- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02601521
Comparative Effectiveness of Two Tobacco Cessation Interventions for Employees of Partners HealthCare, Inc. (PiHQ)
22. februar 2021 opdateret af: Nancy A. Rigotti, Massachusetts General Hospital
Specific Aim: To conduct a randomized controlled trial among permanent employees of Partners HealthCare, Inc., and their adult dependents, who are current tobacco smokers.
The trial will compare two interventions designed to help smokers stop using tobacco: (1) External Coaching Program (Standard Care) and (2) Internal Coaching Program, a chronic disease management strategy for treating tobacco use and dependence.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
106
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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Massachusetts
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Boston, Massachusetts, Forenede Stater, 02114
- Massachusetts General Hospital
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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
18 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Current permanent employee of Partners Healthcare, Inc. or their adult dependent
- Current tobacco smoker (smoked a cigarette, even a puff, in the past 30 days)
Exclusion Criteria:
- Temporary, per diem or former employee of Partners Healthcare, Inc.
- Plan to leave Partners employment in the next 12 months
- Inability to give informed consent or participate in counseling due to serious psychiatric disorder or cognitive disorder
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: Internal coaching program
The internal coaching program uses a chronic disease management strategy to treat tobacco use and dependence.
The program provides evidence-based treatment consisting of up to 12 months of services from a tobacco coach based at Partners HealthCare.
The tobacco coach offers (1) repeated smoking cessation counseling delivered by proactive telephone calls, emails, and interactive voice response [automated phone calls] and (2) facilitated access to a new Partners HealthCare Inc., health insurance benefit that provides access to all FDA-approved smoking cessation medications without copay or prior approval.
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The internal coaching program will provide cognitive-behavioral counseling and medication adherence support for smokers who are ready to quit in the next 3 months It consists of:
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Aktiv komparator: External coaching program
The external coaching program consists of referral to the Massachusetts Tobacco Control Program's Smokers Helpline, a free program offering multi-session proactive telephone counseling for 3 months to individuals who are ready to quit smoking.
Individuals in this arm also receive information about Partners HealthCare, Inc.'s new health insurance benefit that provides access to all FDA-approved smoking cessation medications without copay or prior approval.
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Referral to Massachusetts Smokers Helpline (telephone quitline operated by the Massachusetts Tobacco Control Program) for proactive telephone counseling.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Tobacco abstinence for the past 30 days
Tidsramme: 6 months after enrollment
|
6 months after enrollment
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Tobacco abstinence for the past 30 days
Tidsramme: 3 months after enrollment
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3 months after enrollment
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Tobacco abstinence for the past 30 days
Tidsramme: 12 months after enrollment
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12 months after enrollment
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Quit attempt
Tidsramme: Intentional tobacco abstinence for at least 24 hours since enrollment
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Intentional tobacco abstinence for at least 24 hours since enrollment
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Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Duration of use of tobacco cessation pharmacotherapy
Tidsramme: at 3 months and at 6 months after enrollment
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Includes any FDA-approved product (nicotine patch, gum, lozenge, inhaler, nasal spray or bupropion or varenicline
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at 3 months and at 6 months after enrollment
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Smoking cessation counseling contacts
Tidsramme: at 3 months and at 6 months after enrollment
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Number of telephone calls with an internal or external tobacco coach to address smoking cessation
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at 3 months and at 6 months after enrollment
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
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)
1. november 2015
Primær færdiggørelse (Faktiske)
1. september 2019
Studieafslutning (Faktiske)
1. marts 2020
Datoer for studieregistrering
Først indsendt
9. november 2015
Først indsendt, der opfyldte QC-kriterier
9. november 2015
Først opslået (Skøn)
10. november 2015
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
24. februar 2021
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
22. februar 2021
Sidst verificeret
1. februar 2021
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2015P000002/MGH
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 .