| 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
|
|
|
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 |