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Recruiting NCT05645146

Enhancing Long-Term Smoking Abstinence Among Cervical Cancer Survivors (Project ACCESS)

Conditions: Smoking Cessation, Cervical Cancer, High Grade Cervical Dysplasia

Sex: Female
Ages: 18 Years – N/A
Phase: NA
Enrollment: 360
Sponsor: H. Lee Moffitt Cancer Center and Research Institute

Location: United States

Summary

The goal of this research study is to compare the efficacy of a treatment approach that comprises both Motivation And Problem-Solving (MAPS)-based telephone counseling and a personally-tailored SMS-delivered text-based approach to quitline-delivered smoking cessation treatment to help participants with a history of cervical cancer or high-grade cervical dysplasia quit smoking.

Eligibility Criteria

Inclusion Criteria:At least 100 cigarettes or more smoked in participants lifetimeSpeaks EnglishCurrently smoke 1 cigarette or more in the past 30 daysHistory of cervical cancer or high grade cervical dysplasiaHas a working smartphoneHas a valid home address in the State of FloridaExclusion Criteria:Medical condition precluding nicotine replacement therapyReceiving behavioral or pharmacological tobacco treatmentHousehold member enrolled in this study

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05645146). StuddyBuddy aggregates publicly available trial information.