- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT04340102
Development of a Scalable Intervention to Improve Smoking Cessation in Persons With Serious Mental Illness
4 november 2020 uppdaterad av: Melanie Bennett, University of Maryland, Baltimore
All patients with serious mental illness are abstinent while in the hospital for a psychiatric admission yet almost all return to smoking after discharge.
The investigators propose to adapt a digital intervention both to the needs of SMI smokers and to being introduced in the inpatient psychiatric setting through a collaboration between experts in SMI and the Truth Initiative, a pre-eminent tobacco control organization.
The investigators believe this will bridge the inpatient to outpatient gap in cessation services and will help people remain abstinent following hospital discharge.
Studieöversikt
Detaljerad beskrivning
Persons with serious mental illness (SMI, schizophrenia, bipolar disorder, recurrent depression) are a socioeconomically disadvantaged group and die on average 10-15 years earlier than those in the general population, many from cancer.
The prevalence of smoking in persons with SMI is approximately 3 times that in the general population; smoking is the is the strongest risk factor for elevated mortality in this population.
Psychiatric inpatient admissions are common in SMI and the hospital is an optimal place to provide smoking cessation services.
All patients are abstinent while in the hospital.
The key challenge is how to continue to engage these patients in cessation services to support continued abstinence.
While most receive refer to telephone quitline at discharge, quitlines are not as effective with SMI smokers and almost all return to smoking.
Introducing hospitalized SMI patients to cessation services that can be easily accessed when they leave the hospital offers the best chance of converting initial abstinence into sustained abstinence post-discharge.
A digital intervention that incorporates web-delivered evidence-based smoking cessation practices, digital coaching, and mobile text messaging is a scalable and sustainable way to bridge the inpatient to outpatient gap in cessation services.
Currently there is no digital cessation program that addresses the needs of SMI smokers.
The investigators propose to adapt a digital intervention both to the needs of SMI smokers and to being introduced in the inpatient psychiatric setting through a collaboration between experts in SMI and the Truth Initiative, a pre-eminent tobacco control organization.
The investigators will build upon a well-established, evidence-based, cessation website, BecomeAnEX.org (EX), that offers individualized quit plans, an active social community, text and email messaging support, and digital coaching.
Integrating input from different stakeholders, the investigators will develop adaptations so that EX components and language are in line with principles of mental health recovery and will successfully engage SMI smokers with digital coaching that will support use of other EX services.
The investigators will develop automated and integrated procedures for identifying hospitalized SMI smokers and registering them with EX.
The investigators will then examine the feasibility and acceptability of the adapted intervention to engage and retain 60 smokers with SMI after hospital discharge.
Studietyp
Interventionell
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
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Maryland
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Baltimore, Maryland, Förenta staterna, 21201
- University of Maryland School of Medicine
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Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år och äldre (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- Age 18 or greater
- Diagnosis of serious mental illness (schizophrenia, schizoaffective disorder, bipolar disorder, or major depression)
- Current smoker [prior to admission, smoked at least one cigarette or small cigar per day in the past month (unless restricted, e.g. due to ER/hospital visit) and smoked at least 100 cigarettes lifetime]
- Interested in remaining quit after hospital discharge or quitting within the following 30 days
- Expected Internet use at least several times a week post-discharge and ownership of mobile device with text messaging plan post-discharge
- Sufficiently stable and cooperative to engage in the intervention, operationalized as not on a nursing observation level that indicates high acuity/safety concerns and has participated in a majority of hospital unit activities as documented in the chart during the hospital stay so far
Exclusion Criteria:
- Intellectual disability (DSM5 317, 318), traumatic brain injury, or deafness.
- Homeless prior to admission or anticipated to be homeless at discharge.
- Discharge to a residential setting where smoking is prohibited.
- Medical condition for which the use of nicotine replacement therapy (NRT) is contraindicated including pregnant, planning to become pregnant, or breastfeeding; within 4 weeks post myocardial infarction; severe arrhythmia, severe angina pectoris; peptic ulcer; severe renal failure; poorly controlled insulin-dependent diabetes; severely uncontrolled hypertension; peripheral vascular disease.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
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Experimentell: BecomeAnEx
Participants will have three individual meetings with a research staff person while they are in the hospital.
At these meetings participants will answer questions about their smoking and interest in quitting, learn about BecomeAnEx, and register with the BecomeAnEx program so that they can use it when you leave the hospital.
Participants will be given two weeks of nicotine replacement therapy when they leave the hospital.
Participants will be asked to use BecomeAnEx as much as they want when they leave the hospital program.
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This research study is focused on a smoking cessation program called BecomeAnEx.
We are studying how to adapt BecomeAnEx for people with a mental health disorder who want to reduce or quit their tobacco smoking.
BecomeAnEx includes a website that provides education about smoking and quitting.
It also has a text messaging program that delivers personalized information.
Persons in the program have access to real-time digital coaching with a remote coach who has experience helping people quit smoking.
In addition, the program has an on-line community of current and former smokers that can provide support and encouragement.
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
---|---|---|
Feasibility of recruitment
Tidsram: 2 months
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Rate of recruitment
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2 months
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Feasibility of registration
Tidsram: 2 months
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Time to register with the web based intervention
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2 months
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Acceptability
Tidsram: 2 months
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Satisfaction with the web based intervention using the Client Satisfaction Questionnaire
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2 months
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Acceptability
Tidsram: 2 months
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Satisfaction with the web based intervention using the Services Satisfaction Questionnaire
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2 months
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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Förväntat)
1 juli 2020
Primärt slutförande (Förväntat)
1 juni 2022
Avslutad studie (Förväntat)
1 juni 2022
Studieregistreringsdatum
Först inskickad
1 april 2020
Först inskickad som uppfyllde QC-kriterierna
6 april 2020
Första postat (Faktisk)
9 april 2020
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
6 november 2020
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
4 november 2020
Senast verifierad
1 november 2020
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 1R21CA237468-01A1
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
NEJ
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
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Nej
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