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effect of non pharmacological (5A)intervention in smokeless tobacco userS

Efficacy of 5A intervention on smokeless tobacco cessation on dental outpatients: A randomized controlled study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/060208
Enrollment
60
Registered
2023-11-23
Start date
Unknown
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

Health Condition 1: F172- Nicotine dependence

Interventions

Intervention1: 5A Intervention: Step 1: Ask the patient about his smoking status Step 2: ADVISE - Provide clear, strong advice to quit with personalized messages about the impact of smoking and quitt

Sponsors

AIIMS New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 18 to 60 years. Male Current (last 1 month) users of Smokeless tobacco and those who report daily use of smokeless tobacco in the past 1 year. Diagnosed with nicotine dependence as per ICD-11 criteria. Currently receiving dental treatment in CDER. Patients who have to follow up for dental treatment at CDER (center for dental education and research). Willing to participate in telephonic follow up at 4 weeks and in-person follow up at 12 weeks.

Exclusion criteria

Exclusion criteria: History of co-morbid psychiatric illnesses (as assessed by WHO self-report questionnaire) Patient unable to chew tobacco and or smoke due to oral lesions Smoked tobacco in the past 1 year WHO- ASSIST scores more than or equal to 10 for alcohol or more or equal to 4 for other substances except tobacco. Has ever received tobacco cessation intervention (except simple advice from a health care professional) in the past Presence of any terminal condition for e.g. malignancy Unwilling to give informed consent for the study Unable to understand and communicate with the interviewer

Design outcomes

Primary

MeasureTime frame
7 day point prevalence of abstinence Ascertained by screening for the salivary cotinine. Reduction in smokeless tobacco use as measured by the number of chews per day Timepoint: 4 weeks and 12 weeks

Secondary

MeasureTime frame
Change in the stage of motivation Number of quit attempts lasting more than 24 hours Timepoint: 4 weeks,12 weeks

Countries

India

Contacts

Public ContactNew fight Seth

AIIMS, New Delhi

shalin.achra@gmail.com9810114818

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026