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Participatory action research for health capability in a Swazi community caring for children affected by HIV and AIDS- a project ethnography
thesis
posted on 2017-01-09, 05:58authored byMichelle Rhonda Brear
This thesis
provides an ethnographic account, and reports the findings, of
qualitatively-driven mixed-methods participatory action research (PAR) for
health capability. The research aims were to generate knowledge about: (1) the
process and outcomes of PAR, including empowerment; and (2) health capability,
its enablers and deprivations; in a community caring for children affected by
HIV and AIDS. Participatory action research aims for empowering community
participation in all aspects of the research process. Health capability is a
social justice philosophy that conceives health as the realisation of civil,
social, economic and political entitlements.
The research was conducted over an 18
month period, in partnership with lay “co-researchers” from a rural Swazi
community caring for children affected by HIV and AIDS. The ethnography
involved 76 instances of participant observation of, and 22 focus group
discussions about, the dynamics of participation in, and the knowledge creation
and human development (particularly empowerment) outcomes of, the PAR process.
The PAR involved a demographic and health census of the population and 18 focus
group discussions about health capability in the community.
Co-researchers participated in numerous
activities in each aspect of the PAR process. Their participation had negative
and positive, knowledge creation and human development outcomes. It enabled the
development of a unique sampling technique and research instruments that
captured emic (community) perspectives and enhanced the PAR’s cultural
sensitivity. However, there were possible tensions between cultural sensitivity
and implementing scientifically and ethically rigorous PAR, in a culture where
gender equality, voluntary informed consent and participatory governance were
unfamiliar concepts. Positive human development outcomes reminiscent of
empowerment occurred for co-researchers but were limited for the community as a
whole, due to lack of material resources. Health capability deprivations in the
community were widespread, and associated with poverty, lack of material resources
and modern infrastructure, and discriminatory norms, including over-reliance on
the unpaid labour of marginalised community members, particularly women.
The ethnographic and PAR findings
demonstrate that, from the perspective of community members and co-researchers,
empowerment, as a multidimensional theoretical construct should be conceived
as: a process of human development towards; and/or an outcome representing the
realisation of, health capability for all. For co-researchers, individual
empowerment transcended the previously hypothesised personal, psychological
processes; it also involved interactions with, and emotional responses to,
others. The results indicate that organisational and community empowerment are
both forms of group empowerment that depend on the groups’ values, and
expertise and the actions and interactions they have opportunities to, and
actually do, engage in.
Empowering groups, including communities
caring for children affected by HIV and AIDS, is a long term human development
process that must involve the exchange of social and material resources, which
enhance health capability for all, including children’s caregivers. Extensive
participation in PAR can enhance scientific knowledge creation and contribute to
the empowerment of co-researchers. However, it does not negate the need for
improved access to material resources to create enabling environments and
secure empowerment, that is, health capability for all, in communities caring
for children affected by HIV and AIDS.