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An Exercise Intervention to Improve the Eating Patterns of Preadolescent Children at High Risk for Obesity

13. september 2022 opdateret af: Nichole Kelly, University of Oregon

An Exercise Intervention to Improve the Eating Patterns of Preadolescent Children

Children in rural communities experience significant obesity-related health disparities; they are 26%-55% more likely to be obese and less likely to have health insurance and access to weight management specialists than are their urban peers. Geographic-specific disparities in obesity may be due, in part, to variations in eating behaviors. Children in rural communities describe purchasing and consuming significantly more energy-dense, low-nutrient food items relative to their urban peers. Existing behavioral strategies for improving children's EI patterns have largely been ineffective in reducing risk for excess weight gain. The primary aim of the proposed study is to test the effects of a brief, novel strategy for improving rural children's eating behaviors. Specifically, the study aims to harness the well-documented benefits of an acute bout (20 min) of moderate physical exercise on children's executive functioning, and to see if these cognitive changes lead to better self-regulation of eating. If 20 min of moderate physical exercise is associated with observed improvements in preadolescent children's eating secondary to increases in executive functioning, these data may offer explicit targets for an obesity prevention trial in rural Oregon elementary schools.

Studieoversigt

Status

Afsluttet

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

92

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • Oregon
      • Eugene, Oregon, Forenede Stater, 97401
        • University of Oregon

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

8 år til 10 år (Barn)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion criteria:

  • 8-10 years (block recruited to ensure 50% female, 50% obese)
  • Rural geographic location (≥ 10 miles from a city of ≥ 40,000)
  • Understand English

Exclusion criteria

  • BMI < 5th percentile
  • Major medical condition, current full-threshold psychiatric diagnosis, or moderate suicide risk (e.g., plan or intent)
  • Current or recent use (< 3 months) of medication known to affect body weight or energy intake
  • Recent brain injuries that would be expected to affect neuropsychological functioning
  • Mobility impairments that would impede their ability to walk on a treadmill
  • Estimated full-scale intelligence quotient score ≤ 70
  • History of pregnancy
  • Significant food allergies that would prevent them from safely consuming the study's breakfast and lunch meals
  • Responses on a food preference questionnaire that suggest that they do not like (i.e., rated them below 6 on a scale from 1 to 10) at least 50% of the food items offered in the lunch test meal

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Forebyggelse
  • Tildeling: Randomiseret
  • Interventionel model: Crossover opgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Acute moderate physical activity
Participants will walk at a moderate intensity for 20 minutes on a treadmill
For 20 minutes, participants will walk on a treadmill at a moderate intensity based on a combination of evidence-based and pre-determined parameters, including ratings of perceived exertion and heart rate
Ingen indgriben: Sedentary activity
Participants will be permitted to read books and/or draw for 20 minutes

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Energy intake
Tidsramme: up to 14 days
total kcal consumed during a laboratory test meal after each of two conditions
up to 14 days

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Executive functioning
Tidsramme: Assessed immediately after each of the two experimental conditions administered during two separate study visits approximately 14 days of each other
executive functioning performance assessed with a 3-minute task immediately after each of two conditions
Assessed immediately after each of the two experimental conditions administered during two separate study visits approximately 14 days of each other

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Nichole R Kelly, PhD, University of Oregon

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 (Faktiske)

14. juni 2017

Primær færdiggørelse (Faktiske)

4. august 2021

Studieafslutning (Faktiske)

4. august 2021

Datoer for studieregistrering

Først indsendt

27. juli 2018

Først indsendt, der opfyldte QC-kriterier

7. august 2018

Først opslået (Faktiske)

8. august 2018

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

15. september 2022

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

13. september 2022

Sidst verificeret

1. september 2022

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • 04252017.043

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

UBESLUTET

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

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Kliniske forsøg med Spiseadfærd

Kliniske forsøg med Acute moderate physical activity

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