- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07838142
Improving Diet Quality of Community-Dwelling Seniors Using a Community-Based Participatory Approach
This study implements a community co-designed educational intervention program to improve diet quality of community-dwelling seniors.
Studienübersicht
Status
Intervention / Behandlung
Studientyp
Einschreibung (Geschätzt)
Phase
- Unzutreffend
Kontakte und Standorte
Studienkontakt
- Name: Zoe Lim, PhD
- Telefonnummer: +6583586255
- E-Mail: zoe.lim@geri.com.sg
Studienorte
-
-
Singapore
-
Singapore, Singapore, Singapur, 768024
- Geriatric Education & Research Institute, Yishun Community Hospital
-
Kontakt:
- Zoe Lim, PhD
- Telefonnummer: +6583586255
- E-Mail: zoe.lim@geri.com.sg
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
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
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: 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. |
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Global Diet Quality Score (GDQS)
Zeitfenster: 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.
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Knowledge and Literacy
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
|
Mitarbeiter und Ermittler
Mitarbeiter
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 2025-0092
Plan für individuelle Teilnehmerdaten (IPD)
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Beschreibung des IPD-Plans
Ethics approval limits data use to the original study team, thus consent does not cover data sharing.
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