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Phone-based Smoking Cessation Intervention for Patients With Chronic Pancreatitis.(START)

Phone-based Smoking Cessation Intervention for Patients With Chronic Pancreatitis :a Prospective Multicenter Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05940987
Enrollment
382
Registered
2023-07-12
Start date
2023-06-28
Completion date
2025-02-25
Last updated
2025-04-01

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

Conditions

Pancreatitis, Chronic

Keywords

Smoking Cessation, Phone-based intervention

Brief summary

This study aims to explore whether regular telephone intervention in patients with chronic pancreatitis can improve their smoking cessation rate.

Detailed description

Chronic pancreatitis(CP) is a chronically progressive disease characterized by pancreatic fibrosis and inflammation, and its basic pathological features include chronic inflammatory damage to the pancreatic parenchyma, interstitial fibrosis, pancreatic parenchymal calcification, pancreatic duct dilation, and pancreatic duct stones. Environmental factors such as alcoholism,smoking and genetic factors are the main causative factors of CP. Clinical studies have found that smoking can not only accelerate the course of CP, but also increase the risk of CP-related complications. Some scholars believe that smoking cessation may be a potential way to prevent the progression of CP and improve the prognosis of CP. Although there is no evidence to verify whether smoking cessation will improve the clinical course of CP, the latest ACG Clinical Guideline strongly recommends CP patients quit smoking. In 2016,a prospective study of smoking cessation interventions in CP patients showed that 27 enrolled patients had a smoking cessation rate of 0% after 6 months of smoking cessation intervention, indicating that smoking cessation is a huge challenge for CP patients. The investigators propose to conduct a randomized controlled trial to investigate the effects of telephone intervention on smoking cessation in patients with CP and explore the impact of smoking cessation on their clinical course and prognosis.

Interventions

BEHAVIORALPhone-based smoking cessation intervention

Participants who allocate to the intervention group will receive regular phone-based smoking cessation intervention by professional team.

Sponsors

Changhai Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

1.18 years of age and older living; 2.Patients diagnosed as chronic pancreatitis; 3.Self-reported smoking ≥ 5 cigarettes; 4.Urine cotinine levels ≥ 200 ng/mL; 5.Owning a phone; 6.Willing to provide informed consent to participate in the study.

Exclusion criteria

1. Patients diagnosed as pancreatic cancer within 2 years after diagnosing chronic pancreatitis; Patients diagnosed as groove pancreatitis or autoimmune pancreatitis; 2. Pregnant or lactating women; 3. Patients with life expectancy ≤ 12 months; 4. Comorbidities such as Alzheimer's disease, end-stage cancer, HIV, end-stage congestive heart failure, end-stage chronic obstructive pulmonary disease, uncompensated cirrhosis, renal failure; 5. Smoking e-cigarettes or other forms of non-burning tobacco. 6. Patients refused to participate.

Design outcomes

Primary

MeasureTime frameDescription
Biochemically Validated of 7-day Point Abstinence12 monthsThe primary outcome will be biochemical validation of Self-reported 7-day point-prevalence abstinence at month 2, 6, 12 after quit date.

Secondary

MeasureTime frameDescription
Self-reported 7-day Point Abstinence12 monthsSelf-reported 7-day point-prevalence abstinence at month 2, 6, 12 after quit date.
Number of cigarettes smoked per day12 monthsMean number of cigarettes smoked per day among participants still smoking at 12 months.
Fagerstrom Test of Nicotine Dependence (FTND) scores12 monthsThe FTND is a validated, 6-item self-report instrument that evaluates the intensity of physical addiction to nicotine. The scores will be assessed at month 2, 6, 12 after quit date.Three items are rated yes/no (0/1), and the other three items are rated on a scale from 0-3. Items are summed to yield a total score of 0-10, with higher scores reflecting greater nicotine dependence. This outcome variable will be reported as the difference in FTND total score between the intervention condition and the control condition.

Other

MeasureTime frameDescription
Reduction in Tobacco Consumption12 monthsThe number of CP patients who self-reported a 50% reduction in tobacco consumption at 2, 6 and 12 months after quit date.
Times of hospitalizations12 monthsThe times of hospitalizations for episodes of chronic pancreatitis at 12 months after quit date.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026