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CTRI Number  CTRI/2025/02/080243 [Registered on: 10/02/2025] Trial Registered Prospectively
Last Modified On: 23/01/2025
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Behavioral 
Study Design  Randomized, Parallel Group, Active Controlled Trial 
Public Title of Study   A clinical trial to study the effects of two methods, a behavioral support intervention and only brief advice for persons with severe mental illness and tobacco use disorder 
Scientific Title of Study   The SCIMITAR South Asia programme to address tobacco related multiple long term conditions in Severe Mental Illness 
Trial Acronym  SCIMITAR-SA 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Prof Pratima Murthy 
Designation  Senior Professor of Psychiatry and Director, NIMHANS 
Affiliation  NIMHANS, Bengaluru 
Address  Department of Psychiatry, NIMHANS Hosur Road Bengaluru

Bangalore
KARNATAKA
560029
India 
Phone  08026995001  
Fax    
Email  pratimamurthy@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Prof Pratima Murthy 
Designation  Senior Professor of Psychiatry and Director, NIMHANS 
Affiliation  NIMHANS, Bengaluru 
Address  Department of Psychiatry, NIMHANS Hosur Road Bengaluru

Bangalore
KARNATAKA
560029
India 
Phone  08026995001  
Fax    
Email  pratimamurthy@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Prof Pratima Murthy 
Designation  Senior Professor of Psychiatry and Director, NIMHANS 
Affiliation  NIMHANS, Bengaluru 
Address  Department of Psychiatry, NIMHANS Hosur Road Bengaluru

Bangalore
KARNATAKA
560029
India 
Phone  08026995001  
Fax    
Email  pratimamurthy@gmail.com  
 
Source of Monetary or Material Support  
National Institute for Health and Care Research, Grange House, 15 Church Street, Twickenham, Pin: TW1 3NL United Kingdom through the Department of Health Sciences, Seebohm Rowntree Building, University of York, Heslington, York, Pin: YO10 5DD, United Kingdom  
 
Primary Sponsor  
Name  Prof Pratima Murthy 
Address  Senior Professor of Psychiatry and Director, NIMHANS, Hosur Road, Bengaluru 560029 
Type of Sponsor  Other [SELF] 
 
Details of Secondary Sponsor  
Name  Address 
Dr Krishna Prasad M  Department of Psychiatry, NIMHANS, Hosur Road, Bengaluru  
 
Countries of Recruitment     Bangladesh
India
Pakistan  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Pratima Murthy  NIMHANS, Bengaluru  Department of Psychiatry, Hosur Road, Bengaluru 560029
Bangalore
KARNATAKA 
08026995001

pratimamurthy@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Ethics Committee (Behavioural Sciences Division), NIMHANS, Bengaluru  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: F317||Bipolar disorder, currently in remission, (2) ICD-10 Condition: F333||Major depressive disorder, recurrent, severe with psychotic symptoms, (3) ICD-10 Condition: F172||Nicotine dependence, (4) ICD-10 Condition: F200||Paranoid schizophrenia, (5) ICD-10 Condition: F250||Schizoaffective disorder, bipolartype,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  Brief advice  It will include a brief conversation on the harmful effects of tobacco and advice to stop using tobacco, consistent with the 3A protocol (Ask about tobacco use, advise patient on personal health benefits, and act on their response). BA will be delivered by trained healthcare staff in a one off, 5 minute interaction. Participants will receive an information leaflet with written advice to take home. 
Intervention  SCIMITAR SA Intervention  The behavioural support offered in SCIMITAR SA will comprise up to 15 one-to-one counselling sessions with a trained healthcare worker, over three months. Each session will last between 15 to 40 minutes, delivered either face to face or remotely using telephone or video calling (via platforms such as WhatsApp and or Zoom). 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  60.00 Year(s)
Gender  Both 
Details  Adults (more than or equal to 18 years) receiving outpatient care at the study site
Confirmed diagnosis of one or more SMI (schizophrenia, schizoaffective disorder, bipolar affective disorder,
psychosis, severe depression with psychosis) by healthcare staff self reported current users of smoking (including
cigarettes, bidis, waterpipe) and/or smokeless forms of tobacco (such as betel-quid, naswar, gutkha, zarda) for at least
six months.
Mentally stable at the time of recruitment and able to provide informed consent
Willing to quit tobacco use and able to attend up to 10 face to face or telephone based counselling sessions with trained
healthcare staff. 
 
ExclusionCriteria 
Details  We will restrict trial participation to one member per household (to avoid contamination) and exclude those with comorbid drug and/or alcohol use (ascertained by the mental health
specialist), as these individuals would require more specific intervention. We will also exclude those who are currently under
treatment for tobacco dependence. 
 
Method of Generating Random Sequence   Stratified block randomization 
Method of Concealment   Centralized 
Blinding/Masking   Outcome Assessor Blinded 
Primary Outcome  
Outcome  TimePoints 
The primary trial outcome is biochemically verified, continuous abstinence from all tobacco products at six months
post-randomisation. 
Data will be collected at baseline, three and six months 
 
Secondary Outcome  
Outcome  TimePoints 
Secondary outcomes include self-reported abstinence at 12 months, and changes in physical health, mental health, and quality of life at six and 12 months.  Data will be collected at baseline, three, six and twelve months 
 
Target Sample Size   Total Sample Size="1450"
Sample Size from India="290" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   Phase 3 
Date of First Enrollment (India)   01/08/2026 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  01/08/2026 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="4"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)   Not Yet Recruiting 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  
Research Question: Can we treat tobacco dependence among individuals in South Asia with the most severe forms of mental illnesses, in order to prevent the onset and progression of tobacco-related multiple-long term conditions (MLTCs)?
Background: Tobacco dependence is a chronic relapsing condition and a precursor to several MLTCs. In people with severe mental illness (SMI), tobacco use exacerbates health inequalities and reduces life expectancy. Efforts for tobacco cessation are
critical in addressing MLTCs in SMI populations, particularly in low-resource settings like South Asia, which have a high burden of tobacco-related morbidity and mortality.
Aims and objectives: We have previously adapted a behavioural intervention for smoking cessation in people with SMI (SCIMITAR UK) for India and Pakistan. We will now:
1. Further adapt the intervention (to be called SCIMITAR-South Asia[SA]) for all forms of tobacco users (including smokeless tobacco) and for SMI populations in Bangladesh.
2. Design contextually tailored implementation strategies to deliver SCIMITAR-SA in mental health services in Bangladesh, India and Pakistan.
3. Test the feasibility, acceptability and clinical effectiveness of SCIMITAR-SA, delivered face-to-face or remotely to individuals with SMI in mental health settings
4. Establish the cost-effectiveness of SCIMITAR-SA, understand the economic and distributional health gains of tobacco cessation in SMI and estimate the costs of scaling-up of tobacco cessation services across mental health facilities
5. Systematically assess the contextual barriers and drivers to delivering SCIMITAR-SA in order to guide further adaptations and tailoring of implementation strategies.
We will also build capacity in tobacco cessation and applied research in mental and physical multimorbidity.
Methods and timelines: In year 1, we will review evaluations of existing behavioural interventions for tobacco cessation in South Asia, hold consensus workshops with experts for adapting intervention content and delivery, and produce the SCIMITAR-SA
intervention package, logic model and fidelity index. Stakeholder workshops will identify implementation strategies for SCIMITAR-SA.
In year 2, we will conduct a pilot trial of SCIMITAR-SA compared to brief advice (n=100, with three and six months follow-ups) in Bangladesh, India and Pakistan to evaluate recruitment and retention, primary outcome data, and the feasibility and acceptability of SCIMITAR-SA.
In years 3-4, we will conduct a fully powered trial of SCIMITAR-SA with an embedded process evaluation, recruiting and randomising 1450 participants in Bangladesh, India and Pakistan to SCIMITAR-SA or brief advice. We will assess tobacco
abstinence at three, six (primary outcome) and 12 months. Qualitative methods will explore barriers and drivers to implementation, and identify an evidence-informed list of strategies to strengthen and scale-up implementation. An economic
evaluation will identify the cost-effectiveness of SCIMITAR-SA and its distributional health impacts from a health systems perspective. Throughout the programme, we will build research and clinical capacity and pathways to impact.
Anticipated Impact and Dissemination: SCIMITAR -SA has promising prospects of clinical and cost-effectiveness; we will ensure its sustainability through clinical capacity building and identifying appropriate methods for its wider implementation in South Asia. Through stakeholder engagement, we will ensure knowledge translation into practice and policy. We will enhance capacity in South Asia for applied health research
 
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