A randomised trial comparing the effect of self-directed online learning using a web-based resource with a classroom-based interactive workshop, on the knowledge and search skills of healthcare professionals

ISRCTN ISRCTN52541826
DOI https://doi.org/10.1186/ISRCTN52541826
Protocol serial number N0643164123
Sponsor Record Provided by the NHSTCT Register - 2006 Update - Department of Health
Funder Thames Valley Primary Care Research Partnership (UK)
Submission date
29/09/2006
Registration date
29/09/2006
Last edited
12/05/2017
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Other
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 Nicola Bexon
Scientific

Williams Room
Badenoch Building
Old Road Campus
Headington
Oxford
OX3 7LF
United Kingdom

Phone +44 (0)1865 227044
Email nicola.bexon@his.ac.uk

Study information

Primary study designInterventional
Study designRandomised controlled trial
Secondary study designRandomised controlled trial
Study type Participant information sheet
Scientific titleA randomised trial comparing the effect of self-directed online learning using a web-based resource with a classroom-based interactive workshop, on the knowledge and search skills of healthcare professionals
Study objectivesIs there a difference in terms of knowledge and skills, between self-directed learning using web-based resource directed by students, compared with a classroom based interactive workshop directed by tutors?
Ethics approval(s)Not provided at time of registration
Health condition(s) or problem(s) studiedKnowledge and skill education
InterventionAt each location participants will be randomised into two groups:
1. Group one: access to a search-skills web resource (e-group)
2. Group two: receive a search workshop taught by a librarian (workshop group)

The e-learning resource and the workshop will have the same objectives and cover the same content. Each intervention group will attend one group session - the e-group will be shown a demonstration of the e-learning resource and asked to complete as much of the module as they can over the next week; the workshop group will receive a three-hour taught workshop with handouts and slides. At the beginning of these sessions, each participant will complete a pre-intervention search test (baseline) using a clinical scenario. One week after these initial sessions, a post-intervention search test should be completed by both groups. Pre- (baseline) and post-intervention search results will be compared. Follow-up tests will be sent at 4 weeks, 8 weeks (and 12 weeks if time allows).
Intervention typeOther
Primary outcome measure(s)

Not provided at time of registration

Key secondary outcome measure(s)

Not provided at time of registration

Completion date30/04/2005

Eligibility

Participant type(s)Health professional
Age groupAdult
SexAll
Key inclusion criteriaHealth professionals
Key exclusion criteriaNot provided at time of registration
Date of first enrolment01/03/2005
Date of final enrolment30/04/2005

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

Williams Room
Oxford
OX3 7LF
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?
Participant information sheet Participant information sheet 11/11/2025 11/11/2025 No Yes

Editorial Notes

12/05/2017: No publications found, verifying study status with principal investigator.