CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 396 enrolled
Drug / intervention
Nicotine polacrilex +5 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02602288
NCT02602288N/ACompleted

Multilevel Tobacco Intervention in Community Clinics for Underserved Families

Temple University·interventional·Posted Nov 11, 2015·Updated Mar 15, 2022

In Brief

A clinical study evaluating Ask, Advise, Refer, Telebased tobacco counseling, and 4 other interventions for Second Hand Tobacco Smoke and Nicotine Dependence. Completed, enrolled 396 participants across 2 sites.

Detailed Summary

The purpose of this randomized controlled trial is to develop and test the efficacy of a multilevel, multimodal intervention designed to modify maternal smoking behavior to reduce children's exposure to secondhand tobacco smoke (primary outcome) and promote their smoking cessation (secondary outcome). Low-income mothers who smoke will be enrolled. Mothers will be recruited from the supplemental nutrition program, Women, Infants and Children (WIC) clinics. All mothers visiting WIC clinics will receive a clinic-level intervention, which consists of nutrition counselors following an "ask, advise, and refer" protocol to identify if their children are exposed to secondhand tobacco smoke, advise mothers who smoke about the harms of such exposure and the benefits of reducing exposure, and referring mothers to the trial. Screened eligible mothers will be consented and randomized to an attention control condition focused on nutrition (CTL) or to an experimental (EXP) multimodal behavioral intervention that integrates telebased counseling to promote the reduction of child secondhand smoke exposure (SHSE) and maternal smoking with an adjunct smoking cessation mobile app and nicotine replacement therapy use. The investigators will test the primary hypothesis that relative to children in the CTL condition, those in the EXP condition will have lower exposure SHSE as measured by mothers' reports and child cotinine levels. The investigators will also test the secondary hypothesis that relative to mothers in the CTL condition, those in the EXP condition will have higher bioverified 7-day point prevalence quit rates. In addition, the study will: (a) evaluate if specific psychosocial and behavioral factors-- social support, urge coping skills, self-efficacy, and SHSe protective behaviors--mediate the effects of the EXP intervention on outcomes and (b) explore whether other residential smokers, level of nicotine dependence, depressive/anxious symptoms, weight concerns, intervention dosage, and pregnancy status predict outcomes and moderate treatment effects.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsN.O.R.T.H., Inc.

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedNov 11, 2015
Enrollment StartFeb 1, 2016
Primary CompletionOct 23, 2019
TodayJul 2, 2026
Enrollment to primary: 3.7 yearsPosted 10.6 years ago

Interventions

Ask, Advise, Referbehavioral

WIC clinic staff ask about children's secondhand smoke exposure (SHSe), advise about harms of SHSe, and refer to smoking cessation resources

Telebased tobacco counselingbehavioral

Telephone counseling to promote parent's smoking cessation and behaviors to protect children from secondhand tobacco smoke

Telebased nutrition counselingbehavioral

Telephone counseling to promote nutritious eating practices in the family.

Mobile phone smoking cessation applicationdevice

Smartphone based application to support smoking cessation efforts

Mobile phone nutrition applicationdevice

Smartphone based application to support healthy eating habits

Nicotine polacrilexdrug

Over the counter nicotine replacement therapy in gum or lozenge form.