Abstract
The purpose of the current study was to critically assess the gaps in the existing methodologies of dietary data collection for diet diversity indicators. The study proposed the importance of smartphone application to overcome the drawbacks. The review paper identified and assessed the conventional methodologies used in diet diversity indicators including Minimum Dietary Diversity for Women (MDD-W), Minimum Dietary Diversity of Infant and Young Child Feeding Practices (IYCF-MDD), and Household Dietary Diversity Score (HDDS). The 80 research studies from 38 countries were critically assessed on the basis of their research aim, study design, target audience, dietary data collection methodology, sample size, dietary data type, dietary data collection frequency, and location point of dietary data collection. Results indicated that most studies employed interviewer-administered 24-h recall assessing the dietary diversity. The review paper concluded that smartphone application had potential to overcome the identified limitations of conventional methodologies including recall bias, social-desirability bias, interviewer training, and cost–time constraints.
Keywords: diet diversity, diet assessment, MDD-W, IYCF-MDD, HDDS, smartphone application
1. Introduction
Micronutrient malnutrition arises when individuals lack diet diversity and diet quality, despite having sufficient energy intake (1). An individual’s physical health, psychological health, and working capacity are correlated with nutrition status. Maintaining good health in women of reproductive age is important not only for themselves, but also for the development, growth, and long-term health of their children. Fetal development, growth, brain development, and survival rate can all be improved by adequate nutrition during the first 1000 days of a child’s life (2). Child development is vulnerable between the age of 6 and 24 months, as it involves the transition in child feeding practices from exclusive breastfeeding to the consumption of complementary foods (3). Low protein and carbohydrate diets would make women chronically malnourished mothers with a higher risk of infant mortality. Additionally, households may lack access to nutritionally adequate food during the times of food scarcity, resulting in decreased nutrient intake and diet diversity among all members of household (4). Children under the age of 5, and adults over the age of 60 are particularly sensitive to the negative effects of a poor diet (5). Diets containing a little amount of fruits, vegetables, and animal origin products, put them at greater risk of micronutrient insufficiency (6). Many households worldwide, even those with the means to eat better, consume a diet high in carbohydrates and low in nutrient-rich foods, resulting in malnutrition (7). Diet quality is a term that is often used for referring to nutrient adequacy. Diet diversity is one of the key features of diet quality (8). Diets that include a variety of food groups are critical for resisting malnutrition and foster better health in individuals and their offspring (9).
Deficits and differences in nutrition consistency at individual and household level have been known for a long time. Around 2 billion people worldwide suffer from micronutrient deficiencies, a large portion of which is attributed to monotonous diets comprising of nutrient-deficit staple crops (10, 11). As a result, the number of programmatic interventions that aim at improving diet diversity and nutrition has increased with time, as has the demand for indicators that track their impact and progress (12). Although a variety of diet diversity indicators have been developed and implemented in both research and programmatic contexts, only a few indicators have been established for use at population level in resource-poor settings. These indicators include Minimum Dietary Diversity for Women (MDD-W), Minimum Dietary Diversity of Infant and Young Child Feeding Practices (IYCF-MDD), and Household Dietary Diversity Score (HDDS). MDD-W is a dichotomous indicator of whether women 15–49 years of age have consumed at least five out of 10 defined food groups in last 24-h. The 10 defined food groups are: Grains, Roots, and Tubers; Pulses; Nuts and Seeds; Dairy; Meat, Poultry, Fish; Eggs; Dark green leafy vegetables; Other Vitamin A-rich fruits and vegetables; Other fruits; Other vegetables (13). Minimum dietary diversity (MDD) is one of the eight core indicators of Infant and Young Child Feeding Practices (IYCF) (14). MDD is defined as whether children aged between 6 and 23 months have consumed at least five out of eight defined food groups over the period of last 24-h. The eight food groups are: Breast milk; Grains, roots and tubers; Legumes and nuts; Dairy products (milk, yogurt, cheese); Flesh foods (meat, fish, poultry and liver/organ meats); Eggs; Vitamin-A rich fruits and vegetables; and Other fruits and vegetables. The proportion of women 15–49 years of age and children 6–23 months of age, who achieve this threshold in a population, can be used as a proxy indicator for higher micronutrient adequacy, one important dimension of diet quality (13). On the other hand, HDDS is an attractive proxy indicator of diet diversity representing the entire household. It computes the diet diversity score by aggregating different food groups, out of 12, consumed by all members of household over a 24-h period. Traditionally, diet diversity indicator’s dietary data is collected by written or orally reported methods from a female member or household head by employing interviewer-administered questionnaires. These questionnaires can be open recall-based or list-based (8). In open recall, interviewer asks respondent to recall all food items/ beverages consumed in the last 24 h and categorizes different constituents in their respective food groups on the questionnaire. Open recall-based questionnaires are usually administered by the multiple-pass method for 24-h recalls. The multiple-pass method consists of five steps that are followed in chronological order: quick listing of food, recalling forgotten foods, asking time and occasion of consumption, a thorough analysis of food composition, and ultimately a final review of all food items (15). On the other hand, in list-based method, the interviewer pre-defines a list of food items within each food group, and the respondent simply responds “yes” or “no” after listening to the list (16).
However, the dietary data collection methodology used traditionally has a range of drawbacks, such as respondent and researcher burden (17). The precision of 24-h recalls is hampered by memory and attention (18). Additionally, the success of method depends on persistence of the interviewer. Interviewers need to identify food ingredients and categorize them into appropriate food groups. Hiring and training educated enumerators for conducting 24-h recalls is a costly process (19) that is challenging in resource-constrained environments. Moreover, it has been confirmed that using 24-h recalls as the sole method of diet assessment results in systemic negative bias. The bias consequently leads to a significant decrease in average daily energy and nutrient intake in rural populations (20). Respondents with unstructured eating habits and regular snacking are more likely to under-report their diets (21). The feeding of 24-h recall questionnaires on a computer for analysis requires expertise and can be a time-consuming chore (22). The time and resources necessary for an interviewer-administered 24-h recall have limited its application for dietary assessment at national and subnational levels (18).
To overcome these gaps, smartphone applications can be employed as a substitute for conventional interviewer-administered 24-h recalls (23). According to Statista, there are currently 3.8 billion mobile users worldwide, which equates to 48.33 per cent of the global population. With time, smartphone capabilities have advanced, allowing them to link with the internet and run a complete operating system. Smartphone applications that enable users to track their food and beverage intake can be an easy and cost-effective way to conduct a dietary assessment (23). Smartphones not only capture food entries faster than traditional methods but also collect real-time data and substantially reduce the researcher burden (24). The ‘Eat and Track’ (EaT) (23), ‘My Meal Mate’ (24), ‘Electronic Dietary Intake Assessment’ (25, 26), ‘Easy Diet Diary’ (27), and ‘Electronic Carnet Alimentaire’ (e-CA) (28) are few dietary tracking mobile applications that have been validated with 24-h dietary recall as a reference process. Among these studies, ‘My Meal Mate’, ‘Easy Diet Diary’, and ‘Electronic Carnet Alimentaire’ (e-CA) had 72, 62.5, and 62% of participants as women, respectively (24, 26, 28).
To the best of our knowledge, this is the first study that examines the existing methodologies of diet diversity indicator’s and proposes the importance of replacing traditional methods with a smartphone application. The findings of this review paper helped us to identify and analyze the potential gaps in traditional methodologies. In the second stage, we propose that using a smartphone application for diet diversity indicators to capture and analyze data in real-time would help in overcoming the constraints of traditional methods, while improve the quality of data collection by increasing efficiency and limiting the misreporting errors.
2. Materials and methods
2.1. Literature search
The goal of the literature search was to identify and assess the methodologies employed in studies that implement MDD-W, IYCF-MDD, and HDDS as diet diversity indicator for women, children, and households, respectively. Relevant literature includes the FAO report “Moving forward on choosing a standard operational indicator of women’s dietary diversity” (29), the “Nutrition baseline survey summary report” (30) and systematic reviews of research on nutrition-sensitive agriculture that aided in the development of search strategy (31–34). Keywords search in Scopus, MDPI Nutrients, Web of Science, PubMed, ScienceDirect, Agris (a literature search portal of the United Nations Food and Agriculture Organization), and Google Scholar was conducted in May 2021 to include peer-reviewed studies published in English. The keywords employed in the literature search were “women,” “children,” “households,” “MDD-W,” “MDD,” “HDDS,” “nutrition-sensitive interventions,” “dietary diversity,” “dietary quality,” “food consumption,” “food variety,” “24-h dietary recall,” and “food frequency questionnaire.” The literature search was carried out over a time period of 11 months. This review considered all types of research designs related to diet diversity indicators, ranging from cross-sectional to cohort studies, as well as other impact evaluation or intervention studies.
2.2. Data screening and classification
All research papers were screened twice. In the initial screening stage, titles and abstracts were reviewed, and studies unrelated to the evaluation process were excluded. This was followed by a comprehensive text screening to ensure that studies met the second-stage eligibility criteria: studies that scrutinized, evaluated, associated, or validated either of diet diversity indicator among MDD-W, IYCF-MDD, and HDDS, with or without other household or individual diet diversity/ diet quality indicators, factors, or characteristics. The following data was tabulated to aid the full-text screening: (i) Research aim (purpose of the study); (ii) Study design (e.g., baseline survey of an intervention); (iii) Country (location of the study); (iv) Target audience [subject, e.g., pregnant women (15–49 years)]; (v) Dietary data collection methodology (e.g., 24-h dietary recall using the multiple-pass method); (vi) Sample size (number of participants involved, e.g., N = 558); (vii) Dietary data type (e.g., Quantitative or Qualitative); (viii) Dietary data collection frequency (number of times dietary data collected, e.g., once every year, for 3 years; (ix) Dietary data collection point (place where data was collected, e.g., household).
After screening, 80 studies were chosen to be included in this review. The applicability and methodology of these studies were assessed critically. To begin classification, studies were categorized according to methodology, whether the dietary data was gathered using an interviewer-administered recall (n = 78), self-administered recall (n = 2), or both (n = 0). The studies were further classified into four categories: 24-h (24-h) dietary recall, 48-h (48-h) dietary recall, 7-day (7-d) dietary recall, 30-day (30-d) dietary recall, and 1-year (1-y) dietary recall. Dietary data was classified as quantitative if the portion estimation of food was done by weighing scale, food photo atlas, or standard household utensils, including pots, plates, bowls, cups, or spoons. On the contrary, portion estimate was classed as semi-quantitative if it was performed solely to get an idea of the food quantity, else, it was categorized as qualitative. Dietary data collection frequency was classified as consecutive, if diets were recorded on sequential days, otherwise, it was classified as non-consecutive.
All critical assessment disagreements among the reviewing co-authors were settled through discussion.
3. Results
3.1. Description of the studies
The context and methodology used in the 80 research studies included in this review are summarized in Table 1. The studies have evidence from 38 countries, including one from Oceania (Fiji), two from North America (United States and Costa Rica), seven from South America (Brazil, Chile, Colombia, Ecuador, Peru, Suriname, and Venezuela), 12 from Asia (Bangladesh, Cambodia, China, India, Indonesia, Iran, Laos, Lebanon, Nepal, Pakistan, Philippines, and Sri Lanka) and 16 from Sub-Saharan Africa (Benin, Burkina Faso, Ethiopia, Ghana, Kenya, Malawi, Mali, Mozambique, Nigeria, Rwanda, Somalia, South Africa, Tanzania, Uganda, Zambia, and Zimbabwe). Seven studies present findings from multiple countries (54, 66, 73, 75, 100). In terms of their purpose, there was significant heterogeneity across 80 studies regarding association with micronutrient adequacy, household food insecurity, agricultural food production diversity, seasonal food patterns, food purchasing practices, women empowerment, antenatal care practices, maternal health care, child growth, child stunting, prevalence of anemia, and bone fractures. Two studies were designed in response to an increased demand for an indicator that can be expressed in terms of the prevalence of meeting a minimum acceptable level of diet diversity in women of reproductive age, resulting in the development of MDD-W as a dichotomous indicator (73, 75). Most of the studies were cross-sectional surveys that looked at association rather than causation. With sample sizes ranging from 40 in a pregnancy cohort study (76) to 41,101 in a prospective study (36), the number of households or individuals surveyed in these studies varied substantially.
Table 1.
An overview of context and methodology of 80 research studies included in this review.
| S. No. | Author/year | Research aim | Study design | Country | Target audience | Dietary data | ||||
|---|---|---|---|---|---|---|---|---|---|---|
| Methodology | Type | Collection frequency | Collection point | Sample size | ||||||
| 1 | Melby et al. (2020) (35) | To establish relationship among agricultural food production diversity (FPD), Diet Diversity (DD), and household food insecurity (HFI) | Cross-sectional survey | Ecuador | Non-pregnant women (18–85 years) | 24-h dietary recall Multiple pass |
Quantitative | 1 day | Household | N = 558 |
| 2 | Jones et al. (2018) (36) | To establish association of farm level agricultural biodiversity with DD and Diet Quality (DQ) To assess the effect of market orientation on this association |
Cross-sectional survey | Peru | Households with woman (18–49 years) | 24-h dietary recall questionnaire. Multimodule household survey questionnaire |
Quantitative | Non-consecutive 2 days |
Household | N = 100 |
| 3 | Zhang et al. (2020) (37) | To investigate effect of DD on any type of fracture in adults | Secondary analysis of cross-sectional survey | China | Adults (40 + years) | 24-h dietary recall questionnaire Household food weight inventory |
Quantitative | Consecutive 3 days |
Household |
N = 10,192 (4,795 Men; 5,397 Women) |
| 4 | Nguyen et al. (2018) (38) | -To compare micronutrient adequacy between pregnant adolescent girls and women -To check performance of Women Diet Diversity Score in predicting mean probability of adequacy -To check performance of MDD-W in pregnant adolescent girls and women |
Secondary analysis of cross-sectional survey | Bangladesh | Pregnant women (18 + years) | 24-h dietary recall Multiple pass 24-h dietary recall List-based questionnaire |
Quantitative | Twice, same day | Household | N = 600 |
| 5 | Seiermann et al. (2021) (39) | To check effect of dietary changes on women’s health during Ramadan | Secondary analysis of repeated cross-sectional survey | Bangladesh | Married women | 24-h dietary recall | Qualitative | Once every 2 months, for 5 years | Household | N = 852 |
| 6 | Sultana et al. (2019) (40) | To assess DD and nutrition status of residential students | Cross-sectional survey | Bangladesh | Women (18–26 years) | 24-h dietary recall -Multiple pass | Quantitative | Consecutive 3 days | University | N = 160 |
| 7 | Bellon et al. (2016) (41) | To investigate relationship of diversity of plant species raised and variety of foods purchased by women of rural households on DD under different market conditions | Cross-sectional survey | Benin | Households with women (15–49 years) | 24-h dietary recall Semi-structured questionnaire Food frequency questionnaire (FFQ) | Qualitative | −15 days (Farm diversity) −7 day (Market diversity) −1 day (Diet diversity) | Household | N = 652 |
| 8 | Diop et al. (2021) (42) | To examine performance of indicators in predicting micronutrient adequacy | Baseline survey of an intervention | Burkina Faso | Pairs of children (24–59 months old) and women | 24-h dietary recall Computer assisted personal interviewing |
Quantitative | Non-consecutive 2 days | Household | N = 1,066 |
| 9 | Custodio et al. (2020) (43) | To check association of MDD-W with food security and purchasing practices | Secondary analysis of repeated Cross-sectional survey | Burkina Faso | Women (15–49 years) | 24-h dietary recall | Qualitative | Once every year, for 3 years | Household | N = 12,754 |
| 10 | Getacher et al. (2020) (44) | To determine prevalence of MDD-W and associated factors among lactating mothers | Cross-sectional survey | Ethiopia | Women (15–49 years) | 24-h dietary recall | Qualitative | 1 day | Household | N = 652 |
| 11 | Hanley-Cook et al. (2020) (45) | To assess validity of List-based and Open recall-based methods with weighed food record for MDD-W | Cross-sectional survey | Cambodia Ethiopia Zambia |
Women (15–49 years) | 24-h dietary recall Weighed food records |
Quantitative | 1 day | Household | N = 1,337 |
| 12 | Girma et al. (2019) (46) | To check nutrition and other factors that contribute to low birth weight in newborns | Cross-sectional survey | Ethiopia | Women and Newborn infants | 24-h dietary recall Questionnaires on socio-economic, medical, behavior, environment, and infant related factors |
Qualitative | 1 day | Health care facilities | N = 279 |
| 13 | Gyimah et al. (2021) (47) | To understand factors contributing to DD in pregnant women | Longitudinal study | Ghana | Pregnant adolescents | 24-h dietary recall Questionnaire on socio-demographic factors |
Quantitative | 3 days | Health care facilities | N = 416 |
| 14 | Agbozo et al. (2020) (48) | To determine link between maternal food habits, antenatal care practices and the prevalence of anemia in the first, second, and third trimesters of pregnancy | Prospective study | Ghana | Women (15–49 years) | 24-h dietary recall FFQ |
Qualitative | 1 day | Health care facilities | N = 415 |
| 15 | Saaka et al. (2021) (49) | To determine the independent predictors of DD and their agreement in nutrition status of pregnant women | Cross-sectional survey | Ghana | Women (15–49 years) | 24-h dietary recall −7-day FFQ |
Quantitative | 1 day | Household | N = 423 |
| 16 | Ayensu et al. (2020) (50) | To determine the prevalence of anemia and dietary micronutrient intakes in pregnant women | Cross-sectional survey | Ghana | Pregnant women (15–49 years) | 24-h dietary recall -FFQ |
Quantitative | Non-consecutive 3 days |
Household | N = 379 |
| 17 | Bukari et al. (2021) (51) | To examine diet quality and its association with household factors and gestational age | Cross-sectional survey | Ghana | Pregnant women (15–49 years) | 24-h dietary recall Questionnaires on socio-demographic characteristics |
Qualitative | 1 day | Health care facilities | N = 403 |
| 18 | Saaka et al. (2017) (52) | To evaluate maternal dietary intake and its association with nutrition status | Cross-sectional survey | Ghana | Households with pregnant women (15–49 years) | 24-h dietary recall -FFQ |
Qualitative | 1 day | Household | N = 400 |
| 19 | Gupta et al. (2019) (53) | To examine women’s agricultural empowerment and iron in-sufficiency | Agriculture-nutrition study (Cross-sectional survey) | India | Non-pregnant Non-lactating (NPNL) women (15–49 years) | 24-h dietary recall -FFQ |
Quantitative | 1 day | Household | N = 960 |
| 20 | Nguyen et al. (2020) (54) | To evaluate performance of list-based and quantitative open recall-based methods in predicting micronutrient adequacy | Secondary analysis of baseline survey | Bangladesh India |
Pregnant women | 24-h dietary recall Qualitative list-based and quantitative open-recall based questionnaire |
Quantitative | 1 day Repeated for 10% (Non-consecutive day) |
Household | N = 1,255 |
| 21 | Ghosh-Jerath et al. (2021) (55) | To determine link between production and access to food, DD, and nutrient intake | Cross-sectional survey | India | Households with Non-pregnant (56) woman (15–49 years) and child (6–54 months) | 24-h dietary recall Multiple pass -FFQ |
Quantitative | Non-consecutive 2 days |
Household | N = 201 |
| 22 | Diana et al. (2019) (56) | To analyze DD and DQ among women | Cross-sectional survey | Indonesia | Anemic pregnant women | 24-h dietary recall | Quantitative | 2 days | Household | N = 152 |
| 23 | Gitagia et al. (2019) (57) | To record Agrobiodiversity, DD and factors influencing them | Cross-sectional survey | Kenya | Women (18–49 years) | 24-h dietary recall Semi quantitative questionnaire |
Semi-quantitative | 1 day | Household | N = 384 |
| 24 | Lamanna et al. (2019) (19) | To check degree of agreement between Computer Assisted Telephone Interviewing (CATI) and Traditional methods | Validation study | Kenya | Households with woman (15–49 years) and child (6–23 months) | 24-h dietary recall -CATI |
– | 2 days | Household | N = 1,821 |
| 25 | Jomaa et al. (2020) (58) | To investigate the links between household food insecurity (HFI) and mother’s sociodemographic, anthropometric, and dietary intakes | Secondary analysis of cross-sectional survey | Lebanon | Households with mother and their child (4–18 years) | 24-h dietary recall | Quantitative | 1 day | Household | N = 1,204 |
| 26 | Adubra et al. (2019) (59) | To investigate agreement of MDD-W with household food insecurity and farm production diversity | Baseline survey of a 3-year intervention (Cross-sectional survey) | Mali | Households with mother–child pair | 24-h dietary recall Android tablet |
Qualitative | 1 day | Household | N = 5,046 |
| 27 | Dulal et al., (2017) (60) | To check association between Enhanced Homestead Food Production (EHFP) and DD of mother and child | Evaluation of ongoing intervention (Repeated cross-sectional survey) | Nepal | Mothers and children (6–23 months) | 7-day dietary recall | – | 2 days | Household | N = 3,095 (2,101 mothers; 994 children) |
| 28 | Shrestha et al. (2021) (61) | To assess DD and associated factors in hilly regions with urban municipality | Cross-sectional survey | Nepal | Pregnant women | 24-h dietary recall | Semi-quantitative | 1 day | Household | N = 327 |
| 29 | Samuel et al. (2019) (62) | Comparison of DD in Cassava value chain households and non-Cassava value chain households | Descriptive cross-sectional survey | Nigeria | Households | 24-h dietary recall -FFQ |
– | Non-consecutive 2 days |
Household | N = 572 |
| 30 | Brazier et al. (2020) (63) | To assess DD and nutritional status of women in marginalized community | Repeated cross-sectional survey | Pakistan | Households with NPNL women (16–49 years) | 24-h dietary recall Multiple pass method |
Semi-quantitative | 5 days | Household | N = 47 |
| 31 | Nsereko et al. (2020) (64) | To discover modifiable risk factors for targeted interventions that aim to reduce Preterm birth | Prospective, longitudinal study | Rwanda | Pregnant women (18–49 years) | 24-h dietary recall FFQ |
– | 1 day | University | N = 367 |
| 32 | Chakona and Shackleton (2017) (65) | To assess DD and establish relation between MDD-W and Household characteristics | Cross-sectional survey | South Africa | Women (15–49 years) | 48-h dietary recall -FFQ |
– | 4 days | Household | N = 554 |
| 33 | Gómez et al. (2020) (66) | To establish relation between MDD-W and micronutrient adequacy among women from Latin American countries | Secondary analysis of cross-sectional survey | Brazil, Colombia, Costa Rica, Chile, Ecuador, Peru, Venezuela | NPNL women (15–49 years) | 24-h dietary recall Multiple pass method |
Quantitative | Non-consecutive 2 days |
Household | N = 3,704 |
| 34 | Weerasekara et al. (2020) (67) | To evaluate DD, nutrient adequacy, dietary and traditional food patterns in marginalized areas | Cross-sectional survey | Sri Lanka | Women (18–49 years) | 24-h dietary recall Multiple pass method |
Quantitative | 1 day | Household | N = 400 |
| 35 | Madzorera et al. (2020) (68) | To establish link among maternal DD, DQ with birth outcomes in pregnant women | Secondary analysis of placebo-controlled study | Tanzania | Pregnant women (18–49 years) | 24-h dietary recall | Quantitative | Once in a month, for 6 months | Health care facilities | N = 7,553 |
| 36 | Conti et al. (2021) (69) | To inspect factors contributing to micronutrient adequacy in women | Cross-sectional survey | Tanzania | Women (14–49 years) | 24-h dietary recall | Quantitative | 1 day | Household | N = 141 |
| 37 | Huang et al. (2018) (70) | To recognize factors of maternal DD and its association with child growth outcomes | Longitudinal survey | Tanzania | Mother–child (under 24 months) pairs | 30-day dietary recall FFQ |
Qualitative | 1 day | Health care facilities | N = 361 |
| 38 | Madzorera et al. (2021) (71) | To examine role of prenatal maternal DD in infant growth | Secondary analysis of a birth cohort study | Uganda | Pregnant women (15–49 years) | 24-h dietary recall | – | 1 day | Household | N = 3,291 |
| 39 | Arimond et al. (2010) (72) | To create simple indicator that can be served as proxy to measure the micronutrient of women’s diets | Secondary analysis of 24-h recalls (collected for distinct purposes) | Bangladesh, Burkina Faso, Mali, Mozambique, Philippines | Women (15–49 years) | 24-h dietary recall | Quantitative | Non-consecutive 2 days |
Household | N = 2,560 |
| 40 | Yves Martin-Prevel et al. (2017) (73) | To develop dichotomous indicator for assessing DD in women of reproductive age | Secondary analysis of 24-h recalls (collected for distinct purposes) | Bangladesh Burkina Faso Mali Mozambique Philippines Uganda |
Women (15–49 years) | 24-h dietary recall -Multiple pass method |
Quantitative | Non-consecutive 2 days |
Household | N = 4,166 |
| 41 | Ahern et al. (2021) (74) | To investigate seasonal variations in MDD-W and food group intake in regions where seasonal agricultural production and food availability have significant impact on DD | Repeated cross-sectional survey | Malawi Zambia |
Women (15–49 years) | 24-h dietary recall | Qualitative | Once every month, for 11 rounds | Household | N = 200 |
| 42 | Kornatowski and Comstock (2018) (75) | To assess DD in women during their third trimester of pregnancy and establish relation with pre-pregnancy Body Mass Index | Secondary analysis of pregnancy cohort study | United States | Women (18+ years) | 24-h dietary recall Self-administered questionnaires |
Qualitative | 1 day | Health care facilities | N = 40 |
| 43 | Gicevic et al. (2018) (76) | To assess bonding of DD and DQ scores with gestational diabetes mellitus and hypertensive disorders of pregnancy | Prospective study | United States | Women (24–44 years) | 1-year dietary recall FFQ Self-administered questionnaires |
Semi-quantitative | Once every year, for 4 years | Health care facilities | N = 41,101 |
| 44 | Paré et al. (2019) (77) | To determine the prevalence of wasting in children aged 6–23 months | Secondary analysis of Cross-sectional survey | Burkina Faso | Households with children 6–23 months of age | 24-h dietary recall | Qualitative | 1 day | Household | N = 956 |
| 45 | Hipgrave et al. (2014) (78) | To assess IYCF and anemia in central and western China | Cross-sectional survey | China | Households with children 6–23 months of age | 24-h dietary recall FFQ |
Semi-quantitative | 1 day | Household | N = 2,244 |
| 46 | Wuneh et al. (2019) (79) | To assess Minimum Meal Frequency (MMF) and MDD | Cross-sectional survey | Ethiopia | Households with children 6–23 months of age | 24-h dietary recall Open recall-based questionnaire |
Qualitative | 1 day | Household | N = 807 |
| 47 | Guja et al. (2021) (80) | To examine concordance between mother and child diet diversity for designing intervention programs | Cross-sectional survey | Ethiopia | Mother and child pair (6–23 months age) | −24-h dietary recall -FFQ |
Qualitative | 1 day | Household | N = 796 |
| 48 | Kim et al. (2016) (81) | To evaluate the effect of interventions on IYCF practices and anthropometry | Repeated cross-sectional survey | Ethiopia | Households with children 0–59 months of age | 24-h dietary recall | Qualitative | Twice, at baseline and endline of intervention | Household | N = 2,969 |
| 49 | Kamran et al. (2017) (82) | To assess determinants of complementary feeding practices | Cross-sectional survey | Iran | Mothers of children aged 6–23 months | 24-h dietary recall -FFQ |
Qualitative | 1 day | Household | N = 576 |
| 50 | Chama (2020) (83) | To determine the contribution of edible non-timber forest products to nutritional status | Cross-sectional survey | Zambia | Households with mother and child (6–23 months) pair | 24-h dietary recall List-based questionnaire -FFQ |
Both Qualitative and Quantitative | 1 day | Household | N = 158 |
| 51 | Modugu et al. (2022) (84) | To determine influence of gender, and migration on IYCF practices | Cross-sectional survey | India | Households with mother and child (6–23 months) pair | 24-h dietary recall FFQ |
Both qualitative and quantitative | 1 day | Household | N = 325 |
| 52 | Wormer et al. (2021) (85) | To determine the association between respiratory tract infections and IYCF practices | Cross-sectional survey | Suriname | Households with mother and child (12 months) pair | 24-h dietary recall | Qualitative | 1 day | Household | N = 763 |
| 53 | Kogade et al. (2019) (86) | To evaluate association of IYCF practices with sociocultural determinants | Cross-sectional survey | India | Mothers of children aged 0–23 months of age | 24-h dietary recall | – | 1 day | Household | N = 612 |
| 54 | Solomon et al. (2017) (87) | To assess the level of MDD and associated factors | Cross-sectional survey | Ethiopia | Mothers of children aged 6–23 months of age | 24-h dietary recall | Quantitative | 1 day | Health care facility | N = 352 |
| 55 | Molla et al. (2021) (88) | To determine DD and associated factors | Cross-sectional survey | Ethiopia | Households with mother and child (6–23 months) pair | 24-h dietary recall | Qualitative | 1 day | Household | N = 665 |
| 56 | Dangura (2017) (89) | To determine DD level and associated factors in Gorche district | Cross-sectional survey | Ethiopia | Households with mother and child (6–23 months) pair | 24-h dietary recall | Quantitative | 1 day | Household | N = 417 |
| 57 | Mekonnen et al. (2017) (90) | To determine MMF, MDD and associated factors | Cross-sectional survey | Ethiopia | Households with mother/caregiver and child (6–23 months) pair | 24-h dietary recall -FFQ |
– | 1 day | Household | N = 623 |
| 58 | Belew et al. (2017) (91) | To determine MMF, MDD and associated factors | Cross-sectional survey | Ethiopia | Households with mother and child (6–23 months) pair | 24-h dietary recall Open recall-based questionnaire |
Qualitative | 1 day | Household | N = 1,034 |
| 59 | Gezahegn and Tegegne (2020) (92) | To determine DD and associated predictors in Gorche district | Cross-sectional survey | Ethiopia | Households with mother and child (6–23 months) pair | 24-h dietary recall Open recall-based questionnaire |
– | 1 day | Household | N = 517 |
| 60 | Blackstone and Sanghvi (2018) (3) | To measure maternal, household, and MDD characteristics | Secondary analysis of cross-sectional survey | Bangladesh | Households with mother and child (6–23 months) pair | 24-h dietary recall | – | Twice in 4 years | Household | N1 = 2,925 N2 = 2,908 |
| 61 | Zhao et al. (2021) (93) | To determine relation between dietary diversity, meal frequency, and early childhood developmental outcomes | Secondary analysis of cross-sectional survey | China | Households with mother and child (6–23 months) pair | 24-h dietary recall | Qualitative | 1 day | Village clinic | N = 1,534 |
| 62 | Chilinda et al. (2021) (94) | To explore the effect of household water access on MDD standards | Secondary analysis of cross-sectional survey | Malawi | Households with mother and child (6–23 months) pair | 24-h dietary recall | Qualitative | 1 day | Household | N = 4,727 |
| 63 | Di Marcantonio et al. (2020) (95) | To assess DD and identify the associated factors | Cross-sectional survey | Somalia | Households with mother and child (6–23 months) pair | 24-h dietary recall | – | 1 day | Household | N = 2,922 |
| 64 | Rubhara et al. (2020) (96) | To assess the impact of cash crop production on household food security | Cross sectional survey | Zimbabwe | Households | 24-h dietary recall | Qualitative | 1 day | Household | N = 281 |
| 65 | Gandure et al. (2010) (97) | To analyze food security indicators used to assess households | Cross sectional survey | Zimbabwe | Households | 24-h dietary recall | Qualitative | 1 day | Household | N = 178 |
| 66 | Cheteni et al. (2020) (98) | To determine HDDS and food security | Cross sectional survey | South Africa | Households | 7-d dietary recall | Qualitative | 1 day | Household | N = 296 |
| 67 | Kennedy et al. (2010) (99) | To provide an overview and compare the performance of HDDS and Food Consumption Score (FCS) | Cross sectional survey | Burkina Faso Lao PDR Uganda |
Households | 24-h dietary recall 7-d dietary recall FFQ List-based questionnaire |
Qualitative | 1 day | Household | N = 3,913 |
| 68 | McDonald et al. (2015) (100) | To identify correlates of household food insecurity and poor dietary diversity | Baseline survey of an intervention | Cambodia | Households | 24-h dietary recall | Quantitative | 1 day | Household | N = 900 |
| 69 | Schwei et al. (2017) (7) | To define a relationship between HDDS, food security, and consumption of Vitamin A-rich foods | Cross sectional survey | Ethiopia | Households | 24-h dietary recall List-based questionnaire |
Qualitative | 1 day | Household | N = 300 |
| 70 | Aweke et al. (2021) (101) | To examine the impact of agricultural technologies on household food and nutrition security | Cross sectional survey | Ethiopia | Households | 24-h dietary recall 7-d dietary recall -FFQ |
Quantitative | 1 day | Household | N = 248 |
| 71 | Melaku et al. (2018) (102) | To use dietary patterns as alternative to diet diversity scores, and investigate their association with childhood stunting | Cross sectional survey | Ethiopia | Households with mother child pair | 24-h dietary recall | Qualitative | 1 day | Household | N = 3,788 |
| 72 | O’Meara et al. (2019) (103) | To examine diet diversity in indigenous food-producing households | Cross sectional survey | Fiji | Households | 24-h dietary recall Open recall-based questionnaire |
Qualitative | 1 day | Household | N = 161 |
| 73 | Mahmudiono et al. (2017) (104) | To explore the relationship between child stunting and household dietary diversity | Cross sectional survey | Indonesia | Households with children below 5 years of age | 24-h dietary recall | Qualitative | 1 day | Household | N = 736 |
| 74 | Jones et al. (2014) (105) | To explore relationship and identify determinants between production diversity of household farms and HDDS | Secondary analysis of Cross-sectional survey | Malawi | Households | 24-h dietary recall 7-d dietary recall -FFQ |
Quantitative | 1 day | Household | N = 6,623 |
| 75 | Nkonde et al. (2021) (106) | To determine effect of agricultural diversification on household dietary diversity | Secondary analysis of Longitudinal survey | Zambia | Households with children below 5 years of age | 24-h dietary recall | Qualitative | 1 day | Household | N = 7,934 |
| 76 | Khumalo and Sibanda (2019) (107) | To determine the contribution of agriculture in food security status of households | Cross sectional survey | South Africa | Households | 24-h dietary recall Open based and list-based questionnaire 4-w dietary recall |
Quantitative | 1 day | Household | N = 208 |
| 77 | Cordero-Ahiman et al. (2021) (5) | To analyze different factors determining HDDS | Cross sectional survey | Ecuador | Households | 7-d dietary recall | Qualitative | 1 day | Household | N = 383 |
| 78 | Roba et al. (2019) (108) | To assess different indicators of household and individual food security status | Longitudinal survey | Ethiopia | Households | 24-h dietary recall 7-d dietary recall 1-m dietary recall -FFQ |
Qualitative | Twice (before and after harvest season) | Household | N = 800 |
| 79 | Hirvonen et al. (2016) (109) | To assess role of seasonality on sources, intake of energy (per capita), and HDDS | Cross sectional survey | Ethiopia | Households | 4-d dietary recall | Quantitative | Twice a week in every month for 1 year | Household | N = 27,835 |
| 80 | Ngema et al. (2018) (110) | To assess the determinants of food security status of households | Cross sectional survey | South Africa | Households | 24-h dietary recall | Qualitative and Quantitative | 1 day | Household | N = 495 |
3.2. Critical appraisal of dietary data collection methodology
For data collection, 78 of the 80 studies employed well-trained interviewers to deliver face-to-face interviews to respondents, while two studies employed self-administered recalls. Three studies reported data collection through tablet-based surveys (19, 36, 45). Only one study, among the 80, used computer-assisted telephone interviewing in addition to interviewer-assisted face-to-face recall (19). All food items in dietary recalls were classified into major food groups as defined in the MDD-W, IYCF-MDD, and HDDS guidelines. Traditional and mixed foods, such as chicken curry and pizza, were disaggregated into respective ingredients and then included in their relevant food groups. The diet diversity score was then calculated by adding the total number of food groups consumed by an individual or the household in a 24-h period. Interviewers were required to attend training sessions on the study objective, data collection procedure, sampling method, ethical issues, data entry, and data management before traveling into the field in almost all the 78 studies. In two studies, employing self-administered recalls (75, 76), trained professionals were required at later stages to assess dietary data from forms. It should be highlighted that, unlike most studies, neither of these two kinds of research were undertaken in resource-poor settings. In the context of recalls, 67 studies employed 24-h recalls, three studies employed 7-d recall, five studies employed both 24-h and 7-d recall, and the remaining five studies employed 48-h recall, 4-d recall, 30-d recall, 1-y recall, and both 24-h and 4-w recall, respectively. The recalls were administered using list-based, open recall-based, or food frequency questionnaires. Although quantitative recalls can be challenging, especially in settings with low literacy rate, recalls practiced in 28 studies were quantitative, 33 were qualitative, five were semi-quantitative, three were both quantitative and qualitative, and 11 studies did not report on the type of recall. Dietary data was collected once in 52 studies, twice in 15 studies, and more than twice in the remaining studies. Data was collected from respondent’s household in 68 studies, health care facilities in 10 studies, and universities in two studies.
Among different methodologies, although there is no fixed gold standard diet evaluation method, the quantitative 24-h recall has been frequently employed in variety of applications such as describing intakes, examining associations, and evaluating the effects of interventions. Nevertheless, we cannot rule out the possibility of recall bias since retrospective methods tend to underestimate or overestimate actual food consumption for various reasons, including forgetfulness (111). Workshops for interviewers, including classroom training and fieldwork are required for the collection of high-quality data with minimal bias (45). Three studies reviewed in this paper evaluate the validity of different methodologies used for data collection (19, 45, 54). Hanley-Cook et al. (45) assessed the relative validation of qualitative list-based and open recall-based methods with reference to weighed food records. It was discovered that in these three countries (Cambodia, Ethiopia, and Zambia), both list-based and open recall-based methods were prone to misreport consumption of certain food groups. Reporting of food items that were not consumed in sufficient quantity, i.e., less than 15 grams for MDD-W, resulted in overreporting for both methods by 10%. These results were consistent with the findings of the second validation study conducted in India and Bangladesh (54), in which they assessed validation of qualitative list-based with reference to quantitative open recall-based methodology. The third validation study evaluated the performance of computer-assisted telephone interviewing (CATI) for collecting dietary data from African women in large-scale studies (19). The findings of this study revealed that switching from traditional in-person interviews increased the diet diversity scores by 11–14% in some indicators. This discrepancy could be the consequence of sensitive probes, which may unveil unfavorable information about the responder. The responses demonstrated a significant social-desirability bias, which can be mitigated by changing the mode of data collection.
4. Discussion
The review has attempted to describe all methodological aspects applied in diet diversity indicator studies, to critically assess the limitations of traditional methodology. According to findings of the review, most studies have employed interviewer-administered 24-h recalls to assess dietary diversity. However, every method possesses constraints that affect data collection and thus undermine conclusions of the research, especially if reported errors are not addressed to the maximum extent possible, using appropriate tool selection. Since they rely on memory and social perception of questions asked, major drawbacks include recall (51) and social-desirability bias (19). Furthermore, traditional methodology necessitates a significant amount of effort on part of the interviewer to probe and transcribe the respondent’s dietary intake, which comes with a high chance of errors and time-related costs (18). Technology adaptation has resulted in notable changes in dietary assessment methodologies, all of which have a favorable effect on cost, respondent-researcher workload, efficiency of data collection, coding and processing of dietary intakes, response rates, and the consistency of assessment measures (112). Since personal digital assistants (PDAs), tape recorders, scan- and sensor-based technologies have all become outdated, and all operations of web-based or computer-based platforms/ software can now be performed on smartphones, dietary evaluation via a smartphone-based application has a great potential (28). According to prior studies, smartphones are convenient, easy to use, and handy, thus preferred over conventional methodologies for recording dietary data (24). Additionally, smartphones possess the ability to overcome the shortcomings of conventional methodologies (113).
4.1. Respondent bias
4.1.1. Recall
Dietary recalls ask respondents to remember and report all foods and beverages consumed in a specific time period, usually the preceding day’s 24 h. Dietary recalls are conducted without prior notice, eliminating the risk of reactivity (18). The use of a local interviewer to administer recall minimizes the literacy barrier and aids recall. However, many respondents have trouble distinguishing between what they consume habitually and what they ate the day before, leaving the door open to omissions and intrusions (114). The human ability to recall events fades over time, beginning within an hour after the meal consumption (115). It can be deduced that longer the recall period, greater is the bias (60). Furthermore, recalling foods eaten away from home is equally dependent on memory, which may reduce the validity of dietary recalls (37). Recall accuracy can be enhanced if executed several times over 24 h, hence minimizing the intrusion rate by shifting to a record-like approach from the recall approach (116). This can be accomplished by using a smartphone application that, due to its portability, can be always carried around by respondents and collects real-time self-administered dietary data on foods consumed via digital recording rather than through paper questionnaires. This will reduce the amount of effort and time required to fill out and decipher conventional forms in 24-h recall interviews, while increasing respondent motivation to record meals (28).
4.1.2. Social-desirability
Social-desirability bias is the tendency of respondents to answer questions in a way they hope will be considered favorable by others (117). Generally, when the survey process is more socialized, respondents are more likely to give answers that are considered desirable by society (19). In dietary surveys, the bias can appear as over-reporting of “healthy diets” and under-reporting of “unhealthy diets.” Additionally, biases based on the sex of the interviewer are becoming more prevalent in the developing world. In one of the MDD-W studies, evidence was found that male interviewers were more likely to record lower diet diversity scores than female interviewers (19). At the point, when respondents are unsure about the interviewer’s probable response, or when the noting cycle does not include any relationship with others, the responses are based more on what respondents actually know or consume (118). The main cause of social-desirability bias, such as the presence of an acquaintance or interactions with the interviewer (44), can be avoided by switching from current traditional practices to technology-based methodologies. By ensuring respondent’s privacy, a smartphone app that allows them to record their dietary data without engaging in face-to-face interactions, by logging into their personal account, could help reduce social-desirability and sex-bias. Such biases in data recording are well documented, but the link between them and data collection methodology needs to be investigated further.
4.2. Interviewer training and burden
In-person interviews using traditional list-based or open recall-based questionnaires have their own set of functional benefits and drawbacks. The list-based methodology demands less interviewer capacity and training time; nonetheless, its implementation can be more time-consuming and prone to food misclassification, particularly for foods taken in little amounts (54, 119). For example, in a study conducted in India, milk added to tea, and onions or tomatoes added in mixed dishes were not identified by the list-based method (54). On the other hand, an open recall-based methodology can provide a more accurate and comprehensive recall of all food items consumed; however, it requires additional training and more skilled enumerators who have a working knowledge of local foods and recipes (120). In most of the studies, workshops on training and confidence-building were required during the preparatory phase to ensure precise and effective data collection. Following the collection of dietary information, incomplete columns were cross-checked, and paper questionnaires were meticulously numbered to preserve the record and privacy of respondents (44). Moreover, to ensure consistency, educated local personnel were required to develop questionnaires first in English, followed by a translation in local language, and finally back to English (44, 46, 60). In one study (45), the interviewers accompanied the respondents to measure the portion of foods consumed away from the household. To enhance interviewer confidence and assess the validity of data collection, some studies conducted small pilot surveys prior to the actual surveys. All these factors together add up to a significant increase in interviewer effort and time to collect the data. An interviewer-administered 24-h dietary recall via the ‘Automated Multiple-Pass Method’ (AMPM) can take 45–60 min in completion (121), increasing both respondent and interviewer burden. On the other hand, smartphone applications that ask structured questions about date/time, occasion of consumption, food name, constituent ingredients, portion size or number of servings, and where the meal was prepared or consumed, would not only reduce the interviewer’s workload, but also allow respondents to track their meals in their own time. Dietary planning is predominantly the duty of women in resource-poor settings. As a result, male interviewers can be less knowledgeable about the constituents of mixed dishes (19). A robust database containing the nutritional content of cooked and uncooked local foods linked with the application might reduce the labor involved in data collection, coding, analysis and provide the results at same time. This will result in a decrease in the dietary data’s reliance on the interviewer’s skill and ability. Prior studies have found a high level of agreement between traditional and modern approaches, with the latter being preferred by a majority of participants.
4.3. Cost–time constraints
In the field of dietary assessment, there is increasing pressure to enhance the accuracy, while lowering the data collection and processing cost involved in traditional methodologies (122). Training and data collection, which involves interviewing, coding, processing, and quality control, demands a significant amount of cost, and time during the research process. Dietary assessment studies commonly adopt technology to reduce the cost and complexity involved in collecting and processing dietary intake data (18). A study comparing different sampling methods among wine consumers claimed that the cost of a face-to-face survey was 2–2.5 times higher than the online surveys (123). In Kenya, while comparing the strengths and limitations of CATI with reference to face-to-face interviews, it was revealed that the former was determined to cost 5 US$ per survey and the latter was determined to cost 16 US$ per survey (19). Recently, a large number of 24-h recalls, and FFQ are being administered via modern technologies pertaining to lower costs (18). Furthermore, the primary disadvantage in the majority of the diet diversity indicator studies assessed was single-day data collection and limited sample sizes, which can be suppressed by smartphone applications, since no significant supplementary cost is required to expand the number of entries or participants. Researchers leading the development of ‘Automated Self-Administered 24-h Recall’ (ASA24) pointed out that research opportunities may arise from significant cost savings provided by newer technologies when compared to the equivalent quality of data (124).
Although most of the studies reviewed in this paper have not mentioned about how long the interviews took, studies conducted in Ethiopia (44) and Lebanon (58) revealed that interviews lasted an average of 30-min and 45-min, respectively. Longer interviews can be a demotivating element for respondents taking part in nutritional surveys. Respondents who are preoccupied with their work, may systematically disregard traditional time-consuming surveys and prefer smartphones over them. Smartphone applications can help in speeding up the data collection and analysis process. ‘My Meal Mate,’ (24) a weight-loss smartphone app, took an average of 7 min to record a meal, compared to 8.5 min for ‘DietMatePro’ (125) and 5 min for the ‘Wellnavi’ Personal Digital Assistant (PDA) device (126). Respondents reported spending an average of 22 min per day using the ‘My Meal Mate’ smartphone application for recording meals, which is comparable to a 24-h recall. However, the amount of time spent manually coding the data collected in the traditional method is far longer than with the smartphone application, which does not require any additional coding effort.
Also, the present situation of a novel virus, COVID-19, which spreads by encountering droplets of infected fluid (127), respondents might not be interested in participating in dietary surveys involving face-to-face interactions. A recent review centered on the efficiency and quality of data collection of studies during the COVID-19 pandemic revealed that 92% of studies collected data through web-based or app-based surveys (128).
Despite increasing popularity and ownership, smartphones are still not universal and have some limitations. There were legitimate concerns that new technology acceptance would be low among various population segments (even with access), notably among those who were not technologically skilled or knowledgeable (129). Prior research has demonstrated that respondents who were not using mobile devices, stated that they will not participate in a survey that does not allow them to maintain a paper diary, as an alternative to the technology-based approach (129). Switching from traditional methods may necessitate respondent training on tool usability and might increase their workload in absence of the interviewer (130). ‘Response fatigue’ is associated with self-administered respondent recordings, that last more than four consecutive days (131). Therefore, as the week progresses, the accuracy of dietary data being recorded by the respondent might more likely be compromised. Moreover, it has been acknowledged that well-off, educated, and knowledgeable respondents tend to make a major proportion of technology-based surveys (132). Being more informative, they can have better dietary habits and diet diversity scores. Consequently, collecting data via smartphone applications can be biased if the population that can be reached via smartphone differs from the general population (non-coverage bias) or if the responding population differs from the non-responding population (non-response bias) (19).
However, the collection of data by mobile phones has evolved over time, from a rarely used and frequently criticized method to a dominant mode of data collection all over the world (123). By reducing the duration involved in collecting and reporting food consumption data, while enhancing the quality by limiting misreporting errors, newer technologies have gained an edge over traditional methodology (132). Automated dietary assessment methods have the potential to reduce respondent and researcher burden while giving the flexibility of a prospective method in terms of food reporting (24). Even though the methodological features of smartphone applications and traditional methods might frequently overlap, smartphones have the potential to improve dietary assessment by allowing lesser respondent-researcher burden, more cost- and time-effective data collection, a wider geographic reach, and greater respondent acceptability.
5. Conclusion
The review has attempted to describe all methodological aspects implemented in MDD-W, IYCF-MDD, and HDDS studies to critically assess the limitations in traditional methodology and fill the gap with inventive smartphone application that works in tandem with technology and modernity. Traditional methods have inherent limitations, such as recall bias, social desirability bias, interviewer burden, and cost–time constraints, which impair data collection and thus undermine the research conclusions. Smartphone adaptation might result in notable changes in dietary assessment methodologies to make a favorable effect on cost, respondent-researcher workload, efficiency of data collection, coding and processing of dietary intakes, response rates, and the consistency of assessment measures. In conclusion, while the transition from conventional to smartphone applications is recommended for collecting dietary data, the relationship between the efficiency, effectiveness, and quality of data collection using both methodologies warrants further investigation.
Author contributions
SM, EK, and MN: conceptualization. SM, CK, EK, and MN: methodology, formal analysis, and investigation. SM, CK, MN: data curation. SM, CK, and EK: writing–original draft preparation. CK, EK, and MN: writing–review and editing and supervision. MN: funding acquisition. All authors contributed to the article and approved the submitted version.
Funding Statement
This research was funded by the International Funds for Agricultural Development.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
- 1.Byerlee D, De Janvry A, Sadoulet E, Townsend R, Klytchnikova I. World development report 2008: agriculture for development. Washington, DC: The World Bank; (2008). [Google Scholar]
- 2.World Health Organization . Guiding principles for feeding infants and young children during emergencies. Geneva: World Health Organization; (2004). [Google Scholar]
- 3.Blackstone S, Sanghvi T. A comparison of minimum dietary diversity in Bangladesh in 2011 and 2014. Matern Child Nutr. (2018) 14:e12609. doi: 10.1111/mcn.12609, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Rome F. Declaration on world food security and world food summit plan of action. World Food Summit. (1996) 1996:13–7. [Google Scholar]
- 5.Cordero-Ahiman OV, Vanegas JL, Franco-Crespo C, Beltrán-Romero P, Quinde-Lituma ME. Factors that determine the dietary diversity score in rural households: the case of the Paute River basin of Azuay Province, Ecuador. Int J Environ Res Public Health. (2021) 18:2059. doi: 10.3390/ijerph18042059, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Bhandari S, Sayami JT, Thapa P, Sayami M, Kandel BP. Banjara MRJAoph. Arch. Belges (Brussels, Belgium). (2016) 74:1–11. doi: 10.1186/s13690-016-0114-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Schwei RJ, Tesfay H, Asfaw F, Jogo W, Busse H. Household dietary diversity, vitamin a consumption and food security in rural Tigray, Ethiopia. Public Health Nutr. (2017) 20:1540–7. doi: 10.1017/S1368980017000350, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Ruel MT, Harris J, Cunningham K. Diet quality in developing countries: Diet quality. Berlin: Springer, pp. 239–261. (2013). [Google Scholar]
- 9.Kennedy G, Fanou-Fogny N, Seghieri C, Arimond M, Koreissi Y, Dossa R, et al. Food groups associated with a composite measure of probability of adequate intake of 11 micronutrients in the diets of women in urban Mali. J Nutr. (2010) 140:2070S–8S. doi: 10.3945/jn.110.123612, PMID: [DOI] [PubMed] [Google Scholar]
- 10.Haas JD, Luna SV, Lung'aho MG, Wenger MJ, Murray-Kolb LE, Beebe S, et al. Consuming iron biofortified beans increases iron status in Rwandan women after 128 days in a randomized controlled feeding trial. J Nutr. (2016) 146:1586–92. doi: 10.3945/jn.115.224741, PMID: [DOI] [PubMed] [Google Scholar]
- 11.Ritchie H, Roser M. Micronutrient deficiency. Our World in data (2017).
- 12.Ruel MT, Alderman H, Maternal and Child Nutrition Study Group . Nutrition-sensitive interventions and programmes: how can they help to accelerate progress in improving maternal and child nutrition? Lancet. (2013) 382:536–51. doi: 10.1016/S0140-6736(13)60843-0, PMID: [DOI] [PubMed] [Google Scholar]
- 13.FAO . Minimum dietary diversity for women: a guide for measurement. Rome, Italy: FAO; (2016). [Google Scholar]
- 14.World Health Organization . Indicators for assessing infant and young child feeding practices: Part 1: Definitions: Conclusions of a consensus meeting held 6–8 November 2007. Washington, DC: World Health Organization; (2008). [Google Scholar]
- 15.Raper N, Perloff B, Ingwersen L, Steinfeldt L, Anand J. An overview of USDA's dietary intake data system. J Food Comp Anal. (2004) 17:545–55. doi: 10.1016/j.jfca.2004.02.013 [DOI] [Google Scholar]
- 16.Thompson FE, Subar AF. Dietary assessment methodology. In: Coulston A, Boushey C, Ferruzzi M. Nutrition in the prevention and treatment of disease. Amsterdam, Netherlands: Elsevier, pp. 5–48. (2017). [Google Scholar]
- 17.Touvier M, Kesse-Guyot E, Méjean C, Pollet C, Malon A, Castetbon K, et al. Br J Nutr. (2011) 105:1055–64. doi: 10.1017/S0007114510004617 [DOI] [PubMed] [Google Scholar]
- 18.Thompson FE, Subar AF, Loria CM, Reedy JL, Baranowski T. Need for technological innovation in dietary assessment. J Am Diet Assoc. (2010) 110:48–51. doi: 10.1016/j.jada.2009.10.008 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Lamanna C, Hachhethu K, Chesterman S, Singhal G, Mwongela B, Ng’endo M, et al. Strengths and limitations of computer assisted telephone interviews (CATI) for nutrition data collection in rural Kenya. PLoS One. (2019) 14:e0210050. doi: 10.1371/journal.pone.0210050 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Poslusna K, Ruprich J, de Vries JH, Jakubikova M, Van’t Veer P. Misreporting of energy and micronutrient intake estimated by food records and 24 hour recalls, control and adjustment methods in practice. Br J Nutr. (2009) 101:S73–85. doi: 10.1017/S0007114509990602, PMID: [DOI] [PubMed] [Google Scholar]
- 21.Boushey CJ, Kerr DA, Wright J, Lutes KD, Ebert DS, Delp E. Use of technology in children’s dietary assessment. Eur J Clin Nutr. (2009) 63:S50–7. doi: 10.1038/ejcn.2008.65 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Buzzard M. 24-hour dietary recall and food record methods. Epidemiol Biostat. (1998) 30:50–73. [Google Scholar]
- 23.Wellard-Cole L, Chen J, Davies A, Wong A, Huynh S, Rangan A, et al. Relative validity of the eat and track (eat) smartphone app for collection of dietary intake data in 18-to-30-year olds. Nutrients. (2019) 11:621. doi: 10.3390/nu11030621 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Carter MC, Burley V, Nykjaer C, Cade J. My meal mate’(MMM): validation of the diet measures captured on a smartphone application to facilitate weight loss. Br J Nutr. (2013) 109:539–46. doi: 10.1017/S0007114512001353 [DOI] [PubMed] [Google Scholar]
- 25.Rangan AM, Tieleman L, Louie JC, Tang LM, Hebden L, Roy R, et al. Electronic dietary intake assessment (e-DIA): relative validity of a mobile phone application to measure intake of food groups. Br J Nutr. (2016) 115:2219–26. doi: 10.1017/S0007114516001525, PMID: [DOI] [PubMed] [Google Scholar]
- 26.Rangan AM, O'Connor S, Giannelli V, Yap ML, Tang LM, Roy R, et al. Electronic dietary intake assessment (e-DIA): comparison of a mobile phone digital entry app for dietary data collection with 24-hour dietary recalls. JMIR Mhealth Uhealth. (2015) 3:e98. doi: 10.2196/mhealth.4613 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Ambrosini GL, Hurworth M, Giglia R, Trapp G, Strauss P. Feasibility of a commercial smartphone application for dietary assessment in epidemiological research and comparison with 24-h dietary recalls. Nutr J. (2018) 17:1–10. doi: 10.1186/s12937-018-0315-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Della Torre SB, Carrard I, Farina E, Danuser B, Kruseman M. Development and evaluation of e-CA, an electronic Mobile-based food record. Nutrients. (2017) 9:10076. doi: 10.3390/nu9010076 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Martin-Prével Y, Allemand P, Wiesmann D, Arimond M, Ballard T, Deitchler M, et al. Moving forward on choosing a standard operational indicator of women’s dietary diversity. Rome, Italy: FAO (2015). [Google Scholar]
- 30.Kennedy G, Keding G, Evang E, Nodari GR, Scheerer LJBDGfIZ. Nutrition baseline survey summary report. (2017).
- 31.Pandey VL, Dev SM, Jayachandran U. Impact of agricultural interventions on the nutritional status in South Asia: A review. Food Policy. (2016) 62:28–40. doi: 10.1016/j.foodpol.2016.05.002 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Bird FA, Pradhan A, Bhavani R, Dangour AD. Interventions in agriculture for nutrition outcomes: a systematic review focused on South Asia. Food Policy. (2019) 82:39–49. doi: 10.1016/j.foodpol.2018.10.015 [DOI] [Google Scholar]
- 33.Verger EO, Ballard TJ, Dop MC, Martin-Prevel Y. Systematic review of use and interpretation of dietary diversity indicators in nutrition-sensitive agriculture literature. Glob Food Secur. (2019) 20:156–69. doi: 10.1016/j.gfs.2019.02.004 [DOI] [Google Scholar]
- 34.Fiorella KJ, Chen RL, Milner EM, Fernald LC. Agricultural interventions for improved nutrition: a review of livelihood and environmental dimensions. Glob Food Secur. (2016) 8:39–47. doi: 10.1016/j.gfs.2016.03.003 [DOI] [Google Scholar]
- 35.Melby CL, Orozco F, Averett J, Muñoz F, Romero MJ, Barahona A. Agricultural food production diversity and dietary diversity among female small holder farmers in a region of the Ecuadorian Andes experiencing nutrition transition. Nutrients. (2020) 12:2454. doi: 10.3390/nu12082454, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Jones AD, Creed-Kanashiro H, Zimmerer KS, De Haan S, Carrasco M, Meza K, et al. Farm-level agricultural biodiversity in the Peruvian Andes is associated with greater odds of women achieving a minimally diverse and micronutrient adequate diet. J Nutr. (2018) 148:1625–37. doi: 10.1093/jn/nxy166 [DOI] [PubMed] [Google Scholar]
- 37.Zhang J, Liang D, Zhao A. Dietary diversity and the risk of fracture in adults: a prospective study. Nutrients. (2020) 12:3655. doi: 10.3390/nu12123655, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Nguyen PH, Huybregts L, Sanghvi TG, Tran LM, Frongillo EA, Menon P, et al. Dietary diversity predicts the adequacy of micronutrient intake in pregnant adolescent girls and women in Bangladesh, but use of the 5-group cutoff poorly identifies individuals with inadequate intake. J Nutr. (2018) 148:790–7. doi: 10.1093/jn/nxy045, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Seiermann AU, Al-Mufti H, Waid JL, Wendt AS, Sobhan S, Gabrysch S. Women's fasting habits and dietary diversity during Ramadan in rural Bangladesh. Matern Child Nutr. (2021) 17:e13135. doi: 10.1111/mcn.13135, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 40.Sultana M, Hasan T, Shaheen N. Dietary diversity and nutritional status of female residential students in University of Dhaka, Bangladesh. Curr Res Nutr Food Sci. (2019) 10:644. doi: 10.5958/0976-5506.2019.01349.4 [DOI] [PubMed] [Google Scholar]
- 41.Bellon MR, Ntandou-Bouzitou GD, Caracciolo F. On-farm diversity and market participation are positively associated with dietary diversity of rural mothers in southern Benin, West Africa. PLoS One. (2016) 11:e0162535. doi: 10.1371/journal.pone.0162535, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Diop L, Becquey E, Turowska Z, Huybregts L, Ruel MT, Gelli A. Standard minimum dietary diversity indicators for women or infants and young children are good predictors of adequate micronutrient intakes in 24–59-month-old children and their nonpregnant nonbreastfeeding mothers in rural Burkina Faso. J Nutr. (2021) 151:412–22. doi: 10.1093/jn/nxaa360, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Custodio E, Kayikatire F, Fortin S, Thomas AC, Kameli Y, Nkunzimana T, et al. Minimum dietary diversity among women of reproductive age in urban Burkina Faso. Matern Child Nutr. (2020) 16:e12897. doi: 10.1111/mcn.12897, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Getacher L, Egata G, Alemayehu T, Bante A, Molla A. Minimum dietary diversity and associated factors among lactating mothers in Ataye district, north Shoa zone, Central Ethiopia: a community-based cross-sectional study. J Nutr Metab. (2020) 2020:1–10. doi: 10.1155/2020/1823697, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45.Hanley-Cook GT, Tung JYA, Sattamini IF, Marinda PA, Thong K, Zerfu D, et al. Minimum dietary diversity for women of reproductive age (MDD-W) data collection: validity of the list-based and open recall methods as compared to weighed food record. Nutrients. (2020) 12:2039. doi: 10.3390/nu12072039, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 46.Girma S, Fikadu T, Agdew E, Haftu D, Gedamu G, Dewana Z, et al. Factors associated with low birthweight among newborns delivered at public health facilities of Nekemte town, West Ethiopia: a case control study. BMC Pregnancy Childbirth. (2019) 19:1–6. doi: 10.1186/s12884-019-2372-x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Gyimah LA, Annan RA, Apprey C, Edusei A, Aduku LNE, Asamoah-Boakye O, et al. Dietary diversity and its correlates among pregnant adolescent girls in Ghana. PLoS One. (2021) 16:e0247979. doi: 10.1371/journal.pone.0247979, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Agbozo F, Abubakari A, Der J, Jahn A. Maternal dietary intakes, red blood cell indices and risk for anemia in the first, second and third trimesters of pregnancy and at predelivery. Nutrients. (2020) 12:777. doi: 10.3390/nu12030777, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Saaka M, Mutaru S, Osman SM. Determinants of dietary diversity and its relationship with the nutritional status of pregnant women. Journal of nutritional. Science. (2021) 10:e14. doi: 10.1017/jns.2021.6 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Ayensu J, Annan R, Lutterodt H, Edusei A, Peng LS. Prevalence of anaemia and low intake of dietary nutrients in pregnant women living in rural and urban areas in the Ashanti region of Ghana. PLoS One. (2020) 15:e0226026. doi: 10.1371/journal.pone.0226026, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Bukari M, Saaka M, Masahudu A, Ali Z, Abubakari AL, Danquah LO, et al. Household factors and gestational age predict diet quality of pregnant women. Matern Child Nutr. (2021) 17:e13145. doi: 10.1111/mcn.13145, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Saaka M, Oladele J, Larbi A, Hoeschle-Zeledon I. Dietary diversity is not associated with haematological status of pregnant women resident in rural areas of northern Ghana. J. Nutr. Metab. (2017) 2017:1–10. doi: 10.1155/2017/8497892, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53.Gupta S, Pingali P, Pinstrup-Andersen P. Women’s empowerment and nutrition status: the case of iron deficiency in India. Food Policy. (2019) 88:101763. doi: 10.1016/j.foodpol.2019.101763 [DOI] [Google Scholar]
- 54.Nguyen PH, Martin-Prevel Y, Moursi M, Tran LM, Menon P, Ruel MT, et al. Assessing dietary diversity in pregnant women: relative validity of the list-based and open recall methods. Curr. Dev. Nutr. (2020) 4:nzz134. doi: 10.1093/cdn/nzz134 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55.Ghosh-Jerath S, Kapoor R, Singh A, Downs S, Goldberg G, Fanzo J. Agroforestry diversity, indigenous food consumption and nutritional outcomes in Sauria Paharia tribal women of Jharkhand, India. Matern Child Nutr. (2021) 17:e13052. doi: 10.1111/mcn.13052, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56.Diana R, Khomsan A, Anwar F, Christianti DF, Kusuma R, Rachmayanti RD. Dietary quantity and diversity among anemic pregnant women in Madura Island, Indonesia. J. Nutr. Metab. (2019) 2019:1–7. doi: 10.1155/2019/2647230, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57.Gitagia MW, Ramkat RC, Mituki DM, Termote C, Covic N, Cheserek MJ. Determinants of dietary diversity among women of reproductive age in two different agro-ecological zones of Rongai Sub-County, Nakuru, Kenya. Food Nutr Res. (2019) 63:63. doi: 10.29219/fnr.v63.1553 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58.Jomaa LH, Naja FA, Kharroubi SA, Diab-El-Harake MH, Hwalla NC. Food insecurity is associated with compromised dietary intake and quality among Lebanese mothers: findings from a national cross-sectional study. Public Health Nutr. (2020) 23:2687–99. doi: 10.1017/S1368980020000567, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 59.Adubra L, Savy M, Fortin S, Kameli Y, Kodjo NE, Fainke K, et al. The minimum dietary diversity for women of reproductive age (MDD-W) indicator is related to household food insecurity and farm production diversity: evidence from rural Mali. Curr Dev Nutr. (2019) 3:nzz002. doi: 10.1093/cdn/nzz002 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 60.Dulal B, Mundy G, Sawal R, Rana PP, Cunningham K. Homestead food production and maternal and child dietary diversity in Nepal: variations in association by season and agroecological zone. Food Nutr Bull. (2017) 38:338–53. doi: 10.1177/0379572117703264, PMID: [DOI] [PubMed] [Google Scholar]
- 61.Shrestha V, Paudel R, Sunuwar DR, Lyman ALT, Manohar S, Amatya A. Factors associated with dietary diversity among pregnant women in the western hill region of Nepal: a community based cross-sectional study. PLoS One. (2021) 16:e0247085. doi: 10.1371/journal.pone.0247085, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Samuel FO, Akinwande BA, Opasola RO, Azeez LA, Abass AB. Food intake among smallholder cassava value chain households. Nutr Food Sci. (2019) 49:1051–62. doi: 10.1108/NFS-11-2018-0310 [DOI] [Google Scholar]
- 63.Brazier AK, Lowe NM, Zaman M, Shahzad B, Ohly H, McArdle HJ, et al. Micronutrient status and dietary diversity of women of reproductive age in rural Pakistan. Nutrients. (2020) 12:3407. doi: 10.3390/nu12113407, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Nsereko E, Uwase A, Mukabutera A, Muvunyi CM, Rulisa S, Ntirushwa D, et al. Maternal genitourinary infections and poor nutritional status increase risk of preterm birth in Gasabo District, Rwanda: a prospective, longitudinal, cohort study. BMC Pregnancy Childbirth. (2020) 20:1–13. doi: 10.1186/s12884-020-03037-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 65.Chakona G, Shackleton C. Minimum dietary diversity scores for women indicate micronutrient adequacy and food insecurity status in south African towns. Nutrients. (2017) 9:812. doi: 10.3390/nu9080812, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66.Gómez G, Nogueira Previdelli Á, Fisberg RM, Kovalskys I, Fisberg M, Herrera-Cuenca M, et al. Dietary diversity and micronutrients adequacy in women of childbearing age: results from ELANS study. Nutrients. (2020) 12:1994. doi: 10.3390/nu12071994, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 67.Weerasekara PC, Withanachchi CR, Ginigaddara G, Ploeger A. Understanding dietary diversity, dietary practices and changes in food patterns in marginalised societies in Sri Lanka. Food Secur. (2020) 9:1659. doi: 10.3390/foods9111659, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 68.Madzorera I, Isanaka S, Wang M, Msamanga GI, Urassa W, Hertzmark E, et al. Maternal dietary diversity and dietary quality scores in relation to adverse birth outcomes in Tanzanian women. Am J Clin Nutr. (2020) 112:695–706. doi: 10.1093/ajcn/nqaa172, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 69.Conti MV, De Giuseppe R, Monti MC, Mkindi AG, Mshanga NH, Ceppi S, et al. Indigenous vegetables: a sustainable approach to improve micronutrient adequacy in Tanzanian women of childbearing age. Eur J Clin Nutr. (2021) 75:1475–82. doi: 10.1038/s41430-021-00865-x, PMID: [DOI] [PubMed] [Google Scholar]
- 70.Huang M, Sudfeld C, Ismail A, Vuai S, Ntwenya J, Mwanyika-Sando M, et al. Maternal dietary diversity and growth of children under 24 months of age in rural Dodoma, Tanzania. Food Nutr. Bull. (2018) 39:219–30. doi: 10.1177/0379572118761682, PMID: [DOI] [PubMed] [Google Scholar]
- 71.Madzorera I, Ghosh S, Wang M, Fawzi W, Isanaka S, Hertzmark E, et al. Prenatal dietary diversity may influence underweight in infants in a Ugandan birth-cohort. Matern Child Nutr. (2021) 17:e13127. doi: 10.1111/mcn.13127, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 72.Arimond M, Wiesmann D, Becquey E, Carriquiry A, Daniels MC, Deitchler M, et al. Simple food group diversity indicators predict micronutrient adequacy of women's diets in 5 diverse, resource-poor settings. J Nutr. (2010) 140:2059S–69S. doi: 10.3945/jn.110.123414 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 73.Martin-Prevel Y, Arimond M, Allemand P, Wiesmann D, Ballard TJ, Deitchler M, et al. Development of a dichotomous indicator for population-level assessment of the dietary diversity of women of reproductive age. Curr Dev Nutr. (2017) 1:1701. doi: 10.3945/cdn.117.001701 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 74.Ahern MB, Kennedy G, Nico G, Diabre O, Chimaliro F, Khonje G, et al. Women’s dietary diversity changes seasonally in Malawi and Zambia. (2021).
- 75.Kornatowski BM, Comstock SS. Dietary diversity is inversely correlated with pre-pregnancy body mass index among women in a Michigan pregnancy cohort. PeerJ. (2018) 6:e5526. doi: 10.7717/peerj.5526, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 76.Gicevic S, Gaskins AJ, Fung TT, Rosner B, Tobias DK, Isanaka S, et al. Evaluating pre-pregnancy dietary diversity vs. dietary quality scores as predictors of gestational diabetes and hypertensive disorders of pregnancy. PLoS One. (2018) 13:e0195103. doi: 10.1371/journal.pone.0195103, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 77.Paré BC, Dahourou DL, Ahmed Kabore AS, Kinda R, Ouaro B, Dahany M-M, et al. Prevalence of wasting and associated factors among 6 to 23 months old children in the Sahel region of Burkina Faso. Pan Afr Med J. (2019) 34:34. doi: 10.11604/pamj.2019.34.164.19886 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 78.Hipgrave D, Fu X, Zhou H, Jin Y, Wang X, Chang S, et al. Poor complementary feeding practices and high anaemia prevalence among infants and young children in rural central and western China. Eur J Clin Nutr. (2014) 68:916–24. doi: 10.1038/ejcn.2014.98, PMID: [DOI] [PubMed] [Google Scholar]
- 79.Wuneh AG, Ahmed W, Bezabih AM, Reddy PS. Dietary diversity and meal frequency practices among children aged 6-23 months in agro pastoral communities in Afar region, Ethiopia: a cross-sectional study. Ecol Food Nutr. (2019) 58:575–96. doi: 10.1080/03670244.2019.1644328, PMID: [DOI] [PubMed] [Google Scholar]
- 80.Guja T, Melaku Y, Andarge E. Concordance of mother-child (6–23 months) dietary diversity and its associated factors in Kucha District, Gamo zone, southern Ethiopia: a community-based cross-sectional study. J Nutr Metab. (2021) 2021:1–11. doi: 10.1155/2021/8819846, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 81.Kim SS, Rawat R, Mwangi EM, Tesfaye R, Abebe Y, Baker J, et al. Exposure to large-scale social and behavior change communication interventions is associated with improvements in infant and young child feeding practices in Ethiopia. PLoS One. (2016) 11:e0164800. doi: 10.1371/journal.pone.0164800, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 82.Kamran A, Sharifirad G, Nasiri K, Soleymanifard P, Savadpour M, Akbar HM. Determinants of complementary feeding practices among children aged 6-23: a community based study. Int J Pediatr. (2017) 5:4551–60. [Google Scholar]
- 83.Chama I. The role of edible non timber forest products in maternal and child diets in rural households of Chongwe district. Zambia: The University of Zambia; (2020). [Google Scholar]
- 84.Modugu HR, Khanna R, Dash A, Manikam L, Parikh P, Benton L, et al. Influence of gender and parental migration on IYCF practices in 6–23-month-old tribal children in Banswara district, India: findings from the cross-sectional PANChSHEEEL study. BMC Nutr. (2022) 8:1–16. doi: 10.1186/s40795-021-00491-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 85.Wormer JR, Shankar A, Van Hensbroek MB, Hindori-Mohangoo AD, Covert H, Lichtveld MY, et al. Poor adherence to the WHO guidelines on feeding practices increases the risk for respiratory infections in Surinamese preschool children. Int J Environ Res Public Health. (2021) 18:10739. doi: 10.3390/ijerph182010739, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 86.Kogade P, Gaidhane A, Choudhari S, Khatib MN, Kawalkar U, Gaidhane S, et al. Socio-cultural determinants of infant and young child feeding practices in rural India. Med Sci. (2019) 23:1015–22. [Google Scholar]
- 87.Solomon D, Aderaw Z, Tegegne TK. Minimum dietary diversity and associated factors among children aged 6–23 months in Addis Ababa, Ethiopia. Int J Equity Health. (2017) 16:1–9. doi: 10.1186/s12939-017-0680-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 88.Molla W, Adem DA, Tilahun R, Shumye S, Kabthymer RH, Kebede D, et al. Dietary diversity and associated factors among children (6–23 months) in Gedeo zone, Ethiopia: cross-sectional study. Ital J Pediatr. (2021) 47:1–10. doi: 10.1186/s13052-021-01181-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 89.Dangura D, Gebremedhin S. Dietary diversity and associated factors among children 6-23 months of age in Gorche district. South Ethiopia. (2017) 17:1–7. doi: 10.1186/s12887-016-0764-x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 90.Mekonnen TC, Workie SB, Yimer TM, Mersha WF. Meal frequency and dietary diversity feeding practices among children 6–23 months of age in Wolaita Sodo town, southern Ethiopia. J Health Popul Nutr. (2017) 36:1–8. doi: 10.1186/s41043-017-0097-x [DOI] [PMC free article] [PubMed] [Google Scholar]
- 91.Belew AK, Ali BM, Abebe Z, Dachew BA. Dietary diversity and meal frequency among infant and young children: a community based study. Ital J Pediatr. (2017) 43:1–10. doi: 10.1186/s13052-017-0384-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 92.Gezahegn H, Tegegne M. Magnitude and its predictors of minimum dietary diversity feeding practice among mothers having children aged 6–23 months in Goba town, Southeast Ethiopia, 2018: a community-based cross-sectional study. Nutr Diet Suppl. (2020) 12:215–22. doi: 10.2147/NDS.S243521 [DOI] [Google Scholar]
- 93.Zhao C, Guan H, Shi H, Zhang J, Huang X, Wang X. Relationships between dietary diversity and early childhood developmental outcomes in rural China. Matern Child Nutr. (2021) 17:e13073. doi: 10.1111/mcn.13073, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 94.Chilinda ZB, Wahlqvist ML, Lee M-S, Huang Y-C. Optimal household water access fosters the attainment of minimum dietary diversity among children aged 6–23 months in Malawi. Nutrients. (2021) 13:178. doi: 10.3390/nu13010178, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 95.Di Marcantonio F, Custodio E, Abukar Y. Child dietary diversity and associated factors among children in Somalian IDP camps. Food Nutr Bull. (2020) 41:61–76. doi: 10.1177/0379572119861000, PMID: [DOI] [PubMed] [Google Scholar]
- 96.Rubhara TT, Mudhara M, Oduniyi OS, Antwi MA. Impacts of cash crop production on household food security for smallholder farmers: a case of Shamva District, Zimbabwe. Agriculture. (2020) 10:188. doi: 10.3390/agriculture10050188 [DOI] [Google Scholar]
- 97.Gandure S, Drimie S, Faber M. Food security indicators after humanitarian interventions including food aid in Zimbabwe. Food Nutr Bull. (2010) 31:513–23. doi: 10.1177/156482651003100405 [DOI] [Google Scholar]
- 98.Cheteni P, Khamfula Y, Mah G. Exploring food security and household dietary diversity in the eastern Cape Province, South Africa. Sustain For. (2020) 12:1851. doi: 10.3390/su12051851 [DOI] [Google Scholar]
- 99.Kennedy G, Berardo A, Papavero C, Horjus P, Ballard T, Dop M, et al. Proxy measures of household food consumption for food security assessment and surveillance: comparison of the household dietary diversity and food consumption scores. Public Health Nutr. (2010) 13:2010–8. doi: 10.1017/S136898001000145X, PMID: [DOI] [PubMed] [Google Scholar]
- 100.McDonald CM, McLean J, Kroeun H, Talukder A, Lynd LD, Green TJ. Correlates of household food insecurity and low dietary diversity in rural Cambodia. Asia Pac J Clin Nutr. (2015) 24:720–30. doi: 10.6133/apjcn.2015.24.4.14, PMID: [DOI] [PubMed] [Google Scholar]
- 101.Aweke CS, Hassen JY, Wordofa MG, Moges DK, Endris GS, Rorisa DT. Impact assessment of agricultural technologies on household food consumption and dietary diversity in Eastern Ethiopia. J Agric Food Res. (2021) 4:100141. doi: 10.1016/j.jafr.2021.100141 [DOI] [Google Scholar]
- 102.Melaku YA, Gill TK, Taylor AW, Adams R, Shi Z, Worku A. Associations of childhood, maternal and household dietary patterns with childhood stunting in Ethiopia: proposing an alternative and plausible dietary analysis method to dietary diversity scores. Nutr J. (2018) 17:1–15. doi: 10.1186/s12937-018-0316-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 103.O’Meara L, Williams SL, Hickes D, Brown P. Predictors of dietary diversity of indigenous food-producing households in rural Fiji. Nutrients. (2019) 11:1629. doi: 10.3390/nu11071629, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 104.Mahmudiono T, Sumarmi S, Rosenkranz RR. Household dietary diversity and child stunting in East Java, Indonesia. Asia Pac J Clin Nutr. (2017) 26:317–25. doi: 10.6133/apjcn.012016.01, PMID: [DOI] [PubMed] [Google Scholar]
- 105.Jones AD, Shrinivas A, Bezner-Kerr R. Farm production diversity is associated with greater household dietary diversity in Malawi: findings from nationally representative data. Food Policy. (2014) 46:1–12. doi: 10.1016/j.foodpol.2014.02.001 [DOI] [Google Scholar]
- 106.Nkonde C, Audain K, Kiwanuka-Lubinda RN, Marinda P. Effect of agricultural diversification on dietary diversity in rural households with children under 5 years of age in Zambia. Food Sci Nutr. (2021) 9:6274–85. doi: 10.1002/fsn3.2587 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 107.Khumalo NZ, Sibanda M. Does urban and peri-urban agriculture contribute to household food security? An assessment of the food security status of households in Tongaat, eThekwini municipality. Sustain For. (2019) 11:1082. doi: 10.3390/su11041082 [DOI] [Google Scholar]
- 108.Roba KT, O’Connor TP, O’Brien NM, Aweke CS, Kahsay ZA, Chisholm N, et al. Seasonal variations in household food insecurity and dietary diversity and their association with maternal and child nutritional status in rural Ethiopia. Food Secur. (2019) 11:651–64. doi: 10.1007/s12571-019-00920-3 [DOI] [Google Scholar]
- 109.Hirvonen K, Taffesse AS, Hassen IW. Seasonality and household diets in Ethiopia. Public Health Nutr. (2016) 19:1723–30. doi: 10.1017/S1368980015003237, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 110.Ngema PZ, Sibanda M, Musemwa L. Household food security status and its determinants in Maphumulo local municipality, South Africa. Sustain For. (2018) 10:3307. doi: 10.3390/su10093307 [DOI] [Google Scholar]
- 111.Jt D, Gardner J, Halvorsen K, Ea K, Cohen A, Valadian I. Memory of food intake in the distant past. Am J Epidemiol. (1989) 130:1033–46. doi: 10.1093/oxfordjournals.aje.a115404 [DOI] [PubMed] [Google Scholar]
- 112.Long JD, Boswell C, Rogers TJ, Littlefield LA, Estep G, Shriver BJ, et al. Effectiveness of cell phones and mypyramidtracker. Gov to estimate fruit and vegetable intake. Appl Nurs Res. (2013) 26:17–23. doi: 10.1016/j.apnr.2012.08.002, PMID: [DOI] [PubMed] [Google Scholar]
- 113.Illner A, Freisling H, Boeing H, Huybrechts I, Crispim S, Slimani N. Review and evaluation of innovative technologies for measuring diet in nutritional epidemiology. Int J Epidemiol. (2012) 41:1187–203. doi: 10.1093/ije/dys105, PMID: [DOI] [PubMed] [Google Scholar]
- 114.Guinn CH, Baxter SD, Hardin JW, Royer JA, Smith AF. Intrusions in children's dietary recalls: the roles of BMI, sex, race, interview protocol, and social desirability. Obesity. (2008) 16:2169–74. doi: 10.1038/oby.2008.293, PMID: [DOI] [PMC free article] [PubMed] [Google Scholar]
- 115.Baxter SD, Thompson WO, Davis HC, Johnson MH. Impact of gender, ethnicity, meal component, and time interval between eating and reporting on accuracy of fourth-graders’ self-reports of school lunch. J Am Diet Assoc. (1997) 97:1293–8. doi: 10.1016/S0002-8223(97)00309-X, PMID: [DOI] [PubMed] [Google Scholar]
- 116.Lu C, Pearson M, Renker S, Myerburg S, Farino C. A novel system for collecting longitudinal self-reported dietary consumption information: The internet data logger (i DL). J Expo Sci Environ Epidemiol. (2006) 16:427–33. doi: 10.1038/sj.jes.7500479 [DOI] [PubMed] [Google Scholar]
- 117.Krumpal I. Determinants of social desirability bias in sensitive surveys: a literature review. Qual Quant. (2013) 47:2025–47. doi: 10.1007/s11135-011-9640-9 [DOI] [Google Scholar]
- 118.Cerri J, Testa F, Rizzi F, Frey M. Factorial surveys reveal social desirability bias over self-reported organic fruit consumption. Br Food J. (2019) 121:897–909. doi: 10.1108/BFJ-04-2018-0238 [DOI] [Google Scholar]
- 119.Martin-Prevel Y, Becquey E, Arimond M. Food group diversity indicators derived from qualitative list-based questionnaire misreported some foods compared to same indicators derived from quantitative 24-hour recall in urban Burkina Faso. J Nutr. (2010) 140:2086S–93S. [DOI] [PubMed] [Google Scholar]
- 120.Gibson RS, Charrondiere UR, Bell W. Measurement errors in dietary assessment using self-reported 24-hour recalls in low-income countries and strategies for their prevention. Adv Nutr. (2017) 8:980–91. doi: 10.3945/an.117.016980 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 121.Galea LM, Beck EJ, Probst YC, Cashman C. Whole grain intake of Australians estimated from a cross-sectional analysis of dietary intake data from the 2011–13 Australian health survey. Public Health Nutr. (2017) 20:2166–72. doi: 10.1017/S1368980017001082 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 122.Eldridge AL, Piernas C, Illner A-K, Gibney MJ, Gurinović MA, De Vries JH, et al. Evaluation of new technology-based tools for dietary intake assessment–an ILSI Europe dietary intake and exposure task force evaluation. Nutrients. (2019) 11. doi: 10.3390/nu11010055 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 123.Szolnoki G, Hoffmann D. Online, face-to-face and telephone surveys–comparing different sampling methods in wine consumer research. Wine Econ Policy. (2013) 2:57–66. doi: 10.1016/j.wep.2013.10.001 [DOI] [Google Scholar]
- 124.Kirkpatrick SI, Subar AF, Douglass D, Zimmerman TP, Thompson FE, Kahle LL, et al. Performance of the automated self-administered 24-hour recall relative to a measure of true intakes and to an interviewer-administered 24-h recall. Am J Clin Nutr. (2014) 100:233–40. doi: 10.3945/ajcn.114.083238 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 125.Beasley JM, Riley WT, Davis A, Singh J. Evaluation of a PDA-based dietary assessment and intervention program: a randomized controlled trial. J Am Coll Nutr. (2008) 27:280–6. doi: 10.1080/07315724.2008.10719701 [DOI] [PubMed] [Google Scholar]
- 126.Wang D-H, Kogashiwa M, Kira S. Development of a new instrument for evaluating individuals’ dietary intakes. J Am Diet Assoc. (2006) 106:1588–93. doi: 10.1016/j.jada.2006.07.004 [DOI] [PubMed] [Google Scholar]
- 127.World Health Organization . Getting your workplace ready for COVID-19: How COVID-19 spreads, 19 March 2020. Geneva: World Health Organization; (2020). [Google Scholar]
- 128.Lin Y-H, Chen C-Y, Wu SI. Efficiency and quality of data collection among public mental health surveys conducted during the COVID-19 pandemic: systematic review. J Med Internet Res. (2021) 23:e25118. doi: 10.2196/25118 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 129.Timmins KA, Vowden K, Husein F, Burley V. Making the best use of new technologies in the National Diet and nutrition survey: A review. (2014).
- 130.Ortega RM, Pérez-Rodrigo C, López-Sobaler A. Dietary assessment methods: dietary records. Nutr Hosp. (2015) 31:38–45. doi: 10.3305/nh.2015.31.sup3.8749 [DOI] [PubMed] [Google Scholar]
- 131.Gersovitz M, Madden JP, Smiciklas-Wright H. Validity of the 24-hr. dietary recall and seven-day record for group comparisons. J Am Diet Assoc. (1978) 73:48–55. [PubMed] [Google Scholar]
- 132.Amoutzopoulos B, Steer T, Roberts C, Cade J, Boushey C, Collins C, et al. Traditional methods v. new technologies–dilemmas for dietary assessment in large-scale nutrition surveys and studies: A report following an international panel discussion at the 9th international conference on diet and activity methods (ICDAM9), Brisbane, 3 September 2015. pp. 7. (2018). [DOI] [PMC free article] [PubMed]
