Using a screening questionnaire to reduce non-attendances at first appointments for smoking cessation advice clinics in general practice: a clustered randomised controlled trial
| ISRCTN | ISRCTN05348847 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN05348847 |
| Protocol serial number | N0026186755 |
| Sponsor | Record Provided by the NHSTCT Register - 2007 Update - Department of Health |
| Funders | Air Balloon Surgery, Avon Primary Care Research Collaborative |
- Submission date
- 28/09/2007
- Registration date
- 28/09/2007
- Last edited
- 17/10/2016
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Mental and Behavioural Disorders
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year
Plain English summary of protocol
Not provided at time of registration
Contact information
Dr Carole Langley
Scientific
Scientific
Air Balloon Surgery
Kenn Road
St George
Bristol
BS5 7PD
United Kingdom
| Phone | +44 0117 9199914 |
|---|---|
| clangley@airballoon.cix.co.uk |
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Clustered randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Study type | Participant information sheet |
| Scientific title | Using a screening questionnaire to reduce non-attendances at first appointments for smoking cessation advice clinics in general practice: a clustered randomised controlled trial |
| Study objectives | 1. Can a short pre-booking questionnaire be used to reduce wastage due to non-attendance of first appointments for smoking cessation advice? 2. Does screening for readiness by using a questionnaire have an impact on successful quit rate and waiting list? |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Smoking cessation |
| Intervention | The study will be a controlled trial that will take place in general practices in Bristol. In order to avoid contamination, randomisation will take place at the practice level. The intervention practices will use a short questionnaire which has been designed to assess readiness to quit, as a screening tool, while the smoking cessation advice clinics in control practices will continue to take referrals according to usual practice and supply their audit data at the end of a 6 month period. The trial will take place over a six-month period. |
| Intervention type | Other |
| Primary outcome measure(s) |
The primary outcome measure will be the percentage of missed first appointments compared with corresponding pre-trial periods. The waiting list and the audited quit rates will also be examined. Analysis will also compare the questionnaire scores with a successful quit attempt. It is anticipated that this will be used to contribute to the validation of the questionnaire. |
| Key secondary outcome measure(s) |
Not provided at time of registration |
| Completion date | 30/09/2007 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Sex | Not Specified |
| Key inclusion criteria | Patients who think they may like to make an appointment for the smoking advice sessions in 15 Bristol general practices. |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 01/10/2006 |
| Date of final enrolment | 30/09/2007 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
Air Balloon Surgery
Bristol
BS5 7PD
United Kingdom
BS5 7PD
United Kingdom
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | Not provided at time of registration |
| IPD sharing plan |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Participant information sheet | Participant information sheet | 11/11/2025 | 11/11/2025 | No | Yes |
Editorial Notes
17/10/2016: No publications found in PubMed, verifying study status with principal investigator.