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Web-Delivered Acceptance & Commitment Therapy for Smokers With Bipolar Disorder

Web-Delivered Acceptance & Commitment Therapy for Smokers With Bipolar Disorder

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02750904
Acronym
WebQuit Plus
Enrollment
51
Registered
2016-04-26
Start date
2017-04-03
Completion date
2019-05-14
Last updated
2019-10-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bipolar Disorder, Smoking

Keywords

Smoking Cessation, Acceptance & Commitment Therapy, Cognitive Behavioral Therapy, Bipolar Disorder

Brief summary

This purpose of the study is to develop and test a new website to help people who have bipolar disorder quit smoking.

Detailed description

The study consist of two separate phases. Phase I consists of website usability testing. Investigators will collect feedback and incorporate the feedback into our website that is tailored for people with bipolar disorder. In Phase II investigators will be comparing quit rates of two groups both utilizing Nicotine Replacement Therapy and a website.

Interventions

BEHAVIORALExperimental plus Nicotine Replacement Therapy

Behavioral: Experimental plus Nicotine Replacement Therapy will be built to specifically address challenges of smoking cessation for individuals with bipolar disorder. Includes four in person and four phone visits. Therapy information is withheld to protect the integrity of the study.

BEHAVIORALControl plus Nicotine Replacement Therapy

Includes four in-person and four phone visits

Sponsors

Palo Alto Veterans Institute for Research
CollaboratorOTHER
Bedford Research Corporation, Inc.
CollaboratorOTHER
Jefferson Center, Community Mental Health Clinic
CollaboratorUNKNOWN
VA Central Western Massachusetts Healthcare System
CollaboratorUNKNOWN
Fred Hutchinson Cancer Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age 18 or older 2. Daily smoker for the past year, averaging at least 5 cigarettes per day for the past 30 days, with expired-air carbon monoxide (CO) level ≥ 4 ppm 3. Motivated to quit smoking (i.e., endorse plans to quit in the next 30 days at the time of phone pre-screening) 4. Meets lifetime criteria for bipolar I or II disorder, based on DSM-V criteria 5. Willing to be randomly assigned to either treatment group 6. Has at least weekly access to a high-speed Internet connection via a tablet, laptop or desktop computer 7. Willing and able to read in English 8. Is under care of a clinician for the treatment of bipolar disorder 9. Willing to authorize communication with the clinician regarding study participation and clinical deterioration 10. Willing to use the nicotine patch to help quit smoking

Exclusion criteria

1. Participating in other smoking cessation interventions 2. Currently using any pharmacotherapies for smoking cessation 3. Previous use of the Smokefree.gov website 4. Meets DSM-V criteria for current mania 5. Meets DSM-V criteria for a current major depressive episode and symptoms are currently severe (Patient Health Questionnaire-9 score \> 14) 6. Current psychotic symptoms 7. Psychiatric hospitalization within one month prior to enrollment 8. Current suicidal or homicidal ideation 9. Meets criteria for a DSM-V diagnosis of a moderate or severe substance use disorder in past month prior to enrollment 10. Unstable medical condition 11. Any medical or psychiatric condition that, in the opinion of the investigator, is severe enough to interfere with protocol adherence or ability to benefit from the intervention 12. Any medical conditions that would preclude use of the nicotine patch (e.g., recent myocardial infarction, significant skin disorder, previous severe adverse reaction to nicotine patch, pregnant or breast feeding, assessed with our standard protocol for determining NRT eligibility) 13. Employee or family member of the investigator or study center, or member of the same household as another research participant

Design outcomes

Primary

MeasureTime frameDescription
RecruitmentWeek -1 (Visit 0)Number approached, screened, eligible, and consented; reasons for ineligibility or refusal
Completion of the experimental interventionWeek 10Completion of the core treatment program
Retention in studyWeek 10Percentage of participants in each arm completing outcome assessments at end of treatment visit
Treatment satisfactionWeek 1012 item survey used in our prior work assessing satisfaction with the assigned treatment
Treatment utilizationWeek 10Server-recorded log-ins to the assigned treatment
Change in acceptance of smoking triggersWeek 10Change in acceptance scores between baseline and end of treatment
Change in commitment to quitWeek 10Change in commitment scores between baseline and end of treatment
CO-confirmed 7-day point prevalence abstinence from cigarette smokingWeeks 10Preliminary efficacy for smoking cessation
Change in bipolar disorder symptomsWeek 10Change in mania and depression scale scores

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026