Effective practice? A randomised trial of dissemination and implementation strategies for guidelines for the appropriate extraction of third molar teeth

ISRCTN ISRCTN81740528
DOI https://doi.org/10.1186/ISRCTN81740528
Protocol serial number IMP R2-64 Pitts
Sponsor Record Provided by the NHS R&D 'Time-Limited' National Programme Register - Department of Health (UK)
Funder NHS Evaluation of Methods to Promote the Implementation of Research Findings (National Programme) (UK) (ref: IMP R2-64 Pitts)
Submission date
23/01/2004
Registration date
23/01/2004
Last edited
13/05/2008
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Oral Health
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data

Plain English summary of protocol

Not provided at time of registration

Contact information

Prof Nigel Pitts
Scientific

University of Dundee
Dundee Dental Hospital and School
Park Place
Dundee
DD1 4HR
United Kingdom

Phone +44 (0)1382 635994
Email n.b.pitts@dundee.ac.uk

Study information

Primary study designInterventional
Study designA pragmatic, cluster randomised controlled trial (RCT), 2 x 2 factorial design
Secondary study designRandomised controlled trial
Scientific title
Study objectivesTo investigate the effectiveness and cost-effectiveness of different guideline implementation strategies, using the Scottish Intercollegiate Guidelines Network (SIGN) Guideline 42: Management of unerupted and impacted third molar teeth (published 2000) as a model.
Ethics approval(s)Ethical approval was obtained from The Multicentre Research Ethics Committee for Scotland (MREC) and the relevant local research ethics committees.
Health condition(s) or problem(s) studiedOral health/stomatognathic diseases
InterventionIntervention groups as follows:
1. Control (paper copy of guidelines and opportunity to attend a postgraduate course)
2. Audit and feedback
3. Patient specific prompts/restructured records
4. Computer aided learning with decision support
Intervention typeOther
Primary outcome measure(s)

The proportion of patients whose treatment complied with the guideline.

Key secondary outcome measure(s)

No secondary outcome measures

Completion date31/12/2000

Eligibility

Participant type(s)Patient
Age groupAdult
SexAll
Target sample size at registration60
Key inclusion criteria1. Randomly selected from the Scottish Dental Practice Board list and invited to participate in the trial by mail
2. Written informed consent
Key exclusion criteriaDoes not comply with above inclusion criteria
Date of first enrolment01/01/1999
Date of final enrolment31/12/2000

Locations

Countries of recruitment

  • United Kingdom
  • Scotland

Study participating centre

University of Dundee
Dundee
DD1 4HR
United Kingdom

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
IPD sharing plan

Study outputs

Output type Details Date created Date added Peer reviewed? Patient-facing?
Results article Results 11/12/2004 Yes No