Pregnancy Related, Smoking Cessation
Conditions
Brief summary
The aim of this study is to investigate the feasibility and likelihood of success of a narrative and image-based intervention, administered via text messages, for smoking cessation in pregnant women, prior to undertaking a large scale trial of its effectiveness. A feasibility and pilot trial will be undertaking involving 70 pregnant women who smoke in two NHS Boards.
Detailed description
Smoking during pregnancy carries serious risks to mother and infant health. More babies whose mothers smoke are stillborn or die within the first year of life. Smoking during pregnancy results in increased rates of intrauterine growth retardation, preterm birth, and babies' longer-term risk of developing heart disease and diabetes. Pregnant women who smoke are more likely to experience miscarriage, placental abruption, pregnancy-induced hypertension and later conditions such as lung cancer and heart disease. Reduction in smoking in pregnancy has been a long standing health policy target however there is limited evidence of effectiveness of many smoking cessation interventions and their uptake is generally low. We have developed, and carried out initial testing of an intervention to support smoking cessation in pregnant women using narrative, story-telling delivered via automated text-messages. The intervention aims to alter women's perceptions of risk, social norms, outcomes and self-efficacy using three key elements. 1. a narrative story of a fictional young pregnant woman 'Megan' trying to stop smoking by overcoming a series of commonplace barriers. 2) images showing the size of their fetus and its stage of development 3) an interactive 'help' function to receive a supportive, tailored response. Behaviour change techniques for smoking cessation in pregnancy are embedded in the intervention. A randomised controlled trial is required to test the effectiveness of the intervention in reducing smoking in pregnancy. The aim of this study is to investigate the feasibility and likelihood of success of the narrative and image-based intervention for smoking cessation in pregnant women. If successful the intervention will be tested in a full-scale (Phase III) multi centre randomised controlled trial. Objectives: 1. To assess acceptability and willingness to be randomised to the narrative and image based intervention or usual care. 2. To assess and compare the feasibility of recruitment strategies, the level of participants' retention in the study and engagement with the intervention. 3. To assess the acceptability and likely impact of the intervention among pregnant smokers. 4. To estimate the required sample size for a full trial.
Interventions
BEHAVIORALSKIP-IT
A theory-based intervention using narrative, images and embedded behaviour change techniques, delivered via text-messaging.
Sponsors
Glasgow Caledonian University
University of Dundee
University of Southampton
Edinburgh Napier University
University of Stirling
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Intervention model description
Behaviour change
Eligibility
Sex/Gender
FEMALE
Age
16 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Women 16 years of age or over, 2. Live within the catchment areas of study sites, 3. Up to and including 14 weeks of pregnancy, 4. Current smoker, 5. Own or regularly use a mobile phone with media capability, 6. Understand written English, 7. Able to give informed consent.
Exclusion criteria
1. Women who do not currently smoke, 2. Live outside the catchment areas of study sites, 3. Over 14 weeks of pregnancy, 4. Do not use or have access to a mobile phone with media capability, 5. Cannot understand written English, 6. Not able to give informed consent, 7. Already enrolled in an alternative formal smoking cessation trial at the time of referral to the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Recruitment rate | 23 months | Progression to a full trial will require recruitment ≥50% of women who give permission to have their details passed to the research team (i.e. those who express initial interest in the study). |
| Drop out rate | 23 months | Progression to a full trial will require \<30% dropout |
| Direction of effect | 23 months | Progression to a full trial will require direction of effect on smoking cessation rate in favour of the intervention. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Engagement | 23 months | Engagement in the intervention will be assessed using data captured by the computer system which monitors the text message responses. |
| Acceptability | 23 months | Acceptability of the intervention will be assessed in short interviews conducted with intervention group participants at the follow-up points |
Other
| Measure | Time frame | Description |
|---|---|---|
| Smoking cessation outcomes | At each subsequent data collection time-point (4 weeks post-randomisation, 36 weeks of pregnancy, 6-7 weeks post due-date, 12-13 weeks post due-date) | 1. The Russell Standard abstinence question: if they have smoked at all since the last data collection point (with answers being reported as: 'no, not a puff; 1-5 cigarettes; more than 5 cigarettes'). \[self-reported abstinence\] 2. How many times they have purposefully not smoked for more than 24 hrs since the last data collection time point. \[Self-reported 24hr quit attempts\] |
Countries
United Kingdom
Outcome results
None listed