asked to complete an AMS knowledge survey and pre-prescribing guidelines survey after PPS is conducted. Then, paper-based prescribing guidelines in both adult and paediatric versions (one adult guideline and one paediatric guideline) are distributed to all doctors at participating hospitals, followed by guideline introductory session of the guidelines. After introduction of the paper-based guidelines, all six hospitals are formally included in the reference period. | |
| Intervention phase | Experimental |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Antimicrobial prescribing guideline mobile phone application (MicroGuide) | Device | This session is given to all hospital doctors in all study hospitals at the start of the intervention period of each paired hospital. All participating hospitals will join AMS knowledge survey three times during the study period (1st time= at the start of the project, 2nd time= before entering to the intervention period and 3rd time= at the end of the project). |
| Measure | Description | Time Frame |
|---|---|---|
| Proportion of antimicrobial prescriptions adherent with prescribing guidelines | Point prevalence surveys of hospital antimicrobial prescribing in both in- and outpatients (every 4 months until month 16) | 16 months (12 months' exposure in each group) |
| Measure | Description | Time Frame |
|---|---|---|
| Antimicrobial defined daily doses (DDDs) | Point prevalence surveys of hospital antimicrobial prescribing in both in- and outpatients (every 4 months until month 16) | 16 months (12 months' exposure in each group) |
| Proportion of antimicrobials oral administration |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Vilada Chansamouth | Lao-Oxford-Mahosot Hospital Wellcome Trust Research Unit | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Lao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit (LOMWRU) | Vientiane | Vientaine | 0103 | Laos |
we are not recruiting individual participants. Therefor, this is not applicable and data will be shared according to Mahidol Oxford Tropical Medicine Research Unit (MORU) data sharing policy
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| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| Prot_SAP | Yes | Yes | No | Study Protocol and Statistical Analysis Plan | Jun 13, 2020 | Feb 16, 2022 | Prot_SAP_000.pdf |
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| ID | Term |
|---|---|
| D003141 | Communicable Diseases |
| ID | Term |
|---|---|
| D007239 | Infections |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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The study design is an open cohort stepped wedge cluster randomized controlled trial (SW-CRT) in six central/provincial hospitals across Laos. SW-CRT is appropriate in the Lao context because it requires fewer sites than a parallel cluster trial, but has similar observational periods for reference and intervention phases. As the interventions are delivered by one team travelling to each cluster in turn, implementing in stages is more practical. In addition, all participating hospitals have access to the novel interventions at the end of the study. Prescribers are allowed to move in and out of clusters during the trial.
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Point prevalence surveys of hospital antimicrobial prescribing in both in- and outpatients (every 4 months until month 16) |
| 16 months (12 months' exposure in each group) |
| AMS knowledge level of prescribers | Antimicrobial stewardship knowledge survey (month 0, before the implementation of the mobile phone app guidelines and AMS training and at month 16) | 16 months (12 months' exposure in each group) |
| Prescriber satisfaction/acceptability of the prescribing guidelines | Prescriber surveys (month 0, paper-based antimicrobial prescribing guidelines survey before the implementation of the mobile phone app guidelines, mobile phone app-based antimicrobial prescribing guidelines survey 4 month after the implementation of the mobile phone app guidelines | 16 months (12 months' exposure in each group) |
| Total costs of antimicrobials prescribed | Point prevalence surveys of hospital antimicrobial prescribing and antimicrobial costing in both in- and outpatients (every 4 months until month 16) | 16 months (12 months' exposure in each group) |
| Proportion of antimicrobial prescription pre-trial versus trial | Point prevalence surveys of hospital antimicrobial prescribing in both in- and outpatients (every 4 months until month 16) | 16 months |