A survey to assess how user-friendly is the mobile phone app created to help people quit tobacco

Not Applicable

Completed

Conditions: Health Condition 1: Z789- Other specified health status

Registration Number: CTRI/2023/08/056661

Lead Sponsor: FTB COLAB PRIVATE LIMITED

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Completed

Sex: Not specified

Target Recruitment: 100

Inclusion Criteria

Patients meeting following inclusion criteria will be eligible for participation in the study:

Age

1. Male and female subjects in the age group = 18 years.

usage.

5. Subjects who are educated and who are able to read, type and understand instructions in English language given in cab read and understand instructions and information given via poster, videos, chatbot and other sections in smartphone application, and be able to give their feedback on the application.

6. Subject having a smartphone Android - OS Version 9.0 or above, or iOS – OS Version 11.0 or above.

7. Subject/ Legally Acceptable Representative (LAR) of the subject willing to sign the informed consent form

8. Interested in learning, knowing and following tips to quit tobacco smoking and/or smokeless tobacco use. 9. Not participating in any other tobacco cessation interventions study

Exclusion Criteria

the give inclusion criteria number 2 and 3.

2. Subject had cognitive impairment or a substance use disorder (e.g., alcohol, cannabis, and opioid)

3. Subject is a pregnant woman/lactating mother.

4. Individuals with mental health complications that have been managed for less than 6-months

5. Hearing and/or vision disabilities in receiving intervention assessment such as videos or podcasts

6. Inability to read, type, speak and understand instructions and concepts in English language.

7. Using any other tobacco cessation interventions (including apps or our other intervention studies)

8. Subject who are not willing to spend or follow the protocol procedure.

9. Subject who is illiterate.

Study & Design

Study Type: Observational

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To evaluate the acceptability & perceived usability & appeal, assessed during a single interaction, of the smartphone/mobile application specifically designed to reduce the prevalence of tobacco consumption.Timepoint: There is only one visit.

Secondary Outcome Measures