Enhancing Smoker Utilization of the Minnesota Quitline Through Support Persons

This study has been completed.
Sponsor:
Collaborator:
ClearWay Minnesota
Information provided by:
Mayo Clinic
ClinicalTrials.gov Identifier:
NCT01311830
First received: March 8, 2011
Last updated: March 22, 2011
Last verified: March 2011
  Purpose

This study will develop an intervention for adults who want to support a smoker. The goal of the intervention is for the support person to motivate & encourage their smoker to call the state Quitline funded by Minnesota ClearWay. The study will examine the efficacy of a telephone based intervention for support persons compared to a self-help intervention (written materials only).


Condition Intervention
Tobacco Use
Behavioral: Telephone Counseling
Behavioral: Written Materials

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Enhancing Smoker Utilization of the Minnesota Quitline Through Support Persons

Further study details as provided by Mayo Clinic:

Primary Outcome Measures:
  • proportion of smokers in each group who call the Minnesota Quitline, and changes in supportive behaviors among the support persons as measured by the Support Provided Measure. [ Time Frame: 6 months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • quit attempts and changes in readiness to quit among the smokers [ Time Frame: 6 months ] [ Designated as safety issue: No ]

Enrollment: 534
Study Start Date: September 2007
Study Completion Date: April 2010
Primary Completion Date: April 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Telephone Counseling Behavioral: Telephone Counseling
Placebo Comparator: Written Materials Behavioral: Written Materials

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. reside in Minnesota
  2. be 18 years of age or older
  3. provide written informed consent
  4. be a never or former cigarette smoker (no cigarette smoking in the past 6 months)
  5. be interested in supporting a current cigarette smoker (has smoked a total of >1 cigarettes during the past 7 days) who is 18 years of age or older and who resides in Minnesota
  6. be able and willing to participate in all aspects of the study
  7. have access to a working telephone
  8. have current and anticipated contact (any combination of face-to-face, telephone, or electronic mail) with the smoker on at least 3 days a week for the 26 week study duration.

Individuals will be excluded if another support person from the same household has enrolled.

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01311830

Locations
United States, Minnesota
Mayo Clinic
Rochester, Minnesota, United States, 55905
Sponsors and Collaborators
Mayo Clinic
ClearWay Minnesota
  More Information

No publications provided by Mayo Clinic

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Christi Patten, Mayo Clinic
ClinicalTrials.gov Identifier: NCT01311830     History of Changes
Other Study ID Numbers: 06-005379
Study First Received: March 8, 2011
Last Updated: March 22, 2011
Health Authority: United States: Institutional Review Board

Additional relevant MeSH terms:
Tobacco Use Disorder
Substance-Related Disorders
Chemically-Induced Disorders
Mental Disorders

ClinicalTrials.gov processed this record on August 01, 2014