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Workstation Pilot Study

13. september 2022 opdateret af: Pennington Biomedical Research Center

WorkStation Pilot Study

This is a pilot study to assess the feasibility of using treadmill desks (Workstations) within a Louisiana office workplace and to determine the effects of walking while working in overweight or obese, sedentary individuals.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

Eligible participants will be randomized by chance to the WorkStation Intervention Group or to a Usual Working Condition Group.

The WorkStation Intervention Group will be asked to walk for up to 1.5 hours per day during the work week of Monday through Friday on the treadmill. Participants will complete two sessions per day for up to 45 minutes per session, tracking time and speed.

Usual Working Condition Group will be asked to continue working in usual environment and accustomed manner.

Regardless of which group the participants are assigned to, the participants will be asked to complete baseline and follow up assessment visits. Months 3 and 6 for approximately 1 hour for Body measurements (height, weight and waist circumference), body fat percent, gait speed, questionnaires, and accelerometry.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

41

Fase

  • Ikke anvendelig

Kontakter og lokationer

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

Studiesteder

  • Forenede Stater
    • Louisiana
      • Baton Rouge, Louisiana, Forenede Stater, 70808
        • Pennington Biomedical Research Center

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 og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Males or females
  • BMI ≥ 25 kg/m2
  • Willing to give informed consent
  • Willing to accept randomization to group assignment and willing to follow the protocol for the group to which they have been assigned
  • Willing to maintain fulltime employment at the company for the next 6 months
  • Willing to receive frequent contacts and communication from study staff over the next 6 months

Exclusion Criteria:

  • Current participation in other Pennington Biomedical research studies
  • BMI < 25 kg/m2
  • Type 1 diabetes
  • Average step count of ≥ 7,500 steps/day
  • Self-reporting exercising > 20 minutes on 3 or more days/wk, within the past 6 months
  • Unable to walk 45 minutes continuously without taking a rest
  • Unable to walk without the use of an assistive device, such as a cane or walker
  • Have had a cardiovascular event (stroke or heart attack) in the past 6 months
  • Have a pacemaker or any other internal electrical medical device
  • Have been diagnosed with Schizophrenia or bipolar disorder
  • Have any condition that would limit participation in a physical activity program
  • Women who are pregnant, have been pregnant in the last 6 months, or are breastfeeding
  • Actively participating in a weight loss program
  • Plan to move out of the study area within the next 6 months or plan to be away from work for more than 4 weeks in the next 6 months
  • Have another member of household participating in the study
  • Have any condition, which, in the opinion of the investigator would impede competence or compliance or possibly hinder completion of the study

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Andet
  • Tildeling: Randomiseret
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Placebo komparator: Usual Working Condition Group
Participants assigned to the usual working condition control group will continue to work in their usual environment and accustomed manner. The control group participants will have access to the Workstations at the completion of study.
Adfærdsmæssigt: Usual Working Condition
Participants will be asked to continue working at their desk in their usual manner.
Aktiv komparator: WorkStation Intervention Group
Participants will be asked to walk for up to 1.5 hours per day on the treadmill. This will be split into two 45 minute sessions per day. Behavioral support will focus on adherence to frequency (attending scheduled sessions). Participants self-select speed of walking and time (they have up to 45 minutes allotted, but may choose less as they like).
Adfærdsmæssigt: WorkStation
Participants will be asked to attend 2 scheduled sessions per day of treadmill walking, which will replace their sitting desk time. Participants will complete 2 sessions per day for 6 months.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Waist
Tidsramme: 6 months
Waist circumference will decrease in workers assigned to the WorkStation working condition relative to the usual working condition.
6 months

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Weight Assessments
Tidsramme: 6 months
Weight will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
6 months
Body Fat Percent
Tidsramme: 6 months
Body fat percent will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
6 months
Accelerometry
Tidsramme: 6 months
Participants' activity level measured by the accelerometer will increase in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
6 months
Gait Speed
Tidsramme: 6 months
Participants' gait speed will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
6 months
Stress
Tidsramme: 6 months
Participants' stress level will decrease in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
6 months
Fatigue
Tidsramme: 6 months
Participants' fatigue level will decrease in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
6 months
Quality of life Questionnaire
Tidsramme: 6 months
Participants' quality of life will improve in workers assigned to the WorkStation Group relative to the Usual Working Condition Group.
6 months

Samarbejdspartnere og efterforskere

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

Sponsor

Pennington Biomedical Research Center

Efterforskere

  • Ledende efterforsker: Catrine Tudor-Locke, PhD, Principal Investigator

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 2012

Primær færdiggørelse (Faktiske)

1. februar 2013

Studieafslutning (Faktiske)

1. februar 2013

Datoer for studieregistrering

Først indsendt

25. april 2012

Først indsendt, der opfyldte QC-kriterier

25. april 2012

Først opslået (Skøn)

27. april 2012

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

Nøgleord

Andre undersøgelses-id-numre

  • PBRC 12015

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 .

Kliniske forsøg med Usual Working Condition

Søg i lignende forsøg

Sponsorer og samarbejdspartnere

Medicinske tilstande

Narkotikainterventioner

CROs by country

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Betingelser

Sjældne sygdomme

Narkotikainterventioner

Kosttilskud

Sponsor / samarbejdspartnere

Placeringer

Abonner