- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00998452
Dissemination of a Weight Management Program Among US Veterans
21. april 2017 opdateret af: University of North Carolina, Chapel Hill
This study is being conducted with the Veterans Affairs National Center for Health Promotion and Disease Prevention (VANCP), which is overseeing the current dissemination of MOVE! (Managing Overweight/Obesity for Veterans Everywhere), a national weight management program for veterans.
It will be based at 10 local sites in the national network of VA medical settings and community-based outpatient clinics and will compare two different models for disseminating and implementing MOVE! using a randomized experimental design.
One study arm will implement the MOVE* VETS! (Volunteer Education and Tailored Self-management and support) model that includes tailored newsletters and peer counseling MI calls and activities, and the other will receive the standard MOVE!
program.
Studieoversigt
Detaljeret beskrivelse
The purpose of this research is to study the dissemination and implementation of MOVE!.
MOVE! is a national weight management program for veterans that has moved form pilot to full dissemination.
Overweight and obesity are rapidly rising in the United States and interventions to combat this epidemic are desperately needed.
Within the VA population, approximately 70% of veterans are overweight and or obese.
Participants will be male and female Veterans, aged 21 and over receiving health services at one of the 10 study sites, who qualify for the MOVE! program.
We are recruiting a minimum of 800 -1000 Veterans to complete a baseline survey at the 10 VA sites participating in the study.
Participants at the 10 VA sites are recruited during a primary care visit by primary care provider, they will not be chosen based on the presence or absence of any disease, thus health status will vary.
The primary outcome measures will be participation after enrollment into MOVE! and participant weight loss.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
732
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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California
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West Los Angeles, California, Forenede Stater, 90073
- West LA VAMC
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Connecticut
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West Haven, Connecticut, Forenede Stater, 06516
- West Haven VAMC
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Illinois
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Chicago, Illinois, Forenede Stater, 60612
- Jesse Brown VAMC
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Hines, Illinois, Forenede Stater, 60141
- Edward Hines Jr. VAMC
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Massachusetts
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Boston, Massachusetts, Forenede Stater, 02130
- Boston Vamc
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Minnesota
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Minneapolis, Minnesota, Forenede Stater, 55417
- Minneapolis VAMC
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Nebraska
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Omaha, Nebraska, Forenede Stater, 68105
- Omaha VAMC
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North Carolina
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Chapel Hill, North Carolina, Forenede Stater, 27599-7294
- Lineberger Comprehensive Cancer Center at UNC-CH
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Texas
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San Antonio, Texas, Forenede Stater, 78229
- Audie L. Murphy VAMC
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Utah
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Salt Lake City, Utah, Forenede Stater, 84148
- George E. Wahlen VAMC
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Washington
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Seattle, Washington, Forenede Stater, 98108
- VA Puget Sound HCS
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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
21 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Receiving primary care at the one of the 10 selected VA centers
- BMI 25 or over
- 21 years old, no upper age limit
- Pregnant women may participate in the study with the approval of the VA medical staff
Exclusion Criteria:
- Not a patient at one of the 10 VA sites
- BMI less than 25
- Under 21 years of age
- Pregnant without medical approval to participate
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: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Ingen indgriben: MOVE!
Participants will receive the usual VA MOVE! Program.
These elements include a baseline assessment, brief clinic counseling session about weight, printed targeted health information on weight management and behaviors, and opportunities to participate in group sessions at the VA site and telephone follow-up from MOVE! clinic staff.
|
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Aktiv komparator: MOVE*VETS
Participants will receive the same MOVE!
program as the control group plus 4 tailored newsletters on the study health behavior topics created from the baseline survey.
Also 2-4 counseling calls from volunteer veteran peer counselors.
|
Receiving 4 tailored newsletters on the study health behavior topics created from the baseline survey.
Also 2-4 counseling calls from peer counselors.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
Primary study outcome measures at the participant level will be program participation and effectiveness in achieving weight loss.
Tidsramme: At enrollment and 6 months post-enrollment
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At enrollment and 6 months post-enrollment
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Sekundære resultatmål
Resultatmål |
Tidsramme |
---|---|
Secondary outcome measures include improved self-management behaviors (diet and physical activity),psychosocial factors, awareness and utilization of program components/activities, and perceptions of the program/organization.
Tidsramme: enrollment to 6 months post-enrollment
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enrollment to 6 months post-enrollment
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: Bryan Weiner, PhD, UNC Chapel Hill
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. december 2009
Primær færdiggørelse (Faktiske)
1. august 2012
Studieafslutning (Faktiske)
1. august 2012
Datoer for studieregistrering
Først indsendt
19. oktober 2009
Først indsendt, der opfyldte QC-kriterier
19. oktober 2009
Først opslået (Skøn)
20. oktober 2009
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
25. april 2017
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
21. april 2017
Sidst verificeret
1. februar 2013
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 06-0350
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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