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Introduction
and Overview
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Workshop at a Glance (short agenda) Full Agenda (with presentation abstracts) Summary
and Recommendations
From September 9-11 2002, a group of 70 people (including representatives from 22 PVOs, six cooperating agencies, and five independent consultants) met in Silver Spring, Maryland to learn from each other on using data to improve child health.
1.
Clearinghouse of tools and
training manuals/Database of tools and experiences Create
a clearinghouse of tools and training manuals including reviews (peer
and expert) for information systems, social autopsies. Create a database
of tools and experiences in community-based health information systems
(CB-HIS). Responsible organizations: CSTS, CORE MEWG, users. Tools should
be sent to CSTS. Tools presented during the Data for Action workshop
should be available by January 2003. The database should be useable
by September 2003. 2.
Toolkit/resource/compendium
of qualitative research Develop
a toolkit/resource/compendium of qualitative research including guidelines
for standardized reporting of qualitative data. Include:
Responsible
organizations: CSTS, and the CORE Group’s Social and Behavior Change
Working Group. No date was set. 3. Toolkit/resources on cost effectiveness and applied analysis Develop
a toolkit/resources (including economists) on determining cost effectiveness
and applied analysis which would go beyond facility-based actions. Conduct
a survey of PVO tools and activities. Responsible organizations: CSTS
working with the CORE Group’s Monitoring and Evaluation Working Group,
which could develop a Taskforce on Cost/Analysis Effectiveness with
responsibility to define the product(s).Also consider Abt, URC, and QAP. No date was
set. 4.
Collection of best-practices Develop
guidelines and disseminate best practices on CB-HIS including how the
community defines priorities and parameters. Include mechanisms to collect
information on community feedback on program strategies. Responsible
organization: The CORE Group. Completion by September 2003.
5.
Inventory of CB-HIS Hold
country-wide meetings in the spring/summer of 2003, for preparing an
inventory of CB-HIS in 2-3 countries, and make recommendations. In preparation,
PVOs active in those countries should complete an inventory during the
winter of 2002-2003. As a suggestion, they could use the inventory found
on p. 23 of the draft CB-HIS CSTS/JHU SOTA papers. Responsible organizations:
The CORE Group PVOs and their NGOs/partners; CORE/CORE-lettes; with
the CORE Group Monitoring and Evaluation Working Group as facilitator. Participants
also requested a centralized, easy-to-access point of contact or resource
with expertise in operations research (OR), who can share information
and answer questions ranging from estimating costs of studies to issues
relating to the implementation of studies, to tools, etc. This would
also serve as a valuable mechanism to disseminate results and lessons
learned from OR. As there is a level of effort of writing and costs
involved, participants described a non-competitive small grants mechanism
be developed, with a special emphasis on building OR capacity at the
field level. Data
for Action: A Historical Perspective
Within
the child survival context, the period 1985-1998 was an era of data
proliferation. The standardization and evolution of the knowledge, practice,
coverage (KPC) methodology provided useful data on maternal knowledge
and practice to guide project planning and setting quantitative population-based
objectives. Follow-up KPCs assessed achievement of population-based
objectives; progress was sometimes assessed through a mid-term KPC as
well. Nevertheless, outside of USAID guidelines there appeared to be
limited program focus on systematic methods to monitor and improve
project performance between the baseline and final KPC surveys. Further,
there was growing concern that data were not used on any type of routine
basis to improve implementation. Beginning
in a concerted way in 1998, PVOs, USAID, and others in the child survival
community engaged in a process of extended dialogue on designing and
implementing child survival activities with the greatest long-term impact.
This has corresponded to a shift away from direct service delivery to
partnership models, which has precipitated a focus on improving partner
capacity to manage for results, and the facilitation of community use
of data to manage their own health and nutrition. PVOs are now often
assessing their partner(s) capacity at baseline/end of project, and using
data to inform partner relationships. At the same time PVOs have begun
routinely using available data including Demographic Health Surveys
(DHS) and Multiple Indicator Cluster Surveys (MICS) for situational
analyses. More recently, PVOs have begun to estimate and track coverage
or behaviors for sub-project areas. In
June 1998, the CORE Group and BASICS held an “Expert Consultation on
High Impact PVO Child Survival Programs.” Technical experts and field
practitioners sought to identify the essential elements of successful child
survival projects and to recommend how those lessons could be used in
the design and implementation of child survival activities in the future.
These addressed the effectiveness, sustainability, and spread (coverage)
of PVO child survival programs. Presented programs used a variety of
strategies including integration of services, partnering with government,
participatory community approaches, operations research, management
by information, and a perinatal focus. Two
strategies of project success related to the use of data emerged: (1)
using information and management to detect and diagnose problems, provide
feedback, and conduct situational analysis; and (2) problem-focused
operations research[1]. The
Expert Consultation concluded that future child survival efforts should
have a strong emphasis on assessment, monitoring, and evaluation, including
built-in operations research. It was recommended that PVOs develop a
research agenda, test various program models in different settings,
and document failures as well as successes. These
three organizational levels served as useful discussion platforms for
the Data for Action workshop. Again following a worldwide call for abstracts,
16 papers were selected. Looking at the level of either their own PVO,
local partner(s), or communities, presenters highlighted the types of
data they collected periodically or routinely. Examples included a range
of qualitative and quantitative information including results of operational
research, lessons learned, study of better practices, and applications
of new or established approaches and tools. Presenters then discussed
their organizational use of data to improve child survival project design
(for example, setting health priorities and policies, and planning for
sustainability and scale-up); effectively implement/manage activities
(such as cost-effective allocation of resources); and to maximize outcomes
in terms of target children.
Peter Winch of the Johns Hopkins University Bloomberg School of Public
Health identified several continuing challenges in the ongoing shift
from service delivery to partnership. These include
Each of the presentations made at the workshop addressed questions of data use, and how data were used in decision-making at the various levels of involvement. The presentations are included on this CD in various forms: All of the papers are available in Microsoft Word, presentations are available in PowerPoint, and, if the presentations were recorded, links to streaming audio are included as well. If you have any questions regarding this workshop or the outcomes, please send your questions to the Child Survival Technical Support Project, 11785 Beltsville Drive, Suite 300, Calverton, MD 20866 <csts@macrointernational.com> [1] The complete list of conclusions and recommendations from the Expert Consultation can be found athttp://www.basics.org/publications/abs/abs_pvo.html
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