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。

Improving Diet Quality of Community-Dwelling Seniors Using a Community-Based Participatory Approach

2026年10月3日 更新者:Zoe Lim、Geriatric Education and Research Institute

This study implements a community co-designed educational intervention program to improve diet quality of community-dwelling seniors.

調査の概要

状態

まだ募集していません

研究の種類

介入

入学 (推定)

50

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。

研究連絡先

研究場所

    • Singapore
      • Singapore、Singapore、シンガポール、768024
        • Geriatric Education & Research Institute, Yishun Community Hospital
        • コンタクト:

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

60年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

はい

受講資格のある性別

全て

説明

Inclusion Criteria (Senior Participants):

  • aged 60 years and above
  • have at least one social risk factor as assessed by community-based providers, based on criteria defined by Singapore's Agency for Integrated Care
  • able to understand and provide consent

Inclusion Criteria (Center Staff and Volunteers):

  • aged 21 years and above,
  • Active Ageing Centre (AAC) staff member, micro-jobber or volunteer
  • able to understand and provide consent.

Exclusion Criteria (Senior Participants):

  • living with helpers
  • require diet with modified consistencies due to swallowing impairment
  • moderate-severe dementia
  • multiple or severe food allergies
  • Stages 3, 4 or 5 Chronic kidney disease (CKD), or other medical conditions deemed unsuitable for participation
  • concurrently participating in other nutrition and food literacy programmes, and
  • unable to converse in English or Chinese

Exclusion Criteria (Center Staff and Volunteers):

  • require diet with modified consistencies due to swallowing impairment
  • moderate-severe dementia
  • multiple or severe food allergies
  • Stages 3, 4 or 5 Chronic kidney disease (CKD), or other medical conditions deemed unsuitable for participation
  • concurrently participating in other nutrition and food literacy programmes, and
  • unable to converse in English or Chinese

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:処理
  • 割り当て:なし
  • 介入モデル:単一グループの割り当て
  • 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

This is a single-arm trial and so all participants will be in the intervention arm.

The intervention is a food literacy workshop comprising 4 sessions held once every 2 weeks, up to 3 hours each. The main workshop themes are: 1) Practical ways to prepare simple and healthy meals; and 2) Basic nutrition knowledge related to the meals prepared, such as their nutrient components, links to chronic conditions and short/long-term health effects. These sessions include hands-on food preparation, tasting sessions, talks, group discussions and/or question and answer. Hands-on food preparation will focus on 'no-equipment' or 'light cooking' recipes. Food tasting involves everyday ingredients such as fruits, vegetables, proteins, nuts, seeds, spices, grains, and condiments. Group discussions will be facilitated by a study team member and will revolve around the specific themes of the workshop delivered on that day.

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
Global Diet Quality Score (GDQS)
時間枠:Baseline to end of 8 weeks.

A questionnaire that captures all foods consumed by the individual respondent during a 24-hour reference period and classifies foods into their corresponding GDQS food groups. The overall GDQS score sums up points across food groups, totaling a possible range of 0-49. Higher scores denote better diet quality.

Baseline to end of 8 weeks.

二次結果の測定

結果測定
メジャーの説明
時間枠
Knowledge and Literacy
時間枠:Baseline to end of 8 weeks.

Knowledge regarding health eating self-rated on a 5-point Likert scale. Higher scores denote better self-rated knowledge

Baseline to end of 8 weeks.
Behavior Change
時間枠:Baseline to end of 8 weeks.

Self-selected factors influencing food choice and frequency of snacking behavior.

Baseline to end of 8 weeks.
Adapted Nutrition Literacy Quiz
時間枠:Baseline to end of 8 weeks.

A quiz that assesses the participant's nutrition literacy.

Baseline to end of 8 weeks.
Adapted Food Literacy Scale
時間枠:Baseline to end of 8 weeks.

A scenario-based assessment that tests the participant's food literacy across 4 domains: Planning, Selection, Preparation, and Eating. Each correct answer will be given one score, totaling a possible range of 0-4.

Baseline to end of 8 weeks.
Brief Pittsburgh' Sleep Quality Index (B-PSQI)
時間枠:Baseline to end of 8 weeks.

Subjective sleep quality is rated from 0 (very bad) to 3 (very good). Sleep duration is rated from < 5 hours (severe sleep deprivation) to > 7 hours (standard healthy recommendations).

Baseline to end of 8 weeks.
Visual Analog Scales (VAS)
時間枠:Baseline to end of 8 weeks.

Three domains (feelings of Stomach discomfort, Energy, and Mood) self-rated on a 0-10 VAS. Higher scores denote less stomach discomfort, better energy or better mood.

Baseline to end of 8 weeks.
Body Mass Index (BMI)
時間枠:Baseline to end of 8 weeks.

Weight (kg) divided by the square of height (m), a measure of obesity and overweightness.

Baseline to end of 8 weeks.
Timed Up and Go (TUG)
時間枠:Baseline to end of 8 weeks.

Participants are timed as they rose from a chair, walked 3-metres to-and-fro, and sat back down on the chair. A measure of physical function and performance.

Baseline to end of 8 weeks.
University of California, Los Angeles (UCLA) 3-Item Loneliness Scale
時間枠:Baseline to end of 8 weeks.

A 3-item questionnaire that assesses an individual's subjective feelings of loneliness and social isolation. Higher scores denote more loneliness. A score of 6-9 out of 9 indicated loneliness

Baseline to end of 8 weeks.
Lubben Social Network Scale (LSNS-6)
時間枠:Baseline to end of 8 weeks.

A 6-item validated instrument designed to measures the size, closeness, and frequency of a person's social interactions with family and friends. Possible range of scores is from 0 to 30. A score of <12 out of 30 indicated poor social network score, or at risk of social isolation.

Baseline to end of 8 weeks.
EuroQol 5-Dimension 5-Level (EQ-5D-5L)
時間枠:Baseline to end of 8 weeks.

A health-related quality of life questionnaire based on five dimensions (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression) across five levels. An index score will be computed based on specific country's value set, where max score is 1.000 (perfect health) and min score could be a negative value (health state that is "worse than dead"). Based on the official Singapore EQ-5D-5L value set, the index scores range from 1.000 down to -0.851. Visual-analogue scale score ranges from 0 to 100, with higher scores denoting better self-rated health.

Baseline to end of 8 weeks.
Program Satisfaction
時間枠:End of 8-week intervention.

Overall satisfaction with intervention program rated on a 5-point Likert scale. Higher point denotes better satisfaction.

End of 8-week intervention.
Self-Efficacy of Health Messages Delivery
時間枠:Baseline to end of 8 weeks.

Confidence in delivering health and nutrition-related messages, rated on 5-point Likert scale.

Baseline to end of 8 weeks.
Adapted Trust in the Community Health Worker Scale
時間枠:End of 8 weeks

An adapted validated scale to measure participant's trust in the trainers. Each item is scored on a 4-point Likert scale. Scores are calculated as a mean of non-missing items, with possible range of score from 1.0 to 4.0. Higher scores denote higher trust.

End of 8 weeks

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。

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 (推定)

2026年9月1日

一次修了 (推定)

2027年3月1日

研究の完了 (推定)

2027年6月1日

試験登録日

最初に提出

2026年9月16日

QC基準を満たした最初の提出物

2026年9月16日

最初の投稿 (実際)

2026年9月24日

学習記録の更新

投稿された最後の更新 (実際)

2026年10月7日

QC基準を満たした最後の更新が送信されました

2026年10月3日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

追加の関連 MeSH 用語

その他の研究ID番号

  • 2025-0092

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?

いいえ

IPD プランの説明

Ethics approval limits data use to the original study team, thus consent does not cover data sharing.

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