Experiences of Pregnant Women Who Use NRT in Pregnancy as Part of a Quit Attempt

This study is largely a qualitative study with a small survey component. The aim of the survey would be to gain a quantitative perspective of how women use NRT after this has been prescribed by stop smoking services (SSS). The aim of the qualitative study would be to enhance knowledge of pregnant smoker's views and attitudes about their experiences of using NRT and in particular to understand why pregnant women who start using NRT often discontinue this early or do not use the medication as it is prescribed. This information is important for a number of reasons; firstly it will help health professionals and researchers gain an in depth understanding about how women experience using NRT, which may be used to help devise strategies for encouraging better adherence and which could be used in future clinical trials to gain a clearer understanding as to whether or not NRT is effective in pregnancy.

Study Overview

• Status: Completed
• Conditions: Pregnancy; Nicotine Replacement Therapy; Qualitative
• Intervention / Treatment: Other: Qualitative and survey

• Study Type: Observational
• Enrollment (Actual): 15

Contacts and Locations

Study Locations

• United Kingdom
  • Nottingham, United Kingdom
    • New Leaf Stop smoking services
  • Nottinghamshire
    • Nottingham, Nottinghamshire, United Kingdom, NG7 2RD
      • University of Nottingham

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 16 years and older (Child, Adult, Older Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: Female

• Sampling Method: Non-Probability Sample

Study Population

Participants will be identified through two identification sites; New Leaf Stop Smoking Services in Nottinghamshire and Nottingham City. The study will consist of a short survey focussing on how NRT is used during pregnancy. As well as providing information the survey responses will also be able to distinguish who is eligible to participate in qualitative telephone interviews. A subsection of these women will be asked to participate in an interview. The survey and interviews will be conducted as close as possible after participants have had an appointment with a smoking cessation advisor and, have given consent for the researcher to contact them, this is likely to be within a two week period.

Description

Inclusion Criteria:

• Quantitative survey;

  • Women who are pregnant
  • Aged 16 or over (no upper age limit)
  • Who have been prescribed NRT (patches/dual therapy) to aid a quit attempt.

Qualitative interview study will include the above plus;

• Women will have used NRT for over 24 hours
• Either not be using NRT as prescribed (as deciphered by the survey questions) or have currently quit NRT (and have either stopped smoking or continue to smoke)

Exclusion Criteria:

• Survey and qualitative interviews

  • Women who cannot understand the study procedure sufficiently in order to provide consent e.g. due to cognitive difficulties
  • Women who are unable to read or understand the consent procedure and study procedures in English.

Study Plan

How is the study designed?

Number of groups / cohorts

1

Cohorts and Interventions

Group / Cohort	Intervention / Treatment
Nicotine Replacement Therapy	Other: Qualitative and survey

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
number of women that use NRT after being prescribed	All women will be asked whether they have used NRT after being given a prescription, this measurement will be obtained within 4 weeks of the participant consenting to take part in the study.	within 4 weeks of taking part in the study

Secondary Outcome Measures

Outcome Measure	Time Frame
Number of women who adhere to NRT	4 weeks

Collaborators and Investigators

• Sponsor: University of Nottingham

Study record dates

Study Major Dates

• Study Start: April 1, 2014
• Primary Completion (Actual): December 1, 2014
• Study Completion (Actual): December 1, 2014

Study Registration Dates

• First Submitted: April 23, 2014
• First Submitted That Met QC Criteria: April 28, 2014
• First Posted (Estimate): April 29, 2014

Study Record Updates

• Last Update Posted (Estimate): December 4, 2014
• Last Update Submitted That Met QC Criteria: December 3, 2014
• Last Verified: December 1, 2014

More Information

Terms related to this study

• Other Study ID Numbers: 14024