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Effectiveness of Behavioral Counselling with Nicotine Gum versus Behavioral Counselling alone for quitting tobacco usage among patients at a Tobacco Cessation Clinic in Delhi.

Effectiveness of Behavioral Counselling with Nicotine Gum versus Behavioral Counselling among patients visiting Tobacco Cessation Clinic in Delhi: a Randomized Clinical Trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/03/012867
Enrollment
120
Registered
2018-03-26
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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 Health Condition 2: null- tobacco users

Interventions

Intervention1: 1.Behavioral counselling, Nicotine Replacement Therapy: NRT Dosage 2mg and 4 mg depending upon the patients tobacco usage. Route of administration - Oral Total duration- 12 weeks. S

Sponsors

Dr Neetu
Lead Sponsor
Department of Public Health DentistryMaulana Azad Institute of Dental Sciences
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. A daily smoker/smokeless/mixed form of tobacco user. 2. Patients reporting to the TCC and found to be tobacco users. 3. Those who will give informed consent and are able to read and write local language. 4. Patients who have medium nicotine dependence score as per Fagerstrom scale for smoking and Modified Fagerstrom scale for smokeless tobacco.

Exclusion criteria

Exclusion criteria: 1. Patient not willing to participate, uncooperative and are edentulous/having TMJ problems/chewing difficulties and any dental emergencies. 2. Patients who are medically compromised and have diseases which are contraindications for NRT use. 3. Patients/Tobacco users who have not participated in any trial or intervention related to tobacco cessation. 4. Patients who report past usage of NRT (with or without prescription) and have experienced side effects.

Design outcomes

Primary

MeasureTime frame
Effectiveness of two methods on the basis of quit status: quit, reduction and status quo.Timepoint: 1st week,2nd week, 3rd week, 3rd month, 6th month

Secondary

MeasureTime frame
Sociodemographic and other related factors, Nicotine dependence, Oral health status and Tobacco related Health Literacy.Timepoint: 1st week,2nd week, 3rd week, 3rd month, 6th month

Countries

India

Contacts

Public ContactNeetu

Maulana Azad Institute of Dental Sciences

vikrantmohanty@gmail.com9654700983

Outcome results

None listed

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