Status:

COMPLETED

Efficacy of Tobacco Quitline for Cancer Survivors

Lead Sponsor:

St. Jude Children's Research Hospital

Collaborating Sponsors:

National Cancer Institute (NCI)

Conditions:

Smoking Cessation

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The proposed study is a two-armed randomized controlled clinical trial examining the long-term (one-year) efficacy of telephone intervention conditions for smoking cessation in a high risk medical pop...

Detailed Description

In this study participants (n=1242) will be randomly assigned to a Counselor-Initiated Tobacco Quit Line (QL;) in which the counselor contacts the client with the standardized intervention protocol, o...

Eligibility Criteria

Inclusion

  • Participants smokes cigarettes
  • Participants is a cancer survivor
  • Participant must be at least 18 years of age.
  • Childhood cancer survivors must be at least one year out active cancer treatment.
  • Participant understands consent procedures.
  • Participant speaks English.
  • Participant must have access to a telephone for participation

Exclusion

  • Inability to understand consent procedures
  • Participants with a known contraindication or sensitivity to nicotine replacement therapy may participate in this study; however they will not receive nicotine replacement therapy (NRT) as part of their smoking cessation program.
  • Since our participants are childhood cancer survivors and they can be medically fragile and we are interested in providing all eligible participants with NRT to enhance their ability to quit smoking, we added a cautionary conditions list to the recruitment screening form. Those with severe arrhythmias, myocardial infarction, unstable angina, cerebrovascular incident, blood vessel disease, phaeochromocytoma, diabetes, hyperthyroidism, abnormal kidney or liver function, or history of gastritis or peptic ulcers, or who smoke less than 5 cigarettes per day will not receive NRT.
  • Patients with questionable NRT eligibility will be discussed/reviewed on a case by case basis with the Staff Family Physician

Key Trial Info

Start Date :

October 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 1 2013

Estimated Enrollment :

946 Patients enrolled

Trial Details

Trial ID

NCT00827866

Start Date

October 1 2008

End Date

November 1 2013

Last Update

November 25 2014

Active Locations (1)

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St. Jude Children's Research Hospital

Memphis, Tennessee, United States, 38105