Information needs and access of Members of Vigilante in Adamawa State, North -East Nigeria

ABSTRACT The study investigated the Information needs and access of Members of Vigilante in Adamawa state, North-eastern Nigeria, one of the three states bedeviled by the Boko Haram insurgency. Quantitative research methodology and Cross-sectional survey design was applied for the study. The population of the study comprised of One Thousand Four Hundred Members (1400) drawn from Nineteen (19) local governments areas in the state. Krejcie and Morgan Table (1970) was used to draw (302) members as sample of the population, while Walpole’s (1982) formula for proportions was used in arriving at a sample for each stratum (i.e. each local government area). In collecting data, a total of Three Hundred and Two (302) copies of questionnaires were administered, and Two Hundred and Forty 240 copies (79.47%) were returned and found useful. The data collected was analyzed using descriptive statistics. The outcome of the study revealed that the information needs of members were daily mainly work related and from informal sources, as there were no public libraries/information centers in 17 local governments’ areas of the state. The outcome of the research also revealed barriers to information access to include general lack of formal information infrastructure such as libraries/information centers, poor and unreliable informal information sources, as well as lack of training on information literacy skills for members of Vigilante. It is recommended that there is a need for those involved in vigilante information delivery to continuously examine and identify evolving information needs of members of vigilante in order to meet such needs. Government should resuscitate the dying public libraries in all the local government areas of Adamawa state to provide information services. Libraries should organize training on information literacy and other information use skills for members of vigilante, because if this is done, it will enhance and improve information access across communities in Adamawa state. Finally, information resources be repackaged in order to take care of challenges of proximity to sources of information, language barrier and other challenges faced by members of vigilante

Shaping solutions with a community: the research design using design science research (DSR) and case study research with an ICT4D project

This paper describes the research design of a mixed method information and communication technology for development (ICT4D) study using design science research (DSR) and case study research in the pragmatic tradition. The study participants are a group of women working as domestic workers in Johannesburg, South Africa and a selected group of organisations. The organisations are included to gain an understanding of their approach to information inclusivity and to evaluate the resulting artefact. The novelty of this study is the combination of DSR with ICT4D, the use of journals as a self-documentation technique to collect data, followed by a design thinking workshop and interviews. The problem that the study addresses is how should the information needs that are meaningful to women working as domestic workers, be effectively translated through the use of ICT in order to enhance their experience of the good life as defined by Sen’s capability approach (1999) and to contribute to the success and social value of ICT4D projects

The information needs of people with albinism in Khomas Region, Namibia

The dissertation is a report of an investigation of the information needs of people with albinism in Khomas region, Namibia. The investigation aims to ascertain the information needs of people with albinism (PWA), including the kind of information needs they have. It also seeks to establish the mechanisms used by PWA to seek information and to determine who initiates their information-seeking activities. Furthermore, the study identifies the challenges PWA in Khomas region face on a daily basis when seeking information and recommends information services that could be suitable for PWA in Khomas region. For its theoretical framework, the study applies Moore (2002) and Wilson’s (1996) model of information behaviour. It is situated within the interpretivism paradigm following a qualitative approach. The research design is that of a case study with aspects of autoethnography resulting from the researcher’s personal memory of her lived experiences of albinism as a mother of two children with albinism. Face-to-face interviews were conducted with sixteen people with albinism; six parents of children with albinism (CWA); and two key informants from associations dealing with PWA in Namibia. The findings reveal that PWA have information needs related to their condition, specifically skin and eye care, as well as other basic needs, such as shelter, employment opportunities, education prospects and the process of their acquisition of identity and travel documents. The study revealed that the internet (especially Google), the radio and television, healthcare professionals and Support in Namibia of Albinism Sufferers Requiring Assistance (SINASRA) and Namibia Albino Association Trust (NAAT) are some of the sources and mechanisms used by participants when searching for information. The organisational participants revealed that they provide a range of services to PWA, including information about skin care and protective clothing, as well as applications for disability grants. PWA who participated in the study indicated that they encounter problems when accessing information. These include the long distances between information seekers and providers, time constraints and the cost associated with accessing information. Language was identified as a major barrier to information access because most of the content is in English. Lack of awareness of information sources coupled with poor eyesight for PWA the reading of information in small fonts that is not provided in alternative formats a glaring challenge. The study concluded that information about albinism is critical not only for PWA, but also to an African society that often subjects PWA to grievous harm, simply because it still holds myths and stigma about albinism. Therefore, the study recommends that it is crucial to provide information to PWA, including their family members through platforms such as open days, sensitisation meetings, and the creation of WhatsApp groups. These interventions should also be directed at society at large in order to create a sense of belonging and get rid of isolation suffered by PWA. The study also recommends that an information booklet be developed by the ministry of health and social services. This booklet should contain information on different types of disabilities that can affect unborn children, in order to prepare the parents