Ignite Creation Date:
2024-05-06 @ 4:05 PM
Last Modification Date:
2024-10-26 @ 2:03 PM
Study NCT ID:
NCT04867772
Status:
COMPLETED
Last Update Posted:
2021-04-30
First Post:
2021-04-27
Brief Title:
Community Based Rehabilitation After Knee Arthroplasty
Sponsor:
University of Oxford
Organization:
University of Oxford
Study Overview
Official Title:
COmmunity Based Rehabilitation After Knee Arthroplasty CORKA A Prospective Two Arm Individually Randomised Controlled Trial
Status:
COMPLETED
Status Verified Date:
2021-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
CORKA
Brief Summary:
Background The CORKA study was developed in response to a commissioned call by the National Institute for Health Research NIHR Health Technology Assessment HTA programme for research into a functional home based rehabilitation programme for patients who may be at risk of poor outcome after knee arthroplasty
Design The CORKA trial is a prospective individually randomised controlled trial with blinded outcome assessment at baseline 6 and 12 months The study will also include a qualitative and a health economic analysis Participants will be randomised to one of two arms home-based rehabilitation or Usual Care Those in the usual care arm will receive a minimum of 1 and a maximum of 6 sessions of physiotherapy as delivered locally eg class one to one etc Those in the intervention arm will receive 7 sessions of a functional rehabilitation programme over a 12 week timescale The intervention will be delivered using physiotherapists and physiotherapy assistants in the participants home Participants will be followed up at 6 months and 12 months
Design The CORKA trial is a prospective individually randomised controlled trial with blinded outcome assessment at baseline 6 and 12 months The study will also include a qualitative and a health economic analysis Participants will be randomised to one of two arms home-based rehabilitation or Usual Care Those in the usual care arm will receive a minimum of 1 and a maximum of 6 sessions of physiotherapy as delivered locally eg class one to one etc Those in the intervention arm will receive 7 sessions of a functional rehabilitation programme over a 12 week timescale The intervention will be delivered using physiotherapists and physiotherapy assistants in the participants home Participants will be followed up at 6 months and 12 months
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None