- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02567097
Evaluating Specific Plans to Increase Smoking Quit Attempts in Prison
The Role of Self-Incentives in Smoking Cessation: A Randomised Controlled Trial Within a Local Prison
Study Overview
Detailed Description
The research aims to test the role of self-incentivising implementation intentions in smoking cessation among prisoners aged 18 and over, enrolling on a stop smoking programme provided by Livewire within Risley Prison. The effectiveness of self-incentives has been successfully seen previously within health behaviour change, but not within smoking cessation (ongoing randomised controlled trial in alongside community stop smoking services, and local workplaces). This research will build on this by testing the effectiveness of self-incentives in prisoners' stop smoking attempts.
This study is a randomised controlled trial with the between participants factor of condition which has four levels:
1. Control (plan) 2 Self-generated implementation intention (if-then plan) 3. Weekly self-incentivising implementation intention 4. Monthly self-incentivising implementation intention
The within participants' factor will be time which has three levels:
- Baseline (T1)
- Follow-up (T2) (end of stop smoking programme)
- Follow-up (T3) (six months post quit date)
An ethical concern is that participants in the control condition may struggle more to quit smoking as they will not have the additional benefits of being within an experimental condition which uses self-incentives to aid their quit attempt. A control condition is needed to monitor if quitting smoking is due to the use of self-incentives or another behaviour change technique.
The recruitment process will involve the researcher (Emma Brown) administering study packs to the potential participants. The participant information sheet will be read to each participant and time will be provided to ask any questions. If the participant agrees to take part in the research and complete the questionnaire, then this will be completed with the help of the researcher (Emma Brown) if required. Questionnaires will be placed in a sealed envelope and returned to the University of Manchester by the researcher (Emma Brown).
All participants who are able to provide informed consent and are over the age of 18 years old are eligible to take part in the study. Unfortunately, the study does not cater for people who cannot understand English at the present time, although this will be monitored for amendments in future studies. The study will use a paper format as not to exclude those participants who have limited or no access to the internet.
The participant information sheet included within the study pack alongside the questionnaire includes details about the study, costs and benefits of taking part in the study, and the right to consent and withdraw at any point throughout the study. There are no risks involved in taking part in the study. There is a minimal burden in time taken to complete the baseline questionnaire to take no longer than 15 minutes and the further two follow-up questionnaires to take no longer than 10 minutes.
In terms of confidentiality, participants are asked to form a personal identification code to match baseline and follow-up questionnaires once completed.
There are no conflicts of interest. Results will be fed back to all participating services and participants involved in the study, should they indicate for a summary of the results.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Cheshire
-
Warrington, Cheshire, United Kingdom, WA3 6BP
- Risley Prison
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Aged 18 or over
- Able to understand verbal English
- Competent to provide informed consent
- Attending or previously attended the stop smoking services provided
Exclusion Criteria:
- Not aged 18 or over
- Not able to understand verbal English
- Not competent to provide informed consent
- Not attending or previously attended the stop smoking services provided
Study Plan
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Control
Participants read a brief statement designed to encourage them to quit smoking (we would like you to plan to quit smoking).
Participants are then asked to form their plan to quit smoking.
|
Participants are asked to form plans to quit smoking using various descriptions specified dependent on the arm in which they are randomised.
|
|
Active Comparator: Implementation Intention
Participants read a brief statement designed to encourage them to quit smoking (we would like you to plan to quit smoking).
Participants are then asked to form a specific 'if-then' plan using an implementation intention basis.
|
Participants are asked to form plans to quit smoking using various descriptions specified dependent on the arm in which they are randomised.
|
|
Experimental: Weekly Self-Incentivising
Participants read a brief statement designed to encourage them to quit smoking (we would like you to plan to quit smoking).
Participants are then asked to specify a self-incentive on which they could implement at the end of each week which they have been successful in not smoking.
|
Participants are asked to form plans to quit smoking using various descriptions specified dependent on the arm in which they are randomised.
|
|
Experimental: Monthly Self-Incentivising
Participants read a brief statement designed to encourage them to quit smoking (we would like you to plan to quit smoking).
Participants are then asked to specify a self-incentive on which they could implement at the end of each month which they have been successful in not smoking.
|
Participants are asked to form plans to quit smoking using various descriptions specified dependent on the arm in which they are randomised.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Smoking status
Time Frame: up to 6-months
|
up to 6-months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Amount of cigarettes smoked at both followup time periods
Time Frame: up to 6-months
|
up to 6-months
|
|
Smoking behaviour (habitual)
Time Frame: up to 6-months
|
up to 6-months
|
|
Intentions to stop smoking
Time Frame: up to 6-months
|
up to 6-months
|
|
Self-regulation strategies used
Time Frame: up to 6-months
|
up to 6-months
|
|
Source of motivation to quit smoking
Time Frame: up to 6-months
|
up to 6-months
|
|
Compliance to self-incentivise
Time Frame: up to 6-months
|
up to 6-months
|
|
Frequency of self-incentivisation
Time Frame: up to 6-months
|
up to 6-months
|
|
Self-incentives used
Time Frame: up to 6-months
|
up to 6-months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Christopher J Armitage, University of Manchester
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 15428
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Health Behaviour
-
Western University, CanadaNot yet recruitingSedentary Behaviour | Health Behaviour ChangeCanada
-
Kristiania University CollegeHorten municipalityActive, not recruiting
-
Health HQCompletedHealth BehaviourAustralia
-
Sakarya UniversityThe Scientific and Technological Research Council of TurkeyNot yet recruitingHealth Behaviour | Risk Behavior, Health
-
University of GuelphCompletedHealth Behaviour | Nutrition Intervention | Impaired Health
-
W.J. PasmanCompletedHealth Behaviour Change | Self-monitoring of HealthNetherlands
-
Singapore Management UniversityRecruitingHealth Behaviour ChangeSingapore
-
Queen's University, BelfastCompletedPhysical Activity | Health BehaviourUnited Kingdom
-
Western University, CanadaCompletedSedentary Lifestyle | Health Behaviour ChangeCanada
-
Seçil HürCompletedHygiene | Health Behaviour | Peer MentoringTurkey (Türkiye)
Clinical Trials on Self-Incentive
-
Centre Hospitalier Universitaire DijonCompleted
-
Emory UniversityCompleted
-
University of ManchesterEconomic and Social Research Council, United KingdomCompletedWillingness to ParticipateUnited Kingdom
-
Johns Hopkins Bloomberg School of Public HealthIfakara Health Institute; Pontificia Universidad Javeriana; The Bloomberg Family...CompletedNoncommunicable Diseases | Surveys and QuestionnairesTanzania, Colombia
-
University of PennsylvaniaCompleted
-
Johns Hopkins Bloomberg School of Public HealthIfakara Health Institute; Pontificia Universidad Javeriana; The Bloomberg Family...CompletedNoncommunicable Diseases | Surveys and QuestionnairesTanzania, Colombia
-
University of PennsylvaniaDeloitteCompletedObesityUnited States
-
University of California, San FranciscoUniversity of California, Los AngelesCompletedDental Caries | Parent-Child Relations | Oral Hygiene | Dental Plaque | ToothbrushingUnited States
-
Carnegie Mellon UniversityUniversity of VirginiaCompletedSocial Isolation | Activity, MotorUnited States