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Study of adherence to smoking cessation treatment in two groups of patients, one with treatment determined by physician and the other with a patient participation in decisions .

Study of adherence to smoking cessation treatment in two groups of patients, one with treatment determined by physician and the other with a shared decision.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3nqdw5
Enrollment
Unknown
Registered
2016-10-11
Start date
2015-10-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Smoking

Interventions

Intervention group consist of 50 participants. Before starting treatment, intervention group participants will receive an educational session for 1 hour and 30 minutes using visual audio material and
Behavioural

Sponsors

Faculdade de Medicina da Universidad Federal da Bahia
Lead Sponsor
Programa de Pos-graduação em Medícina e Saude
Collaborator
Coordenação de aperfeiçoamento de pessoal de nivel superior
Collaborator

Eligibility

Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Having diagnosis of dependence Tobacco according to the DSM-5 V and the "Smoking Treatment Guide" by INCA; Want to quit smoking (the patient should be in the contemplation or action stage )

Exclusion criteria

Exclusion criteria: Patients with a mental disorder that compromises the decision making about treatment; patients who have criteria for abuse and / or dependence on other drugs that compromise the decision-making about treatment; patients who in the moment are in treatment for smoking (Patients transferred).

Design outcomes

Primary

MeasureTime frame
Absolute risk reduction (ARR) of nonadherent patients rate to cognitive behavioral therapy (CBT) using shared decision (intervention group) compared to the control group. They will be considered adherent patient at patients who participated in four sessions during four initial weeks (all sessions during the first 4 weeks) and at the end of 12 weeks more than 8 session (over 70% of sessions). With RAR, we will calculate the number needed to treat (NNT) to have one adherent patient to CBT. Absolute risk reduction (ARR) of cognitive behavioral therapy (CBT) dropout using shared decision (intervention group) compared to control group, will be declared as dropout if patients participate under 6 sessions (50% of CBT) in end of treatment. With RAR, we will calculate the number needed to treat (NNT) to have one patient that not dropout therapy. Absolute risk reduction (ARR) nonadherent patients to drug therapy, verified by Moriski Green Portuguese version scale, participants with score of 0 will be considered as adherents and the different values of 0 will be considered nonadherents. With RAR, we will calculate the number needed to treat (NNT) to have one adherent patient to drug therapy

Secondary

MeasureTime frame
Means difference self reported number of cigarettes smoked at the end of treatment at least less than 50% of the initial consumption. Number needed to treat NNT to have a abstinent patient using shared decision-employment (intervention group) compared to the control group, patients will be considered abstinent with self-reported quit smoking during cognitive behavioral therapy. concordance rate between the type of treatment chosen in both groups front National Cancer Institute of Brazil protocol; values equals 0 = no agreement, 0-.19 = poor agreement, from .20 to .39 = poor agreement .40 to .59 moderate agreement, 0.60 to 0.79 substantial agreement, 0, 80-1 = perfect agreement.

Countries

Brazil

Contacts

Public ContactJuan Aguilar Ticona

Programa de Pos-graduação em Medícina e Saude

pkjpablo@gmail.com+55 (71) 984318399

Outcome results

None listed

Source: REBEC (via WHO ICTRP)