Simplified Treatment Protocol for Acute Malnutrition in Venezuela

Sponsor
UNICEF - Venezuela (Other)
Overall Status
Recruiting
CT.gov ID
NCT05543759
Collaborator
(none)
310
1
11.9
26.1

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Ready-To-Use Therapeutic Food (RUTF)

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).

The protocol will be implemented by health professionals from each institution, duly previously trained in applying the study protocol.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
310 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Simplified Combined Protocol for the Identification and Treatment of Acute Malnutrition in Venezuela
Actual Study Start Date :
Sep 5, 2022
Anticipated Primary Completion Date :
Jun 1, 2023
Anticipated Study Completion Date :
Sep 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Cases

Children aged 6-59 months of both sexes from households established permanently in the catchment area of the selected health posts or health centers, meeting the SAM or MAM acute malnutrition case definitions described below with no medical complications and disability, and whose caregiver has granted consent to participate.

Dietary Supplement: Ready-To-Use Therapeutic Food (RUTF)
SAM [MUAC <115mm or WHZ <-3 or oedema (+/++)] = Two 92g sachets RUTF/day (Approx. 1000 kcal/day). MAM [MUAC 115mm<125mm or WHZ <-2] = One 92g sachet RUTF/day (Approx. 500 kcal/day).

Outcome Measures

Primary Outcome Measures

  1. Recovery rate [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.

  2. Weight gain [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

  3. MUAC gain [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

  4. Duration of the treatment [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

  5. Prevalence of relapse after discharge from the treatment [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

  6. Number of RUTF delivered per child [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)

  7. Cost per child [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 Outcome Measures

  1. 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]

    This indicator is defined for each child as the number of visits during which nutritional wasting is observed divided by the total number of monthly visits made.

  2. 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]

    Proportion of children with Height-for-age Z-score (LAZ)<-2 (according to the 2006 World Health Organization reference) at the end of the study

  3. 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]

    Defined by the number of days with symptoms of acute respiratory infections, fever, diarrhea (three or more loose or liquid stools per day) and malaria divided by the total number of days observed/reported in the recall period

  4. Prevalence of readmission [Up to 6 months, at 24 weeks after the admission]

    Prevalence of children readmitted to the treatment within six months after after the admission

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Months to 59 Months
Sexes Eligible for Study:
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Distrito Capital, La Guaira, Miranda Caracas Distrito Capital Venezuela 1060

Sponsors and Collaborators

  • UNICEF - Venezuela

Investigators

  • Principal Investigator: Zulay Gonzalez, MSc, UNICEF - Venezuela

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
UNICEF - Venezuela
ClinicalTrials.gov Identifier:
NCT05543759
Other Study ID Numbers:
  • 291021
First Posted:
Sep 16, 2022
Last Update Posted:
Sep 16, 2022
Last Verified:
Sep 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by UNICEF - Venezuela
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 16, 2022