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Clinical Trials/NCT02433860
NCT02433860CompletedNot Applicable

Evaluation of the Effectiveness of Pharmacists in Implementing the Smoking Cessation and Reduction in Pregnancy and Treatment (SCRIPT) Protocol

Providence Medical Research Center2 sites in 1 country8 target enrollmentStarted: January 1, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
8
Locations
2
Primary Endpoint
quit rates for nicotine for pregnant women

Study Overview

Brief Summary

There is a significant need for nicotine cessation programs for pregnant women in Spokane County. SCRIPT has been proven to be an effective method for smoking cessation in pregnant women. This study will evaluate the success of SCRIPT delivered by pharmacists. At the end of the study, the investigators hope to have three questions answered: 1) what is the quit rate of pregnant women in the Spokane area who receive the SCRIPT intervention delivered by pharmacists? 2) How does the quit rate compare to the quit rates of SCRIPT programs delivered by other health care providers as documented in the literature? And 3) Does the SCRIPT intervention have a significant effect on quit rates for pregnant women compared to current Spokane county quit rates? Urine cotinine tests will be used to document smoking status before delivery of the SCRIPT program, approximately one week after quit date and at >36 wks gestation or at delivery for study participants.

Detailed Description

  1. The goal of this project is to evaluate the success of pharmacists in delivering the SCRIPT smoking cessation program. The research questions that need to be addressed are: i. What is the quit rate of pregnant women in the Spokane area who receive the SCRIPT intervention delivered by a pharmacist? ii. How does this quit rate compare to the quit rates of other SCRIPT programs given by other health care providers (social workers, nurses, etc.)? iii. Does the SCRIPT intervention have a significant effect on quit rates for smoking pregnant women compared to current Spokane county quit rates?

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • nicotine use
  • English speaking
  • 18 years of age or older

Exclusion Criteria

  • Males due to pregnancy status not applicable

Arms & Interventions

pregnant nicotine users

Experimental

watch video and tobacco cessation counselling using SCRIPT protocol

Intervention: pharmacist nicotine cessation counseling using SCRIPT protocol (Behavioral)

Outcomes

Primary Outcomes

quit rates for nicotine for pregnant women

Time Frame: 2 yrs

1. The quit rates of pregnant women in this program will be compared to SCRIPT studies to evaluate the effectiveness of pharmacists providing this program.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Providence Medical Research Center
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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