Intervention for Smoking Cessation in Pre-Surgical Patients.
NCT05961813 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 232
Last updated 2023-07-27
Summary
The goal of this clinical trial is to assess efficacy of an intensive pre-surgical intervention to quit smoking in smoking patients who will be operated on implant orthopedic surgery or general and urological surgery. The main question\[s\] it aims to answer are:
* Evaluate the efficacy of intensive pre surgical intervention to quit smoking compared to a brief intervention
* Evaluate the implementation of this protocol.
Participants will be randomized to 2 intervention groups (patients programmed for protesic implant orthopedic surgery in the first group, and general and urological surgery) and 2 control groups (stratified in the same manner as the intervention groups), and will be monitored through telematic check ups via phone calls.
Conditions
- Smoking
- Smoking Cessation
- Surgical Procedure, Unspecified
Interventions
- BEHAVIORAL
-
Intensive intervention for smoking cessation
Patients will be given a brochure and presentation on smoking cessation and will complete 6 visits (2 before surgical intervention, 4 visits within the following 12 months), as well as follow up phone calls for progressi monitorization.
- BEHAVIORAL
-
Brief intervention for smoking cessation
Patients will be given a brochure and presentation on smoking cessation 4 weeks before surgery, as well as follow up phone calls for progressi monitorization.
Sponsors & Collaborators
-
Hospital Universitari Vall d'Hebron Research Institute
lead OTHER
Principal Investigators
-
Eva Gavilán Castillo, RN; MSN · Vall d'Hebron Hospital
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-05-20
- Primary Completion
- 2025-06-01
- Completion
- 2026-01-01
Countries
- Spain
Study Locations
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