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

Running, not enrolling · Not applicable

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

In brief

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.

Key facts

Study ID

NCT05645146

Run by

H. Lee Moffitt Cancer Center and Research Institute

People needed

360

Starts

2022-11-29

Expected to finish

2028-01-01

Last updated by the study team

2026-04-01

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• At least 100 cigarettes or more smoked in participants lifetime
• Speaks English
• Currently smoke 1 cigarette or more in the past 30 days
• History of cervical cancer or high grade cervical dysplasia
• Has a working smartphone
• Has a valid home address
• Reside in Florida at the time of study enrollment

You may not qualify if…

• Receiving behavioral or pharmacological tobacco treatment
• Household member enrolled in this study

Where it is running

• Moffitt Cancer Center — Tampa, Florida, United States

Full record on ClinicalTrials.gov

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