Study of Effect of Microfinance on Under 5 Health in Rural India
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| ClinicalTrials.gov Identifier: NCT01845545 |
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Recruitment Status :
Completed
First Posted : May 3, 2013
Last Update Posted : February 13, 2017
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| Tracking Information | ||||
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| First Submitted Date ICMJE | April 24, 2013 | |||
| First Posted Date ICMJE | May 3, 2013 | |||
| Last Update Posted Date | February 13, 2017 | |||
| Study Start Date ICMJE | August 2013 | |||
| Actual Primary Completion Date | March 2016 (Final data collection date for primary outcome measure) | |||
| Current Primary Outcome Measures ICMJE |
Weight for height z-score of children under five years of age [ Time Frame: 18 months ] mean weight for height z-score (WHZ) of children under five years of age in the paired early and late intervention tolas at 18 months after the scheme has been implemented in the early intervention tolas
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| Original Primary Outcome Measures ICMJE |
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| Change History | ||||
| Current Secondary Outcome Measures ICMJE |
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| Original Secondary Outcome Measures ICMJE |
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| Current Other Pre-specified Outcome Measures | Not Provided | |||
| Original Other Pre-specified Outcome Measures | Not Provided | |||
| Descriptive Information | ||||
| Brief Title ICMJE | Study of Effect of Microfinance on Under 5 Health in Rural India | |||
| Official Title ICMJE | A Feasibility and Pilot Study of the Effects of Microfinance on Under 5 Mortality and Nutrition, Amongst the Very Poor in India | |||
| Brief Summary | Investigators propose a feasibility and pilot study for a cluster randomised controlled trial. The proposed trial will evaluate the effects of an economic intervention (microfinance) in self-help groups of poor and marginalised women in three provinces in northern India, upon the health of these communities, with a focus on children under five years. This feasibility and pilot study will determine whether accurate data can be collected on mortality by means of a house to house survey or from the register of births and deaths. The feasibility stage will also determine whether village volunteers can accurately weigh children under five and record their weights alongside the financial data already recorded by the self-help group. If these data are accurate and can be collected reliably, the investigators will calculate the power and sample size needed for a future cluster randomised trial, as well as analysing preliminary results from the current project. The investigators will evaluate health outcomes, relating to two Millennium Development Goals: number of children under five years of age who are underweight and the under five mortality rate. | |||
| Detailed Description | Background Microfinance is a process whereby small loans are given to the poorest families in developing countries to help overcome short term economic shocks (natural disasters or ill health) or to make small investments to improve their standard of living (eg in livestock. Microfinance has been shown to contribute to reducing poverty (particularly of female participants) and to improve the health of village economies. The Rojiroti scheme of microfinance has been running in several impoverished states in Northern India for ten years. This low cost scheme has been active in the states of Bihar, Madhya Pradesh and Uttar Pradesh and serves much poorer beneficiaries than those reached by mainstream microfinance. It works through establishing self-help groups (predominantly women from scheduled castes). Initially the members of these groups contribute their own money - a very small sum per week. After 3-6 months they become eligible for emergency loans for medical emergencies and general purpose loans, for investment in livestock etc.. These loans are administered locally by the charity "Centre for Promoting Sustainable Livelihoods" (CPSL). Rojiroti UK have just received a grant from the Department for International Development (DfID) for a 3 year expansion of the Rojiroti programme. Most of the participants in the Rojiroti scheme live in rural hamlets or "tolas", comprising several hundred people who earn a living by share cropping, as tenant farmers. The investigators will evaluate the feasibility of collecting mortality data (both directly in the tola and through registered deaths) and the feasibility of a village volunteer weighing children under five and recording their weights, along with other self-help group data. If data collection proves feasible, the investigators will conduct a pilot cluster randomised trial of immediate vs. delayed microfinance in 50 tolas in Bihar. Trial outcomes will be mortality and weight for age Z score, weight for height z-scores and mid upper arm circumference in children less than 5 years of age. Main centres Rojiroti is already established in northern Indian provinces of Bihar, Madhya Pradesh and Uttar Pradesh. In this study, the investigators plan to enrol tolas from Bihar. In the feasibility study there will be 10 tolas in each arm. If the data reach acceptable standards of accuracy and completeness, the investigators will continue the study in a further 40 tolas in each arm (total 50 tolas per arm, 100 altogether). The data analysis will be undertaken in the School of Medicine, University of Nottingham. Design A feasibility and pilot study for a cluster randomised controlled trial (RCT). The unit of randomisation is the tola. A control tola, paired with each intervention tola, will be randomly selected to have similar characteristics (size and agroeconomic zone) to the early intervention tola. The control tola will be at least 15km away from the intervention site (to avoid self-help groups being set up by word of mouth) but close enough to be practical for data collection. The control tola will receive the microfinance intervention 18 months after randomisation. Selection and randomisation of intervention sites The investigators will select tolas in Bihar province for the feasibility study (10 intervention and 10 control). It is important to include the control tolas at the feasibility stage, as the investigators think the challenges to complete and accurate data collection will be greater in the control tolas. Pairs of tolas will be selected by CPSL and the details provided to the team at the University of Nottingham in a secure, password protected spreadsheet, with each tola identified by a code number. The Nottingham team will randomise one of each pair to intervention or control group. Randomisation will be stratified by agroeconomic region (low, moderate and heavy annual rainfall). Consent and randomisation Initial discussions will take place between CPSL staff and women in the tolas prior to randomisation. The project will only proceed in that tola if sufficient village women (around 10) have expressed an interest in participating in self-help groups. The idea of the immediate and delayed intervention groups will be discussed with the women, by the CPSL staff. Women will have the option to agree to go ahead with the self-help groups, with or without randomisation and collection of health outcome data. The investigators will keep a record of the demographic characteristics of any tola which does not take part as well as those which do. Tolas agree to participate before they are randomised to immediate or delayed intervention groups. Randomisation will take place remotely and tolas are then informed through CPSL to which study arm they have been randomised. Evaluating the accuracy and completeness of data collection More than one self-help group may be set up in each tola but outcome data will be collected for the tola as a whole, in order to measure the effects of the intervention on those families in the self-help group and any the indirect effects on tola dwellers who are not part of the groups. Accuracy of data collection and recording will be evaluated through a field visit by CPSL staff. At this baseline visit, the CPSL staff and the village volunteer will independently:
These data will then be entered in a spreadsheet by CPSL staff and transferred to the team in Nottingham who will calculate the percentage concordance. Concordance of 75% or greater between the records of the CPSL worker and the village volunteer for population and mortality data will be deemed of acceptable accuracy. Concordance of the under five weights (to one decimal place) for 75% of children will be taken as acceptable. As well as checking the accuracy of weighing and weight recording, the CPSL staff will determine the number of children under five have not been weighed (e.g. children who are temporarily absent from the village and those who are ill). Data will also be collected on immunisation rates. The investigators will apply for access to data on registered deaths in each tola, from the provincial government and the investigators will use these to check the validity of the mortality data obtained from questionnaires. Statistical analysis plan Sample size and power calculations: This will be performed to inform a future RCT, using the data collected as part of the current study. If there are sufficient, reliable data available at the end of the feasibility stage, a preliminary power calculation will be performed to determine whether the pilot study might detect a clinically important difference in mortality, proportion underweight or weight for age z score. If so, the trial will move from pilot status to definitive trial. Published estimates of nutrition in Bihar date back to 2006 and suggest that 55% of under fives in Bihar are underweight (61% amongst children from scheduled castes). This may well have changed considerably in the last 6 years. This pilot study will provide a current estimate of the baseline prevalence of mortality and underweight. The sample size calculation for cluster randomised trials described by Hayes et al will be used. Type of analysis: In the pilot study and any future trial, intention to treat analysis will be used where possible i.e. where a tola has been randomised to receive microfinance early or late, their data will be included irrespective of whether the self-help group and microfinance have run successfully. Statistics tests: We will compare the proportion of children who are underweight and the mortality rate in the last year (deaths in the past year / population of the tola) in intervention and control tolas. This will be done at baseline and 18 months after the establishment of a self-help group in the early intervention tola. In order to estimate current tola population, the investigator will use a questionnaire administered by the CPSL worker when the children are weighed. An adjusted risk ratio (RR) with 95% confidence interval will be calculated, allowing for potential confounding effects of the pre-intervention prevalence of underweight or the mortality rate. As this is a cluster randomised trial based in small population units (tolas), the investigators will allow for correlation within zones. Planned exploratory analyses: The investigators will explore whether data can be collected on maternal literacy and years of schooling received. If the data are available, the investigators will compare the effectiveness of the intervention according to whether the mother was literate or illiterate and whether or not she had received at least 5 years of schooling. Change in primary outcome: In the initial study protocol, the primary outcome measures were mortality rate among children under five years of age and the overall mortaility in the tola. However, on further consideratation, this was changed to mean weight for height z-score (WHZ) if children under five years of age. Given the short duration of the study period (18 months), it was thought that any effect of the intervention on mortaility rates may not be evident in the study period. WHZ is a marker of acute malnutrion and wasting and Children with severe wasting (WHZ < -3 SD) have a 9.4-fold higher chance of dying while those with moderate wasting (WHZ -3 to -2 SD) have a 3.0-fold higher chance of dying when compared with their nonmalnourished counterparts. WHZ was therefore selected to be the primary outcome measure as it is strongly associated with mortality and may be affected by the intervention within the short duration of the study period. This change in protocol was made prior to randomisation and baseline data collection and is reported in the protocol publication. |
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| Study Type ICMJE | Interventional | |||
| Study Phase ICMJE | Not Applicable | |||
| Study Design ICMJE | Allocation: Randomized Intervention Model: Parallel Assignment Masking: Single (Outcomes Assessor) Primary Purpose: Other |
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| Condition ICMJE |
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| Intervention ICMJE | Other: Early provision of microfinance
The CPSL staff will support the formation of the self-help groups from the start of the study. The women in this group will have access to microfinance from the first 18 months of the study and will be eligible for emergency loans (up to Rs3000) and general purpose loans, (Rs50-3000) after 3-6 months of starting the self-help group.
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| Study Arms ICMJE |
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| Publications * |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | ||||
| Recruitment Status ICMJE | Completed | |||
| Actual Enrollment ICMJE |
2469 | |||
| Original Estimated Enrollment ICMJE |
800 | |||
| Actual Study Completion Date ICMJE | March 2016 | |||
| Actual Primary Completion Date | March 2016 (Final data collection date for primary outcome measure) | |||
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Sex/Gender ICMJE |
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| Ages ICMJE | 1 Day to 5 Years (Child) | |||
| Accepts Healthy Volunteers ICMJE | Yes | |||
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects | |||
| Listed Location Countries ICMJE | India | |||
| Removed Location Countries | ||||
| Administrative Information | ||||
| NCT Number ICMJE | NCT01845545 | |||
| Other Study ID Numbers ICMJE | UoN-J18102012 | |||
| Has Data Monitoring Committee | Yes | |||
| U.S. FDA-regulated Product | Not Provided | |||
| IPD Sharing Statement ICMJE | Not Provided | |||
| Current Responsible Party | University of Nottingham | |||
| Original Responsible Party | Same as current | |||
| Current Study Sponsor ICMJE | University of Nottingham | |||
| Original Study Sponsor ICMJE | Same as current | |||
| Collaborators ICMJE | Not Provided | |||
| Investigators ICMJE |
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| PRS Account | University of Nottingham | |||
| Verification Date | February 2017 | |||
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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