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

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.

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

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.

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