The smoking cessation in pregnancy incentives trial (CPIT): study protocol for a phase III randomised controlled trial.
Adolescent
Adult
Clinical Trials, Phase III as Topic
Cost-Benefit Analysis
England
Equivalence Trials as Topic
Female
Financial Support
Follow-Up Studies
Humans
Motivation
Multicenter Studies as Topic
Northern Ireland
Pragmatic Clinical Trials as Topic
Pregnancy
Prenatal Care
/ methods
Randomized Controlled Trials as Topic
Scotland
Smoking
/ adverse effects
Smoking Cessation
/ economics
State Medicine
/ economics
Young Adult
Financial incentives
Intervention
Maternal and child health
Outcomes
Pregnancy
Prevention
Randomised controlled trial
Smoking cessation
Journal
Trials
ISSN: 1745-6215
Titre abrégé: Trials
Pays: England
ID NLM: 101263253
Informations de publication
Date de publication:
14 Feb 2020
14 Feb 2020
Historique:
received:
30
09
2019
accepted:
30
12
2019
entrez:
16
2
2020
pubmed:
16
2
2020
medline:
15
12
2020
Statut:
epublish
Résumé
Eighty per cent of UK women have at least one baby, making pregnancy an opportunity to help women stop smoking before their health is irreparably compromised. Smoking cessation during pregnancy helps protect infants from miscarriage, still birth, low birth weight, asthma, attention deficit disorder and adult cardiovascular disease. UK national guidelines highlight lack of evidence for effectiveness of financial incentives to help pregnant smokers quit. This includes a research recommendation: within a UK context, are incentives an acceptable, effective and cost-effective way to help pregnant women who smoke to quit? The Cessation in Pregnancy Incentives Trial (CPIT) III is a pragmatic, 42-month, multi-centre, parallel-group, individually randomised controlled superiority trial of the effect on smoking status of adding to usual Stop Smoking Services (SSS) support, the offer of up to £400 of financial voucher incentives, compared with usual support alone, to quit smoking during pregnancy. Participants (n = 940) are pregnant smokers (age > 16 years, < 24 weeks pregnant, English speaking), who consent via telephone to take part and are willing to be followed-up in late pregnancy and 6 months after birth. The primary outcome is cotinine/anabasine-validated abstinence from smoking in late pregnancy. Secondary outcomes include engagement with SSS, quit rates at 4 weeks from agreed quit date and 6 months after birth, and birth weight. Outcomes will be analysed by intention to treat, and regression models will be used to compare treatment effects on outcomes. A meta-analysis will include data from the feasibility study in Glasgow. An economic evaluation will assess cost-effectiveness from a UK NHS perspective. Process evaluation using a case-study approach will identify opportunities to improve recruitment and learning for future implementation. Research questions include: what is the therapeutic efficacy of incentives; are incentives cost-effective; and what are the potential facilitators and barriers to implementing incentives in different parts of the UK? This phase III trial in Scotland, England and Northern Ireland follows a successful phase II trial in Glasgow, UK. The participating sites have diverse SSS that represent most cessation services in the UK and serve demographically varied populations. If found to be acceptable and cost-effective, this trial could demonstrate that financial incentives are effective and transferable to most UK SSS for pregnant women. Current Controlled Trials, ISRCTN15236311. Registered on 9 October 2017.
Sections du résumé
BACKGROUND
BACKGROUND
Eighty per cent of UK women have at least one baby, making pregnancy an opportunity to help women stop smoking before their health is irreparably compromised. Smoking cessation during pregnancy helps protect infants from miscarriage, still birth, low birth weight, asthma, attention deficit disorder and adult cardiovascular disease. UK national guidelines highlight lack of evidence for effectiveness of financial incentives to help pregnant smokers quit. This includes a research recommendation: within a UK context, are incentives an acceptable, effective and cost-effective way to help pregnant women who smoke to quit?
METHODS
METHODS
The Cessation in Pregnancy Incentives Trial (CPIT) III is a pragmatic, 42-month, multi-centre, parallel-group, individually randomised controlled superiority trial of the effect on smoking status of adding to usual Stop Smoking Services (SSS) support, the offer of up to £400 of financial voucher incentives, compared with usual support alone, to quit smoking during pregnancy. Participants (n = 940) are pregnant smokers (age > 16 years, < 24 weeks pregnant, English speaking), who consent via telephone to take part and are willing to be followed-up in late pregnancy and 6 months after birth. The primary outcome is cotinine/anabasine-validated abstinence from smoking in late pregnancy. Secondary outcomes include engagement with SSS, quit rates at 4 weeks from agreed quit date and 6 months after birth, and birth weight. Outcomes will be analysed by intention to treat, and regression models will be used to compare treatment effects on outcomes. A meta-analysis will include data from the feasibility study in Glasgow. An economic evaluation will assess cost-effectiveness from a UK NHS perspective. Process evaluation using a case-study approach will identify opportunities to improve recruitment and learning for future implementation. Research questions include: what is the therapeutic efficacy of incentives; are incentives cost-effective; and what are the potential facilitators and barriers to implementing incentives in different parts of the UK?
DISCUSSION
CONCLUSIONS
This phase III trial in Scotland, England and Northern Ireland follows a successful phase II trial in Glasgow, UK. The participating sites have diverse SSS that represent most cessation services in the UK and serve demographically varied populations. If found to be acceptable and cost-effective, this trial could demonstrate that financial incentives are effective and transferable to most UK SSS for pregnant women.
TRIAL REGISTRATION
BACKGROUND
Current Controlled Trials, ISRCTN15236311. Registered on 9 October 2017.
Identifiants
pubmed: 32059684
doi: 10.1186/s13063-019-4042-8
pii: 10.1186/s13063-019-4042-8
pmc: PMC7023794
doi:
Types de publication
Clinical Trial Protocol
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
183Subventions
Organisme : Chief Scientist Office
ID : HIPS/16/01
Pays : United Kingdom
Organisme : CSRD VA
ID : 1
Pays : United States
Organisme : Medical Research Council
ID : MR/K025643/1
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C48006/A20863
Pays : United Kingdom
Organisme : HSC Research and Development Division
ID : COM/5352/17
Organisme : Lullaby Trust
ID : 272
Organisme : Chief Scientist Office, Scottish Government Health and Social Care Directorate
ID : HIPS/16/1
Organisme : Department of Health
ID : 10/31/02
Pays : United Kingdom
Organisme : Chest Heart and Stroke Northern Ireland
ID : 2017_09
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