Suaahara Impact Evaluation: End-line Survey

NCT05448287 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 2480

Last updated 2023-01-06

No results posted yet for this study

Summary

Suaahara's primary aim is to reduce the prevalence of stunting, wasting, and underweight among children under 5 years of age and to reduce the prevalence of anemia among women of reproductive age and children 6-59 months of age. For this, the program uses a multi-sectoral approach to achieve four key intermediate results: 1) improved household nutrition, sanitation, and health behaviors; 2) increased use of quality nutrition and health services by women and children; 3) improved access to diverse and nutrient-rich foods by women and children; and 4) accelerated roll-out of the Multi-Sectoral Nutrition Plan (MSNP) through strengthened local governance

Conditions

  • Nutritional Stunting
  • Feeding Behavior

Interventions

BEHAVIORAL

Health and family planning

Promotion of health and family planning behaviors

BEHAVIORAL

Nutrition

Promotion of maternal, infant, and young child feeding behaviors and nutrition

BEHAVIORAL

Agriculture and homestead food production

Promotion of knowledge and practices about homestead food production

BEHAVIORAL

Water, sanitation, and hygiene

Promotion of behaviors to improve water, sanitation, and hygiene

Sponsors & Collaborators

  • Helen Keller International

    collaborator OTHER
  • University of South Carolina

    lead OTHER

Principal Investigators

  • Edward A Frongillo, PhD · University of South Carolina

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
0 Months
Max Age
60 Months
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-06-17
Primary Completion
2022-09-30
Completion
2022-09-30

Countries

  • Nepal

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05448287 on ClinicalTrials.gov