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QuitSure Smoking Cessation Mobile App Effectiveness Trial.

Randomized Controlled Trial for Smartphone-based Smoking Cessation Program – QuitSure

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/05/052863
Enrollment
500
Registered
2023-05-18
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

None listed

Interventions

Intervention1: QuitSure Mobile Application : For Intervention group Name: QuitSure Mobile App usage for 7 days Duration: 7 days Mode of administration: Digital media/ phone/online/ Condition/Disease T

Sponsors

IIT BOMBAY
Lead Sponsor
MS Rapidkart Online Private Limited
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: (i) Smokes at least 1 cigarette per day on average and has smoked at least 100 cigarettes till date. (ii) Agrees to participate in a smoking cessation treatment program with written informed consent (iii) Must be an adult over 18 years of age (iv) Are, at minimum, proficient in the written and spoken English Language (v) Must be an everyday smoker: Should currently smoke 01 (one) or more cigarettes per day on an average (indicating sufficient dependence on nicotine) and have smoked at least 100 cigarettes (indicating sufficient exposure of the body to nicotine) on a regular basis. (vi) Have daily access to an Android or iOS smartphone. (vii) Salivary cotinine test positive on the first visit. (viii) Can use a smartphone without difficulty. (ix) Rinsed mouth thoroughly with water 10 minutes before sample is collected. (x) Inclusion criteria for controls: Age and gender matched controls.

Exclusion criteria

Exclusion criteria: (i) Has already quit smoking and is currently not smoking. (ii) If a doctor has advised the participant not to quit cold-turkey. (iii) History of severe mental illness/ psychiatric illness or under current treatment for psychiatric illness such as schizophrenia or other primary psychotic disorders, BPAD, catatonia, OCD, dissociative disorders, eating disorders, personality disorders. (iv) Unable to attend follow-up clinic visits during the study period. (v) Started taking a smoking cessation medication within 1 year before the registration. (vi) Planned to use any smoking cessation aids and/or to participate in any kind of smoking-cessation activities (not limited to smoking cessation therapy) outside of the trial. (vii) Consumed a major meal within 60 minutes before the test. (viii) Consumed alcohol within 12 hours before the test. (ix) Consumed foods like broccoli, cabbage, mustard, garlic, radishes, almonds and horseradish within 12 hours. (x) Persons working with metal, the related occupations include electroplaters and people who refine precious metals. (xi) Tobacco workers.

Design outcomes

Primary

MeasureTime frame
cessation of smoking.Timepoint: after 4 weeks and 24 weeks.

Secondary

MeasureTime frame
Any form of nicotine and / or smokeless tobacco consumption.Timepoint: 06 months and 12 months.

Countries

India

Contacts

Public ContactDr Aniket Kundu

IIT BOMBAY

drarnab.edu@gmail.com9168219911

Outcome results

None listed

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