Health impacts related to smoking
Conditions
Interventions
Group 1:Assess for readiness and identify barriers and facilitators +Alter incentive/allowance structures
Group 2:Assess for readiness and identify barriers and facilitators + Identify and prepare champions + Alter incentive/allowance structures
Group 3:Assess for readiness and identify barriers and facilitators + Identify and prepare champions + Conduct educational meetings
Group 4:Assess for readiness and identify barriers and facilitators
Group 5:Assess for readiness and identify barriers and facilitators + Identify and prepare champions + Alter incentive/allowance structures +Conduct education
Group 6:Assess for readiness and identify barriers and facilitators +Alter incentive/allowance structures +Conduct educational meetings
Group 7:Assess for readiness and identify barriers and facilitators +Conduct educational meetings
Group 8:Assess for readiness and identify barriers and facilitators + Identify and prepare champions
Sponsors
Southern Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Practicing physicians or assistant practicing physicians from community health service centers/stations and township health centers; 2. Certified village doctors in village clinics/health rooms (referring to doctors who can practice medicine in village-level medical institutions even without a medical license) and health workers in village clinics/health rooms (referring to uncertified village doctors who need to work under the supervision of certified village doctors); 3. All medical workers holding physician qualification certificates in primary and secondary hospitals as well as maternal and child health care hospitals. In addition, the research subjects must also meet the following inclusion criteria: having engaged in clinical work for at least six months; Provide outpatient and primary medical services.
Exclusion criteria
Exclusion criteria: 1.Have received relevant training on smoking cessation or participated in similar trials; 2. Absence from work for one month or more due to certain reasons; 3. Non-regular employees, such as temporary workers or rotational staff; 4. Currently participating in other studies related to the specific implementation techniques tested in this trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinician-asked·smoking status;Clinician-advised·to·quit; | — |
Secondary
| Measure | Time frame |
|---|---|
| Sustainability of BISC delivery;Clinician- Provided a referral;Cost of BISC Delivery;Daily cigarette consumption;Acceptance of BISC Delivery;Patient satisfaction with the BISC provided by the clinician;Sustainment of BISC delivery;7-day point abstinence status;Clinician-discussed the hams and benefits of quitting;Applicability of BISC Delivery;Clinician-asked about number of cigarettes smoked;Coverage of BISC Delivery; | — |
Countries
China
Contacts
Public ContactJiangyun Chen
Southern Medical University
Outcome results
None listed