Hostname: page-component-586b7cd67f-g8jcs Total loading time: 0 Render date: 2024-11-28T17:43:56.808Z Has data issue: false hasContentIssue false

A questionnaire for screening the micronutrient intake of economically active South African adults

Published online by Cambridge University Press:  27 March 2009

Marjanne Senekal*
Affiliation:
Division of Human Nutrition, Department of Human Biology, Faculty of Health Sciences, University of Cape Town, Anzio Road, 8001 Cape Town, South Africa
Nelia P Steyn
Affiliation:
Chronic Diseases of Lifestyle Unit, Medical Research Council, Cape Town, South Africa
Johanna Nel
Affiliation:
Department of Logistics, University of Stellenbosch, Stellenbosch, South Africa
*
*Corresponding author: Email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Objective

The aim of the present study was to develop (phase 1) and validate (phase 2) a screening questionnaire to assess the adequacy of micronutrient intake of economically active South African adults.

Design

For identification of indicator foods to be included in the screening questionnaire (phase 1), a comprehensive, eighty-six-item, quantified FFQ that reflected the food sources of thirteen selected micronutrients associated with the nutrition-related health status of South Africans was developed and completed by 554 adults of all four major ethnic groups. Resulting dietary data were subjected to stepwise regression analyses to identify indicator foods to be included in the final screening questionnaire. For validation of frequency of intake reporting of specific food items included in the screening questionnaire (phase 2), a sample of sixty-six African and eighty-four white adult volunteers of both genders completed a 7 d record as well as the screening questionnaire. The frequency of intake of specific food items derived from the two methods was then compared using Spearman correlation coefficients.

Results

Phase 1 identified thirty indicator foods that formed the basis of the screening questionnaire. In phase 2, significant correlations were found for the total group for twenty-two out of the thirty items in the questionnaire, with correlations being the best for white females and the poorest for African males and females.

Conclusions

A screening questionnaire (thirty-item FFQ) that can be used by researchers and health professionals to assess an individual’s risk of inadequate micronutrient intake was developed and validated.

Type
Research Paper
Copyright
Copyright © The Authors 2009

Primary prevention (health promotion), as opposed to secondary prevention (risk reduction) and tertiary prevention (treatment and rehabilitation), aims to ensure the health and well-being of groups of people(Reference Mahan and Escott-Stump1). One of the most important aspects to be addressed in primary intervention initiatives is adequate food intake (quantity and quality) to ensure optimal intake of energy, macro- and micronutrients. Adequate intake of micronutrients, including vitamins and minerals, is important not only to prevent the development of deficiency diseases such as vitamin A deficiency and Fe-deficiency anaemia, but also contributes to the prevention of chronic diseases of lifestyle(Reference Mahan and Escott-Stump1).

One method that can be utilized to facilitate the early detection of nutritional imbalances is the use of screening procedures, including dietary evaluations(Reference Block, Clifford, Naughton, Henderson and McAdams2, Reference Sahyoun, Jaques, Dallal and Russel3). Screening instruments can be completed by the subject/client or administered by an interviewer/health professional(Reference Lee and Nieman4). The purpose of a dietary screening tool is usually not to produce accurate estimates of nutrient intake by individuals or groups, nor to rank or categorise people accurately on that variable. The purpose is rather to identify individuals or groups at risk of low intakes. On the basis of this type of assessment, groups can be monitored to study the association between their health and indicators of dietary intake; or individuals can be counselled or subjected to an intervention programme; or individuals can be subjected to second-stage screening for more precise assessment of dietary intake and nutritional risk before action is taken(Reference Block, Clifford, Naughton, Henderson and McAdams2, Reference Lee and Nieman4). Self-administered screening instruments can also be regarded as valuable educational tools in that awareness can be created regarding the adequacy and healthfulness of an individual’s dietary intake(Reference Sahyoun, Jaques, Dallal and Russel3). The present paper describes the development (phase 1) and validation (phase 2) of a self- or health worker-administered questionnaire for screening the micronutrient intake of South African adults. As self-administration of the questionnaire would require a reasonable level of literacy (reading and writing), the target group for this research was specified to be economically active South Africans, who were assumed to have the required literacy and comprehension level.

Phase 1: development of the screening questionnaire

Methods of phase 1

Following consultation with a panel of three dietary methodology experts, it was decided that the screening questionnaire to be developed should comply with the following criteria: (i) it had to be short and easy to complete without supervision; (ii) it had to reflect usual dietary intake; (iii) it had to be ethnically/culturally sensitive (recognition and accommodation of different South African population groups); and (iv) it had to facilitate the identification of potential problems with micronutrient intake. The expert panel recommended that a short, semi-quantified, FFQ format had the potential to meet these stated criteria.

An FFQ includes a list of food items known to be the major sources of the dietary components (micronutrients) in question(Reference Lee and Nieman4, Reference Nelson and Bingham5). The validity of any FFQ depends largely on the completeness/adequacy of this food list(Reference Baghurst6, Reference Willett7). The expert panel recommended that in order to develop a list of indicator foods to be included in the screening questionnaire, a comprehensive quantified FFQ that included important sources of micronutrients related to common nutrition-related health problems experienced by South Africans should first be developed and tested. The resulting data could then be subjected to stepwise regression analyses to identify the necessary indicator foods.

Compilation of the comprehensive quantified FFQ

To identify micronutrients that needed to be included in the comprehensive list of food items, the main nutrition-related chronic diseases of lifestyle relevant to South Africans were first identified from a South African Medical Research Council report of the Chronic Diseases of Lifestyle Unit(Reference Fourie and Steyn8). These diseases include hypertension, dyslipidaemia, diabetes mellitus and impaired glucose tolerance, lifestyle-induced cancers, stroke and osteoporosis. Micronutrients that are typically associated with the development/prevention of these diseases include the following thirteen nutrients: Ca, Mg, Zn, Fe, vitamin A, vitamin E, thiamin, riboflavin, niacin, vitamin B6, vitamin B12, folate and vitamin C(Reference Mahan and Escott-Stump1, Reference Fourie and Steyn8, Reference Vorster, Jerling, Oosthuizen, Becker and Wolmerans9). Second, micronutrient deficiencies that are endemic in South African populations, namely Fe and vitamin A deficiencies, were identified from a meta-analysis of dietary surveys(Reference Vorster, Jerling, Oosthuizen, Becker and Wolmerans9) as well as national nutritional status surveys(10, Reference Labadarios11).

Subsequently, the main sources of the thirteen nutrients were identified from the South African food composition tables(Reference Langenhoven, Kruger, Gouws and Faber12) and nutrition textbooks(Reference Mahan and Escott-Stump1, Reference Smolin and Grosvenor13). The criteria formulated by Willett(Reference Willett7) were used to guide this process: (i) the food must have a substantial content of the nutrient(s) of interest; (ii) the food should be eaten reasonably often by an appreciable number of the target group; and (iii) the use of the food must vary from person to person. To ensure cultural/ethnic sensitivity(Reference Teufel14), the foods most commonly consumed by the different ethnic groups in South Africa were identified from reports by the National Programme for Nutrition Intervention of the South African Medical Research Council(Reference Wolmerans, Langenhoven, Benade, Swanepoel, Kotze and Rossouw15Reference Bourne, Langenhoven, Steyn, Jooste, Nesamvuni and Laubscher17). All of this information was combined to compile a list of eighty-six food items that are commonly consumed by adult South Africans and can be regarded as important sources of the identified micronutrients. Items such as sugar, candy, jams, syrup and energy drinks that are not micronutrient-dense were not included in the food list. For frequency of intake reporting, the following response categories were selected based on the evaluation of a number of FFQ(Reference Eck, Klesges, Hanson, Slawson, Portis and Lavasque18Reference Wilson and Howarth23): seldom/never, 1–3 times/month, 1–3 times/week, 4–6 times/week, 1 time/d, 2 times/d and 3 or more times/d. For portion size estimation an average serving size was specified in the questionnaire. These serving sizes were calculated using exchange lists adapted for mean portion sizes reported in South African dietary surveys(Reference Wolmerans, Langenhoven, Benade, Swanepoel, Kotze and Rossouw15Reference Bourne, Langenhoven, Steyn, Jooste, Nesamvuni and Laubscher17, Reference Vorster, Oosthuizen, Jerling, Veldman and Burger24). In this regard it is important to note that most of the variation in the intake of a food item in an FFQ is explained by frequency of intake and not necessarily by estimated portion size(Reference Willett7). Accurate frequency estimation should therefore be a key focus in ensuring the validity of dietary data generated using an FFQ.

The resulting draft questionnaire was completed by twenty African and sixteen white South Africans of both genders as a pilot test, after which a few minor changes were made.

Sample for completion of the comprehensive FFQ and subsequent generation of the screening questionnaire

The sample for phase 1 of the study was randomly drawn from the South African National Database, which is the largest consumer database in South Africa and comprised a sampling frame of more than 7 million economically active adults, i.e. consumers between the ages of 18 and 65 years, at the time of the study. The sampling frame included names and addresses of 52 % white, 30 % mixed ancestry, 11 % Asian and 6 % African South Africans. A random sample of 2100 was drawn to be proportionally representative of all ethnic groups in the database, and to include at least one small town and one city from each of the nine provinces in the final sample. Since mailed questionnaires are known to have a poor response, a very large sample was mailed to ensure a response of at least 25 % (n ≈ 500).

Ethical issues

The research proposal was approved by the Ethics Committee of the University of Limpopo, South Africa. Detailed information concerning the aim of the research was included in an introductory letter that accompanied the eighty-six-item quantified FFQ. Confidentiality and anonymity were ensured. The completion and return of the questionnaire served as indication of voluntary participation and informed consent.

Data collection and processing

The FFQ was mailed to respondents together with a prepaid return envelope. General instructions regarding completion of the questionnaire as well as specific guidelines for portion size estimation were included on the cover page of the questionnaire. After the due date for return of questionnaires had passed, a reminder was mailed to the non-responders. A second reminder followed the first one. The main researcher scrutinised each questionnaire for completeness and quality. Twenty-six out of the 580 returned questionnaires were not included in the analyses. A questionnaire was excluded from analysis if the following was found: (i) whole page(s) not completed; (ii) the same frequency of intake indicated for a number of consecutive items on the list; and (iii) unrealistically high frequencies indicated. For quantification purposes the specified serving size was multiplied with the frequency of intake. In cases where the frequency was specified as a range e.g. 1–3 times/month, the frequency was taken as the midpoint of the range.

Statistical analysis for generation of the screening questionnaire from the dietary intake database

Statistical analyses were conducted using the SAS statistical software package version 6·11 (SAS Institute Inc., Cary, NC, USA). To identify food items that were the most important sources of each nutrient in question, stepwise regression analyses were performed as described by Willett(Reference Willett7). According to this procedure, the food item that explains the most between-person variance in the intake of a specific nutrient is identified as the first independent variable, the food item that explains the most variance not accounted for by the first food is the second independent variable, and so on. The contribution made by a specific food item is reflected in the change in the cumulative R 2. When the cumulative R 2 for a specific nutrient in the analyses reached 0·7, which is indicative of a correlation coefficient of 0·84, the food items in the regression model were taken as the best sources of a particular nutrient. This method identifies the food items that discriminate most between individuals rather than those that contribute to absolute intake. It should be kept in mind that the R 2 value will accumulate more rapidly for those nutrients that are highly concentrated in a few foods, e.g. vitamin C, than for those that are dispersed throughout many foods, e.g. thiamin. According to Willett(Reference Willett7) a limitation of this method is that if several hundred food variables are included in an original list of potential foods, some will enter as ‘statistically significant’ predictors on the basis of chance alone. The shorter the list of foods and the larger the sample size, the smaller is the chance of including unimportant contributors of a nutrient. The regression analyses were completed for the total group as well as for each ethnic group separately. Prominent differences in the rankings of food items between the four ethnic groups were taken into consideration in the final selection of food items to be included in the screening questionnaire.

Results and discussion of phase 1

A sociodemographic profile of the participants in phase 1 of the development procedure is presented in Table 1. The proportions from the various ethnic groups who participated were: Africans 27 %, Indians 12 %, mixed ancestry 18 % and whites 43 %. It must be borne in mind that the ethnic profile of economically active South Africans represented in the South African National Database does not reflect the country’s general demographic profile, which was 78 % African of whom 31 % were unemployed and 54 % were literate at the time of the study(Reference Lehohla25, 26). It can therefore be said that the sample was more representative of the educated employed South African, irrespective of ethnic group, and the application of the screening questionnaire should be aimed at this particular group. Although the response rate was only 28 %, the sample size was large enough to enable us to conduct meaningful statistical analyses to derive the screening questionnaire.

Table 1 Sociodemographic profile (column %) of the study population involved in phase 1 of the study: development of the screening questionnaire (n 554)

*χ 2 = 49·7 (df = 12), P < 0·0001.

χ 2 = 125·0 (df = 9), P < 0·0001.

χ 2 = 67·6 (df = 9), P < 0·0001.

The most important food sources of each of the selected thirteen micronutrients identified by the regression analyses are presented in Table 2. A food item was finally selected for the screening questionnaire by the expert panel if it was the primary source of one or two nutrients, or a secondary source of a number of nutrients. Descriptions of preparation methods and fat content of food items were not included in the final version of the screening questionnaire (Table 3). It was also decided to limit the recall period of the screening questionnaire to one week to reduce the memory burden on the respondent and to simplify the frequency concept. Except for the 1–3 times/month category, all the response categories included in the eighty-six-item FFQ were retained. In the final version of the screening questionnaire the respondent is not expected to indicate portion size.

Table 2 Indicator food itemsFootnote * identified through stepwise regression analyses for each of the specified micronutrients (n 528)

* Food items indicated in italics were included in the final version of the screening questionnaire.

Fortification of fruit juice with Ca could be responsible for high Ca values in citrus.

Table 3 Final thirty-item FFQ for the screening of the micronutrient intake of economically active adults (=screening questionnaire)

For quantitative micronutrient risk assessment purposes, the daily intake of each of the thirteen micronutrients reflected by the thirty food items in the screening questionnaire can be computed by using either a standard dietary assessment program or a tailored calculation program. The actual calculation should be based on the frequency of intake indicated by the respondent using standard portion sizes. Micronutrient intake can then be compared to the relevant dietary reference intake (Recommended Dietary Allowance (RDA) or Adequate Intake (AI)) for individual risk assessment(27). Suggested cut-off points are: serious risk, <67 % of RDA or AI; mild risk, ≥67 % and <100 % of RDA or AI; no risk, ≥100 % RDA or AI(Reference Nel and Steyn28).

Phase 2: assessment of the validity of frequency reporting in the screening questionnaire

Methods of phase 2

The underlying question addressed by this phase of the study was whether the screening questionnaire provided a true reflection of the usual intake of the selected micronutrients by an individual. Construct, face and content validity of the instrument, i.e. whether it actually had the potential to reflect the usual intake of the micronutrients in question, were ensured by the process that was followed in the development of the questionnaire in phase 1. However, whether the concept of ‘frequency of intake’ was well understood, and whether the frequency indicated in the questionnaire was a true reflection of actual frequency of intake, needed to be assessed.

Sample

For these purposes a sample of sixty-six African and eighty-four white adult volunteers of both genders, with a sociodemographic profile comparable to that of respondents who participated in phase 1 of the study, was recruited. Recruitment drives focused on employees of two South African universities. Potential participants for the validation study were invited to attend a session during which the aim and procedures of the study were explained, after which they could volunteer for participation.

Validation method

According to Brants et al.(Reference Brants, Löwik, Brussaard and Kistemaker29), the dietary record method is the best comparison/calibration dietary method for an FFQ because the sources of error associated with both methods are largely independent. Therefore participants in this validation study were requested to keep a 7 d estimated food record to determine usual frequency of intake of the food items included in the screening questionnaire. Each participant received a booklet that included the necessary recording guidelines, which were explained to them by a registered dietitian trained for this purpose. The respondents completed the screening questionnaire two weeks after completion of the 7 d record during a personal session with the dietitian.

Ethical issues

The protocol for phase 2 of the study was also approved by the Ethics Committee of the University of Limpopo. Each participant signed a consent form.

Data processing and analysis

Statistical analyses were conducted using the SAS statistical software package version 6·11 (SAS Institute Inc.). The 7 d records were analysed to generate an indication of frequency of intake of specific food items. For example, the number of times red meat was eaten during the recording week was counted, irrespective of the preparation method, to generate an indication of the frequency of red meat intake. Spearman correlation coefficients were computed to determine the relationship between the frequency of intake indicated in the screening questionnaire for a particular food item and the frequency of intake derived from the 7 d records.

Results and discussion of phase 2

The sociodemographic profile of the study population of phase 2 of the study, presented in Table 4, indicates that the majority of participants were employed and educated at secondary and tertiary levels. The correlations between frequency of intake of specific food items recorded on the screening questionnaire and that derived from the 7 d record are presented in Table 5. Significant Spearman correlation coefficients were found for twenty-two of the thirty items (r ranging from 0·24 to 0·62) in the total group (n 150), for nineteen of the thirty items (r ranging from 0·27 to 0·66) among females (n 81) and for fifteen of the thirty items (r ranging from 0·25 to 0·77) among males (n 69). When considering the gender groups within the two ethnic groups, it becomes evident that the best correlations were found for white females and the poorest for both African males and females. Generally the strongest correlations were found for food items such as red meat, milk, cheese, bread, breakfast cereal, margarine, some vegetables, citrus fruit, bananas and pears/apples. The weakest correlations were found for most vegetables, tinned fish, chicken, legumes and orange/guava juice. When interpreting these results it should be borne in mind that the screening questionnaire requests the respondent to report on frequency of intake of specific food items over the ‘past week’. As the 7 d food record was completed two weeks before the screening questionnaire was completed, food items that are consumed only two times or less per month could have been recorded using one method but not the other, which could explain low correlation coefficients for some items. Many of the food items for which no significant correlations were found are in fact items that are consumed less frequently by South Africans(Reference Nel and Steyn28). These include the following: tinned fish, peas, mixed vegetables, peanuts and nuts, sweet potatoes, fruit juices, eggs, legumes and tomatoes.

Table 4 Sociodemographic profile (column %) of the study population involved in phase 2 of the study: validation of the frequency reporting in the screening questionnaire (n 150)

*χ 2 = 20·3 (df = 5), P = 0·001.

χ 2 = 11·0 (df = 3), P = 0·01.

χ 2 = 11·8 (df = 5), P = 0·04.

Table 5 Comparison (Spearman correlation coefficients) of frequency of intake reported in the thirty-item screening questionnaire and the frequency of intake derived from the 7 d estimated record (n 150)

Correlation was statistically significant: *P ≤ 0·05, **P ≤ 0·01, ***P ≤ 0·001, ****P ≤ 0·0001.

†Not consumed by African men participating in the study.

‡Not consumed by any person, not in season.

Conclusions and recommendations for application: phases 1 and 2

A comprehensive procedure was followed to develop a questionnaire to screen the micronutrient intake of economically active South Africans. The result is a brief thirty-item FFQ (screening questionnaire) on which respondents indicate frequency of intake of each food item. Micronutrient intakes can then be computed using the indicated frequency of intake and standard portion sizes. Intakes should be compared with reference standards (i.e. dietary reference intakes) to provide an indication of deficiency risk for each specified micronutrient. The screening questionnaire can be used by researchers and health professionals to assess the micronutrient intake risk of individuals in a simplified and quick manner. The possibility of publishing the screening questionnaire, as well as appropriate guidelines to improve micronutrient intake where necessary in the lay media or on the Internet, can be considered.

Finally, as the screening questionnaire was developed for use in economically active South Africans, its application in screening the micronutrient intake of other groups of South Africans individuals, including those in the lowest socio-economic groups who may be less economically active and even illiterate, is not recommended without further assessment of the screening questionnaire’s validity in such groups of individuals.

Acknowledgements

The study was funded by the Vitamin Information Service, Roche Laboratories and the Universities of Limpopo and Stellenbosch. There is no conflict of interest. M.S. planned the study, helped with data analyses and was the main author. N.P.S. helped in planning, carried out the field work and assisted in writing up the study. J.N. undertook the data analyses and interpretation of the data.

References

1.Mahan, LK & Escott-Stump, S (2008) Krause’s Food Nutrition and Diet Therapy, 12th ed. Philadelphia, PA: Mosby Saunders Elsevier Inc.Google Scholar
2.Block, G, Clifford, C, Naughton, MD, Henderson, M & McAdams, M (1989) A brief dietary screen for high fat intake. J Nutr Educ 21, 199207.Google Scholar
3.Sahyoun, NR, Jaques, PF, Dallal, GE & Russel, RM (1997) Nutrition screening initiative checklist may be a better awareness/educational tool than a screening one. J Am Diet Assoc 97, 760764.Google Scholar
4.Lee, RD & Nieman, DC (2003) Nutritional Assessment, 3rd ed. London: McGraw-Hill.Google Scholar
5.Nelson, M & Bingham, S (1997) Assessment of food consumption and nutrient intake. In Design Concepts in Nutritional Epidemiology, 2nd ed., pp. 123169 [BM Margetts and M Nelson, editors]. Oxford: Oxford University Press.CrossRefGoogle Scholar
6.Baghurst, KI (1992) The food frequency technique and its relevance to population surveys in Australia. Aust J Nutr Diet 49, 101105.Google Scholar
7.Willett, W (1998) Nutritional Epidemiology, 2nd ed. Oxford: Oxford Press.Google Scholar
8.Fourie, J & Steyn, K (1995) South African Research Council Technical Report: Chronic Diseases in South Africa. Parow: Medical Research Council.Google Scholar
9.Vorster, HH, Jerling, JC, Oosthuizen, W, Becker, P & Wolmerans, P (1995) Nutrient Intakes of South Africans: An Analysis of the Literature (SANNS Group Report). Isando: Roche.Google Scholar
10.South African Vitamin A Consultative Group (1996) Child malnutrition in South Africa. Nutriview 1, 13.Google Scholar
11.Labadarios, D (editor) (2000) The National Food Consumption Survey (NFCHS): Children aged 1–9 years, South Africa. Pretoria: Department of Health.Google Scholar
12.Langenhoven, M, Kruger, M, Gouws, E & Faber, M (1991) MRC Food Composition Tables, 3rd ed. Parow: Medical Research Council.Google Scholar
13.Smolin, LA & Grosvenor, MB (2003) Nutrition: Science & Applications, 4th ed. London: Saunders College Publications.Google Scholar
14.Teufel, NI (1997) Development of culturally competent food-frequency questionnaires. Am J Clin Nutr 65, Suppl., 1173S1178S.Google Scholar
15.Wolmerans, P, Langenhoven, ML, Benade, AJS, Swanepoel, ASP, Kotze, TJ & Rossouw, JE (1988) Intake of macronutrients and their relationship with total cholesterol and high-density lipoprotein cholesterol. S Afr Med J 73, 140148.Google Scholar
16.Langenhoven, ML, Steyn, K & van Eck, M (1988) The food and meal pattern in the Cape Peninsula coloured population. Ecol Food Nutr 22, 107116.Google Scholar
17.Bourne, LT, Langenhoven, ML, Steyn, K, Jooste, PL, Nesamvuni, AE & Laubscher, JA (1994) The food and meal pattern in the urban African population of the Cape Peninsula, South Africa: The Brisk study. S Afr Med J 40, 140148.Google Scholar
18.Eck, LH, Klesges, RC, Hanson, CL, Slawson, D, Portis, L & Lavasque, ME (1991) Measuring short-term dietary intake: development and testing of a 1-week food frequency questionnaire. J Am Diet Assoc 50, 220228.Google Scholar
19.Hammond, J, Nelson, M, Chinn, S & Rona, RJ (1993) Validation of a food frequency questionnaire for assessing dietary intake in a study of coronary heart disease risk factors in children. Eur J Clin Nutr 47, 242250.Google Scholar
20.Jacques, PF, Sulsky, SI, Sadowski, JA, Phillips, JC, Rush, D & Willet, WC (1993) Comparison of micronutrient intake measured by a dietary questionnaire and biochemical indicators of micronutrient status. Am J Clin Nutr 57, 182189.CrossRefGoogle ScholarPubMed
21.Caan, B, Coates, A & Schaffer, D (1995) Variations in sensitivity, specificity, and predictive value of a dietary fat screener modified from Block et al. J Am Diet Assoc 95, 564568.CrossRefGoogle ScholarPubMed
22.Subar, AF, Thompson, FE & Smith, AF (1995) Improving food frequency questionnaires: a qualitative approach using cognitive interviewing. J Am Diet Assoc 95, 781788.Google Scholar
23.Wilson, P & Howarth, C (1996) Validation of a short frequency questionnaire for assessment of dietary calcium intake in women. Eur J Clin Nutr 50, 220228.Google Scholar
24.Vorster, HH, Oosthuizen, W, Jerling, JC, Veldman, FJ & Burger, HM (1997) The Nutritional Status of South Africans: A Review of the Literature (Part II). Durban: Health Systems Trust.Google Scholar
25.Lehohla, P (2005) ‘Race’ is just one variable in monitoring change. Statistics South Africa. http://www.statssa.gov.za/news_archive/12may2005_1.asp (accessed May 2008).Google Scholar
26.Development Bank of Southern Africa (1994) Race Relations Survey 1993/1994. Johannesburg: SAIRR.Google Scholar
27.Institute of Medicine, Food and Nutrition Board (1998) Dietary Reference Intakes. Washington, DC: National Academy Press.Google Scholar
28.Nel, JH & Steyn, NP (2002) Report on South African Food Consumption Studies Undertaken Amongst Different Population Groups (1983–2000). Pretoria: Department of Health.Google Scholar
29.Brants, HAM, Löwik, MRH, Brussaard, JH, Kistemaker, C & Van Erp-Baart AMJ (1997) Food consumption methods. Development, reproducibility and validation of a food frequency questionnaire for vitamin B6. Eur J Clin Nutr 51, Suppl., S12S18.Google Scholar
Figure 0

Table 1 Sociodemographic profile (column %) of the study population involved in phase 1 of the study: development of the screening questionnaire (n 554)

Figure 1

Table 2 Indicator food items* identified through stepwise regression analyses for each of the specified micronutrients (n 528)

Figure 2

Table 3 Final thirty-item FFQ for the screening of the micronutrient intake of economically active adults (=screening questionnaire)

Figure 3

Table 4 Sociodemographic profile (column %) of the study population involved in phase 2 of the study: validation of the frequency reporting in the screening questionnaire (n 150)

Figure 4

Table 5 Comparison (Spearman correlation coefficients) of frequency of intake reported in the thirty-item screening questionnaire and the frequency of intake derived from the 7 d estimated record (n 150)