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Babies Living Safe and Smokefree (BLiSS)

Primary Purpose

Second Hand Tobacco Smoke, Nicotine Dependence

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Ask, Advise, Refer
Telebased tobacco counseling
Telebased nutrition counseling
Mobile phone smoking cessation application
Mobile phone nutrition application
Nicotine polacrilex
Sponsored by
Temple University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Second Hand Tobacco Smoke

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • English speaking
  • female
  • at least 18 years of age
  • parent or legal guardian of child under 6 yrs old who lives with them at least 4 days/wk
  • smokes

Exclusion Criteria:

  • non-nicotine drug dependence
  • active psychiatric disturbance (bipolar, schizophrenia, psychosis)
  • inadequate health literacy
  • pregnant
  • no smartphone

Sites / Locations

  • Temple University
  • N.O.R.T.H., Inc.

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

AAR+Behavioral Intervention (EXP)

AAR+Attention Control Intervention (CTL)

Arm Description

Ask Advise Refer (AAR): WIC clinic staff ask about children's secondhand smoke exposure (SHSe), advise about harms of SHSe, and refer to smoking cessation resources. Telebased tobacco counseling: Telephone counseling to promote parent's smoking cessation and behaviors to protect children from secondhand tobacco smoke. Mobile phone smoking cessation application: Smartphone based application to support smoking cessation efforts. Nicotine polacrilex: Over the counter nicotine replacement therapy in gum or lozenge form.

Ask Advise Refer (AAR): WIC clinic staff ask about children's secondhand smoke exposure (SHSe), advise about harms of SHSe, and refer to smoking cessation resources. Telebased nutrition counseling: Telephone counseling to promote nutritious eating practices in the family. Mobile phone nutrition application: Smartphone based application to support healthy eating habits

Outcomes

Primary Outcome Measures

Child Urine Cotinine
Child urine cotinine is a biomarker for assessing secondhand smoke exposure. The investigators anticipate the EXP group will evidence a greater reduction in child urine cotinine over time than the CTL group. Cotinine values were log transformed to normalize distributions.
Cigarettes/Day
Parental report of cigarettes child is exposed to each day in the home and car and other locations by all sources during the 7 days prior to assessment. The investigators anticipate the EXP group will evidence greater reductions in child secondhand smoke exposure over time than the CTL group.

Secondary Outcome Measures

Parent-reported Cotinine-verified 7-day Point Prevalence Abstinence
When a participant reports smoking abstinence, the investigators will bioverify their smoking status.

Full Information

First Posted
November 9, 2015
Last Updated
February 15, 2022
Sponsor
Temple University
Collaborators
N.O.R.T.H., Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT02602288
Brief Title
Babies Living Safe and Smokefree
Acronym
BLiSS
Official Title
Multilevel Tobacco Intervention in Community Clinics for Underserved Families
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
February 2016 (undefined)
Primary Completion Date
October 23, 2019 (Actual)
Study Completion Date
October 23, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Temple University
Collaborators
N.O.R.T.H., Inc.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Second Hand Tobacco Smoke, Nicotine Dependence

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
396 (Actual)

8. Arms, Groups, and Interventions

Arm Title
AAR+Behavioral Intervention (EXP)
Arm Type
Experimental
Arm Description
Ask Advise Refer (AAR): WIC clinic staff ask about children's secondhand smoke exposure (SHSe), advise about harms of SHSe, and refer to smoking cessation resources. Telebased tobacco counseling: Telephone counseling to promote parent's smoking cessation and behaviors to protect children from secondhand tobacco smoke. Mobile phone smoking cessation application: Smartphone based application to support smoking cessation efforts. Nicotine polacrilex: Over the counter nicotine replacement therapy in gum or lozenge form.
Arm Title
AAR+Attention Control Intervention (CTL)
Arm Type
Active Comparator
Arm Description
Ask Advise Refer (AAR): WIC clinic staff ask about children's secondhand smoke exposure (SHSe), advise about harms of SHSe, and refer to smoking cessation resources. Telebased nutrition counseling: Telephone counseling to promote nutritious eating practices in the family. Mobile phone nutrition application: Smartphone based application to support healthy eating habits
Intervention Type
Behavioral
Intervention Name(s)
Ask, Advise, Refer
Intervention Description
WIC clinic staff ask about children's secondhand smoke exposure (SHSe), advise about harms of SHSe, and refer to smoking cessation resources
Intervention Type
Behavioral
Intervention Name(s)
Telebased tobacco counseling
Intervention Description
Telephone counseling to promote parent's smoking cessation and behaviors to protect children from secondhand tobacco smoke
Intervention Type
Behavioral
Intervention Name(s)
Telebased nutrition counseling
Intervention Description
Telephone counseling to promote nutritious eating practices in the family.
Intervention Type
Device
Intervention Name(s)
Mobile phone smoking cessation application
Intervention Description
Smartphone based application to support smoking cessation efforts
Intervention Type
Device
Intervention Name(s)
Mobile phone nutrition application
Intervention Description
Smartphone based application to support healthy eating habits
Intervention Type
Drug
Intervention Name(s)
Nicotine polacrilex
Other Intervention Name(s)
nicotine gum, nicotine lozenge
Intervention Description
Over the counter nicotine replacement therapy in gum or lozenge form.
Primary Outcome Measure Information:
Title
Child Urine Cotinine
Description
Child urine cotinine is a biomarker for assessing secondhand smoke exposure. The investigators anticipate the EXP group will evidence a greater reduction in child urine cotinine over time than the CTL group. Cotinine values were log transformed to normalize distributions.
Time Frame
3 months and 12 months
Title
Cigarettes/Day
Description
Parental report of cigarettes child is exposed to each day in the home and car and other locations by all sources during the 7 days prior to assessment. The investigators anticipate the EXP group will evidence greater reductions in child secondhand smoke exposure over time than the CTL group.
Time Frame
3 months and 12 months
Secondary Outcome Measure Information:
Title
Parent-reported Cotinine-verified 7-day Point Prevalence Abstinence
Description
When a participant reports smoking abstinence, the investigators will bioverify their smoking status.
Time Frame
7 days prior to 3 month and 12 month assessments

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: English speaking female at least 18 years of age parent or legal guardian of child under 6 yrs old who lives with them at least 4 days/wk smokes Exclusion Criteria: non-nicotine drug dependence active psychiatric disturbance (bipolar, schizophrenia, psychosis) inadequate health literacy pregnant no smartphone
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephen J Lepore, PhD
Organizational Affiliation
Temple University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Temple University
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19122
Country
United States
Facility Name
N.O.R.T.H., Inc.
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19132
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35196033
Citation
Collins BN, Lepore SJ, Egleston BL. Multilevel Intervention for Low-Income Maternal Smokers in the Special Supplemental Nutrition Program for Women, Infants, and Children (WIC). Am J Public Health. 2022 Mar;112(3):472-481. doi: 10.2105/AJPH.2021.306601.
Results Reference
derived
PubMed Identifier
34255698
Citation
Lepore SJ, Collins BN, Killam HW, Barry B. Supportive Accountability and Mobile App Use in a Tobacco Control Intervention Targeting Low-Income Minority Mothers Who Smoke: Observational Study. JMIR Mhealth Uhealth. 2021 Jul 2;9(7):e28175. doi: 10.2196/28175.
Results Reference
derived
PubMed Identifier
28288601
Citation
Collins BN, Lepore SJ. Babies Living Safe & Smokefree: randomized controlled trial of a multilevel multimodal behavioral intervention to reduce low-income children's tobacco smoke exposure. BMC Public Health. 2017 Mar 14;17(1):249. doi: 10.1186/s12889-017-4145-7.
Results Reference
derived

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Babies Living Safe and Smokefree

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