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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
ClinicalTrials.gov identifier
Public 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
Scientific title
Acronym N/A
Serial number at source N0026186755
Study hypothesis 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 Not provided at time of registration
Study design Clustered randomised controlled trial
Countries of recruitment United Kingdom
Disease/condition/study domain Mental and Behavioural Disorders: Smoking cessation
Participants - inclusion criteria Patients who think they may like to make an appointment for the smoking advice sessions in 15 Bristol general practices.
Participants - exclusion criteria Not provided at time of registration
Anticipated start date 01/10/2006
Anticipated end date 30/09/2007
Status of trial Completed
Patient information material
Target number of participants Not provided at time of registration
Interventions 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.
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.
Secondary outcome measure(s) Not provided at time of registration
Sources of funding Air Balloon Surgery
Avon Primary Care Research Collaborative
Trial website
Publications
Contact name Dr  Carole  Langley
  Address Air Balloon Surgery
Kenn Road
St George
  City/town Bristol
  Zip/Postcode BS5 7PD
  Country United Kingdom
  Tel +44 0117 9199914
  Fax +44 0117 9086660
  Email clangley@airballoon.cix.co.uk
Sponsor Record Provided by the NHSTCT Register - 2007 Update - Department of Health
  Address The Department of Health, Richmond House, 79 Whitehall
  City/town London
  Zip/Postcode SW1A 2NL
  Country United Kingdom
  Tel +44 (0)20 7307 2622
  Fax +44
  Email dhmail@doh.gsi.org.uk
  Sponsor website: http://www.dh.gov.uk/Home/fs/en
Date applied 28/09/2007
Last edited 22/10/2007
Date ISRCTN assigned 28/09/2007
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