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Recruitment Messages for Current Smokers Recently Diagnosed With Cancer

A Multimethod Evaluation of Tobacco Treatment Trial Recruitment Messages for Current Smokers Recently Diagnosed With Cancer: Pilot Factorial Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05471284
Enrollment
99
Registered
2022-07-22
Start date
2019-02-11
Completion date
2019-04-02
Last updated
2022-07-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tobacco Smoking, Health Behavior

Keywords

Cancer, Digital outreach, Multimethod randomized trial, Factorial Design, Message Frames, Tobacco use, Smoker enrollment rates

Brief summary

The objective of this study was to conduct a pilot factorial randomized trial to identify the message frames that are most effective in promoting participation in a tobacco treatment trial for current smokers recently diagnosed with cancer. To do so, we used a multimethod approach to evaluate 3 different message frames across evaluation, effectiveness, and outcome measures. We combine findings from a message design experiment with textual analytic software to provide a holistic understanding of how message frames may or may not differentially affect tobacco treatment trial participation within the context of a cancer diagnosis.

Detailed description

Background: A cancer diagnosis can catalyze motivation to quit smoking. Tobacco treatment trials offer cessation resources but have low accrual rates. Digital outreach may improve accrual, but knowledge of how best to recruit smokers with recent diagnoses is limited. Objective: This study aims to identify the message frames that were most effective in promoting intent to talk to a physician about participating in a tobacco treatment trial for smokers recently diagnosed with cancer. Methods: From February to April 2019, current smokers diagnosed within the past 24 months were recruited from a national web-based panel for a multimethod pilot randomized trial (N=99). Participants were randomized to a 2×3 plus control factorial design that tested 3 unique message frames: proximal versus distal threats of smoking, costs of continued smoking versus benefits of quitting, and gains of participating versus losses of not participating in a tobacco treatment trial.

Interventions

BEHAVIORALProximal

The first factor tested framing of the near, proximal threat of continued smoking.

BEHAVIORALDistal

The first factor tested framing of the long-term, distal threat of continued smoking.

BEHAVIORALCost

Cost framework measures the response efficacy to quitting smoking by displaying costs of continued smoking.

BEHAVIORALBenefit

Benefit framework measures the response efficacy to quitting smoking by displaying benefits of quitting.

BEHAVIORALLoss

The third factor tested framing of the response efficacy of participating in a cessation study by utilizing loss of not participating in a smoking cessation.

BEHAVIORALGain

The third factor tested framing of the response efficacy of participating in a cessation study by utilizing gain of participating in a smoking cessation.

BEHAVIORALControl

Does not include any of the three message factors.

Sponsors

Tufts University
CollaboratorOTHER
Massachusetts General Hospital
CollaboratorOTHER
Memorial Sloan Kettering Cancer Center
CollaboratorOTHER
University of Oklahoma
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Speak and understand English * A recent cancer diagnosis (within the past 24 months) * 18 years or older * Report any cigarette use within the past 30 days

Exclusion criteria

* Do not speak or understand English * Have not been diagnosed with cancer within the past 24 months * Below the age of 18 * Does not report any cigarette use within the past 30 days

Design outcomes

Primary

MeasureTime frameDescription
Difference in intent to talk to a physician about participating in a smoking cessation study between factors.Within 30 minutesThe main effect within each message factor level was examined using ANOVA and compared with the control condition.

Secondary

MeasureTime frameDescription
Predictors of intent to talk to a physician about participating in a smoking cessation study.Within 30 minutesOther message evaluation and effectiveness measures were collected and explored in a multivariable model predicting intent to talk to a physician.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026