Ignite Creation Date:
2024-10-26 @ 3:42 PM
Last Modification Date:
2024-10-26 @ 3:42 PM
Study NCT ID:
NCT06632756
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-10-07
Brief Title:
Positive Psychology for Smoking Cessation
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Positive Psychotherapy for Smoking Cessation A Focus on Strengths to Improve Self-efficacy and Enable Successful Quitting Strategies
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study will examine how Positive Psychotherapy PPT may help people interested in quitting smoking quit
Detailed Description:
This project aims to adapt the Positive Psychotherapy PPT practice for smoking cessation in adults with severe mental illness SMI testing its usability feasibility and acceptability in a mixed-methods feasibility pilot study First we plan to perform qualitative interviews to obtain usability and acceptability input on our adapted PPT manual from 4-5 Peer Providers Then in partnership with The Mental Health Center of Greater Manchester MHCGM we will recruit a group of 6-8 adult smokers with SMI who want to quit smoking in the next month and are willing to use nicotine replacement therapy NRT We will test our 16-week PPT adaptation Positive Recovery for Smoking and assess progress on cessation through interviewer-administered quantitative assessments at baseline 8 and 16 weeks We will also collect data on self-reported cigarettes per day CPD and carbon monoxide CO prior to each group treatment session Informed by the weekly group check-in of cessation progress quitting status we will conduct qualitative interviews at 16 weeks to obtain a more nuanced description of the uptake of the intervention successful quitting strategies and barriers to cessation with this new method We will then adapt our manual and materials based on the feedback from the first group and recruit another group of 6-8 participants to receive the refined intervention and protocol The result of this feasibility pilot will provide data on the adapted PPTs feasibility and acceptability alongside a deep description of strategies used and why and how the treatment was perceived as useful or not to the enrolled participants
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None