TY - JOUR
T1 - The sanitation hygiene infant nutrition efficacy (SHINE) Trial
T2 - Rationale, design, and methods
AU - The Sanitation Hygiene Infant Nutrition Efficacy (SHINE) Trial Team
AU - Humphrey, Jean H.
AU - Jones, Andrew D.
AU - Manges, Amee
AU - Mangwadu, Goldberg
AU - Maluccio, John A.
AU - Mbuya, Mduduzi N.N.
AU - Moulton, Lawrence H.
AU - Ntozini, Robert
AU - Prendergast, Andrew J.
AU - Stoltzfus, Rebecca J.
AU - Tielsch, James M.
AU - Chasokela, Cynthia
AU - Chigumira, Ancikaria
AU - Heylar, William
AU - Hwena, Preston
AU - Kembo, George
AU - Majo, Florence D.
AU - Mutasa, Batsirai
AU - Mutasa, Kuda
AU - Rambanepasi, Philippa
AU - Sauramba, Virginia
AU - Tavengwa, Naume V.
AU - Van Der Keilen, Franne
AU - Zambezi, Chipo
AU - Chidhanguro, Dzivaidzo
AU - Chigodora, Dorcas
AU - Chipanga, Joseph F.
AU - Gerema, Grace
AU - Magara, Tawanda
AU - Mandava, Mandava
AU - Mavhudzi, Tafadzwa
AU - Mazhanga, Clever
AU - Muzaradope, Grace
AU - Mwapaura, Marian T.
AU - Phiri, Simon
AU - Tengende, Alice
AU - Banda, Cynthia
AU - Chasekwa, Bernard
AU - Chidamba, Leah
AU - Chidawanyika, Theodore
AU - Chikwindi, Elisha
AU - Chingaona, Lovemore K.
AU - Chiorera, Courage K.
AU - Dandadzi, Adlight
AU - Govha, Margaret
AU - Gumbo, Hlanai
AU - Gwanzura, Karen T.
AU - Kasaru, Sarudzai
AU - Makasi, Rachel
AU - Smith, Laura E.
N1 - Publisher Copyright:
© 2015 The Author 2015. Published by Oxford University Press for the Infectious Diseases Society of America.
PY - 2015/12/15
Y1 - 2015/12/15
N2 - Child stunting and anemia are intractable public health problems in developing countries and have profound short- and long-term consequences. The Sanitation Hygiene Infant Nutrition Efficacy (SHINE) trial is motivated by the premise that environmental enteric dysfunction (EED) is a major underlying cause of both stunting and anemia, that chronic inflammation is the central characteristic of EED mediating these adverse effects, and that EED is primarily caused by high fecal ingestion due to living in conditions of poor water, sanitation, and hygiene (WASH). SHINE is a proof-of-concept, 2 × 2 factorial, cluster-randomized, community-based trial in 2 rural districts of Zimbabwe that will test the independent and combined effects of protecting babies from fecal ingestion (factor 1, operationalized through a WASH intervention) and optimizing nutritional adequacy of infant diet (factor 2, operationalized through an infant and young child feeding [IYCF] intervention) on length and hemoglobin at 18 months of age. Within SHINE we will measure 2 causal pathways. The program impact pathway comprises the series of processes and behaviors linking implementation of the interventions with the 2 child health primary outcomes; it will be modeled using measures of fidelity of intervention delivery and household uptake of promoted behaviors and practices. We will also measure a range of household and individual characteristics, social interactions, and maternal capabilities for childcare, which we hypothesize will explain heterogeneity along these pathways. The biomedical pathway comprises the infant biologic responses to the WASH and IYCF interventions that ultimately result in attained stature and hemoglobin concentration at 18 months of age; it will be elucidated by measuring biomarkers of intestinal structure and function (inflammation, regeneration, absorption, and permeability); microbial translocation; systemic inflammation; and hormonal determinants of growth and anemia among a subgroup of infants enrolled in an EED substudy. This article describes the rationale, design, and methods underlying the SHINE trial. Clinical Trials Registration.NCT01824940.
AB - Child stunting and anemia are intractable public health problems in developing countries and have profound short- and long-term consequences. The Sanitation Hygiene Infant Nutrition Efficacy (SHINE) trial is motivated by the premise that environmental enteric dysfunction (EED) is a major underlying cause of both stunting and anemia, that chronic inflammation is the central characteristic of EED mediating these adverse effects, and that EED is primarily caused by high fecal ingestion due to living in conditions of poor water, sanitation, and hygiene (WASH). SHINE is a proof-of-concept, 2 × 2 factorial, cluster-randomized, community-based trial in 2 rural districts of Zimbabwe that will test the independent and combined effects of protecting babies from fecal ingestion (factor 1, operationalized through a WASH intervention) and optimizing nutritional adequacy of infant diet (factor 2, operationalized through an infant and young child feeding [IYCF] intervention) on length and hemoglobin at 18 months of age. Within SHINE we will measure 2 causal pathways. The program impact pathway comprises the series of processes and behaviors linking implementation of the interventions with the 2 child health primary outcomes; it will be modeled using measures of fidelity of intervention delivery and household uptake of promoted behaviors and practices. We will also measure a range of household and individual characteristics, social interactions, and maternal capabilities for childcare, which we hypothesize will explain heterogeneity along these pathways. The biomedical pathway comprises the infant biologic responses to the WASH and IYCF interventions that ultimately result in attained stature and hemoglobin concentration at 18 months of age; it will be elucidated by measuring biomarkers of intestinal structure and function (inflammation, regeneration, absorption, and permeability); microbial translocation; systemic inflammation; and hormonal determinants of growth and anemia among a subgroup of infants enrolled in an EED substudy. This article describes the rationale, design, and methods underlying the SHINE trial. Clinical Trials Registration.NCT01824940.
KW - anemia
KW - environmental enteric dysfunction
KW - hygiene
KW - sanitation
KW - stunting
UR - https://www.scopus.com/pages/publications/84950323601
U2 - 10.1093/cid/civ844
DO - 10.1093/cid/civ844
M3 - Article
C2 - 26602296
AN - SCOPUS:84950323601
SN - 1058-4838
VL - 61
SP - S685-S702
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
ER -