- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01414699
The Influence of Dietary Variety and Course Sequence on Fruit Intake in Preschool-Aged Children
3. april 2018 opdateret af: Hollie Raynor, The University of Tennessee, Knoxville
The purpose of this study is to determine the extent to which manipulation of dietary variety and course sequence affects fruit intake and overall energy intake in preschool-aged children.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
In the past two decades overweight and obesity rates in children (ages 2-19) have risen from 5% to 17%, with toddlers (ages 2-5) at 10%.
Among children and adolescents the consumption of low-energy-dense foods, such as fruit and vegetables (F&Vs), remain below current recommendations.
Therefore, strategies to increase low-energy-dense F&V intake and decrease high-energy-dense food intake aimed at young children are essential.
Antecedents, or cues, can trigger eating.
Therefore, manipulating food presentation can be utilized to produce certain behaviors.
Dietary variety and course sequence are two examples of this relationship.
It has been well established that high dietary variety leads to greater consumption patterns compared to low DV diets in adults.
High DV has only been tested with problematic foods, and not with the goal of increasing F&V intake.
Additionally, serving a first course meal can act as a preload to decrease intake of the second course entrée.
Dietary variety and course sequence manipulations have been experimentally tested with caloric intake goals but never with the goal of increasing F&V intake.
Therefore, the purpose of this study is to determine the extent to which manipulation of dietary variety and course sequence affects fruit intake and overall energy intake in preschool-aged children.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
16
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Tennessee
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Knoxville, Tennessee, Forenede Stater, 37916
- Healthy Eating and Activity Laboratory
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
3 år til 6 år (Barn)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- All children that are ≥3 years of age enrolled in the ELC preschool with parental consent can participate.
- Eligible children must also like applesauce, peaches and cheese cubes, and be able to consume foods with a spoon.
Exclusion Criteria:
- Children allergic to applesauce, peaches, or chocolate pudding or who are lactose-intolerant will not be included in the study.
- Did not attend all feeding sessions.
- Did not consume more than 5 grams from any of the foods on an occasion.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Grundvidenskab
- Tildeling: Randomiseret
- Interventionel model: Crossover opgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Aktiv komparator: One-Course, Variety
Participants will receive a snack in one course with a variety of fruit.
|
These conditions will have snack served with an increase of fruit variety.
|
Aktiv komparator: Two-Course, Variety
Participants will receive a snack in two courses with a variety of fruit.
|
These conditions will have snack served with an increase of fruit variety.
|
Aktiv komparator: One-course, Non-Variety
Participants will receive a snack in one course with no variety of fruit.
|
These conditions will receive a snack without a variety of fruit.
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Aktiv komparator: Two-Course, Non-Variety
Participants will receive a snack in two courses with no variety of fruit.
|
These conditions will receive a snack without a variety of fruit.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Total grams of snack consumed.
Tidsramme: 4 weeks
|
Total grams of snack consumed by participants over the 4-week study (with 1 snack per week) period will be determined by subtracting pre- and post-consumption weight of the snack provided.
|
4 weeks
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: Hollie A Raynor, PhD, University of Tennessee, Knoxville
- Ledende efterforsker: Chelsi C Cardoso, BS, University of Tennessee, Knoxville
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. august 2011
Primær færdiggørelse (Faktiske)
1. december 2011
Studieafslutning (Faktiske)
1. december 2015
Datoer for studieregistrering
Først indsendt
10. august 2011
Først indsendt, der opfyldte QC-kriterier
10. august 2011
Først opslået (Skøn)
11. august 2011
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
5. april 2018
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
3. april 2018
Sidst verificeret
1. april 2018
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- 8585B
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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-
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-
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