Evaluation of the Effectiveness and Impact of Community Case Management of Severe Acute Malnutrition
![]() |
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT03043352 |
Recruitment Status :
Completed
First Posted : February 6, 2017
Last Update Posted : February 6, 2017
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
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.
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Severe Malnutrition | Dietary Supplement: Management of SAM at home Dietary Supplement: Management of SAM at facility | Not Applicable |

Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 762 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
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 |
Actual Study Start Date : | April 20, 2015 |
Actual Primary Completion Date : | June 30, 2016 |
Actual Study Completion Date : | June 30, 2016 |

Arm | Intervention/treatment |
---|---|
Experimental: Group A (intervention)
'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.
|
Dietary Supplement: Management of SAM at home
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 |
Active Comparator: Group B (Control)
'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.
|
Dietary Supplement: 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. |
- 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.
- Prevalence of malnutrition [ Time Frame: 18 months ]It will be estimated through cross sectional surveys.
- To evaluate the cost effectiveness of treatment. [ Time Frame: 18 months ]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.
- Relapse from severe acute malnutrition [ Time Frame: 18 months ]
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.
- Default cases of SAM [ Time Frame: 18 months ]Pakistan national guidelines for the community based management of acute malnutrition 2014 will be used to measure this outcome.

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 6 Months to 59 Months (Child) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Born in the study area
- Presence of severe acute malnutrition (SAM).
- Ability of the parents or guardians to provide informed consent.
Exclusion Criteria:
- 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

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03043352
Pakistan | |
Aga Khan University Project Office | |
Khairpur Nathan Shah, Sindh, Pakistan |
Principal Investigator: | Sajid Soofi, FCPS | Aga Khan University |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | Dr Sajid Bashir Soofi, Associate Professor, Aga Khan University |
ClinicalTrials.gov Identifier: | NCT03043352 |
Other Study ID Numbers: |
3276-Ped-ERC-14 |
First Posted: | February 6, 2017 Key Record Dates |
Last Update Posted: | February 6, 2017 |
Last Verified: | February 2017 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Yes |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
SAM Malnutrition LHW CMAM |
Malnutrition Severe Acute Malnutrition Nutrition Disorders |