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Diet, Physical Activity, and Sleep Habits (DPAS)

16. august 2021 opdateret af: Hollie Raynor, The University of Tennessee, Knoxville
This study aims to observe if consistency in a young adult's schedule is related to health factors and outcomes, such as diet quality, amount of physical activity and sleep, and weight.

Studieoversigt

Status

Afsluttet

Betingelser

Detaljeret beskrivelse

During young adulthood, patterns regarding physical activity,1,2 dietary intake,3 and weight status4 are established that track into later life and can impact health. Social and physical cues also impact patterns-particularly those cues that may influence biological and behavioral rhythms which can influence the Circadian Timing System (CTS).5 Chronotype, the timing of sleep patterns, is closely tied to the CTS as it reflects sleep in relation to the light and dark cycle, with morning-type (MT) having a pattern that should assist with better entrainment (sleep better entrained to the physical cues of light/dark).6 Research has found that chronotype is related to several areas important to health, including diet,6-11 physical activity,12-14 weight regulation.15-18. As a whole, research in this area suggests that MT individuals are more likely to consume a healthier eating pattern, be more physically active, and more successfully manage their weight. However, the research in this area for young adults is limited.

While there has been research regarding chronotype and diet, activity, and weight management, there is a paucity of research on the relationship between social cues and social rhythms, which also influence the CTS, and health related outcomes. Social rhythms, as measured by the Social Rhythm Metric (SRM), are related to chronotype, such that MT is related to a higher SRM.19-21 Due to the relationship between SRM and chronotype, and chronotype and diet, physical activity, and weight management, it would be anticipated that SRM is also related to these health outcomes. Specifically, it would be anticipated that more consistent social rhythms (higher SRM) would be related to a healthier eating pattern, greater physical activity, and weight management. However, this relationship has never been investigated.

Therefore, to better understand how social rhythms, which are triggered by social cues, are related to health, this investigation will be assessing both chronotype and SRM and collecting measures on diet quality, via food records, physical activity and sleep, via accelerometers, and anthropometrics, via BMI. The population of interest for this study is specifically young adults because young adulthood is a time period when health patterns are established for the rest of life. This study aims to observe if consistency in a young adult's schedule is related to health factors and outcomes, such as diet quality, amount of physical activity and sleep, and weight.

Undersøgelsestype

Observationel

Tilmelding (Faktiske)

63

Kontakter og lokationer

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

Studiesteder

    • Tennessee
      • Knoxville, Tennessee, Forenede Stater, 37996
        • Healthy Eating and Activity Lab, University of Tennessee

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

18 år til 35 år (Voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

Young adult between the ages of 18 and 35 years, taking classes and/or working, able to engage in physical activity, and having no dietary restrictions.

Beskrivelse

Inclusion Criteria:

  • Between the ages of 18-35 years
  • Able to pass the Physical Activity Readiness Questionnaire for Everyone (PAR-Q+) indicating that they have no health conditions that limit their ability to engage in physical activity
  • Access to an email address and internet each day during their participation
  • An town when all measures are collected
  • Taking classes and/or working a job when all measures are collected

Exclusion Criteria:

  • Pregnant
  • Allergy to stainless steel, making the participant unable to wear Body Media Armband
  • Dietary restrictions of any kind
  • Shift work, here defined as having to work a shift for any period of time between the hours of 12 am and 6 am

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Diet Quality 1
Tidsramme: Through study completion, 1 week
Healthy Eating Index Score calculated using a three-day food record
Through study completion, 1 week
Diet Quality 2
Tidsramme: Through study completion, 1 week
Total energy intake will be assessed using a three-day food record
Through study completion, 1 week
Physical Activity 1
Tidsramme: Through study completion, 1 week
Minutes of moderate to vigorous physical activity will be assessed using SenseWear Armbands
Through study completion, 1 week
Physical Activity 2
Tidsramme: Through study completion, 1 week
Energy expenditure from moderate to vigorous physical activity will be assessed using SenseWear Armbands
Through study completion, 1 week
Sleep 1
Tidsramme: Through study completion, 1 week
Length of sleep will be assessed using SenseWear Armbands
Through study completion, 1 week
Sleep 2
Tidsramme: Through study completion, 1 week
Sleep efficiency will be assessed using SenseWear Armbands
Through study completion, 1 week

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Body Mass Index (BMI)
Tidsramme: Baseline appointment
BMI will be calculated using height and weight measurements
Baseline appointment
Body Composition
Tidsramme: Baseline appointment
Body fat percentage will be assessed using the Body Composition Analyzer TBF-300 (TANITA Corporation, Tokyo, Japan)
Baseline appointment
Chronotype
Tidsramme: Baseline appointment
Chronotype will be assessed using the Composite Score for Morningness
Baseline appointment

Samarbejdspartnere og efterforskere

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

Efterforskere

  • Ledende efterforsker: Hollie Raynor, PhD, 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.

Generelle publikationer

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)

13. juli 2019

Primær færdiggørelse (Faktiske)

16. august 2021

Studieafslutning (Faktiske)

16. august 2021

Datoer for studieregistrering

Først indsendt

13. juli 2019

Først indsendt, der opfyldte QC-kriterier

24. juli 2019

Først opslået (Faktiske)

29. juli 2019

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

18. august 2021

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

16. august 2021

Sidst verificeret

1. august 2021

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • UTK IRB-19-05178-XP

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Ingen

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Ingen

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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