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Clinical Trials/NCT05543759
NCT05543759TerminatedNot Applicable

Simplified Combined Protocol for the Identification and Treatment of Acute Malnutrition in Venezuela

UNICEF - Venezuela1 site in 1 country307 target enrollmentStarted: September 5, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Sponsor
Enrollment
307
Locations
1
Primary Endpoint
Recovery rate

Study Overview

Brief Summary

Global acute malnutrition (GAM) in children under five is defined by being too thin for a given height and/or having the Mid-upper arm circumference less than a given threshold. GAM includes moderate acute malnutrition (MAM) and severe acute malnutrition (SAM). This study has been designed to generate new evidence about the simplified combined protocol for the identification and treatment of GAM in Venezuela. The objective of the study is to document the safety and effectiveness of the Venezuelan simplified treatment protocol for GAM, which includes reduced frequency of follow-up visits, single product use and optimized daily RUTF dose. This prospective longitudinal study was conducted in 19 centers treating GAM in children aged 6-59 months diagnosed with uncomplicated GAM, defined as WHZ <-2 or MUAC <125mm or ++ bilateral edema. Children will be prospectively followed for a total of 6 months, including the treatment phase and the immediate post-discharge weeks until 6 months. The effectiveness of the treatment will be measured by the recovery rate, duration of the treatment and changes in anthropometry (weight, height and arm circumference). Other treatment effects will also be measured, including how many are admitted to the hospital, death and relapse rates from the nutritional program. An economic evaluation component will be incorporated. Total costs will be aggregated and presented as costs per child treated and per child recovered.

Detailed Description

The general objective of the study is to document the safety and effectiveness of Venezuelan simplified treatment protocol for Acute malnutrition of reduced frequency of follow-up visits, single product use and optimized daily RUTF dose.

This will be a prospective longitudinal study assessing the Venezuelan Simplified Combined Protocol among children with uncomplicated acute malnutrition according to the definition case study recently adopted by the Implementation Guidance: Prevention, Early Detection and Treatment of Wasting in Children 0-59 Months through National Health Systems in the Context of Coronavirus Disease, United Nations Children's Fund and World/Health Organization, for a single arm cohort included in treatment.

Children will be prospectively followed for a total of 6 months including the treatment phase and the immediate post-discharge weeks until 6 months.

An economic evaluation component will be incorporated. The economic valuation will be carried out based on quantitative data. Cost data will be collected from accounting records where available and through a series of interviews with key informants including health workers, civil society organizations, relevant staff from non-governmental organizations and United Nations agencies. Total costs will be aggregated and presented as cost per child treated and cost per child per child recovered.

The study will be implemented in 19 Community Health Centers purposively chosen based on their acute malnutrition prevalence and operational constraints. All of them will be proportionally distributed in three central states of Venezuela (Distrito Capital, Miranda, and La Guaira).

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
6 Months to 59 Months (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • The child is between 6 and 23 months of age at inclusion.
  • The mother must live in the study area from the time of inclusion.
  • Mid-upper arm circumference (MUAC) <12.5 cm or WHZ <-2 or bilateral pitting edema.
  • No serious medical complications.
  • Positive appetite test.
  • The consent of the mother or caregiver.

Exclusion Criteria

  • Congenital malformations that make anthropometric measurements impossible.
  • Mother intends to leave the study area before six months.
  • Presence of medical condition requiring referral for hospitalization.

Outcomes

Primary Outcomes

Recovery rate

Time Frame: Up to 4 months, from date of inclusion in the program until the date of recovery or 16th week after inclusion in the program or date of death from any cause, whichever came first

This indicator is defined as the number children who recovered from wasting, MAM and SAM according to national program criteria (WHZ\>-2 and MUAC\>=125mm and absence of bilateral edema for two consecutive visits, within 16 weeks of enrollment in the program) divided by the total number of treatment results recorded.

MUAC gain

Time Frame: Up to 4 months, from date of inclusion in the program until the date of recovery or 16th week after inclusion in the program or date of death from any cause, whichever came first

Average change in MUAC per month

Weight gain

Time Frame: Up to 4 months, from date of inclusion in the program until the date of recovery or 16th week after inclusion in the program or date of death from any cause, whichever came first

Average weight change per month

Duration of the treatment

Time Frame: Up to 4 months, from date of inclusion in the program until the date of recovery or 16th week after inclusion in the program or date of death from any cause, whichever came first

Defined as the average number of weeks spent on treatment (enrollment and discharge) in children 6-59 months of age at enrollment, according to health registers

Prevalence of relapse after discharge from the treatment

Time Frame: at six months after the admission

This indicator is defined as the proportion of children with WHZ-score \<-2 or MUAC \<125 mm or bilateral edema six months after the admission

Number of RUTF delivered per child

Time Frame: Up to 4 months, from date of inclusion in the program until the date of recovery or 16th week after inclusion in the program or date of death from any cause, whichever came first

Average number of RUTF delivered per child (SAM/MAM)

Cost per child

Time Frame: Up to 4 months, from date of inclusion in the program until the date of recovery or 16th week after inclusion in the program or date of death from any cause, whichever came first

Average number of dollars that cost to recovery a child

Secondary Outcomes

  • Prevalence of readmission(Up to 6 months, at 24 weeks after the admission)
  • Prevalence of child morbidity(Up to 6 months, from date of enrolment until the date of last documented progression or date of death from any cause, whichever came first)
  • Prevalence of child stunting(Up to 6 months, from date of enrolment until the date of last documented progression or date of death from any cause, whichever came first)
  • Longitudinal prevalence of wasting(Up to 6 months, from date of enrolment until the date of last documented progression or date of death from any cause, whichever came first)

Investigators

Sponsor
UNICEF - Venezuela
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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