このページは自動翻訳されたものであり、翻訳の正確性は保証されていません。を参照してください。 英語版 ソーステキスト用。

Nutrition Intervention Among Ethnic Minority Children Aged 5-16 Years in Tra Vinh Province, Vietnam

2026年5月8日 更新者:Bui Thi Hoang Lan、University of Medicine and Pharmacy at Ho Chi Minh City

Nutritional Status, Associated Factors, and Preliminary Effectiveness of a Nutrition Health Education Intervention Among Ethnic Minority Children Aged 5-16 Years in Tra Vinh Province, Vietnam

The goal of this study is to evaluate the effectiveness of a nutrition health education intervention among ethnic minority children aged 5-16 years in Tra Vinh Province, Vietnam. It will also assess factors associated with nutritional status in this population.

The main questions it aims to answer are:

Does the nutrition health education intervention improve nutritional status? Does the intervention improve nutrition-related knowledge, attitudes, and practices (KAP)? Does the intervention improve diet quality and physical activity levels among participants?

Researchers will compare participants receiving the nutrition education intervention with control group to evaluate the effectiveness of the intervention.

Participants in intervention group will:

Participate in a structured nutrition education program delivered monthly for 4 months through interactive lessons, videos, and educational materials Receive ongoing support and reinforcement activities for an additional 2 months Attend baseline and follow-up assessments including anthropometric measurements and interviews Complete questionnaires on nutrition knowledge, dietary practices, and physical activity

調査の概要

研究の種類

介入

入学 (実際)

811

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Tra Vinh
      • Thanh pho Tra Vinh、Tra Vinh、ベトナム
        • Community Health Centers in Tra Vinh Province

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 子

健康ボランティアの受け入れ

はい

説明

Inclusion Criteria:

  • Ethnic minority children aged 5-16 years
  • Living in selected communities or attending selected schools
  • Consent from parents/caregivers and assent from children

Exclusion Criteria:

  • Congenital deformities affecting anthropometry
  • Medical conditions affecting body composition measurement
  • Inability to participate in interviews

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:防止
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:intervention group
Participants receive a structured nutrition health education intervention delivered through community-based and school-based models. The program includes four monthly educational sessions using presentations and videos, supported by interactive posters, nutrition leaflets, and dietary and physical activity diaries. The intervention is implemented over four months, followed by a two-month maintenance phase with reinforcement activities involving community health workers, school staff, and family engagement.
A multi-component nutrition health education program delivered through community-based and school-based models. For children aged 5-10 years, both children and their caregivers participate in nutrition education sessions at local health stations. For children aged 11-16 years, the intervention is delivered at ethnic minority boarding schools. The program consists of four monthly structured sessions using presentations and videos, supported by interactive posters, nutrition leaflets, and dietary and physical activity diaries. The key topics include: (1) nutrients and health, (2) prevention of undernutrition and overweight/obesity, (3) healthy dietary habits, and (4) physical activity promotion. The intervention lasts four months, followed by a two-month maintenance phase with reinforcement by community health workers, school staff, and family engagement.
介入なし:control group
Participants do not receive the structured nutrition education intervention. They continue to receive routine health and nutrition education activities available at local community health centers and schools without additional intervention from the study.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change in BMI-for-age z-score
時間枠:Baseline and 6 months
Weight and height will be combined to report BMI in kilogram/meters^2. BMI-for-age z-score calculated according to the 2007 WHO growth standards.
Baseline and 6 months
Change in prevalence of malnutrition (including undernutrition and overweight/obesity)
時間枠:Baseline and 6 months
Proportion of participants with abnormal nutritional status, including undernutrition (stunting, underweight, or thinness) and overweight/obesity, classified according to WHO growth reference standards based on age- and sex-specific z-scores.
Baseline and 6 months

二次結果の測定

結果測定
メジャーの説明
時間枠
Change in nutrition-related knowledge, attitudes, and practices (KAP)
時間枠:Baseline and 6 months

Nutrition knowledge, attitudes, and practices assessed using a structured questionnaire developed based on the Food and Agriculture Organization of the United Nations Guidelines for assessing nutrition-related knowledge, attitudes and practices.

Knowledge scores ranged from 0 to 11, attitude scores from 0 to 17, and practice scores from 0 to 8, with higher scores indicating better nutrition knowledge, more favorable nutrition attitudes, and better nutrition practices.

Baseline and 6 months
Change in diet quality scores
時間枠:Baseline and 6 months

Diet quality was assessed using the Diet Quality Questionnaire (DQQ), including the Dietary Diversity Score (DDS) and the Global Dietary Recommendations (GDR) score.

The Dietary Diversity Score (DDS) ranges from 0 to 10 based on the number of food groups consumed, with higher scores indicating greater dietary diversity.

The Global Dietary Recommendations (GDR) score ranges from 0 to 18 and reflects adherence to global dietary recommendations for protection against non-communicable diseases, with higher scores indicating better adherence to recommended dietary patterns.

Baseline and 6 months
Change in physical activity levels
時間枠:Baseline and 6 months
Physical activity levels assessed using a standardized questionnaire, including frequency and duration of moderate-to-vigorous physical activity.
Baseline and 6 months
Change in skeletal muscle mass
時間枠:Baseline and 6 months
Skeletal muscle mass (SMM), measured in kilograms using bioelectrical impedance analysis with an InBody analyzer.
Baseline and 6 months
Change in body fat mass
時間枠:Baseline and 6 months
Body fat mass (BFM), measured in kilograms using bioelectrical impedance analysis with an InBody analyzer.
Baseline and 6 months
Change in fat-free mass
時間枠:Baseline and 6 months
Fat-free mass (FFM), measured in kilograms using bioelectrical impedance analysis with an InBody analyzer.
Baseline and 6 months

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

捜査官

  • 主任研究者:Truc T Thanh, PhD、University of Medicine and Pharmacy at Ho Chi Minh City

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2024年11月6日

一次修了 (実際)

2025年4月27日

研究の完了 (実際)

2025年4月27日

試験登録日

最初に提出

2026年5月1日

QC基準を満たした最初の提出物

2026年5月8日

最初の投稿 (実際)

2026年5月13日

学習記録の更新

投稿された最後の更新 (実際)

2026年5月13日

QC基準を満たした最後の更新が送信されました

2026年5月8日

最終確認日

2026年5月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

The data presented in this study are available on request from the corresponding author.

IPD 共有時間枠

De-identified individual participant data and supporting documents will be available beginning 6 months after publication and ending 5 years after publication.

IPD 共有アクセス基準

De-identified individual participant data and supporting documents will be available upon reasonable request to the corresponding author for academic research purposes.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • SAP
  • ANALYTIC_CODE

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

購読する