What We Do

The NEWAID Foundation provides research funding to public health students, encouraging their involvement with traditionally neglected infectious diseases in the developing world.

2011-2012 Applications

The NEWAID foundation will not be offering grants for this academic year. Instead, we will be conducting a survey of past grant recipients in an internal review process to determine what past NEWAID Fellows have done with their careers after their research experiences. We hope to offer another round of grants in the 2012-2013 academic year, with applications typically due Jan 31st.

Author Archive

Jan
12

Update: 2012 awards

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The NEWAID foundation will not be offering grants this year. Instead, we will be conducting an internal review, following up with our past fellows to determine what impact our grants have had on their career choices. Ideally, our grants are intended to inspire young professionals to continue to pursue work with neglected infectious diseases in some capacity as they continue their careers and we would like to verify the outcomes of our initial investments as a foundation. Thanks for your understanding. We hope to be offering grants again for the 2012-2013 school year, with application deadlines of around Jan 31 of each year.

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We have selected a final group of applicants and will be releasing the award selections later this week. Please stay tuned, and thank you for your patience.

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Jan
16

Applications Due Jan 31, 2011

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Just a reminder that this year’s application materials are due by Jan 31, 2011. If you have any questions or need assistant, please use the Contact form on this website.

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May
23

2010 NEWAID Finalists

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Below is a summary of the projects to by conducted by the 2010 NEWAID Finalists.

The Impact of Vector Control, Knowledge, and Behavior on Zoonotic Visceral Leishmaniasis in Brazil

Kevin Esch, DVM: University of Iowa / Iowa State University, College of Public Health / Department of Veterinary Pathology

Visceral leishmaniasis (VL), caused by Leishmania chagasi infantum, transmitted by the sand fly, is responsible for deaths in dogs and humans globally. In Brazil, 51,222 new cases of human (VL) were reported between 1980 and 2003. Infected dogs have been identified as a major risk factor for human infection. While the infection rate of dogs in Brazil is high, the number of animals becoming visibly ill is significantly lower. This results in a population of dogs able to spread the disease, while not showing any signs of illness. Risk factors such as malnutrition, home construction, education, income, HIV infection, and knowledge, have also been identified as risk factors for human visceral leishmaniasis.

Our goal is two-fold. First, we will administer a household survey to determine what factors may be leading to VL in the study community, and to evaluate their knowledge of VL and methods of disease prevention in themselves and their pets. This will allow us to identify risk factors specific for VL and aid in developing educational materials directed toward the populations at greatest risk. Secondly, we will draw blood from human and canine study participants to evaluate the frequency of disease in the population at the beginning of the study. We will then begin a canine treatment group on monthly topical insecticide to prevent sand fly feeding, and test for the disease in canines, humans, and sand flies at 3 months, 6 months, and 12 months to determine the impact of preventive treatment on canine and human disease, and the feeding habits of sand flies. This will allow us to determine the effectiveness of insecticides in preventing canine infection, sand fly infection, and human
infection. If successful, our results could be used to further develop educational materials for the population of Rio Grande do Norte, and allow human health professionals and veterinarians make recommendations regarding treatment of dogs to prevent visceral leishmaniasis.

The effect of acute T. cruzi infection on cognitive development in children

Jess Edwards & Lydia Feinstein (Joint Application) , University of North Carolina, Chapel Hill School of Public Health

Chagas disease infects more than 18 million people in Latin America. Because the triatome insect that carries the disease lives primarily in human dwellings with thatched roofs or cracked adobe walls, families living in poverty are at greatest risk for contracting the disease. Neurological effects of Chagas disease have been documented, but the long-term effects on the central nervous system in children are not well understood. This study will assess the relationship between infection with T. cruzi, the parasite responsible for Chagas disease, and cognitive development in children living in rural Nicaragua. We will also document the prevalence of infection with T. cruzi among school-aged children and investigate common risk factors for the disease.

Pathogen Investigation and Discovery Study in Sri Lanka

Wenfeng Gong, Duke Global Health Insitute

Pathogen investigation and discovery refers to the research procedure of recognizing the distribution and transmission patterns of emerging or reemerging pathogens. It is the cornerstone of subsequent actions surrounding emerging infectious disease prevention, including the evaluation of epidemiological potential of local infectious diseases, the redistribution of healthcare infrastructure and workforce, health system strengthening, and policy development and modification. However, pathogen investigation research in developing countries, even where people are facing a deadly threat of emerging/reemerging pathogens, is usually limited in scale and quality, due to insufficient funding, lack of pathogen detection technology and skilled staff, as well as the neglect of policy makers. As a graduate student in Global Health with a biomedical research background, I expect to help address the threat of emerging/reemerging infectious diseases in developing countries by conducting pathogen investigation in a more efficient way.

As one of the innovations of this study, we will utilize the cutting edge molecular pathogen detection and typing system at Duke-NUS Medical School in Singapore to solve the lack of technological support in Sri Lanka. Compared with sending specimens to other countries with advanced facilities, conducting tests in Singapore can largely reduce the shipping cost and days of specimens in storage before being tested. At the same time when samples are collected from patients presenting in the hospital with acute febrile diseases, epidemiological data and clinical symptoms of each patient will also be recorded for systemic analysis. By combining the clinical symptoms, epidemiological histories, and biological features, this study will be able to provide a description of pathogen emergence in Sri Lanka and offer an evaluation of the epidemiological potential by unveiling relationship between emerging pathogen transmission and people’s living pattern.

Novel In Vitro Antimalarial Drug Susceptibility Assays

Kansas Sparks, University of South Florida College of Public Health

Malaria continues to exert a devastating impact on the health of human populations in tropical regions, with over 500 million cases and the death of 1-3 million each year. The hardest hit is sub-Saharan Africa where an estimated 90% of deaths occur, primarily in children less than 5 years old infected with falciparum malaria. Although the burden of disease is in Africa, the impact of malaria in other tropical regions is no less dramatic. The malaria situation in Southeast Asia is particularly important as this region is the focus for the most drug resistant malaria in the world and resistance problems that emerge here can then spread to other regions of the world. The two most important emerging drug resistance issues in SE Asia are clinical resistance to artemisinin combination therapy (ACTs) and mergence of drug resistance in vivax malaria. In order to combat this problem, we propose two aims: 1) to assess a novel in vitro assays for artemisinin resistant falciparum malaria, and 2) to assess the therapeutic potential of two new drug series for chloroquine resistant vivax malaria in a new in vitro assay developed at the Shoklo Malaria Research Unit (SMRU). The population in which we plan to assess both aims will include patients admitted to the local clinic that display symptoms of malaria. In doing so, we hypothesize that the optimization of the methods employed at SMRU will identify both an effective control measure for falciparum malaria and potential new antimalarial drugs for the treatment of vivax malaria.

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May
22

Past NEWAID Fellows: Molly Franke

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Molly Franke was awarded a Masters Research grant in 2007, with continuing support for her PhD research in 2008. Molly’s initial work went on for publication in the journal Clinical Infectious Diseases. The abstract of her project “Risk Factors and Mortality Associated with Default from Multidrug-Resistant Tuberculosis Treatment” can be found below:

Background. Completing treatment for multidrug-resistant (MDR) tuberculosis (TB) may be more challenging than completing first-line TB therapy, especially in resource-poor settings. The objectives of this study were to (1) identify risk factors for default from MDR TB therapy (defined as prolonged treatment interruption), (2) quantify mortality among patients who default from treatment, and (3) identify risk factors for death after default from treatment.

Methods. We performed a retrospective chart review to identify risk factors for default from MDR TB therapy and conducted home visits to assess mortality among patients who defaulted from such therapy.

Results. Sixty-seven (10.0%) of 671 patients defaulted from MDR TB therapy. The median time to treatment default was 438 days (interquartile range, 152–710 days), and 27 (40.3%) of the 67 patients who defaulted from
treatment had culture-positive sputum at the time of default. Substance use (hazard ratio, 2.96; 95% confidence interval, 1.56–5.62; Pp.001), substandard housing conditions (hazard ratio, 1.83; 95% confidence interval, 1.07–3.11; Pp.03), later year of enrollment (hazard ratio, 1.62, 95% confidence interval, 1.09–2.41; Pp.02), and health district (Pp.02) predicted default from therapy in a multivariable analysis. Severe adverse events did not predict default from therapy. Forty-seven (70.1%) of 67 patients who defaulted from therapy were successfully traced; of these, 25 (53.2%) had died. Poor bacteriologic response, !1 year of treatment at the time of default, low education level, and diagnosis with a psychiatric disorder significantly predicted death after default in a multivariable analysis.
Conclusions. The proportion of patients who defaulted from MDR TB treatment was relatively low. The large proportion of patients who had culture-positive sputum at the time of treatment default underscores the public
health importance of minimizing treatment default. Prognosis for patients who defaulted from therapy was poor. Interventions aimed at preventing treatment default may reduce TB-related mortality.

Franke CID 2008

Her other project “Helminth infection and the risk of tuberculosis infection in children” is currently starting enrollment. The abstract for that project is as follows:

In the year 2000, an estimated 884,019 children less than 15 years of age became ill with tuberculosis.  Despite the existence of curative therapy, the World Health Organization (WHO) has estimated that approximately one third of TB cases among children in this age group result in death. The paucity of data describing TB risk factors in children poses a challenge to the design of interventions that could decrease TB disease progression in this group.  The identification of modifiable risk factors might lead to interventions that could substantially decrease TB-related morbidity and mortality in children. Helminth infection, including round worm and hookworm infection, may be one such risk factor. Several recent case-control studies in adults and adolescents suggest that TB disease is associated with both helminth infection and immunological responses consistent with helminth infection. Other studies have found no association between helminth infection and tuberculosis. To date, no studies have examined the association between TB endpoints and helminth infection in children, the group most vulnerable to helminth infection and about which the least is known regarding risk factors for progression to active TB disease.  The general objective of this study is to examine whether helminth infection increases susceptibility to TB disease in children.  We will pursue the following specific aims:  (1) To determine whether helminth infection among children is associated with an increased risk of TB disease; and (2) To examine whether there is a dose-response relationship between the total burden of helminths and/or the number of helminth species with which a child is infected and progression to active TB disease. We will conduct a matched case-control study in Lima, Peru.  We will compare the prevalence of helminth infection among children with and without TB disease.  Cases will be matched to controls by age, neighborhood, and TB contact history.

Molly is currently working with the Department of Global Health and Social Medicine at Harvard Medical School on projects that collaborate with Partners in Health.

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May
04

Decisions have been made

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Our finalists for 2010 have been selected today, and emails will be sent to all applicants later this evening.

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Apr
26

Applications update

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We have received reviews of all applications from our associated faculty and will be meeting this week with our executive board to select all finalists. Please stay tuned and expect an email shortly.

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Feb
04

Thank you to our applicants

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Our 2009-2010 application cycle is now closed, and no additional applications will be accepted. We have received 32 completed applications for this year’s grant cycle and are reviewing them now. Our goal is to reach a decision and notify our finalists by the end of April. Status updates and additional announcements will be posted here.

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Jan
20

Saving your application

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I have received a few emails from people concerned about a notification that says “Your form has been submitted” when they save their application to continue later. Your application has not been submitted, just the “save for later” form information which has been sent in and is being saved. Once you have clicked “Ok” you will receive an email to the email address specified in your application, with a link to continue where you left off. Unfortunately this submission notification is a notification that is built into our application software that can’t be overridden. If you don’t receive the email or can’t access your application let me know and I can try and re-send your access details.

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Our 2009-2010 grant application is now online and available. To access the application click HERE or on the link below. The deadline for applications is Jan 31, 2010. Apply-Now

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