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Incidence of Severe Acute Malnutrition After Treatment: A Prospective Matched Cohort Study in Sokoto, Nigeria 2018-2019

Nigeria, 2018 - 2019
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Reference ID
NGA_2018-2019_CMAM_v01_M
Producer(s)
Oxford Policy Management Ltd.
Metadata
DDI/XML JSON
Created on
Jan 03, 2022
Last modified
Jan 03, 2022
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  • Study Description
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  • Identification

    Survey ID number

    NGA_2018-2019_CMAM_v01_M

    Title

    Incidence of Severe Acute Malnutrition After Treatment: A Prospective Matched Cohort Study in Sokoto, Nigeria 2018-2019

    Country
    Name Country code
    Nigeria NGA
    Study type

    Other Household Health Survey [hh/hea]

    Abstract

    Background

    Acute malnutrition is an important concern for children aged under 5 years, both globally and in Nigeria. Since the 2000s and the advent of Ready-to-Use Therapeutic Foods (RUTF), Severe Acute Malnutrition (SAM) has been commonly addressed through the WHO-recommended approach of Community-based Management of Acute Malnutrition (CMAM). CMAM programs provide treatment for children aged 6-59 months through an outpatient therapeutic program (OTP) service for uncomplicated cases and an inpatient service for complicated cases.

    In Nigeria, children are admitted and discharged from the CMAM program using mid-upper arm circumference (MUAC) as the main criterion. Children with a MUAC <115 mm and no apparent health complications are admitted into the OTP.

    CMAM is evidently effective in resolving SAM. However, evidence exists that children who have gone through an episode of SAM remain at higher risk of morbidity and mortality than children who have not. The evidence on SAM relapse is sparse with a high variation in estimates in the literature due to both contextual and methodological differences. This makes it difficult to understand the persistent risk of a SAM episode after initial recovery from the CMAM program, as well as the associated risk factors. Another important gap in the literature is the absence of comparison groups, making it difficult to determine the excess risk for SAM associated with a recent SAM episode.


    Research objectives

    The primary objective of this study was to assess the persistent and excess risk of SAM among children treated by the CMAM program.
    · The persistent risk was assessed by measuring the 6-month incidence rate of relapse into SAM among children discharged as cured from the OTP services of the CMAM program.
    · Excess risk was assessed by comparing this rate of relapse to the 6-month incidence rate of SAM in a cohort of community controls.
    Our secondary objective was to identify factors that are associated with the risk of relapse.


    Methods

    We conducted a prospective matched cohort study that tracked 553 children who were discharged as cured from OTP and 526 community control children in Sokoto State, Northern Nigeria. Data were collected from September 2018 to May 2019. OTP-cured children were recruited from the health facilities at discharge from OTP. Control children were recruited in the same communities the OTP-cured children lived in. Outcomes and potential risk factors were measured in up to 12 fortnightly home visits, i.e. in a period of up to six months for each child.

    This cohort study was implemented in several phases that took place sequentially, and that included recruitment of OTP-cured children, recruitment of community control children, first home visit (to collect baseline characteristics), and subsequent follow-up home visits. At each phase, different questionnaires were administered.

    Kind of Data

    Sample survey data [ssd]

    Unit of Analysis
    • Households
    • Individuals
    • Children
    • Health facilities

    Version

    Version Description

    V1.1: Edited, anonymous dataset for public distribution

    Version Date

    2021-07-22

    Version Notes

    Version 1.1 consists of five edited and anonymised datasets with the responses to a small number of questions removed; these were removed for confidentiality purposes or because they were not needed for the analysis. Some of the datasets also contain selected constructed indicators prefixed by n_. These constructed indicators are included to save data users time as they require complex reshaping and extraction of data from multiple sources (but they could be generated by data users if preferred).

    Scope

    Topics
    Topic Vocabulary
    Nutrition
    Keywords
    Child nutrition Acute Malnutrition Severe Acute Malnutrition Community-based Management of Acute Malnutrition Outpatient Therapeutic Programme Relapse Post-discharge outcomes Associated factors Cohort study Prospective matched cohort study Survival analysis Nigeria Northern Nigeria

    Coverage

    Geographic Coverage

    This study took place in five rural local government areas (LGAs) in Sokoto State in Northern Nigeria.

    Producers and sponsors

    Primary investigators
    Name
    Oxford Policy Management Ltd.
    Producers
    Name Role
    Valid International Support in research design and analysis
    Funding Agency/Sponsor
    Name
    Children’s Investment Fund Foundation
    Other Identifications/Acknowledgments
    Name Affiliation Role
    United Nations Children's Fund Nigeria UNICEF Support in research implementation

    Sampling

    Sampling Procedure

    Selection of LGAs and health facilities

    This prospective matched cohort study was conducted in five rural local government areas (LGAs) in Sokoto State, northern Nigeria. Nine out of the 23 LGAs in Sokoto State hosted the CMAM program. Of these, four were excluded because they were either hosting another study looking at improving CMAM delivery, were peri-urban, or not easily accessible. In the selected five LGAs, the CMAM program had been running since 2010 and was being implemented throughout the study period. Within each LGA, five health facilities were hosting the CMAM program, and the study covered this exhaustive list of 25 health facilities (i.e. there was no sampling of health facilities within LGAs, all health facilities that were hosting the CMAM program in each LGA were included in the study).

    Selection of children

    The study followed two cohorts of subjects:

    1. First, a cohort of children who were i) admitted into OTP and discharged alive and as cured (children are discharged as cured from OTP if their MUAC is superior or equal to 115mm, and there are no signs of bilateral pitting oedema), ii) were aged 6-59 months at admission into the OTP, iii) had not previously been admitted to the OTP or inpatient care, and iv) whose households resided in the catchment area of the selected health facilities and were not planning to move out. These children are referred to as 'OTP-cured children.'
    2. Second, a cohort of children i) from the same communities as OTP-cured children who had ii) no history of SAM or treatment for SAM, iii) no anthropometric or clinical signs of MAM (MUAC <125 mm) or of severe stunting (height/length-for-age z-score (HAZ/LAZ) <-3 SD) at the time of recruitment into the study, and iv) who were matched to the OTP-cured children based on a set of criteria. Each community control child was matched to an OTP-cured child based on the following criteria: i) residence (living in the same community), ii) age in months (being of similar age, and allowing up to 3-month difference), iii) sex (having same sex), iv) age of the mother (below or above 20 years of age), and v) level of education of the mother (no education, completed primary, and completed secondary or above). These children are referred to as 'community control children.'

    Exclusion criteria for both cohorts of children for enrolment into the study included:
    · Presence of disability or any congenital disease (after clinical examination) that affects growth or prevents accurate anthropometric measurement and/or prevents the child from eating normally;
    · A sibling already enrolled into the study;
    · The biological mother of the child having passed away; or
    · Having a mother <15 years old.

    Note that children were not sampled. Rather:

    1. All OTP-cured children and their caregivers were approached to be included in the study as they were being discharged from the CMAM programme (during our recruitment period) and assessed for eligibility until a maximum number of participants was recruited.
    2. Community control children were purposively recruited into the study within the communities of each OTP-cured child using a snowball approach.

    Sample size (intended)

    The sample size determination was based on the relapse rate as the principal outcome variable.

    The minimum sample size required for this study was calculated to be 500 OTP-cured and 500 community control children across the 25 facilities. This sample size would allow us to detect a 4% point difference in SAM incidence between both cohorts of children with 95% confidence. Calculation parameters were chosen conservatively and assumed an incidence of SAM among community controls of 1%, a total number of 25 clusters (health facilities), a coefficient of variation of cluster sizes of 0.9, and an intra-cluster correlation of 0.02. Sample size calculations were implemented using the clustersampsi tool in Stata.

    With an anticipated loss to follow-up of 20%, the study therefore aimed to recruit 600 children per cohort.

    Representativeness

    It is important to emphasise that the two cohorts of children included in this study are not necessarily representative of the overall population of children in Northern Nigeria or even Sokoto State. On the one hand, children from the OTP-cured cohort were recruited from health facilities in a purposefully selected set of LGAs within that state. Given the way that they were recruited, they do represent a census of OTP-cured children from those health facilities that were discharged as cured during the recruitment phase of this study and that were eligible for the study. However, the level of representativeness beyond that group is unclear. Community control children, on the other hand, were selected using snowball sampling, which essentially implies purposeful sampling within visited communities. Hence, generalising findings beyond the two groups covered in the study should only be done with care.

    Response Rate
    • Out of a total of 645 OTP-cured children that were recruited into the study, 553 were found at the first home visit and deemed eligible, 83 were not found and 9 were later discovered to not be eligible.
    • Out of a total of 543 community children that were recruited into the study (met eligibility criteria and were matched to OTP-cured children) at the first home visit, 17 were discovered later on to not have been eligible (and therefore were dropped).

    Therefore, the sample size of the study (and consequently the number of observations of the published data) consists of 553 OTP-cured children and 526 community control children.

    In terms of the outcomes of children at the end of the study:

    • Of the 553 OTP-cured children, 378 did not experience SAM during the study period and therefore lasted until the 12th home visit; 134 experienced SAM during one of the visits (at which point their inclusion in further follow-up visits ended); 32 dropped out of the study at some point (3 withdrew their consent later, and 29 were no longer traceable); and 9 died during the study period (at which point their inclusion in further follow-up visits ended).
    • Of the 526 community control children, 488 did not experience SAM during the study period and therefore lasted until the 12th home visit; 3 experienced SAM during one of the visits (at which point their inclusion in further follow-up visits ended); 30 dropped out of the study at some point (6 withdrew their consent later, and 24 were no longer traceable); and 5 died during the study period (at which point their inclusion in further follow-up visits ended).
    Weighting

    The collected data does not have any sampling weights. This is due to the nature of child selection, whereby all children that were discharged as cured during the study's recruitment period and were eligible were invited to participate in the study.

    Survey instrument

    Questionnaires

    1. COHORT TIMELINE

      This cohort study was implemented in several phases that took place sequentially, and that included recruitment of OTP-cured children, recruitment of community control children, first home visit (to collect baseline characteristics), and subsequent follow-up home visits. At each phase, different questionnaires were administered.

    At each health facility, a CMAM day is held once a week, rotating through all facilities per LGA so that no two facilities within an LGA have a CMAM day on the same day per week. Children who are enrolled in the CMAM programme and their caregivers attend CMAM days for check-ups and treatment. This study recruited OTP-cured children at these CMAM days, identifying children who were discharged as cured.

    The data collection timeline was as follows:

    1. OTP-cured children were recruited at health facilities on a rolling basis between September and November 2018. There, the study team screened all children who had been discharged as cured on that day for eligibility and consent to participate in the study. This meant enrolling children as they were successfully discharged from the CMAM programme in the 25 health facilities that formed part of this study. At each CMAM day and health facility, teams of two interviewers were present throughout the day to ensure that all children discharged from the programme on that day were screened for possible enrolment into the study and recruited if eligible up until the minimum sample size is reached.

    2. Following recruitment into the study, each OTP-cured child was tracked to their community and visited at their home within 2 to 3 weeks of their initial recruitment. Field teams used the information collected at recruitment to locate children in their community. Most communities were accessed either on foot or by motorcycle. This constituted the first home visit where a long baseline questionnaire was administered.

    3. Immediately after the first home visit of each OTP-cured child, a search for a suitable community control for that child was conducted. For each OTP-cured child, potential community controls were identified using a snowball approach. In essence, this approach meant that interviewers were referred to potential community control children by the mother of the OTP-cured child. Potential community controls were assessed with respect to their eligibility to enter the study and to whether they matched the corresponding OTP-cured child on a set of criteria (mentioned in the sampling section). The first community control to meet both sets of criteria was recruited into the study and the search for a community control for a given OTP-cured child ended at that stage. Once a control child was identified, the same first home (baseline) questionnaire was administered to the household and mother of that child.

    4. Afterwards, both cohorts were followed-up fortnightly for a total of 12 home visits (the 12 visits includes the first baseline home visit).

    5. Participation in the study for both cohorts ended at the 12th home visit, unless a child developed SAM earlier or dropped out of the study (e.g. family no longer consented to participate in the study or moved out of the community, or child had died), whichever came first. In total, children were followed up for a duration of up to six months after discharge from OTP. Within the six months of follow-up, if children were identified as being SAM by the field team, they proceeded to exit the study and interviewers referred those children to CMAM services.


    1. DESCRIPTION OF QUESTIONNAIRES

    There were a number of questionnaires that were used for this study.

    During recruitment of OTP-cured children at the health facility

    A recruitment questionnaire for OTP-cured children was administered to the mother of the child on the day children were discharged and recruited into the study. This questionnaire assessed eligibility of the child and collected some information to help with locating the home of the child.

    Additionally, data on children's health status at admission and discharge from the OTP were also collected from registration and treatment tracking cards kept at the facility by staff (OTP cards and Ration cards). This data was scanned on enumerator's tablets and later on entered into a database by data entry staff. Information that was entered from these records included anthropometric measurements and morbidity at admission, duration of treatment and anthropometric measurements at each visit to the OTP. Note that data from the scanned OTP and Ration cards has not been uploaded for public use due to data quality concerns. The data suffers from many missing observations, given that this data was not directly collected by the enumerators but relied on health facility staff filling in the OTP and Ration cards for the treated children.

    During this phase, a health facility questionnaire was also administered in each health facility to assess adherence of the health facility to the Nigeria CMAM national guidelines and availability of OTP-related drugs and equipment and the general quality of infrastructure and resources. The survey also collected data on shocks that affected the catchment area of facilities in the year prior to the survey, such as drought, floods, sandstorms, and security-related events. In each health facility, this survey was administered once, on the first day the interview team visited the health facility. The survey used direct observation as well as interviews with the head of the health facility and the CMAM focal person in charge. If either of these individuals were not available on the day, other knowledgeable health facility member was asked to respond to the questions.

    During recruitment of community control children

    A recruitment questionnaire for community control children was administered to the mothers of the children to assess eligibility and matching criteria and decide if they can be recruited.

    During the first home visit

    At the first home visit, a long baseline questionnaire was administered to the mother of the recruited child and the household head to collect baseline information across several domains related to the child, mother, and household. Children's MUAC was measured using the WHO/UNICEF-recommended MUAC tape and measurement protocol, whereas height and length were measured with a precision of 0.1 cm, using boards manufactured by SECA: standing boards for children who were able to stand and lying-down boards for children unable to. The domains included in the baseline questionnaire include:

    • Child level: height/length, mid-upper arm circumference; demographics; breastfeeding history; co-morbidities in the 2 weeks prior to the survey; immunization status; dietary diversity (24 hours prior to survey).
    • Mother level: demographics; economic activity and education status; knowledge on child feeding and health-seeking behaviour; reproductive history and care; perceived OTP experience; networks in community.
    • Household level: household demographics and composition; economic activity and education of household head; household assets and wealth; water, sanitation, and hygiene infrastructure; household food security and dietary diversity; deaths in the household in the year prior to the survey.

    During the follow-up home visits

    At each follow-up home visit, a short follow-up questionnaire was administered to the mother of the child to collect child-level co-morbidity data in the 2 weeks preceding the visit (a subset of the questions asked in the baseline questionnaire) and to measure the child's MUAC.

    In the final follow-up visit (i.e. the visit when the child exited the study either because they developed SAM or if they reached the final 12th visit), additional questions were asked of the household including on mother's employment status, changes in the breastfeeding and pregnancy status of mothers, deaths in the household, household food security, child feeding, household and child dietary diversity, and mother's feeding knowledge and practices. These questions were a subset of those asked in the baseline questionnaire and they were added in order to understand if household, mother, or child conditions assessed at the first home visit might have changed at the point of exit. Note that these additional questions were not asked of children who dropped out of the study (because the interviewers would not have known that the previous visit was going to be the final exit visit).

    All questionnaires were administered using the Computer-Assisted Personal Interviewing software CSPro (Version 7.1.3), and OTP and Ration cards were scanned and data entered digitally using the SurveyCTO software. Questionnaires were translated into Hausa and administered to all respondents in Hausa.


    1. NOTE ON THE DEFINITION OF SAM

      SAM was determined using the WHO and national MUAC criteria of MUAC <115 mm. Given that this study's objective was to identify definite relapses and cases of SAM that would require treatment, we classify a child as having SAM if his/her MUAC =112 mm at any home visit or if his/her MUAC is between 112 and 115mm for two consecutive visits. The reason we do this is to account for the possibility of measurement error, i.e. it is difficult to identify whether children around the 115mm MUAC cut-off temporarily dip into SAM or whether they are a certain SAM case that requires treatment.


    1. NOTES ON THE DATA COLLECTION THAT MIGHT BE RELEVANT FOR DATA ANALYSIS

      Survival analysis techniques can be used to analyse the data.

    An important point to emphasise is that for OTP-cured children there was a lag of up to three weeks between their recruitment at the health facility and the first visit at home (where we collected baseline data). Some children had already relapsed into SAM at the first home visit before additional data on these children could be collected. For those children who relapsed between recruitment and the first home visit, it would therefore not be possible to assess whether certain time-varying characteristics collected at the first home visit - e.g. child-level health indicators - materialised as a consequence of relapse or prior to relapse. This is a limitation and could present implications for data analysis, depending on the type of analysis the users of the data wish to conduct. Specifically, it is important for the analysis not to suffer from endogeneity if for instance users are interested in assessing the effect of certain factors on relapse rates. There are options to deal with this limitation, for instance, i) limiting the analysis to the factors/covariates that could reasonably be assumed to be time-invariant between recruitment and the first home visit, or ii) defining the time origin for OTP-cured children as the first home visit (as opposed to their recruitment from the health facility) and restricting the analysis to the subsample of children that had not relapsed into SAM at the first home visit (though this option would entail a significant reduction in sample size).

    Data collection

    Dates of Data Collection
    Start End
    2018-09-03 2019-05-31
    Data Collectors
    Name
    Oxford Policy Management
    Supervision

    Several data quality assurance mechanisms were implemented to ensure data quality throughout the survey:

    1. Data was collected using CAPI, which enabled automated live data checks during implementation of interviews. Extensive validations and cross-checks were programmed into the CAPI software and pre-tested to reduce errors and inaccuracies during the interviews.
    2. Data were uploaded every day, which enabled the survey management team to conduct a range of consistency checks on a daily basis. Any issues identified at this stage were immediately communicated to the relevant team supervisors for action.
    3. A data collection monitoring dashboard on PowerBi was used to daily monitor the progress of data collection as well as the performance of data collection teams and individual enumerators, thus allowing the field management team and team supervisors to give feedback to teams on a regular basis and continuously improve the quality of data collection.
    4. Two measures of MUAC were taken at each visit to minimise the risk of measurement error. A third measure was triggered whenever the difference between the two first measures was more than 5mm.
    5. Team supervisors were trained in quality assurance to control the quality of data collection in their teams and give live feedback to their team members.
    6. The survey management team visited data collection teams at random throughout the implementation of the study to observe interviews and provide additional feedback to team supervisors and teams in general.
    Data Collection Notes

    Pre-tests of instruments

    A number of pre-tests were conducted in Sokoto state during 2018 to test the instruments and protocols. A team of core nutrition and survey specialists and experienced survey supervisors visited facilities and households. The objectives of the pre-tests were to:

    • Understand how children are discharged from OTP and how we can recruit them into the study;
    • Develop criteria to select health facilities from which to recruit;
    • Understand how to follow-up with children over time in their homes;
    • Develop a strategy to find and follow-up with community controls;
    • Understand the community's and household's acceptance to study design;
    • Understand the CMAM delivery model and data sources to cross-reference a child's progress via facility based records;
    • Develop a model for the data collection;
    • Test all of the instruments and test the CAPI application.

    Ethical considerations

    This study met the ethics criteria of the Sokoto State Health Research Ethical Committee and approval was received on 12 March 2018.

    Verbal informed consent was sought and recorded in the questionnaire from mothers during recruitment of children into the study and from household heads at the first home visit. Consent was sought again from households at each follow-up visit. All children who experienced SAM during the study were referred to the nearest OTP services.

    Training and pilot

    Before data collection was conducted, training was organised for the interviewing teams and included a mix of in-class training and piloting. Two trainings were organised: one for the recruitment phase and one for the home visits phase. The main objective of the training was to ensure that the data collection teams mastered the questionnaires, could measure MUAC accurately and implement the survey protocol, and were comfortable using CAPI.

    Classroom training for the recruitment phase was structured following the recruitment and health facility questionnaire: for each module a brief introduction was delivered, then each module question explained, and finally a mock interview between trainees took place. The training ended with a two-day piloting exercise to practice using the instruments and protocols.

    Similarly, classroom training for the home visits phase was structured to follow the long household questionnaire: for each module a brief introduction was delivered, then each module question explained, and finally a mock interview between trainees took place. A full day of training was dedicated to MUAC measurement and young children from Sokoto were invited for in-class practice. The training ended with a two-day piloting exercise to further familiarise trainees with overall survey instruments and protocols.

    A central component of quality assurance was the supervision and feedback that each enumerator received during the training, piloting, and roll-out of the study. At the beginning of every training day, the trainees had to complete a test on the modules covered the previous day and individual feedback was provided daily to identify and resolve any challenges faced by the interviewing team.

    Team supervisors were selected from among the most experienced and best-performing participants, and these individuals completed an additional training module for the extra tasks of coordination and quality assurance.

    Data processing

    Data Editing

    Given the data was electronically collected, it was continually checked, edited and processed throughout the survey cycle.

    A first stage of data checking was done by the survey team which involved
    (i) checking of all IDs;
    (ii) checking for missing observations;
    (iii) checking for missing item responses where none should be missing; and
    (iv) first round of checks for inadmissible/out of range and inconsistent values.

    Additional data processing activities were performed at the end of data collection in order to transform the collected cleaned data into a format that is ready for analysis. The aim of these activities was to produce reliable, consistent and fully-documented datasets that can be analysed throughout the survey and archived at the end in such a way that they can be used by other data users well into the future. Data processing activities involved:

    • Reshaping datasets in order to produce data files for each unit of observation,
    • Anonymising data by removing all variables that identify respondents such as names, address, GPS coordinates, etc.,
    • Classifying non-response and coding them using a pre-determined classification scheme,
    • Reviewing 'Other (specify)' responses by checking if any of the responses fall into existing response categories and can be recoded into the existing category or if there are multiple similar other responses that warrant the creation of a new response category (a decision to be made by the data analysts), and
    • Properly naming and labelling the variables in each dataset.

    The datasets were then sent to the analysis team where they were subjected to a second set of checking and cleaning activities. This included checking for out of range responses and inadmissible values not captured by the filters built into the CAPI software or the initial data checking process by the survey team.

    A comprehensive data checking and analysis system was created including a logical folder structure, the development of a detailed data analysis guide and template syntax files (in Stata), to ensure data checking and cleaning activities were recorded and that all analysts used the same file and variable naming conventions appropriately.

    Data Access

    Access authority
    Name URL Email
    Oxford Policy Management http://www.opml.co.uk/ admin@opml.co.uk
    Access conditions

    The datasets have been anonymised and are available as a Public Use Dataset. They are accessible to all for statistical and research purposes only, under the following terms and conditions:

    1. The data and other materials will not be redistributed or sold to other individuals, institutions, or organisations without the written agreement of Oxford Policy Management Ltd.
    2. The data will be used for statistical and scientific research purposes only. They will be used solely for reporting of aggregated information, and not for investigation of specific individuals or organisations.
    3. No attempt will be made to re-identify respondents, and no use will be made of the identity of any person or establishment discovered inadvertently. Any such discovery would immediately be reported to Oxford Policy Management Ltd.
    4. No attempt will be made to produce links among datasets provided by Oxford Policy Management Ltd, or among data from Oxford Policy Management Ltd and other datasets that could identify individuals or organisations.
    5. Any books, articles, conference papers, theses, dissertations, reports, or other publications that employ data obtained from Oxford Policy Management Ltd will cite the source of data in accordance with the Citation Requirement provided with each dataset.
    6. An electronic copy of all reports and publications based on the requested data will be sent to Oxford Policy Management Ltd.

    The original collector of the data, Oxford Policy Management Ltd, and the relevant funding agencies bear no responsibility for use of the data or for interpretations or inferences based upon such uses.

    Citation requirements

    Oxford Policy Management. Incidence of Severe Acute Malnutrition After Treatment: A Prospective Matched Cohort Study in Sokoto, Nigeria, Version 1.1 of the public use dataset (November 2021). Ref: NGA_2018-2019_CMAM_v01_M. Downloaded from [url] on [date].

    Disclaimer and copyrights

    Disclaimer

    The user of the data acknowledges that the original collector of the data, the authorised distributor of the data, and the relevant funding agency bear no responsibility for use of the data or for interpretations or inferences based upon such uses.

    Copyright

    (c) 2021, Oxford Policy Management Ltd.

    Contacts

    Contacts
    Name Email URL
    Oxford Policy Management admin@opml.co.uk http://www.opml.co.uk/

    Metadata production

    DDI Document ID

    DDI_NGA_2018-2019_CMAM_v01_M

    Producers
    Name Affiliation Role
    Ngowi, Abraham Oxford Policy Management Ltd. Documentation of the study
    Harb, Jana Oxford Policy Management Ltd. Data analyst
    Date of Metadata Production

    2021-11-17

    Metadata version

    DDI Document version

    Version 1.1 (November 2021)

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