Severe MalnutritionNCT03043352
Evaluation of the Effectiveness and Impact of Community Case Management of Severe Acute Malnutrition
A study testing Management of SAM at home and Management of SAM at facility in people with Severe Malnutrition, run by Aga Khan University at 1 site in Pakistan.
Trial summary
HYPOTHESIS: Investigators hypothesize that by provision of care at household level in a community through lady health workers will as effective (recovery rate, burden of SAM, cost effective, coverage) as through health care providers at facility level. OBJECTIVES 1. Read more about this study
- Who is it for?
- Ages 6 to 59 months
- Conditions the study is for
- Severe Malnutrition
- What is being tested?
- Management of SAM at home and Management of SAM at facility
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 762 participants
- Where
- 1 sitePakistan
- Study dates
- 20 Apr 2015to 30 Jun 2016
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 6 to 59 months
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Born in the study area
- Presence of severe acute malnutrition (SAM).
- Ability of the parents or guardians to provide informed consent.
Who cannot join
- Presence of chronic debilitating illness.
- Residence outside of study areas.
- Inability or refusal of the parents or guardians to give informed consent, or refusal of assessment.
- Internally displaced population
Trial locations and contacts
1 site in 1 country.
Pakistan1 site
Aga Khan University Project Office
Khairpur Nathan Shah, Sindh
About this study
Official title: Evaluation of the Effectiveness and Impact of Community Case Management of Severe Acute Malnutrition Through Lady Health Workers As Compared To a Facility Based Program: A Cluster Randomized Controlled Trial
HYPOTHESIS:
Investigators hypothesize that by provision of care at household level in a community through lady health workers will as effective (recovery rate, burden of SAM, cost effective, coverage) as through health care providers at facility level. OBJECTIVES
Read more
- To evaluate the effectiveness (rate of recovery, burden \& coverage), of SAM standard management of children 06-59 months delivered at household level by first level health care providers (Lady health workers) compared with the standard CMAM program delivered at health facility by Govt./ACF staff.
- To evaluate the cost effectiveness of treatment of SAM provided by LHWs at community level versus treatment delivered at health facility by Govt/ACF staff.
STUDY DESIGN:
Cluster randomized controlled trial
SAMPLE SIZE \& RANDOMIZATION:
Investigators took 6% prevalence to calculate the sample size with an expected reduction of 20%. A sample size of 3 clusters per group with 150 individuals per cluster is needed. STUDY METHODOLOGY Intervention (Group A): LHWs will identify and treat all cases of severe acute malnutrition (SAM) as per the study eligibility criteria (MUAC < 11.5 cm) and manage all cases of SAM without complications at home following the national CMAM guidelines. Control (Group B): LHWs will identify SAM as per the CMAM guidelines (MUAC < 11.5 cm) and will refer all cases to the health facility (ACF) for further management and counselling by health workers at facility.
Read the detailed description
INTRODUCTION \& RATIONALE:
There is good evidence of the success of CMAM programs for treating SAM in emergencies and humanitarian crises [1], but little regarding the most cost effective mechanisms to deliver it or of the added value of integrating treatment of acute malnutrition with treatment of common childhood illness and/or extensive communitybased nutritional program.
HYPOTHESIS:
Provision of SAM treatment at household level in a community through lady health workers will be as effective (recovery rate, survival, cost effectiveness, coverage) as treatment provided at facility level.
RESEARCH QUESTION:
Will SAM treatment delivered through LHW at household level be as effective as SAM treatment delivered at facility level by health center staff?
PRIMARY OBJECTIVES:
To evaluate the effectiveness (rate of recovery, relapse \& coverage), of SAM treatment of children 6-59 months delivered at household level by first level health care providers (Lady health workers) compared with the standard CMAM program delivered at health facility by Government and ACF staff. To evaluate the cost effectiveness of treatment of SAM provided by LHWs at community level versus treatment delivered at health facility by Government and ACF staff.
SECONDARY OBJECTIVES:
To evaluate the characterization of the breast feeding and complementary feeding practices in both study arms. To identify the main socio-economic characteristics of the households in both study arms.
STUDY DESIGN:
The study will be a 2-armed cluster randomized controlled trial targeting children 60-59 months and their mothers for the treatment and prevention of acute severe malnutrition in children. Each cluster will be allocated to intervention group A, or control group B.
Cost-effectiveness analysis:
Cost effectiveness will be calculated to reflect the full range of resources required by service providers and households. A societal perspective will be taken with data collected on household costs incurred for participation in community and facility based activities. The approach will capture all resources used regardless of who incurs them, as used for cost analysis of other similar programs. Costs will be calculated with a combination of accounting records and estimates derived with an "ingredients" approach, using unit costs and quantities of inputs. Institutional costs will be estimated via accounting records. Costs which are known to be incurred by the program but which are not reflected in the accounting records (e.g. staff whose salaries are on different budgets, storage space which was not planned for in the original budget, etc.) will be estimated after identifying these costs through discussion with staff and document review. This data will be supplemented with costs calculated via an ingredients approach. Key informant interviews will be held with all key implementing staff to estimate their time allocation to project activities, in order to perform an activity based cost analysis.
Coverage assessment:
Coverage Assessments will be implemented in the two areas at the start the study, at six months of the study beginning and at the end of the study. SQUEAC methodology will be used. Coverage assessments are of particular interest in order to access the population that is not accessing treatment and understand its barriers to access. These assessments will be carried out by trained ACF staff.
MAIN STUDY OUTCOMES:
The key indicators to be captured are:
- Effectiveness - recovery rate (proportion of cured children among SAM enrolled), supplement compliance rate, defaulter rate, relapse rate, Length of stay, average weight gain, hospital admission, and complications
- Coverage rates and barriers to access (estimated using the SQUEAC methodology)
- Health \& Nutrition status of children (prevalence of malnutrition etc.)
- Cost-effectiveness
- Descriptive analysis to assess the distribution of various factors within and between groups, cluster-adjusted analyses will compare SAM rates (recovery, survival, relapse, default) observed in the different arms. Kaplan Meier statistics will be used for the comparison of post-treatment survival.
SAMPLE SIZE \& RANDOMIZATION:
Investigators have calculated the sample size on the basis of SAM as the primary indicator; Investigators took 6% prevalence to calculate the sample size with an expected reduction of 20%. A sample size of 3 clusters per group with 150 individuals per cluster achieves 98% power to detect a difference of 0.200 between the group means when the standard deviation is 0.500 and the intracluster correlation is 0.00100 using a Two-Sided T-test with a significance level of 0.05000.
Definition of cluster:
A union council has been defined as the CLUSTER for the trial, a union council is the smallest administrative unit in the district which usually have a population of about 25000 to 30000, and this population has about 2500-3000 under five children, if Investigators consider the national rates of SAM in Pakistan which is about 6% Investigators will find more than 150 cases of SAM from each union council during the study period which will be enough sample to achieve the objectives of the trial. One union council has usually one health facility Basic health Unit (BHU) or Rural Health Center.
STUDY SITE:
The study will be carried out in Dadu district, a rural district of Sindh province of Pakistan. This district has been selected due to the high global acute malnutrition (GAM) rates, being affected by emergencies. Currently in Sindh, SAM treatment is delivered at health facility level.
BENEFICIARIES:
Main target beneficiaries would be children 6- 59 months of age fulfilling the case definition of severe malnutrition and their mothers.
DELIVERY OF INTERVENTION:
Intervention Arm (A): Lady Health Workers operating at field level in study arm A will be trained at the start of the study. The same training package will be delivered to all LHWs involved in the study regardless of their previous training and the trainings will be delivered by the Department of Health (once officially agreed), by ACF \& AKU. All eligible children in the LHW´s catchment area will be identified and registered by the LHWs as part of their routine activities. In Pakistan national guidelines, SAM treatment admission criteria is MUAC <11.5 cm. Children 6- 59 months, with MUAC less than 11.5 cm and meeting eligibility criteria will be enrolled after obtaining consent and provide treatment of SAM at home and IYCF counseling and follow up till recovery. Children 60-59 months in the criteria for stabilization care will also be referred by the LHW.
The LHW will visit fortnightly to follow up all recruited children with SAM and receiving RUTF in their catchment population. If the child gets severely ill or having any complication the LHW will immediately refer that child to the nearest health facility for hospital based care. The LHW will record MUAC measurements on fortnightly follow up visits and weight and height will be recorded by the data collectors. Control Arm (B): Lady Health Workers operating at field level in study arm B will perform monthly home visit and will recruit and register all eligible children in their catchment area as part of their routine activities. The LHW will identify cases of SAM as per national CMAM guidelines through MUAC measurements and refer them to the nearest health facility where ACF staff will provide treatment in the facility as per standard CMAM guidelines.
DATA COLLECTION:
Data will be collected by an independent team, and not by LHWs. Data collection team will consist of 2 data collectors and a team leader. Data collectors and team leaders will be hired and trained to collect data by the study team.The team will visit identified households and the data will cross validate the LHW activities. The study team will collect information regarding children with SAM at baseline survey and during the study from LHWs and health facilities staff. A trained community health worker will visit the household having child with SAM and will take informed consent and recruit the child in the study.
Baseline Cross Sectional Survey :
A cross sectional survey will be conducted at household level in both arms
Fortnightly follow-up visits :
A fortnightly follow up of children will be carried out by the community health worker until the recovery of child this may takes up to 3-6 months during the first 3 months of the study , the purpose of this follow up is to collect the information regarding, acceptability, compliance, concurrent morbidities if any and record anthropometry (only weight \& MUAC).
Monthly follow-up visits:
Monthly follow ups will be done by data collectors to capture the information on recovery, feeding practices, child's nutritional status morbidities \& mortality. These follow ups will be continued for 6 months from the time of recruitment. Complete anthropometry (MUAC, Height and Weight) will be carried out during monthly follow ups.
Household cost survey:
Towards the end of the intervention, a household survey will be implemented on a random sample of program beneficiaries in both study areas to collect information on the direct and indirect costs they incurred in participating in the program. This will include information on cost of transportation, foods and medicines purchased, and time spent in accessing care.
- Conditions
- Severe Malnutrition
- Being tested
- Management of SAM at home, Management of SAM at facility
- Keywords
- SAM, Malnutrition, LHW, CMAM
- Medical subject headings
- Malnutrition
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Management of SAM at homeDietary supplement
LHWs will identify and treat all cases of severe acute malnutrition (SAM) in children under-five years at household level compared with the standard CMAM program
Management of SAM at facilityDietary supplement
LHWs will identify SAM as per 'Standard CMAM program' (MUAC < 11.5cm) and will refer all cases to the health facility BHU/ satellite site (ACF) for further management and counselling by health workers (ACF CMAM Nurse) at facility level.
| Study group | Role | What they receive |
|---|---|---|
| Group A (intervention) | Experimental | 'Management of SAM at home' LHWs will identify and treat all cases of severe acute malnutrition (SAM) as per the study eligibility criteria (MUAC < 11.5 cm) and manage all cases of SAM without complications at home with 'Standard CMAM program'. The LHWs will also identify SAM with complications for further assessment to the BHU Doctor and subsequent referral to the stabilization center . They will also provide one to one health and Infant and Young Child Feeding (IYCF) counselling to care takers of children in their catchment area. Receives: Dietary Supplement: Management of SAM at home |
| Group B (Control) | Active comparator | 'Management of SAM at facility' LHWs will identify SAM as per 'Standard CMAM program' (MUAC < 11.5cm) and will refer all cases to the health facility BHU/ satellite site (ACF) for further management and counselling by health workers (ACF CMAM Nurse) at facility level. Receives: Dietary Supplement: Management of SAM at facility |
What is being measured
The primary outcome is the main question the study is designed to answer.
To evaluate rate of recovery
To evaluate the rate of recovery of SAM treatment of children 6-59 months old delivered at household level by first level health care providers (Lady Health workers) compared with the standard CMAM program delivered at health facility by Govt and ACF staff.
Pakistan national guidelines for the community based management of acute malnutrition 2014 will be used to measure this outcome.
Measured: 18 months
Secondary outcomes (4)
Prevalence of malnutrition
It will be estimated through cross sectional surveys.
Measured: 18 months
To evaluate the cost effectiveness of treatment.
To evaluate the cost effectiveness of treatment of SAM provided by LHWs at community level versus treatment delivered at health facility by Govt and ACF staff.
Measured: 18 months
Relapse from severe acute malnutrition
To evaluate the relapse of SAM treatment of children 6-59 months old delivered at household level by first level health care providers (Lady Health workers) compared with the standard CMAM program delivered at health facility by Govt and ACF staff.
Pakistan national guidelines for the community based management of acute malnutrition 2014 will be used to measure this outcome.
Measured: 18 months
Default cases of SAM
Pakistan national guidelines for the community based management of acute malnutrition 2014 will be used to measure this outcome.
Measured: 18 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Feb 2017 (estimated)
- Study start20 Apr 2015
- Primary completion30 Jun 2016
- Study completion30 Jun 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Severe MalnutritionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 762 participants (actual)
Sponsor and investigators
- Lead sponsor
- Aga Khan University
- Sponsor type
- University, hospital or other
- Collaborators
- Action Contre la Faim
- Responsible party
- Principal investigator, Dr Sajid Bashir Soofi, Aga Khan University
- Investigators
- Sajid Soofi, FCPS, Principal investigator, Aga Khan University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03043352
- Sponsor's protocol ID
- 3276-Ped-ERC-14
- Status last verified
- Feb 2017
- First submitted
- 11 Nov 2015
- Last updated
- 6 Feb 2017
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes
Publications
Bhutta ZA, Das JK, Rizvi A, Gaffey MF, Walker N, Horton S, Webb P, Lartey A, Black RE; Lancet Nutrition Interventions Review Group, the Maternal and Child Nutrition Study Group. Evidence-based interventions for improvement of maternal and child nutrition: what can be done and at what cost? Lancet. 2013 Aug 3;382(9890):452-477. doi: 10.1016/S0140-6736(13)60996-4. Epub 2013 Jun 6.
PubMed 23746776Rogers E, Guerrero S, Kumar D, Soofi S, Fazal S, Martinez K, Moran JLA, Puett C. Evaluation of the cost-effectiveness of the treatment of uncomplicated severe acute malnutrition by lady health workers as compared to an outpatient therapeutic feeding programme in Sindh Province, Pakistan. BMC Public Health. 2019 Jan 17;19(1):84. doi: 10.1186/s12889-018-6382-9.
PubMed 30654780
Study at a glance
From the registry record, last updated by the sponsor on 6 Feb 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of the Effectiveness and Impact of Community Case Management of Severe Acute Malnutrition Through Lady Health Workers As Compared To a Facility Based Program: A Cluster Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT03043352
- Acronym / sponsor ID
- 3276-Ped-ERC-14
- Conditions
- Severe Malnutrition
- Keywords
- SAM, Malnutrition, LHW, CMAM
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 762 participants (actual)
- Lead sponsor
- Aga Khan UniversityUniversity, hospital or other
- Collaborators
- Action Contre la Faim
- Study start
- 20 Apr 2015 (actual)
- Primary completion
- 30 Jun 2016 (actual)
- Study completion
- 30 Jun 2016 (actual)
- First posted
- 6 Feb 2017 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
HYPOTHESIS:
Investigators hypothesize that by provision of care at household level in a community through lady health workers will as effective (recovery rate, burden of SAM, cost effective, coverage) as through health care providers at facility level. OBJECTIVES
- To evaluate the effectiveness (rate of recovery, burden \& coverage), of SAM standard management of children 06-59 months delivered at household level by first level health care providers (Lady health workers) compared with the standard CMAM program delivered at health facility by Govt./ACF staff.
- To evaluate the cost effectiveness of treatment of SAM provided by LHWs at community level versus treatment delivered at health facility by Govt/ACF staff.
STUDY DESIGN:
Cluster randomized controlled trial
SAMPLE SIZE \& RANDOMIZATION:
Investigators took 6% prevalence to calculate the sample size with an expected reduction of 20%. A sample size of 3 clusters per group with 150 individuals per cluster is needed. STUDY METHODOLOGY Intervention (Group A): LHWs will identify and treat all cases of severe acute malnutrition (SAM) as per the study eligibility criteria (MUAC < 11.5 cm) and manage all cases of SAM without complications at home following the national CMAM guidelines. Control (Group B): LHWs will identify SAM as per the CMAM guidelines (MUAC < 11.5 cm) and will refer all cases to the health facility (ACF) for further management and counselling by health workers at facility.
Detailed description
INTRODUCTION \& RATIONALE:
There is good evidence of the success of CMAM programs for treating SAM in emergencies and humanitarian crises [1], but little regarding the most cost effective mechanisms to deliver it or of the added value of integrating treatment of acute malnutrition with treatment of common childhood illness and/or extensive communitybased nutritional program.
HYPOTHESIS:
Provision of SAM treatment at household level in a community through lady health workers will be as effective (recovery rate, survival, cost effectiveness, coverage) as treatment provided at facility level.
RESEARCH QUESTION:
Will SAM treatment delivered through LHW at household level be as effective as SAM treatment delivered at facility level by health center staff?
PRIMARY OBJECTIVES:
To evaluate the effectiveness (rate of recovery, relapse \& coverage), of SAM treatment of children 6-59 months delivered at household level by first level health care providers (Lady health workers) compared with the standard CMAM program delivered at health facility by Government and ACF staff. To evaluate the cost effectiveness of treatment of SAM provided by LHWs at community level versus treatment delivered at health facility by Government and ACF staff.
SECONDARY OBJECTIVES:
To evaluate the characterization of the breast feeding and complementary feeding practices in both study arms. To identify the main socio-economic characteristics of the households in both study arms.
STUDY DESIGN:
The study will be a 2-armed cluster randomized controlled trial targeting children 60-59 months and their mothers for the treatment and prevention of acute severe malnutrition in children. Each cluster will be allocated to intervention group A, or control group B.
Cost-effectiveness analysis:
Cost effectiveness will be calculated to reflect the full range of resources required by service providers and households. A societal perspective will be taken with data collected on household costs incurred for participation in community and facility based activities. The approach will capture all resources used regardless of who incurs them, as used for cost analysis of other similar programs. Costs will be calculated with a combination of accounting records and estimates derived with an "ingredients" approach, using unit costs and quantities of inputs. Institutional costs will be estimated via accounting records. Costs which are known to be incurred by the program but which are not reflected in the accounting records (e.g. staff whose salaries are on different budgets, storage space which was not planned for in the original budget, etc.) will be estimated after identifying these costs through discussion with staff and document review. This data will be supplemented with costs calculated via an ingredients approach. Key informant interviews will be held with all key implementing staff to estimate their time allocation to project activities, in order to perform an activity based cost analysis.
Coverage assessment:
Coverage Assessments will be implemented in the two areas at the start the study, at six months of the study beginning and at the end of the study. SQUEAC methodology will be used. Coverage assessments are of particular interest in order to access the population that is not accessing treatment and understand its barriers to access. These assessments will be carried out by trained ACF staff.
MAIN STUDY OUTCOMES:
The key indicators to be captured are:
- Effectiveness - recovery rate (proportion of cured children among SAM enrolled), supplement compliance rate, defaulter rate, relapse rate, Length of stay, average weight gain, hospital admission, and complications
- Coverage rates and barriers to access (estimated using the SQUEAC methodology)
- Health \& Nutrition status of children (prevalence of malnutrition etc.)
- Cost-effectiveness
- Descriptive analysis to assess the distribution of various factors within and between groups, cluster-adjusted analyses will compare SAM rates (recovery, survival, relapse, default) observed in the different arms. Kaplan Meier statistics will be used for the comparison of post-treatment survival.
SAMPLE SIZE \& RANDOMIZATION:
Investigators have calculated the sample size on the basis of SAM as the primary indicator; Investigators took 6% prevalence to calculate the sample size with an expected reduction of 20%. A sample size of 3 clusters per group with 150 individuals per cluster achieves 98% power to detect a difference of 0.200 between the group means when the standard deviation is 0.500 and the intracluster correlation is 0.00100 using a Two-Sided T-test with a significance level of 0.05000.
Definition of cluster:
A union council has been defined as the CLUSTER for the trial, a union council is the smallest administrative unit in the district which usually have a population of about 25000 to 30000, and this population has about 2500-3000 under five children, if Investigators consider the national rates of SAM in Pakistan which is about 6% Investigators will find more than 150 cases of SAM from each union council during the study period which will be enough sample to achieve the objectives of the trial. One union council has usually one health facility Basic health Unit (BHU) or Rural Health Center.
STUDY SITE:
The study will be carried out in Dadu district, a rural district of Sindh province of Pakistan. This district has been selected due to the high global acute malnutrition (GAM) rates, being affected by emergencies. Currently in Sindh, SAM treatment is delivered at health facility level.
BENEFICIARIES:
Main target beneficiaries would be children 6- 59 months of age fulfilling the case definition of severe malnutrition and their mothers.
DELIVERY OF INTERVENTION:
Intervention Arm (A): Lady Health Workers operating at field level in study arm A will be trained at the start of the study. The same training package will be delivered to all LHWs involved in the study regardless of their previous training and the trainings will be delivered by the Department of Health (once officially agreed), by ACF \& AKU. All eligible children in the LHW´s catchment area will be identified and registered by the LHWs as part of their routine activities. In Pakistan national guidelines, SAM treatment admission criteria is MUAC <11.5 cm. Children 6- 59 months, with MUAC less than 11.5 cm and meeting eligibility criteria will be enrolled after obtaining consent and provide treatment of SAM at home and IYCF counseling and follow up till recovery. Children 60-59 months in the criteria for stabilization care will also be referred by the LHW.
The LHW will visit fortnightly to follow up all recruited children with SAM and receiving RUTF in their catchment population. If the child gets severely ill or having any complication the LHW will immediately refer that child to the nearest health facility for hospital based care. The LHW will record MUAC measurements on fortnightly follow up visits and weight and height will be recorded by the data collectors. Control Arm (B): Lady Health Workers operating at field level in study arm B will perform monthly home visit and will recruit and register all eligible children in their catchment area as part of their routine activities. The LHW will identify cases of SAM as per national CMAM guidelines through MUAC measurements and refer them to the nearest health facility where ACF staff will provide treatment in the facility as per standard CMAM guidelines.
DATA COLLECTION:
Data will be collected by an independent team, and not by LHWs. Data collection team will consist of 2 data collectors and a team leader. Data collectors and team leaders will be hired and trained to collect data by the study team.The team will visit identified households and the data will cross validate the LHW activities. The study team will collect information regarding children with SAM at baseline survey and during the study from LHWs and health facilities staff. A trained community health worker will visit the household having child with SAM and will take informed consent and recruit the child in the study.
Baseline Cross Sectional Survey :
A cross sectional survey will be conducted at household level in both arms
Fortnightly follow-up visits :
A fortnightly follow up of children will be carried out by the community health worker until the recovery of child this may takes up to 3-6 months during the first 3 months of the study , the purpose of this follow up is to collect the information regarding, acceptability, compliance, concurrent morbidities if any and record anthropometry (only weight \& MUAC).
Monthly follow-up visits:
Monthly follow ups will be done by data collectors to capture the information on recovery, feeding practices, child's nutritional status morbidities \& mortality. These follow ups will be continued for 6 months from the time of recruitment. Complete anthropometry (MUAC, Height and Weight) will be carried out during monthly follow ups.
Household cost survey:
Towards the end of the intervention, a household survey will be implemented on a random sample of program beneficiaries in both study areas to collect information on the direct and indirect costs they incurred in participating in the program. This will include information on cost of transportation, foods and medicines purchased, and time spent in accessing care.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Group A (intervention) | Experimental | Dietary Supplement: Management of SAM at home'Management of SAM at home' LHWs will identify and treat all cases of severe acute malnutrition (SAM) as per the study eligibility criteria (MUAC < 11.5 cm) and manage all cases of SAM without complications at home with 'Standard CMAM program'. The LHWs will also identify SAM with complications for further assessment to the BHU Doctor and subsequent referral to the stabilization center . They will also provide one to one health and Infant and Young Child Feeding (IYCF) counselling to care takers of children in their catchment area. |
| Group B (Control) | Active comparator | Dietary Supplement: Management of SAM at facility'Management of SAM at facility' LHWs will identify SAM as per 'Standard CMAM program' (MUAC < 11.5cm) and will refer all cases to the health facility BHU/ satellite site (ACF) for further management and counselling by health workers (ACF CMAM Nurse) at facility level. |
Who may qualify
- Ages
- 6 to 59 months
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (3 listed)
- Born in the study area
- Presence of severe acute malnutrition (SAM).
- Ability of the parents or guardians to provide informed consent.
Key exclusion criteria (4 listed)
- Presence of chronic debilitating illness.
- Residence outside of study areas.
- Inability or refusal of the parents or guardians to give informed consent, or refusal of assessment.
- Internally displaced population
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Management of SAM at homeLHWs will identify and treat all cases of severe acute malnutrition (SAM) in children under-five years at household level compared with the standard CMAM program | Dietary supplement | Group A (intervention) |
| Management of SAM at facilityLHWs will identify SAM as per 'Standard CMAM program' (MUAC < 11.5cm) and will refer all cases to the health facility BHU/ satellite site (ACF) for further management and counselling by health workers (ACF CMAM Nurse) at facility level. | Dietary supplement | Group B (Control) |
Primary outcome
To evaluate rate of recovery
Time frame: 18 months
To evaluate the rate of recovery of SAM treatment of children 6-59 months old delivered at household level by first level health care providers (Lady Health workers) compared with the standard CMAM program delivered at health facility by Govt and ACF staff. Pakistan national guidelines for the community based management of acute malnutrition 2014 will be used to measure this outcome.
4 secondary outcomes
Prevalence of malnutrition
Time frame: 18 months
To evaluate the cost effectiveness of treatment.
Time frame: 18 months
Relapse from severe acute malnutrition
Time frame: 18 months
Default cases of SAM
Time frame: 18 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Feb 2017.
- Background: PubMed 23746776Bhutta ZA, Das JK, Rizvi A, Gaffey MF, Walker N, Horton S, Webb P, Lartey A, Black RE; Lancet Nutrition Interventions Review Group, the Maternal and Child Nutrition Study Group. Evidence-based interventions for improvement of maternal and child nutrition: what can be done and at what cost? Lancet. 2013 Aug 3;382(9890):452-477. doi: 10.1016/S0140-6736(13)60996-4. Epub 2013 Jun 6.
- Derived from this study: PubMed 30654780Rogers E, Guerrero S, Kumar D, Soofi S, Fazal S, Martinez K, Moran JLA, Puett C. Evaluation of the cost-effectiveness of the treatment of uncomplicated severe acute malnutrition by lady health workers as compared to an outpatient therapeutic feeding programme in Sindh Province, Pakistan. BMC Public Health. 2019 Jan 17;19(1):84. doi: 10.1186/s12889-018-6382-9.
- Individual participant dataSharing planned: Yes
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Sajid Soofi, FCPS principal investigator
Aga Khan University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Management of SAM at home and Management of SAM at facility in people with Severe Malnutrition, run by Aga Khan University at 1 site in Pakistan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 6 Feb 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
To evaluate rate of recovery (time frame: 18 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03043352, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Feb 2017.