Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04271371
Other study ID # 254028
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 8, 2019
Est. completion date December 30, 2023

Study information

Verified date February 2024
Source University of Nottingham
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Prisoners experience huge health inequalities, and their exceptionally high smoking prevalence (five times the national average) contributes significantly to their high mortality. Since the introduction of smoke-free polices across Her Majesty's Prison and Probation Service (HMPPS) in England and Wales, prisoners are now obliged to abstain from smoking while held in prison. This represents a unique opportunity to promote lifelong cessation in this highly disadvantaged and marginalised group. However, evidence suggests most prisoners intend to resume smoking as soon as possible after release. A systematic review of prison smoke-free polices worldwide concluded that there was a need for new research to identify effective strategies to reduce relapse in these individuals.


Description:

The primary objective of this study will be to develop and pilot test the feasibility and acceptability of an intervention to help prevent prisoners relapse to smoking after release. The study will work in accordance with the Medical Research Council (MRC) framework for developing and evaluating complex interventions. The Preventing Relapse tO Smoking among PrisonErs after Release (PROSPER) study consists of three key Phases: 1. Document the support provided to manage nicotine addiction during imprisonment and in the periods immediately before and after release; establish the extent to which prisoners intentionally resume or unintentionally relapse to smoking after release; and obtain views on how relapse might be prevented. 2. Drawing on current literature and findings from Phase 1, develop and design an prototype intervention to prevent smoking relapse after release. 3. To pilot the designed prototype intervention and conduct a process evaluation to inform the development of further work in this area. The research will be carried out in three prisons in the East Midlands. The main duties will include recruitment of participants (HMPPS staff members and prisoners), data collection, data analysis, assist with intervention development and refining related intervention materials/resources, co-facilitate Patient and Public Involvement (PPI) groups, contribute to the ethical application for the pilot intervention, and preparation of manuscripts for peer-review publication.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date December 30, 2023
Est. primary completion date May 1, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years and older
Eligibility Inclusion criteria 2. Release prisoner cohort - All participants are aged 18 or over (no upper age limit) - Are currently residing in one of the three study sites (HMPs Nottingham, Ranby and Sudbury) - Male (women will not be held at any of the study sites) - Have a provisional release date within the next 2 months. - Are capable of understanding and consenting to the study. - Remand and sentenced prisoners. - Who report that they are a current smoker and/or a current smoker prior to entering prison (smoked up to 7 days before entering prison), and/or were in prison (and still on the same sentence) and a current smoker prior to the smoke-free prison policy. 3. Reception prisoner cross-sectional - All participants are aged 18 or over (no upper age limit) - Are currently residing in the open prison study site (HMP Sudbury) - Male (women will not be held at any of the study sites) - Have been in the open prison more than two weeks but for less than 3 months. - Have been transferred from a closed prison. - Are capable of understanding and consenting to the study. - Sentenced prisoners. - Who report that they were a current smoker prior to entering prison (smoked up to 7 days before entering prison), and/or were in prison (and still on the same sentence) and a current smoker prior to the smoke-free prison policy. Exclusion criteria 2. Release prisoner cohort - Present a serious risk of harm to the researchers, highlighted in PNOMIS records or by a member of staff. - Non-smokers. - Being deported post release. - Been in prison for less than four weeks. 3. Reception prisoner cross-sectional - Present a serious risk of harm to the researchers, highlighted in PNOMIS records or by a member of staff. - Been in prison for less than 2 weeks. - Non-smokers.

Study Design


Intervention

Other:
Not yet developed
A prototype intervention will be developed over Phase 1 & 2 and piloted in Phase 3 of this study.

Locations

Country Name City State
United Kingdom University of Nottingham, School of Medicine Nottingham Please Select

Sponsors (5)

Lead Sponsor Collaborator
University of Nottingham Cancer Research UK, Her Majesty's Prison and Probation Service (HMPPS), Plymouth University Peninsula Schools of Medicine & Dentistry (PUPSMD), Public Health England

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary To develop and pilot test the feasibility and acceptability of an intervention to help prevent prisoners relapse to smoking after release. Smoking abstinence rates at 1 week, 1 month and 3 months post release, self-reported. 3 years
Secondary To document prisoners smoking history to date and levels of nicotine addiction. Phase 1 (Scoping stakeholder interviews/Release prisoner cohort/Reception prisoner cross-sectional) 1 year
Secondary To document the support provided to manage nicotine addiction during imprisonment and in the periods immediately before and after release. Phase 1 (Scoping stakeholder interviews/Release prisoner cohort/Reception prisoner cross-sectional) 1 year
Secondary The impact of smoke-free prison policy on prisoners smoking behaviours. Phase 1 (Scoping stakeholder interviews/Release prisoner cohort/Reception prisoner cross-sectional) 1 year
Secondary To establish the extent to which prisoners intentionally resume or unintentionally relapse to smoking after release (and does their intended behaviour pre-release predict post-release behaviour). Phase 1 (Scoping stakeholder interviews/Release prisoner cohort/Reception prisoner cross-sectional) 1 year
Secondary To establish the extent to which prisoners relapse to smoking after transfer to an open prison where smoking is permitted in designated areas. Phase 1 (Scoping stakeholder interviews/Release prisoner cohort/Reception prisoner cross-sectional) 1 year
Secondary To obtain views on triggers to smoking after release (and transfer to an open prison) and how relapse might be prevented. Phase 1 (Scoping stakeholder interviews/Release prisoner cohort/Reception prisoner cross-sectional) 1 year
Secondary For those prisoners who return to smoking after release, at what point do they resume smoking (in days). Phase 1 (Scoping stakeholder interviews/Release prisoner cohort/Reception prisoner cross-sectional) 1 year
Secondary After release do prisoners use cessation pharmacotherapy, electronic cigarettes or NHS SSS support, or any other means of preventing relapse. Phase 1 (Scoping stakeholder interviews/Release prisoner cohort/Reception prisoner cross-sectional) 1 year
Secondary Record and examine other potential predictors (as outlined in the international literature) of relapse to smoking after release from smoke-free prisons, e.g other negative health behaviours. Phase 1 (Scoping stakeholder interviews/Release prisoner cohort/Reception prisoner cross-sectional) 1 year
Secondary For those prisoners who do return to smoking after release, do they smoke less, the same or more as they previously smoked before entering prison/and or before the prison service went smoke-free. Phase 1 (Scoping stakeholder interviews/Release prisoner cohort/Reception prisoner cross-sectional) 1 year
Secondary Review of methods of recruitment in prison and community follow-up (to feed into future pilot intervention study). Phase 1 (Scoping stakeholder interviews/Release prisoner cohort/Reception prisoner cross-sectional) 1 year
Secondary To develop, design, and refine an intervention to prevent smoking relapse after release with input from fellow academics, stakeholders and PPI groups. Phase 2 (Intervention development) 1 year
Secondary To develop logic models to map the problem and the prototype intervention. Phase 2 (Intervention development) 1 year
Secondary To assess any barriers and facilitators to the developed intervention. Phase 3 (Intervention pilot & Intervention process evaluation) 1 year
Secondary To explore any unintended consequences as a result of the intervention. Phase 3 (Intervention pilot & Intervention process evaluation) 1 year
Secondary To identify aspects of the intervention and delivery that could be improved. Phase 3 (Intervention pilot & Intervention process evaluation) 1 year
Secondary Explore smoking abstinence rates at 1 week, 1 month and 3 months post release, self-reported and CO validated. Phase 3 (Intervention pilot & Intervention process evaluation) 1 year
Secondary Explore impact of the intervention on self-reported health, housing, reconviction rates, use of illicit substances in prisoner's post- release. Phase 3 (Intervention pilot & Intervention process evaluation) 1 year
See also
  Status Clinical Trial Phase
Completed NCT03999411 - Smartphone Intervention for Smoking Cessation and Improving Adherence to Treatment Among HIV Patients Phase 4
Completed NCT03931772 - Online Automated Self-Hypnosis Program N/A
Completed NCT02649556 - A 26-week Extension of the ZRHR-ERS-09-US Study Evaluating Biological and Functional Changes in Healthy Smokers After Switching to THS 2.2 N/A
Completed NCT03901066 - Smoking Dependence and Periodontitis
Completed NCT03170752 - Implementing and Testing a Cardiovascular Assessment Screening Program (CASP) N/A
Completed NCT03305978 - Pulmonary Nodule Detection: Comparison of an Ultra Low Dose vs Standard Scan. N/A
Completed NCT00000437 - Tobacco Dependence in Alcoholism Treatment (Nicotine Patch/Naltrexone) Phase 4
Completed NCT06105424 - BRP1602: Evaluation of Technical and Logistical Feasibility to Measure Lung Permeability N/A
Active, not recruiting NCT02752022 - Monitoring the Transition From Smoking to E-cigarettes
Completed NCT04340830 - The Effect of Smoking on Dimensional Changes of Free Gingival Graft Around Dental Implants N/A
Completed NCT02901171 - The Contribution of a Smartphone Application to Acceptance and Commitment Therapy Group Treatment for Smoking Cessation N/A
Completed NCT03206619 - A Health Recommeder System to Tailor Message Preferences in a Smoking Cessation Programme
Completed NCT02912000 - TEACH: Technology Evaluation to Address Child Health N/A
Completed NCT02949648 - Electronic Cigarette Use and Quitting in Youth N/A
Completed NCT02945371 - Tailored Inhibitory Control Training to Reverse EA-linked Deficits in Mid-life N/A
Completed NCT02246114 - Self-Monitoring of Carbon Monoxide to Enhance Reproductive Outcomes in Women N/A
Completed NCT03448900 - Intervention Study for Smoking Cessation in Spanish College Students N/A
Completed NCT01954407 - Young Adults' Responses to Anti-smoking Messages N/A
Completed NCT02008292 - Acetylcholine, Tobacco Smoking, Genes and Nicotinic Receptors N/A
Completed NCT01898507 - Nicotine Metabolism and Low Nicotine Cigarettes N/A