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Effectiveness of four de-addiction methods among patients with addiction to tobacco and alcohol.

Effectiveness of four de-addiction methods among patients admitted with addiction to tobacco and alcohol in two de-addiction centres of Madhya Pradesh â?? An interventional study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/08/035916
Enrollment
169
Registered
2021-08-25
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: null- Patients with moderate to high level of addiction to tobacco and alcohol admitted to two deaddiction ceters in Madhya Pradesh.

Interventions

Intervention1: Two psychological intervention techniques using motivational intervention as control Two pharmacological interventions using tobacco in tapering dose as control.: Study had six interven

Sponsors

Self Financed
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a. Who gave the written informed consent to participate in the study b. With addiction to tobacco and alcohol c. Having a moderate to high level of dependence (Dependence score of more than five) for smoking/smokeless tobacco/ combinations as per Fagerstrom scale d. Who agreed to stay as inpatients in the de-addiction centers for the duration of 25-30 days to receive the assigned intervention.

Exclusion criteria

Exclusion criteria: Study participants a. With addiction only to alcohol and / or other substances (drug addicts) without addiction to tobacco in any form. b. Undergoing any other psychopharmacological interventions during the study period c. With known drug hypersensitivity, epilepsy, pregnancy, lactation, any serious or unstable cardiac, renal, hepatic, hypertensive, pulmonary, endocrine or neurological disorder as these participants were not recruited in to the de-addiction centres till their condition was medically stable.

Design outcomes

Primary

MeasureTime frame
Complete abstinence and partial reduction.Timepoint: one at the time of discharge and one after one month following discharge

Secondary

MeasureTime frame
Change in KAPTimepoint: Baseline, at the time of dischrage and one month after discharge.

Countries

India

Contacts

Public ContactDr Rahul Ganavadiya

JSS Dental College and Hospital

drchandrubr@yahoo.com8197705773

Outcome results

None listed

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