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Data-Informed Platform for Health (DIPH)

25 марта 2022 г. обновлено: Bilal Iqbal Avan, London School of Hygiene and Tropical Medicine

The overall aim of the Data-Informed Platform for Health (DIPH) is to improve Maternal, Newborn and Child Health (MNCH) programmes and services at the district level. The DIPH strategy does this by bringing together data on inputs and processes to promote the use of local data for decision-making, priority-setting, and planning by introducing a structured decision-making process at the district level.

The DIPH is embedded in the existing district decision-making forum- e.g., performance review teams meetings - adding a structured coordination process between different departments and formal data-sharing for evidence-based decision-making, planning, and resource allocation according to local health priorities. Conceptually, the DIPH strategy uses a structured set of processes involving five pre-defined steps and standardised job-aids corresponding to each step to facilitate linking data from health and associated departments and stakeholders. A typical DIPH cycle has five steps around a health theme, which take about four months to complete. Technical assistance is provided by the district stakeholders' induction, orientation, and handholding during the implementation of the initial cycles.

The DIPH job-aids - a set of standardised job-aids (paper forms or web-based interface) - are designed to help organise and interpret data from multiple sectors involved in delivering services around the chosen theme using a common data-sharing platform. They are aimed at district leadership and management teams systematically using, inputting and processing data for decision-making, planning and progress monitoring of the theme.

In Ethiopia, the DIPH intervention research will be employed for four cycles in the North Shoa zone (12 intervention and 12 comparison districts), coupled with process evaluation to understand and improve ongoing implementation issues. In addition, for the impact evaluation of DIPH implementation, a before-and-after comparison of the study outcomes between intervention and comparison study arms will be carried out via district health administration surveys.

This study is a collaboration between the Ethiopian Public Health Institute (EPHI) and the London School of Hygiene and Tropical Medicine (LSHTM).

Обзор исследования

Статус

Активный, не рекрутирующий

Условия

Вмешательство/лечение

Подробное описание

The overall purpose of the Data-Informed Platform for Health - or DIPH - is to improve MNCH programmes and services through data-driven decision-making at the district level. It is a strategy for strengthening health systems. The DIPH does this by bringing together various stakeholders into a single platform and facilitating their understanding and use of key district-level data.

Our focus is MNCH, although the DIPH concept has broad applicability. The primary objectives of the DIPH are to promote the use of local data from programmatic activities for 1) decision-making, priority-setting and planning at the district health administration level; and 2) appraisal of health services and programmes. The DIPH approach will regularly bring governmental and non-governmental service providers to a common forum to share data according to an agreed plan and use the resulting information as a tool in priority-setting for resource allocation and needs assessment for further acquiring funds.

A district is considered an operating unit for the DIPH based on the assumption that this is the lowest administrative level of decision-making in a health system in Ethiopia. The DIPH concept has its roots in the 'District Evaluation Platform approach.' The DIPH does not try to reinvent the wheel - it is embedded in decision-making procedures that already exist at the district level. DIPH adds a structured coordination process between the government and private stakeholders of formal data-sharing for evidence-based decision-making, planning and resource allocation. Moreover, the DIPH is conducted in accordance with local health priorities.

The DIPH is delivered as a package of job aids and guidelines. Structurally, the box is made up of three main elements: Firstly, it involves the grouping of stakeholders who are brought together to deliberate on issues in a virtual platform facilitated by regular meetings. The membership of this virtual platform is flexible and responds to the needs of the problems in focus. Secondly, the DIPH package facilitates these stakeholder meetings in five steps: Assessment, Engagement, Definition, Planning and Follow-up. These five steps together makeup one whole cycle of the DIPH and, in practice, take 3-4 months to complete. Each cycle looks at a specific health theme, identified in the early stages of the cycle itself. Thirdly, the DIPH package also includes a digital interface where everyone involved in the process can regularly review data and check on progress.

Overall aim:

To enhance interaction among district-level health personnel and linkage of databases to improve coordinated decision-making and planning by strengthening health systems through capacity-building and effective use of data for decision-making.

Specific research objectives:

  1. To systematically strengthen the district health system using the DIPH strategy by developing a coordinated decision-making and planning through the Data-Informed Platformfor Health strategy
  2. To evaluate the effectiveness of embedding the Data-Informed Platform for Health within the district health system with respect to improvement in district health performance in terms of data management and data-driven decision-making as compared to Non-DIPH districts.

This is a health system intervention to adapt, implement and evaluate the DIPH approach in Ethiopia, in close collaboration with national and local institutions, and engage key government stakeholders.

Study Design: a randomised controlled study design will employ pre and post-comparisons to establish the effectiveness of DIPH intervention. A district will be considered as a study implementation unit and equal number will be allocated for the presence and absence of intervention arm.

Study area: the study will be implemented in North Shewa, one of the administrative zones in the Amhara region. The study will be conducted in all 24 districts of the Zone by allocating 12 of them in intervention and 12 in non-intervention arms. To reduce subjective allocation, matching will be done based on the district performance level based on HMIS indicators and distance.

The development phase has been successfully completed with formative research, field observations, consultative meetings with district administrations, co-creation workshops with the federal health ministry, and adaptation of the DIPH package according to the Ethiopian district health system.

Implementation phase: four-monthly cycles of DIPH each will be conducted in the 12ditricts of the North Shewa zone over the 16 months. Which will form the basis of formal evaluation of DIPH intervention (An additional 1 four-monthly cycle -Transition cycle -will be conducted to implement and evaluate exit strategy of the DIPH intervention)

Embedding: The Performance Review Team meetings of the district health administration, which is entrusted with integrating planning and facilitating data-driven and collaborative decision-making, will be used as a platform to introduce the DIPH. Activities will focus primarily on:

  1. Strengthening the Performance Review Team forum for the engagement of all government and non-governmental stakeholders to identify challenges and solutions and assess resource allocation and responsibilities. These meetings will be convened to achieve consensus-building and collective decision-making to improve health systems and services in their areas.
  2. Promoting the critical review and regular use of local data to understand health-system progress at the district level.

Training: Before initiating the first DIPH cycle, the district health management staff of DIPH districts will be provided with three days' intensive residential training based on the specifically-designed DIPH training handbook in their zonal city. The overall aim of this curriculum, which is the basis of a training handbook, is to provide tools and knowledge for improved decision-making at the district level, utilising available data. Its target audience is district health officers in administrative and managerial roles within health systems. The first half of the course will cover the four core skills of decision-making, stakeholder engagement, data-use, and monitoring health-system performance. Next, participants will be provided with an overview of district-level organisational structure, followed by an introduction to DIPH, steps in the DIPH cycle, primary and supplementary forms, roles and responsibilities, DIPH meetings, and, finally,, how to use the DIPH interface.

On average, the research team will train five to six staff members per district. Along with the district's health department head, programme officers and an HMIS focal person, experts from the zonal health department will be included in the training. The DIPH research investigators team will conduct the three-day residential training.

Overall, the field team will comprise one DIPH regional coordinator, four DIPH support supervisors and one data manager. Each support supervisor will be assigned three districts to provide overall technical support in implementing the DIPH strategy. This will consist of inducting, orientating and handholding district stakeholders during the implementation of the initial cycles, participating in districts' monthly performance-review meetings, and monitoring collected data. Data collection will be performed on tablets using appropriate software for electronic data collection. Data collected from the field will be sent to EPHI's server daily through the Internet File Streaming System, a technology for transferring data already installed at EPHI.

EVALUATION:

B. Process evaluation will be carried out to understand and address on-going implementation issues and will specially address the following questions:

To what extent is health data used for problem-solving and delivering health services in each DIPH cycle? What is the level of engagement of various health stakeholders? What are the key mechanisms for data-sharing and consensus-building among the range of health-service stakeholders at the district level? What are the facilitators of, and barriers to, sustaining the DIPH strategy?

Data will be collected on semi-structured forms for in-depth interviews by DIPH support supervisors for each cycle throughout the implementation of DIPH. Synthesised findings will be presented periodically to respective district staff so that learning can be used to improve the following DIPH cycle. Post-intervention, end of cycle four, in-depth interviews will be also be conducted with the health administration of 4 selected comparison districts to assess any comparable changes that happened in the decision making and data use culture in the control districts over time.

A. Before-and-after comparison of health-system outcomes employed difference-in-differences estimates in intervention- and comparison-district surveys to assess changes resulting from DIPH implementation, in terms of changes in health information system performance and governance of data-driven decision-making at the district level

Study participants: The survey respondents will be the head of the health department, all programme officers and data managers at the district level. All eligible district staff will be interviewed, except those working in their respective districts for less than six months. IT is anticipated that on average 6 -7 eligible staff would be available in each district and all of them will be included in the study.

The sample size estimations for the required number of districts required per study arm is based on the statistical formula recommended by Hayes et al i.e a minimum sample size of 72 health management staff per study arm (144 in total) would have 80% power to detect a difference of at least 25 percentage points as statistically significant.

Data-collection: After a detailed pilot testing, baseline survey data-collection will be carried out by DIPH field teams. For end-line survey data-collection, an independent team of four data-collectors and one supervisor will be recruited from the zone for one month. Data-collectors will be recruited by EPHI and will, as a minimum, have a Master's degree. Their classroom training on the survey instruments will be followed by a written assessment on the survey contents. Data collectors will be provided with a field manual for reference during fieldwork. Job descriptions - with the roles and responsibilities of each team member and expected day-to-day deliverables - will be provided. The survey will be piloted to test survey procedures and tools, and a detailed standard operating-procedures document for the survey will be provided to the data-collection team.

Data Analysis: For quantitative analysis, the summary measures/indices will be calculated for each of the 24 districts at baseline and endline, ranging from 0-100%. The indexes will also be categorized to create indicators to determine proportion change for before and after comparison to answer the extent to which the DIPH has changed Health Information System performance and data-driven decision-making.

For the qualitative data, a realist evaluation analysis approach principles will be employed to identify prevalent issues that influence the embedding of the DIPH in health facilities and determine the opportunities that can be leveraged to promote DIPH strategy at the district level.

All these findings will inform an additional outcome of the DIPH evaluation, i.e. revision of the DIPH programme theory for the Ethiopian context.

Тип исследования

Интервенционный

Регистрация (Действительный)

24

Фаза

  • Непригодный

Контакты и местонахождение

В этом разделе приведены контактные данные лиц, проводящих исследование, и информация о том, где проводится это исследование.

Места учебы

Критерии участия

Исследователи ищут людей, которые соответствуют определенному описанию, называемому критериям приемлемости. Некоторыми примерами этих критериев являются общее состояние здоровья человека или предшествующее лечение.

Критерии приемлемости

Возраст, подходящий для обучения

  • Ребенок
  • Взрослый
  • Пожилой взрослый

Принимает здоровых добровольцев

Нет

Полы, имеющие право на обучение

Все

Описание

Inclusion Criteria:

  • All districts in the North Shewa zone will be included in the study.
  • All managerial and administrative district staff.

Exclusion Criteria:

  • Study participants who do not consent will be excluded.

Учебный план

В этом разделе представлена ​​подробная информация о плане исследования, в том числе о том, как планируется исследование и что оно измеряет.

Как устроено исследование?

Детали дизайна

  • Основная цель: Исследования в области здравоохранения
  • Распределение: Рандомизированный
  • Интервенционная модель: Параллельное назначение
  • Маскировка: Нет (открытая этикетка)

Оружие и интервенции

Группа участников / Армия
Вмешательство/лечение
Экспериментальный: DIPH-intervention districts
Twelve districts were randomly selected from the North Shewa Zone of the Amhara region, Ethiopia. These districts were matched with the comparison arm based on health system performance and distance. The DIPH intervention is implemented at the district health administration office level.
The DIPH promotes local data use for decision-making, priority-setting, planning and course correction at the district level by introducing a structured and collaborative process within the administration cadre. The DIPH is delivered as a package of job aids and guidelines. It involves grouping stakeholders who are brought together to deliberate on issues in a virtual platform facilitated by regular meetings. The package facilitates stakeholders' meetings in five steps: Assessment, Engagement, Definition, Planning and Follow-up. Together, these steps make up one whole cycle of the DIPH completed over four months. Each cycle looks at a specific health theme, identified in the early stages of the cycle itself. The package also includes a digital interface where everyone can regularly review data and check on progress. Note: LSHTM has exempted this study from having a sponsor, as DIPH is implemented at the health system administration level.
Другие имена:
  • DIPH
Без вмешательства: Non-intervention districts
Twelve districts were randomly selected from the North Shewa Zone of the Amhara region, Ethiopia. These districts were matched with the DIPH intervention arm based on health system performance and distance.

Что измеряет исследование?

Первичные показатели результатов

Мера результата
Мера Описание
Временное ограничение
'Health Information System performance' Index
Временное ограничение: From the randomization of districts to implementation of the DIPH intervention for 16 months (i.e immediately after completing the 4th DIPH cycle).

Conceptually: It refers to Behavioural (e.g. skills, attitudes, values, and motivation of the people who use data) and Technical (e.g. data collection processes, systems, and methods) determinants of the health information system at the district level. It is a survey-based assessment developed by Performance of Routine Information System Management (PRISM) Toolkit ( https://www.measureevaluation.org/resources/publications/tl-18-13/index.html).

Operationally: the summary measures are created of the constructs 1) essential infrastructure for data management, 2) data diversity, 3)reporting timelines, 4) data-quality assessment mechanisms, and 5) data use motivation, i.e. summating the survey item's responses and converting scores to fall on a standardized scale of 0-100. Statistically, the difference-in-differences technique will be employed to compare the change in the outcome in the DIPH intervention arm versus the change occurring in the control arm to assess the net effect.

From the randomization of districts to implementation of the DIPH intervention for 16 months (i.e immediately after completing the 4th DIPH cycle).
'Governance of data-driven decision-making' Index
Временное ограничение: From the randomization of districts to implementation of the DIPH intervention for 16 months (i.e. immediately after completing the 4th DIPH cycle).

Conceptually: it refers to the Organizational determinants of health information system at the district level (i.e., information culture, structure, resources, and roles and responsibilities of key people who use data). It a survey-based assessment developed by Performance of Routine Information System Management (PRISM) Toolkit ( https://www.measureevaluation.org/resources/publications/tl-18-13/index.html).

Operationally: the summary measures are created of the constructs 1) evidence-based decision-making, 2) participatory decision-making, 3) understanding value of data, 4) health system support for data-use/data-driven decision-making, and 5) accountability, i.e. by summating the survey item's responses and converting scores to fall on a standardized scale of 0-100. Statistically, the difference-in-differences technique will be employed to compare the change in the outcome in the DIPH intervention arm versus the change occurring in the control arm to assess the net effect.

From the randomization of districts to implementation of the DIPH intervention for 16 months (i.e. immediately after completing the 4th DIPH cycle).

Соавторы и исследователи

Здесь вы найдете людей и организации, участвующие в этом исследовании.

Следователи

  • Учебный стул: Tanya Marchant, PhD, London School of Hygiene and Tropical Medicine

Публикации и полезные ссылки

Лицо, ответственное за внесение сведений об исследовании, добровольно предоставляет эти публикации. Это может быть что угодно, связанное с исследованием.

Полезные ссылки

Даты записи исследования

Эти даты отслеживают ход отправки отчетов об исследованиях и сводных результатов на сайт ClinicalTrials.gov. Записи исследований и сообщаемые результаты проверяются Национальной медицинской библиотекой (NLM), чтобы убедиться, что они соответствуют определенным стандартам контроля качества, прежде чем публиковать их на общедоступном веб-сайте.

Изучение основных дат

Начало исследования (Действительный)

1 сентября 2020 г.

Первичное завершение (Ожидаемый)

30 апреля 2022 г.

Завершение исследования (Ожидаемый)

30 июня 2022 г.

Даты регистрации исследования

Первый отправленный

10 февраля 2022 г.

Впервые представлено, что соответствует критериям контроля качества

25 марта 2022 г.

Первый опубликованный (Действительный)

5 апреля 2022 г.

Обновления учебных записей

Последнее опубликованное обновление (Действительный)

5 апреля 2022 г.

Последнее отправленное обновление, отвечающее критериям контроля качества

25 марта 2022 г.

Последняя проверка

1 марта 2022 г.

Дополнительная информация

Термины, связанные с этим исследованием

Другие идентификационные номера исследования

  • INV-007644

Планирование данных отдельных участников (IPD)

Планируете делиться данными об отдельных участниках (IPD)?

Да

Описание плана IPD

Two years after the completion of study.

Сроки обмена IPD

Study datasets for the Data-Informed Platform for Health (DIPH) will be made available on LSHTM Data Compass, a research data repository operated by the London School of Hygiene and Tropical Medicine.

Критерии совместного доступа к IPD

To protect participant confidentiality, the de-identified datasets are made available through a controlled access approach. Researchers wishing to access datasets will be asked to apply for access via the repository's data request form, providing information on the variables they wish to access and details of their analysis plan. The request will be sent to the study team (that performed the research and have greatest understanding of the data) and the LSHTM Research Data Manager (who acts as an independent advisor). If the data analysis can be performed in compliance with the study's ethical and legal requirements, the study team will produce a derived dataset that contains the requested variables and work with the applicant to help them to understand the data. If there remains a recognisable risk that the derived dataset contains potentially identifiable information, the applicant will be asked to sign a Data Sharing Agreement before being provided with the dataset.

Совместное использование IPD Поддерживающий тип информации

  • Протокол исследования

Информация о лекарствах и устройствах, исследовательские документы

Изучает лекарственный продукт, регулируемый FDA США.

Нет

Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.

Нет

Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .

Клинические исследования Data informed Platfrom for health

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