ISRCTN ISRCTN81810979
DOI https://doi.org/10.1186/ISRCTN81810979
Protocol serial number 94060025
Sponsor NHS R&D Regional Programme Register - Department of Health (UK)
Funder NHS Executive Northern and Yorkshire (UK)
Submission date
23/01/2004
Registration date
23/01/2004
Last edited
24/10/2019
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Musculoskeletal Diseases
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

Ms Elizabeth Lingard
Scientific

School of Surgical and Reproductive Sciences
The Medical School
University of Newcastle upon Tyne
Newcastle
NE2 4HH
United Kingdom

Study information

Primary study designInterventional
Study designRandomised controlled trial
Secondary study designRandomised controlled trial
Scientific titlePre admission for patients undergoing total knee arthroplasty
Study objectivesThis prospective randomised study will assess the effectiveness of formal pre-admission education for patients awaiting total knee replacement surgery using video presentation and physiotherapist input. The video contains information about the routine admission of a patient undergoing total knee arthroplasty. The emphasis of the video is aimed at educating the patient on what they need to do to achieve the optimal outcome post-operatively. Analysis of patient satisfaction with this method of patient education will be compared between the groups as well as their post-operative rehabilitation progress and length of hospital stay. Results of this project have important implications for improving clinical outcomes, quality assurance and reducing hospital costs within the NHS.
Ethics approval(s)Not provided at time of registration
Health condition(s) or problem(s) studiedMusculoskeletal diseases: Arthritis (rheumatoid); Musculoskeletal diseases: Arthritis (osteo)
Intervention1. Formal pre-admission education programme
2. Standard care
Intervention typeOther
Primary outcome measure(s)

Clinical outcome, quality of life

Key secondary outcome measure(s)

Not provided at time of registration

Completion date31/03/1996

Eligibility

Participant type(s)Patient
Age groupNot Specified
SexNot Specified
Key inclusion criteriaPatients awaiting total knee replacement surgery
Key exclusion criteriaNot provided at time of registration
Date of first enrolment04/01/1994
Date of final enrolment31/03/1996

Locations

Countries of recruitment

  • United Kingdom
  • England

Study participating centre

School of Surgical and Reproductive Sciences,
Newcastle
NE2 4HH
United Kingdom

Results and Publications

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

Editorial Notes

24/10/2019: No publications found. All search options exhausted.