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N/A Completed N=371 Randomized Treatment

Pain and Smoking Study

Source: ClinicalTrials.gov NCT02971137 ↗
Enrolled (actual)
371
Serious AEs
0.0%
Results posted
Jan 2023
Primary outcomePrimary: Number of Participants Who Abstained From Smoking Cigarettes at 6months (Prolonged Abstinence) — 43; 41 Participants

Summary

This purpose of this study is to test the telephone delivery of a cognitive behavioral intervention (CBI), for smoking cessation among Veteran smokers with chronic pain

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants Who Abstained From Smoking Cigarettes at 6months (Prolonged Abstinence)
43; 41
PRIMARY
Number of Participants Who Abstained From Smoking Cigarettes at 12 Months (Prolonged Abstinence)
40; 38
PRIMARY
Number of Participants Who Abstained From Smoking Part of a Cigarette at 6months (30-day Point Prevalence)
23; 11
PRIMARY
Number of Participants Who Abstained From Smoking Part of a Cigarette at 12 Months (30-day Point Prevalence)
25; 18
SECONDARY
Change in Brief Pain Inventory (BPI) Pain Intensity, Difference From Baseline to Follow-up at 6 Months
-0.7; -0.5
SECONDARY
Change in Pain Interference, Difference Between Baseline and Follow-up at 6 Months
-0.72; -0.36
SECONDARY
Change in Brief Pain Inventory (BPI) Pain Intensity, Difference in Pain Intensity Between Baseline and 12 Months
-.044; -0.35
SECONDARY
Change in Pain Interference, Difference Between Baseline and Interference
-.56; -.46

Eligibility Criteria

Inclusion Criteria

  • Veterans enrolled at VA Connecticut or VA Central Western Massachusetts
  • Current Cigarette Smokers
  • Willing to make quit attempt in next 30 days
  • Pain intensity 4 or greater on scale 0-10, self-reported

Exclusion Criteria

  • Non-English speaking
  • No access to telephone/Lack of Telephone Access
  • Severely impaired hearing
  • Active diagnosis
  • Terminal Illness
  • Refusal to provide informed consent
  • Enrolled in concurrent smoking cessation programs/research
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02971137). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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