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Trial · NCT02157610

Smoking Cessation for Cervical Cancer Survivors

NCT02157610, Not applicable, Completed, H. Lee Moffitt Cancer Center and Research Institute; results first posted 2023-04-12

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Smoking Cessation for Cervical Cancer Survivors. Trials, record NCT02157610. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02157610

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Smoking Cessation for Cervical Cancer Survivors
NCT number
NCT02157610
Status
Completed
Phases
Not applicable
Enrollment
202 participants, actual
Lead sponsor
H. Lee Moffitt Cancer Center and Research Institute
Conditions
Cervical Cancer, Tobacco Use, Smoking Cessation
Interventions
Self-Help Materials, Nicotine Patch, REDCap, Saliva Test, Telephone Counseling Sessions, Nicotine lozenge
First posted
2014-06-06
Last updated
2023-07-20
Results first posted
2023-04-12

Source ClinicalTrials.gov

Registered outcomes1

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPercentage of Participants With Smoking Abstinence18 months
To test treatment effect at 18 months, logistic regression analysis conducted with abstinence as outcome variable, and treatment (a two-level categorical variable) as predictor, adjusting for covariates, specifically, factors used in the minimization procedures (race/ethnicity, language, age, education, income, cigarettes/day, cervical cancer stage, and time since diagnosis). A logit link and binomial variance function assumed for generalized linear mixed model (GLMM), regression and parameterize them with blocking on individual nested within treatment conditions. Treatment and time included, as well as their interaction, with adjustment for relevant covariates.

Outcomes1

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYPercentage of Participants With Smoking Abstinence18 monthsparticipants included in analysispercentageNUMBER

Results by group2

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Percentage of Participants With Smoking AbstinenceStandard Treatment (ST)12.9percentage
Percentage of Participants With Smoking AbstinenceMotivation + Problem Solving (MAPS)14.2percentage

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDStandard Treatment (ST)100
Overall StudySTARTEDMotivation + Problem Solving (MAPS)102
Overall StudyCOMPLETEDStandard Treatment (ST)96
Overall StudyCOMPLETEDMotivation + Problem Solving (MAPS)98
Overall StudyNOT COMPLETEDStandard Treatment (ST)4
Overall StudyNOT COMPLETEDMotivation + Problem Solving (MAPS)4

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityStandard Treatment (ST)4100
Total, all-cause mortalityMotivation + Problem Solving (MAPS)4102
Total, other adverse eventsStandard Treatment (ST)00
Total, other adverse eventsMotivation + Problem Solving (MAPS)00
Total, serious adverse eventsStandard Treatment (ST)00
Total, serious adverse eventsMotivation + Problem Solving (MAPS)00

Papers2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
34967755BACKGROUNDPubMed
36921237BACKGROUNDPubMed

Grants1

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal years
R01CA172786Smoking Cessation for Cervical Cancer Survivors in a Safety Net Healthcare SystemVIDRINE, JENNIFER IRVINH. LEE MOFFITT CANCER CTR & RES INSTNATIONAL CANCER INSTITUTE2014 to 2019

Trial comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
Standard Treatment (ST) vs Motivation + Problem Solving (MAPS): deaths from any cause

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT02157610

GET https://conductscience.org/api/trials/v1/NCT02157610/registered