- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02672982
Follow Up of Severely Malnourished Children (FUSAM) (FUSAM)
March 11, 2022 updated by: Action Contre la Faim
Follow Up of Severely Malnourished Children (FUSAM): Effectiveness of a Combined Nutrition Psychosocial Intervention on Health and Development.
The overall objective of the research is to assess the long-term and cost-effectiveness of a combined nutrition psychosocial intervention to a stand-alone nutritional treatment of children with Severe Acute Malnutrition (SAM) aged 6 to 24 months in the Saptari District of Nepal.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
In Nepal, the majority of SAM children are treated with therapeutic food in community/home-based care, and little is known about the long-term sustainability of the nutritional and health benefits of treatment after rehabilitation.
The two treatments will be compared in terms of costs of treatment and convened health benefits (child nutritional status and development, cured rate and relapse, maternal mental health, and family care practices) at both short and long-term periods after admission.
The proposed complementary psychosocial intervention focuses directly on the key underlying determinants of acute malnutrition within children's early years, such as child care practices and stimulation, parent-child relationships and maternal mental health.
It includes the mother/caregiver as patient of psychosocial support, but also empowers her as the key ally in the treatment of the undernourished child.
Adding a brief psychosocial component to the standard medico-nutritional treatment is expected to pay off in terms of sustainable recovery, health, and development outcomes of children.
Study Type
Interventional
Enrollment (Actual)
427
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Kathmandu, Nepal
- ACF, Nepal
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
6 months to 1 year (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Age: 6-23 months
- 2 sexes
- Diagnosis: uncomplicated severe acute malnutrition requiring follow-up outpatient therapeutic feeding unit (OTPs), supported by Action Contre la Faim in Saptari district
- Weight-for-height (WH) <-3 Standard Deviation compared to the WHO reference and/or MUAC <115 mm
- And / or nutritional oedema moderate (+ or + +)
- And successful test of appetite
- And no medical complications
- New cases
- Presence of mother / father or legal guardian aged > 18 years.
- Understanding of the consent and information letter
- Follow-up possible
Exclusion Criteria:
- Age <6 months or> 24 months
- Moderate Acute Malnutrition
- Severe Acute Malnutrition complicated
- Weight for height <-3 Standard Deviation compared to the WHO reference and / or MUAC <115mm but failure to test appetite OR medical complications OR severe oedema + + + OR kwashiorkor, marasmus (malnutrition with the same criteria, with oedema mild or severe).
- Relapse or if already registered in the past two months;
- Any child with developmental anomalies, known chronic illnesses like epilepsy, twins and multiple births, parents not consenting,
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: new combined NUTPSY treatment
2-month combined nutrition and psychosocial intervention
|
The psychosocial component of the new combined treatment involves seven weekly counselling sessions with mothers focused on feeding, emotional attachment, stages of child development, stimulation, emotional responsiveness and interaction, and on concerns/strategies of child care and parenting.
|
|
Active Comparator: standard NUT treatment
2-month of standard nutritional treatment only
|
Only the standard nutritional treatment in the form of Ready-to-use Therapeutic Food (RUTF) is administered.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child motor, cognitive, emotional and social development assessed with Ages and Stages Questionnaire
Time Frame: up to 11 months after inclusion
|
The Ages and Stages Questionnaire (Squires et al, 1999), is a low-cost, easily administered, parent-report screening test of development in communication, motor, problem-solving and personal-social domains.
The questionnaire has been adapted and used in low- and middle-income countries in Africa, Asia and Latin America, where it has demonstrated sensitivity to child nutritional status and psychosocial stimulation.
While it is not a diagnostic test, it offers an opportunity to systematically obtain information about children's development with an instrument that does not require extensive training
|
up to 11 months after inclusion
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child Care Practices
Time Frame: Up to 11 months after inclusion
|
The quality of care practices is measured by assessing the level of knowledge and the practices.
It comprises sub-thematics: care for women, pregnancy and delivery, care for the newborn, breastfeeding and feeding, access to resources for care, as well as child development and psychosocial care.
The Child Care Knowledge & Practices Questionnaire has been developped by Action Contre la Faim.
|
Up to 11 months after inclusion
|
|
Mother-child interaction
Time Frame: Up to 11 months after inclusion
|
Action Contre la Faim's Mother-Child Interaction Grid will be used for assessing the quality of mother-child interactions and interpersonal sensitivity and responsiveness.
|
Up to 11 months after inclusion
|
|
Child stimulation
Time Frame: Up to 11 months after inclusion
|
Family Care Indicators (FCI) (Frongillo et al, 2003) is used to assess the quality of child stimulation
|
Up to 11 months after inclusion
|
|
Maternal perinatal mental health
Time Frame: Up to 11 months after inclusion
|
The Edinburgh Post-natal Depression Scale (Cox et al, 1987) is a valuable and efficient way of identifying mothers at risk for "perinatal" depression.
|
Up to 11 months after inclusion
|
|
Perceived Social Support
Time Frame: Up to 11 months after inclusion
|
The Multidimensional Scale of Perceived Social Support (Zimet et al, 1988) measures perceived support from 3 sources: family, friends and significant others.
|
Up to 11 months after inclusion
|
|
Maternal self-esteem
Time Frame: Up to 11 months after inclusion
|
The Rosenberg self-esteem scale (Rosenberg, 1965) assesses maternal self-esteem.
|
Up to 11 months after inclusion
|
|
Maternal mental health
Time Frame: Up to 11 months after inclusion
|
The WHO Self Reporting Questionnaire (SRQ-20) (WHO, 1994) assesses the frequency of depressive symptoms, anxiety, and psychosomatic complaints in the past month.
The measure has been shown to be an accurate predictor of common mental disorder and has been successfully used in several studies in developing countries.
|
Up to 11 months after inclusion
|
|
Child growth (height)
Time Frame: Up to 11 months after inclusion
|
Child growth measures change in height
|
Up to 11 months after inclusion
|
|
Child nutritional status defined by Mid-Upper Arm Circumference (MUAC)
Time Frame: Up to 11 months after inclusion
|
Comparison of the mean MUAC adjusted to age, sex and height
|
Up to 11 months after inclusion
|
|
Child nutritional status defined by Weight-For-Height Z-score
Time Frame: Up to 11 months after inclusion
|
Comparison of the mean Weight-For-Height Z-score
|
Up to 11 months after inclusion
|
|
Child nutritional status defined by height-for-Age Z score
Time Frame: Up to 11 months after inclusion
|
Comparison of the mean height-for-Age Z score
|
Up to 11 months after inclusion
|
|
Child health status (morbidity rate)
Time Frame: Up to 11 months after inclusion
|
Follow-up of morbidity rate
|
Up to 11 months after inclusion
|
|
Child death (mortality rate)
Time Frame: Up to 11 months after inclusion
|
Follow-up of mortality rate
|
Up to 11 months after inclusion
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Cecile Bizouerne, PhD, Action Contre la Faim
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 8, 2014
Primary Completion (Actual)
January 31, 2017
Study Completion (Actual)
January 31, 2017
Study Registration Dates
First Submitted
January 13, 2015
First Submitted That Met QC Criteria
February 2, 2016
First Posted (Estimate)
February 3, 2016
Study Record Updates
Last Update Posted (Actual)
March 25, 2022
Last Update Submitted That Met QC Criteria
March 11, 2022
Last Verified
March 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ACFInternational
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Severe Acute Malnutrition
-
University of California, San FranciscoEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsCompletedUncomplicated Severe Acute MalnutritionBurkina Faso
-
Society for Applied StudiesWorld Health Organization; Christian Medical College, Vellore, India; ArthCompletedUncomplicated Severe Acute MalnutritionIndia
-
National Institute for Medical Research, TanzaniaLondon School of Hygiene and Tropical Medicine; University of Turku; Rigshospitalet... and other collaboratorsNot yet recruitingSevere Acute Malnutrition in ChildhoodTanzania
-
International Centre for Diarrhoeal Disease Research...UNICEF; NutrisetCompletedSevere Acute Malnutrition in ChildhoodBangladesh
-
UNICEFSave the ChildrenCompletedSevere MalnutritionCongo, The Democratic Republic of the
-
International Centre for Diarrhoeal Disease Research...UNICEFNot yet recruitingMalnutrition SevereBangladesh
-
Aga Khan UniversityAction Contre la FaimCompletedEvaluation of the Effectiveness and Impact of Community Case Management of Severe Acute MalnutritionSevere MalnutritionPakistan
-
Action Against Hunger USAUniversity of Washington; Ethiopian Public Health InstituteRecruitingModerate Acute Malnutrition | Severe Acute MalnutritionEthiopia
-
Microbiome Health Research InstituteUniversity of Cape TownTerminatedModerate Acute Malnutrition | Severe Acute MalnutritionSouth Africa
-
University of OxfordLondon School of Hygiene and Tropical Medicine; University College, London; KEMRI-Wellcome... and other collaboratorsUnknownAntibiotic Resistance | Malnutrition Severe | Antibiotic ToxicityKenya, Uganda
Clinical Trials on NUTPSY treatment
-
PfizerCompleted
-
Chiesi Farmaceutici S.p.A.Completed
-
PfizerCompleted
-
Gilead SciencesCompletedChronic Lymphocytic LeukemiaUnited States
-
JW PharmaceuticalCompletedHealthyKorea, Republic of
-
PfizerCompleted
-
AstraZenecaParexelCompleted
-
Assistance Publique - Hôpitaux de ParisRecruitingIntra-articular Fracture of the Mandibular CondyleFrance
-
New Mexico VA Healthcare SystemCompletedPost Traumatic Stress DisorderUnited States
-
PfizerCompletedHealthy VolunteersUnited States