Cluster randomised, controlled trial of pro-actively identifying smokers and offering evidence based support to stop smoking
| ISRCTN | ISRCTN71514078 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN71514078 |
| Protocol serial number | PG/04/073 |
| Sponsor | University of Nottingham (UK) |
| Funder | British Heart Foundation (UK) (ref: PG/04/073) |
- Submission date
- 15/08/2005
- Registration date
- 07/09/2005
- Last edited
- 06/10/2009
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Other
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Plain English summary of protocol
Not provided at time of registration
Contact information
Dr Sarah Lewis
Scientific
Scientific
Division of Respiratory Medicine
Clinical Sciences Building
City Hospital
Nottingham
NG5 1PB
United Kingdom
| Phone | +44 (0)115 8404761 |
|---|---|
| sarah.lewis@nottingham.ac.uk |
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Cluster randomised controlled parallel group trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | |
| Study objectives | That systematically identifying smokers who want to quit smoking using general practice registers and questionnaires, and pro-actively referring them to use a range of evidence-based smoking cessation interventions will be effective and cost effective in encouraging more widespread smoking cessation. |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Smoking |
| Intervention | Participants in intervention practices will be asked whether they would like help or advice to stop smoking. A research nurse trained in smoking cessation methods will telephone these individuals, provide brief advice on smoking cessation according to evidence-based guidelines and encourage smokers to contact and use the local smoking cessation service, New Leaf. Participants in control practices receive no intervention. |
| Intervention type | Other |
| Primary outcome measure(s) |
Point abstinence (for ≥7 days) at 6 months |
| Key secondary outcome measure(s) |
Access and uptake of smoking cessation services by 6 months. |
| Completion date | 31/01/2007 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Lower age limit | 18 Years |
| Sex | All |
| Target sample size at registration | 24 |
| Key inclusion criteria | Patients within the practice aged 18 or over who are current smokers |
| Key exclusion criteria | Does not match inclusion criteria |
| Date of first enrolment | 01/01/2005 |
| Date of final enrolment | 31/01/2007 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
Division of Respiratory Medicine
Nottingham
NG5 1PB
United Kingdom
NG5 1PB
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? |
|---|---|---|---|---|---|
| Results article | results | 01/06/2008 | Yes | No |
