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Comparison · NCT01737281-3f7ebd94

Proactive Outreach vs Usual Care: Number of Participants With Cotinine-Validated Abstinence From Smoking

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Proactive Outreach vs Usual Care: Number of Participants With Cotinine-Validated Abstinence From Smoking. Trial comparisons, record NCT01737281-3f7ebd94. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01737281-3f7ebd94

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.6790.5450.789wilson
Risk in group 20.6820.5340.8wilson
Risk difference, group 1 minus group 2-0.00257-0.1810.181newcombe hybrid score
Risk ratio, group 1 over group 20.9960.7581.31log
Odds ratio, group 1 over group 20.9880.4192.33log
Number needed to treat, for one fewer participant with the outcome on Proactive Outreach than on Usual Care389from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: usual care.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Proactive Outreach
Intervention arm participants received: (1) 12 sessions of proactive telephone cessation counseling, (2) coordination of cessation medications from a VA provider, (3) mailed stress reduction materials, (4) engagement of their regular mental health provider in the treatment process through CPRS progress notes, to which their provider will be added as signer.
3653OG000
Group 2Usual Care
Control arm participants received a mailed list of local VA and non-VA smoking cessation services that they can access on their own. In addition, patients randomized to the control group received treatment or referrals to treatment from their regular VA providers as part of usual care. Pharmacotherapy is available at all sites in the form of nicotine replacement (patches, gum and lozenges) and bupropion.
3044OG001

Outcome

Type
PRIMARY
Title
Number of Participants With Cotinine-Validated Abstinence From Smoking
Description
The primary outcome will be cotinine-validated abstinence from smoking at 12-month follow-up.
Time frame
12 months
Population
Cotinine samples were obtained by mail from 53/76 people reporting abstinence in the intervention arm and 44/58 people reporting abstinence in the control arm. Note that this reflects a complete case analysis, only including people for whom outcome data are available.

Source ClinicalTrials.gov

Trial

Title
Proactive Outreach for Smokers in VA Mental Health
NCT number
NCT01737281
Phases
NA
Conditions
Smoking
Interventions
Proactive outreach, Usual care
Lead sponsor
VA Office of Research and Development
Results first posted
2019-03-14

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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