Intervention study to find the Nicotine dependence among Smokeless Tobacco users

Effectiveness of Behavioural Intervention on level of Nicotine dependence among Smokeless Tobacco users - NIL/NOT APPLICABLE

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/01/061447

Enrollment

Registered

2024-01-15

Start date

Unknown

Completion date

Unknown

Last updated

2024-09-16

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

Conditions

None listed

Interventions

Intervention1: Behavioural Intervention: Research Process: This study includes Experimental group and the control group, The experimental group will be subjected to Behavioural Intervention for a peri

Eligibility

Inclusion criteria

Inclusion criteria: It includes 1.Participants who use smokeless Tobacco 2. Participants who are in the age group from 18 to 40 years 3. Participants who are willing to take part in the study 4. Participants who knows to read and write Kannada 5. Participants who are available at the time of Intervention

Exclusion criteria

Exclusion criteria: It includes 1. Participants who have medical illness 2. Participants who have any psychiatric disorders 3.Participants who are taking treatment for any other disorders 4.Participants who are available at the time of Intervention 5.Participants who those who have not come for Intervention after three weeks

Design outcomes

Primary

Measure	Time frame
Primary outcomes To evaluate the effectiveness of Behavioural Intervention to reduce the level of Nicotine dependence among Smokeless Tobacco users Timepoint: The experimental group will be subjected to Behavioural Intervention for a period of 3 weeks as one session per week. Baseline outcome measures & nicotine dependence using FTND before Intervention for all the participants. Post-test will be taken up after the 3rd Week by follow up & assessing Nicotine dependence. The effectiveness will be assessed at 3rd & 6th Month through FTND	—

Measure

Time frame

Primary outcomes To evaluate the effectiveness of Behavioural Intervention to reduce the level of Nicotine dependence among Smokeless Tobacco users Timepoint: The experimental group will be subjected to Behavioural Intervention for a period of 3 weeks as one session per week. Baseline outcome measures & nicotine dependence using FTND before Intervention for all the participants. Post-test will be taken up after the 3rd Week by follow up & assessing Nicotine dependence. The effectiveness will be assessed at 3rd & 6th Month through FTND

—

Secondary

Measure	Time frame
To evaluate the Nicotine dependance among Smokeless tobacco users To find the association between the smokeless tobacco users with a selected sociodemographic profile aware about the ill effects of SLT Consumption & attempt to quit.Timepoint: 3 weeks	—

Countries

India

Contacts

Public ContactDr Nalini M

Nitte Usha Institute of Nursing Sciences (NUINS)

nalini@nitte.edu.in8095679510

Outcome results