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Effectiveness of Mindfulness Based Relapse Prevention for Tobacco Dependents (MBRP)

Primary Purpose

Tobacco Use Disorder

Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Mindfulness Based Relapse Prevention
Brazilian Ministry of Health Protocol
Sponsored by
Federal University of São Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Tobacco Use Disorder focused on measuring mindfulness, tobacco dependence, relapse prevention

Eligibility Criteria

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

Inclusion Criteria:

  • Patients with a diagnosis of nicotine dependence;
  • Patients currently smoking at least 10 cigarettes a day;
  • Do not have any current major psychological disorders;
  • Patients undergoing treatment for the first time
  • Be willing to attend treatment and follow-up sessions, complete surveys and expired CO tests;
  • Do not exhibit dependence on other drugs.

Exclusion Criteria:

  • Dependence on other substances;
  • Psychiatric comorbidities;
  • Pregnant women.

Sites / Locations

  • Drug Dependency Unit of the Federal University of São Paulo

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Mindfulness Based Relapse Prevention

Brazilian Ministry of Health Protocol

Arm Description

The Experimental Group (EG) will undergo eight sessions of MBRP after Brazilian Ministry of Health Protocol (BMHP) for Tobacco dependence treatment. MBRP Program: the first three sessions: focus on practicing mindful awareness and integrating mindfulness practices into daily life (body scan, sitting meditation, walking meditation); The next three sessions: emphasize acceptance of present experience and application of mindfulness practices to relapse prevention; The final two sessions: expand to include issues of self-care, support network, and lifestyle balance.

The Control Group (CG) is undergo the protocol of the Brazilian Ministry of Health Protocol (BMHP): clinical evaluation, four sessions of cognitive-behavioral approach and Nicotine Replacement Therapy and/or Bupropion as needed, as the Experimental Group. And during the eight sessions of MBRP (EG) both groups (EG and CG) are subjected to eight maintenance sessions of BMHP.

Outcomes

Primary Outcome Measures

Change in the maintenance of abstinence from Cessation of tobacco use through assessment interviews (self-report and CO monitor will be used), and the point prevalence
We will assess the maintenance of abstinence from tobacco use through assessment interviews (self-report and CO monitor will be used), and the point prevalence will be the primary outcome measure.

Secondary Outcome Measures

Change in smoking urges measured with the self report questionnaire: Questionnaire of Smoking Urges (QSU)
This will be measured with the self report questionnaire: Questionnaire of Smoking Urges (QSU)
Change in Symptoms of Anxiety measured through the The Hospital Anxiety and Depression Scale (HAD)
The symptoms of anxiety will be measured through the The Hospital Anxiety and Depression Scale (HAD)
Change in Symptoms of Depression measured through the Centre for Epidemiologic Studies Depression Scale (CES-D)
The symptoms of depression will be measured through the Centre for Epidemiologic Studies Depression Scale (CES-D)
change in Self report Mindfulness level measured with the self report questionnaire Five Facet Mindfulness Questionnaire (FFMQ)
This will be measured with the self report questionnaire Five Facet Mindfulness Questionnaire (FFMQ)
Maintenance of Abstinence measured by a Bedfont Micro Smokerlyser - CO monitor
Abstinence will be measured by a Bedfont Micro Smokerlyser - CO monitor, to support self-reports of smoking cessation.
Tobacco Dependence measured through The Fagerstrom Test for Nicotine Dependence (FTND)
This will be measured through The Fagerstrom Test for Nicotine Dependence (FTND)
Change in Positive and Negative Affects measured through Positive and Negative Affect Scale (PANAS)
This will be measured through Positive and Negative Affect Scale (PANAS).

Full Information

First Posted
December 21, 2014
Last Updated
July 23, 2020
Sponsor
Federal University of São Paulo
Collaborators
Fundação de Amparo à Pesquisa do Estado de São Paulo, Conselho Nacional de Desenvolvimento Científico e Tecnológico
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1. Study Identification

Unique Protocol Identification Number
NCT02327104
Brief Title
Effectiveness of Mindfulness Based Relapse Prevention for Tobacco Dependents
Acronym
MBRP
Official Title
Evaluation of the Effectiveness of the Program of Mindfulness - Based Relapse Prevention (MBRP) as an Assistant Strategy to the Treatment of Tobacco Dependence
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
October 2012 (undefined)
Primary Completion Date
August 2016 (Actual)
Study Completion Date
August 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federal University of São Paulo
Collaborators
Fundação de Amparo à Pesquisa do Estado de São Paulo, Conselho Nacional de Desenvolvimento Científico e Tecnológico

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The dependence on tobacco is a predictable leading cause of death. The treatment based on the cognitive-behavioral therapy, including relapse prevention, became standard for tobacco dependents; yet scientific advances are still needed. Accordingly, the Mindfulness-Based Relapse Prevention (MBRP) program, adjunct to treatment, has shown promising results. The purpose of this project is to evaluate the effectiveness of the program MBRP as an adjunct in the treatment of smoking cessation instituted by the Ministry of Health, through the Instituto Nacional do Câncer (INCA) in Brazil.There will be a randomized clinical trial, with a simple random allocation. 60 patients will participate in this study receiving treatment (INCA'S standard) randomized between two groups: the MBRP Group (EG), which will undergo eight sessions of MBRP; and the Control Group (CG) that will undergo eight sessions of the traditional model of Relapse Prevention.This study will be conducted at Ambulatory benchmark to smoking cessation treatment in the city of Juiz de Fora (Minas Gerais State- Brazil). Changes will be evaluated on several variables such as cessation of smoking, anxiety, depression, craving, positive and negative affects and will investigate the association of levels of mindfulness with smoking cessation. The data will be assessed at baseline (T0) and four other times: 1 (T1), 3 (T2), 6 (T3) and 12 months (T4) after the initiation of the study, besides being subjected to evaluations of regularly planned maintenance in the protocol of Ministry of Health. For data analysis there will be used Analysis of Variance with Repeated Measures and Longitudinal Logistic Regression, in order to evaluate the effect of two types of intervention on the evolution of comorbidities and abstinence of patients.
Detailed Description
Treatments based on cognitive-behavioral therapy, including relapse prevention, have become standard for smoking cessation in Brazil and many other areas of the world; yet scientific advances are still needed. Mindfulness-based approaches have more recently begun to be assessed and implemented for treatment of addiction. The Mindfulness-Based Relapse Prevention (MBRP) program, which integrates mindfulness practice with cognitive therapy approaches, has shown promising preliminary results in previous studies. The purpose of the current study is to evaluate the effectiveness of the Mindfulness-Based Relapse Prevention program as an adjunct in the standard smoking cessation treatment instituted by the Ministry of Health in Brazil. The study is a randomized clinical trial, with 60 patients diagnosed with nicotine dependence. 60 patients will participate in this study receiving treatment (instituted by the Ministry of Health in Brazil, through the Instituto Nacional do Câncer - INCA'S standard) randomized between two groups: the Experimental Group (EG), which will undergo eight sessions of MBRP; and the Control Group (CG) that will undergo eight sessions of the traditional model of Relapse Prevention (INCA's standard). This will include patients diagnosed with nicotine dependence, who have achieved abstinence. Specific Objetctives: Evaluate the difference in the number of patients who continued abstinence of tobacco; Study the effectiveness MBRP in preventing lapses and relapses; Evaluate the effect of MBRP on the craving and its association with smoking cessation; Evaluate the effect of MBRP in positive and negative affects and its association with smoking cessation; To investigate the association of levels of mindfulness with smoking cessation; Evaluate the effect of MBRP in depressive symptoms, and its possible association with smoking cessation; Evaluate the effect of MBRP in anxiety symptoms, and its possible association with smoking cessation. These will be assessed at baseline (T0) and four other times: 1 (T1), 3 (T2), 6 (T3) and 12 months (T4) after the initiation of the study, besides being subjected to evaluations of regularly planned maintenance in the protocol INCA. Screening instruments: Self Report Questionnaire (SRQ-20); Questionnaire of Smoking Urges (QSU); Hospital Anxiety and Depression Scale (HAD); Center for Epidemiologic Studies Depression Scale (CES-D); Five Facet Mindfulness Questionnaire (FFMQ); Smokerlyser (measuring CO); The Fagerstrom Test for Nicotine Dependence (FTND); Positive and Negative Affect Schedule (PANAS). For data analysis there will be used Analysis of Variance with Repeated Measures and Longitudinal Logistic Regression, in order to evaluate the effect of two types of intervention on the evolution of comorbidities and abstinence of patients. Context: Ambulatory benchmark to smoking cessation treatment in the city of Juiz de Fora, Minas Gerais, Brazil. Participants: • Inclusion: patients with a diagnosis of nicotine dependence;• Exclusion: dependence on other substances, psychiatric comorbidities, pregnant women. •Groups matched for gender, education level and dependence on tobacco level. This initial study will evaluate the feasibility of Mindfulness-Based Relapse Prevention in the context of the Brazilian Public Health system as a supplemental treatment on craving and smoking cessation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tobacco Use Disorder
Keywords
mindfulness, tobacco dependence, relapse prevention

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mindfulness Based Relapse Prevention
Arm Type
Experimental
Arm Description
The Experimental Group (EG) will undergo eight sessions of MBRP after Brazilian Ministry of Health Protocol (BMHP) for Tobacco dependence treatment. MBRP Program: the first three sessions: focus on practicing mindful awareness and integrating mindfulness practices into daily life (body scan, sitting meditation, walking meditation); The next three sessions: emphasize acceptance of present experience and application of mindfulness practices to relapse prevention; The final two sessions: expand to include issues of self-care, support network, and lifestyle balance.
Arm Title
Brazilian Ministry of Health Protocol
Arm Type
Other
Arm Description
The Control Group (CG) is undergo the protocol of the Brazilian Ministry of Health Protocol (BMHP): clinical evaluation, four sessions of cognitive-behavioral approach and Nicotine Replacement Therapy and/or Bupropion as needed, as the Experimental Group. And during the eight sessions of MBRP (EG) both groups (EG and CG) are subjected to eight maintenance sessions of BMHP.
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness Based Relapse Prevention
Intervention Description
The MBRP is an adjuvant treatment for people that have been treated for drug use related problems, and to prevent relapses.
Intervention Type
Other
Intervention Name(s)
Brazilian Ministry of Health Protocol
Intervention Description
The control group will receive maintenance sessions based on the Ministry of Health protocol after the four sessions of cognitive-behavioral approach.
Primary Outcome Measure Information:
Title
Change in the maintenance of abstinence from Cessation of tobacco use through assessment interviews (self-report and CO monitor will be used), and the point prevalence
Description
We will assess the maintenance of abstinence from tobacco use through assessment interviews (self-report and CO monitor will be used), and the point prevalence will be the primary outcome measure.
Time Frame
baseline and twelve months
Secondary Outcome Measure Information:
Title
Change in smoking urges measured with the self report questionnaire: Questionnaire of Smoking Urges (QSU)
Description
This will be measured with the self report questionnaire: Questionnaire of Smoking Urges (QSU)
Time Frame
baseline and twelve months
Title
Change in Symptoms of Anxiety measured through the The Hospital Anxiety and Depression Scale (HAD)
Description
The symptoms of anxiety will be measured through the The Hospital Anxiety and Depression Scale (HAD)
Time Frame
baseline and twelve months
Title
Change in Symptoms of Depression measured through the Centre for Epidemiologic Studies Depression Scale (CES-D)
Description
The symptoms of depression will be measured through the Centre for Epidemiologic Studies Depression Scale (CES-D)
Time Frame
baseline and twelve months
Title
change in Self report Mindfulness level measured with the self report questionnaire Five Facet Mindfulness Questionnaire (FFMQ)
Description
This will be measured with the self report questionnaire Five Facet Mindfulness Questionnaire (FFMQ)
Time Frame
baseline and twelve months
Title
Maintenance of Abstinence measured by a Bedfont Micro Smokerlyser - CO monitor
Description
Abstinence will be measured by a Bedfont Micro Smokerlyser - CO monitor, to support self-reports of smoking cessation.
Time Frame
baseline and twelve months.
Title
Tobacco Dependence measured through The Fagerstrom Test for Nicotine Dependence (FTND)
Description
This will be measured through The Fagerstrom Test for Nicotine Dependence (FTND)
Time Frame
baseline and twelve months
Title
Change in Positive and Negative Affects measured through Positive and Negative Affect Scale (PANAS)
Description
This will be measured through Positive and Negative Affect Scale (PANAS).
Time Frame
baseline and twelve months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with a diagnosis of nicotine dependence; Patients currently smoking at least 10 cigarettes a day; Do not have any current major psychological disorders; Patients undergoing treatment for the first time Be willing to attend treatment and follow-up sessions, complete surveys and expired CO tests; Do not exhibit dependence on other drugs. Exclusion Criteria: Dependence on other substances; Psychiatric comorbidities; Pregnant women.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ana Regina Noto, Doctor
Organizational Affiliation
Federal University of São Paulo
Official's Role
Study Director
Facility Information:
Facility Name
Drug Dependency Unit of the Federal University of São Paulo
City
São Paulo
ZIP/Postal Code
04024-003
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
35420700
Citation
Jackson S, Brown J, Norris E, Livingstone-Banks J, Hayes E, Lindson N. Mindfulness for smoking cessation. Cochrane Database Syst Rev. 2022 Apr 14;4(4):CD013696. doi: 10.1002/14651858.CD013696.pub2.
Results Reference
derived
PubMed Identifier
32222767
Citation
Weiss de Souza IC, Kozasa EH, Bowen S, Richter KP, Sartes LMA, Colugnati FAB, Noto AR. Effectiveness of Mindfulness-Based Relapse Prevention Program as an Adjunct to the Standard Treatment for Smoking: A Pragmatic Design Pilot Study. Nicotine Tob Res. 2020 Aug 24;22(9):1605-1613. doi: 10.1093/ntr/ntaa057.
Results Reference
derived

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Effectiveness of Mindfulness Based Relapse Prevention for Tobacco Dependents

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