NCT00360581

Brief Summary

The purpose of this study is to develop strategies to maintain smoking abstinence initiated in pregnancy and prevent relapse in the postpartum period.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
30

participants targeted

Target at P25-P50 for phase_1

Timeline
Completed

Started Apr 2006

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2006

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

August 2, 2006

Completed
2 days until next milestone

First Posted

Study publicly available on registry

August 4, 2006

Completed
1.4 years until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2008

Completed
Last Updated

February 11, 2008

Status Verified

February 1, 2008

First QC Date

August 2, 2006

Last Update Submit

February 7, 2008

Conditions

Keywords

Smoking abstinence

Outcome Measures

Primary Outcomes (1)

  • smoking abstinence by CO testing

Secondary Outcomes (1)

  • smoking abstinence by self-report

Interventions

Eligibility Criteria

Age18 Years - 45 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Must have the ability to read, write, and understand English.
  • Must have quit smoking during their current pregnancy.
  • Must possess the desire to remain smoke-free after delivery.
  • Obtain permission from obstetrician to participate in yoga.
  • Must be reachable by telephone.
  • If subject becomes pregnant again while in the study, she can still participate with written permission from her primary care physician.

You may not qualify if:

  • Untreated hypertension.
  • A history of: glaucoma, major depression, alcohol abuse or substance disorder, anorexia nervosa, or head trauma.
  • Recent abdominal surgery (such as caesarean section).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Pittsburgh School of Nursing

Pittsburgh, Pennsylvania, 15261, United States

Location

MeSH Terms

Conditions

Smoking Cessation

Interventions

YogaCognitive Behavioral Therapy

Condition Hierarchy (Ancestors)

Health BehaviorBehavior

Intervention Hierarchy (Ancestors)

Mind-Body TherapiesComplementary TherapiesTherapeuticsSpiritual TherapiesExercise Movement TechniquesPhysical Therapy ModalitiesBehavior TherapyPsychotherapyBehavioral Disciplines and Activities

Study Officials

  • Susan A. Albrecht PhD, RN, FAAN

    University of Pittsburgh School of Nursing

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 1
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

August 2, 2006

First Posted

August 4, 2006

Study Start

April 1, 2006

Study Completion

January 1, 2008

Last Updated

February 11, 2008

Record last verified: 2008-02

Locations