Skip to main content
Clinical Trials/ISRCTN18357968
ISRCTN18357968
Completed
未知

Rehabilitation following rotator Cuff repaiR: a multi-centre pilot & feasibility randomised controlled trial with nested qualitative study (the RaCeR study)

niversity of Keele0 sites73 target enrollmentAugust 10, 2018

Overview

Phase
未知
Intervention
Not specified
Conditions
Rehabilitation following rotator cuff repair
Sponsor
niversity of Keele
Enrollment
73
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

2019 Protocol article in https://www.ncbi.nlm.nih.gov/pubmed/31171031 protocol (added 10/06/2019) 2020 Results article in https://pubmed.ncbi.nlm.nih.gov/33356517/ nested qualitative study (added 05/08/2021) 2020 Results article in https://pubmed.ncbi.nlm.nih.gov/33305619/ results (added 05/08/2021)

Registry
who.int
Start Date
August 10, 2018
End Date
July 30, 2020
Last Updated
4 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity of Keele

Eligibility Criteria

Inclusion Criteria

  • 1\. Patients diagnosed with a non\-traumatic symptomatic tear of the RC and listed for surgical repair
  • 2\. RC tear confirmed by ultrasound or MRI
  • 3\. Aged \= 18 years
  • 4\. Patients screened by the surgeon as suitable to participate (an opt\-out scheme will be implemented whereby all patients under the care of a surgeon who is participating in the trial will be eligible unless the surgeon states otherwise in the medical notes at the time of listing for surgery)
  • 5\. Able to return to the recruiting centre or affiliated site for the initial outpatient follow\-up physiotherapy appointment
  • 6\. Access to a mobile phone and willing and able to receive and respond to SMS text messages
  • 7\. Able to understand English

Exclusion Criteria

  • 1\. Traumatic RC tears (e.g. sudden onset of shoulder pain and weakness following a fall), given the different care pathways for such patients (these patients are typically fast\-tracked to surgery)
  • 2\. Patients who are unable to give full informed consent

Outcomes

Primary Outcomes

Not specified

Similar Trials