- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02901171
The Contribution of a Smartphone Application to Acceptance and Commitment Therapy Group Treatment for Smoking Cessation
The Contribution of a Smartphone Application to Acceptance and Commitment Therapy Group Treatment for Smoking Cessation: a Randomised Controlled Trial Investigating Its Efficacy, Mediators and Moderators
Study Overview
Status
Conditions
Detailed Description
Smoking is the single biggest preventable cause of death in Ireland and costs the exchequer approximately €1-2 billion per annum. Currently, 19.2% of Irish people aged 15 and over smoke. Given the magnitude of human suffering and economic cost associated with smoking, the systematic empirical development of cost-effective smoking cessation interventions is a major public health need. Combining a group-based treatment for smoking cessation with a theoretically-consistent smartphone application has the advantage of augmenting therapeutic content delivered in the clinic with on-the-spot assistance in the individual's natural environment. In accordance, this study will evaluate the efficacy of a smartphone application in enhancing Acceptance and Commitment Therapy group treatment for smoking cessation. This study will also elucidate the processes through which the treatment promotes smoking cessation. Identifying such mediators of change can inform the enhancement of subsequent interventions, enabling them to retain efficacious elements and disregard redundant elements. Furthermore, this study will identify the participant characteristics associated with differential response to the treatment. Clarifying such treatment moderators can facilitate practitioners in selecting optimal treatments for individual service users.
Participants will attend a baseline assessment on an individual basis prior to their smoking cessation attempt. During this session, participants will provide a breath sample and complete a series of self-report measures: Fagerström Test of Nicotine Dependence, Commitment to Quitting Scale, smoking-related variables (e.g., years smoking, previous quit attempts, etc.), Avoidance and Inflexibility Scale, Mental Health Continuum-Short Form, Valuing Questionnaire, Present Moment Awareness Subscale of the Philadelphia Mindfulness Scale, and the Cognitive Fusion Questionnaire. Participants will then be randomly allocated to the combined treatment, ACT group treatment or group based Behavioural Support Programme. A post-treatment assessment will be conducted to investigate changes in the variables measured at baseline. In addition, a six-month follow-up assessment will determine whether the effects of the treatments are sustained over an extended period of time.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Leinster
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Dublin, Leinster, Ireland
- University College Dublin
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Aged 18 years or older
- Interested in quitting smoking in the next 30 days
- Smoking 10 or more cigarettes per day for at least the past 12 months
- Daily access to a smartphone that is compatible with applications from iTunes (iPhone) or Google Play (Android)
Exclusion Criteria:
- Currently participating in another smoking cessation intervention
- Failure to the meet inclusion criteria
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Combined Treatment
ACT group treatment combined with smartphone application
|
The Acceptance and Commitment Therapy (ACT) group treatment for smoking cessation will be delivered in six weekly 90-min sessions.
Smoking cessation will be promoted in each session by targeting core processes of the ACT model including acceptance, cognitive defusion, mindfulness, flexible perspective taking, values clarification and committed action.
In addition, participants will receive an ACT-based smartphone application for smoking cessation.
The application will foster core processes of the ACT model through daily exercises, tips and tools.
|
Active Comparator: Acceptance and Commitment Therapy (ACT)
ACT group treatment
|
|
Active Comparator: Behavioural Support Programme
Group based Behavioural Support Programme
|
The Behavioural Support Programme will be facilitated by stop smoking experts and delivered in six weekly 90-min sessions in a group format.
During the sessions, advice, support and information on smoking cessation will be given to participants and behavioural techniques will be reviewed.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Seven-day point-prevalence abstinence
Time Frame: 6 weeks after beginning treatment
|
6 weeks after beginning treatment
|
Seven-day point-prevalence abstinence
Time Frame: 6 months after beginning treatment
|
6 months after beginning treatment
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Positive mental health measured by the Mental Health Continuum-Short Form
Time Frame: 6 weeks after beginning treatment
|
6 weeks after beginning treatment
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Positive mental health measured by the Mental Health Continuum-Short Form
Time Frame: 6 months after beginning treatment
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6 months after beginning treatment
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Cigarettes per day in non-abstinent participants
Time Frame: 6 weeks after beginning treatment
|
6 weeks after beginning treatment
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Cigarettes per day in non-abstinent participants
Time Frame: 6 months after beginning treatment
|
6 months after beginning treatment
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Louise McHugh, Ph.D., University College Dublin
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- moconnor
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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