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Completed

NCT Number: NCT01331226

Support Person Intervention to Promote a Smoking Helpline

This study is designed to examine if a telephone-based intervention delivered to a support person (i.e., friend, spouse of a smoker) increases the smoker's use of the Minnesota helpline. In addition, the study will examine if the rate of smoker calls to the helpline is greater if the support person receives 3 intervention calls, 1 intervention call, or no calls (written materials only, control condition).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mayo CLinic

Rochester, Minnesota, 55905, United States

About this study

We will conduct a randomized clinical trial within the ongoing service of the QUITPLAN® Helpline. Our primary aim is to examine the efficacy of two levels of telephone counseling for support persons (1 or 3 sessions) compared with a control condition on the proportion of smokers who call the Helpline over the 7 month follow-up period. We hypothesize a dose response relationship between number of telephone sessions provided to the support persons and smoker calls to the Helpline. Additional aims are to examine smoker quit attempts and cessation, and cost-effectiveness of the interventions.

Nonsmoking adult support persons (N=1020) residing in Minnesota will be enrolled and randomly assigned to one of three study conditions: (1) control condition -written self-help materials, (2) written materials plus one telephone session, or (3) written materials plus three telephone sessions. Outcome assessments will be completed by support persons and smokers at post-treatment (week 4) and at 7 month follow-up.

This design will allow for evaluation of whether results from our previous trial (Patten et al., in press, AJPM) can be replicated when the intervention is implemented within a "real-world" setting. That is all support person intervention calls will be delivered by the Helpline. Moreover, we will examine the potential efficacy and cost-effectiveness of a streamlined version of the intervention (i.e., 1 call). Furthermore, the proposed study will provide new data on quit attempts and cessation among the smokers. Ultimately, positive findings from this line of research could serve as the basis for expanding the range of helpline services to nonsmokers.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The support person must
  • reside in Minnesota
  • be 18 years of age or older
  • provide written informed consent
  • be a never or former cigarette smoker (no cigarette smoking in the past 6 months)
  • want to support a current cigarette smoker (has smoked a total of >1 cigarettes during the past 7 days) who is 18 years of age or older, resides in Minnesota, and has not been enrolled in a helpline or any other cessation program in the last 3 months
  • be able and willing to participate in all aspects of the study
  • have access to a working telephone
  • have current and anticipated contact (any combination of face-to-face, telephone, text messaging, or electronic mail) with the smoker on at least 3 days a week for the 30 week study duration.

Exclusion criteria

  • Support persons will be excluded if another support person from the same household has enrolled.

Treatment and study plan

telephone counseling 3 sessions

Behavioral

3 sessions of telephone counseling

telephone counseling 1 session

Behavioral

1 session of telephone counseling

written materials only

Behavioral

written materials only

Primary outcomes

  1. helpline utilization

    Time frame: At 7 month follow-up

    smoker calls to the helpline

Secondary outcomes

  1. smoker quit attempts and cessation

    Time frame: 7 month follow-up

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Registry information

Official study title

Support Person Effectiveness Study to Promote Smoker Utilization of the QUITPLAN Helpline

Acronym: ClearWay #4

Important dates

Study start
2011
Primary completion
2015
Study completion
2015
First posted
Apr 7, 2011
Registry last updated
Apr 10, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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