Development of a Personalized Tobacco Cessation Intervention Package (PTCIP) for Persons with Schizophrenia in India.

Stage-based content validity intervention nonpharmacological schizophrenia tobacco cessation

Journal

Indian journal of psychological medicine
ISSN: 0253-7176
Titre abrégé: Indian J Psychol Med
Pays: United States
ID NLM: 7910727

Informations de publication

Date de publication:
Mar 2023
Historique:
entrez: 17 3 2023
pubmed: 18 3 2023
medline: 18 3 2023
Statut: ppublish

Résumé

Among persons with schizophrenia (PwS), tobacco use is higher in comparison to the general population, contributing to greater morbidity and mortality. Pharmacological interventions combined with psychosocial interventions are effective in tobacco cessation. While the effectiveness of extant psychosocial interventions-when used in isolation-seems limited, developing better combinations of interventions could help treatment providers deliver tobacco cessation services to PwS at different stages of motivation to quit. We aimed to develop a personalized tobacco cessation intervention package (PTCIP) for PwS. The stage-based intervention package was developed through a systematic review of interventions for tobacco cessation, the authors' clinical experience, and expert validation. The components of the intervention package, developed for PwS visiting the outpatient psychiatric department, were retained, removed, or added based on the content validity ratio (CVR). The final components included brief advice, principles of motivational interviewing, psychoeducation, decisional balance matrix, positive reinforcement, offering various treatment options, personalized feedback using a smoking-risk calculator, and prediction of cardiovascular risk using the WHO package of essential noncommunicable disease (PEN). The delivery of the intervention package was refined based on pilot testing in eight participants. The tailored package was designed to be delivered by a mental health professional as a single comprehensive 40 min to 45 min face-to-face session, integrated with routine follow-up visits, followed by two telephonic conversations in the second and third week of the initial session. The package needs to be tested in a randomized controlled trial for its effectiveness.

Sections du résumé

Background UNASSIGNED
Among persons with schizophrenia (PwS), tobacco use is higher in comparison to the general population, contributing to greater morbidity and mortality. Pharmacological interventions combined with psychosocial interventions are effective in tobacco cessation. While the effectiveness of extant psychosocial interventions-when used in isolation-seems limited, developing better combinations of interventions could help treatment providers deliver tobacco cessation services to PwS at different stages of motivation to quit. We aimed to develop a personalized tobacco cessation intervention package (PTCIP) for PwS.
Methods UNASSIGNED
The stage-based intervention package was developed through a systematic review of interventions for tobacco cessation, the authors' clinical experience, and expert validation. The components of the intervention package, developed for PwS visiting the outpatient psychiatric department, were retained, removed, or added based on the content validity ratio (CVR).
Results UNASSIGNED
The final components included brief advice, principles of motivational interviewing, psychoeducation, decisional balance matrix, positive reinforcement, offering various treatment options, personalized feedback using a smoking-risk calculator, and prediction of cardiovascular risk using the WHO package of essential noncommunicable disease (PEN). The delivery of the intervention package was refined based on pilot testing in eight participants.
Conclusion UNASSIGNED
The tailored package was designed to be delivered by a mental health professional as a single comprehensive 40 min to 45 min face-to-face session, integrated with routine follow-up visits, followed by two telephonic conversations in the second and third week of the initial session. The package needs to be tested in a randomized controlled trial for its effectiveness.

Identifiants

pubmed: 36925498
doi: 10.1177/02537176221105581
pii: 10.1177_02537176221105581
pmc: PMC10011849
doi:

Types de publication

Journal Article

Langues

eng

Pagination

132-138

Informations de copyright

© 2022 The Author(s).

Déclaration de conflit d'intérêts

The authors declared no potential conflicts of interest concerning this article’s research, authorship, and publication.

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Auteurs

Banu Manickam Rajalu (BM)

Dept. of Psychiatry, National Institute of Mental Health and Neurosciences, Bangalore, Karnataka, India.

Deepak Jayarajan (D)

Dept. of Psychiatry, National Institute of Mental Health and Neurosciences, Bangalore, Karnataka, India.

Krishna Prasad Muliyala (KP)

Dept. of Psychiatry, National Institute of Mental Health and Neurosciences, Bangalore, Karnataka, India.

Priyamvada Sharma (P)

Dept. of Clinical Pharmacology and Neurotoxicology, National Institute of Mental Health and Neurosciences, Bangalore, Karnataka, India.

Sailaxmi Gandhi (S)

Dept. of Nursing, National Institute of Mental Health and Neurosciences, Bangalore, Karnataka, India.

Prabhat Kumar Chand (PK)

Dept. of Psychiatry, National Institute of Mental Health and Neurosciences, Bangalore, Karnataka, India.

Classifications MeSH