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Clinical Trials/NCT05597046
NCT05597046
Completed
Not Applicable

PLANNING PHASE- Qualitative Interviews With Healthcare Professionals to Assist in the Development of a New Patient Reported Outcome Measure (PROM) to Assess Patient's Emotional Wellbeing, and Perceptions of Total Knee Replacement (TKR) Surgery for the Treatment of Knee Arthritis.

Invibio Ltd1 site in 1 country6 target enrollmentNovember 3, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Total Knee Replacement
Sponsor
Invibio Ltd
Enrollment
6
Locations
1
Primary Endpoint
Interview
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

PLANNING PHASE- Qualitative interviews with Healthcare Professionals to assist in the development of a new Patient Reported Outcome Measure (PROM) to assess patient's emotional wellbeing, and perceptions of Total Knee Replacement (TKR) surgery for the treatment of knee arthritis.

Detailed Description

The interviews for the SYNC01-PP-USA project will be conducted in person at the American Association of Hip and Knee Surgeons (AAHKS) annual conference in Dallas, Texas, USA during the 3rd, 4th, and 5th November 2022. The interviews will take approximately 30 minutes.

Registry
clinicaltrials.gov
Start Date
November 3, 2022
End Date
November 5, 2022
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Healthcare Professionals who currently care for patients who have undergone Total Knee Replacement surgery.
  • Healthcare Professionals who, in the opinion of the Investigator, can understand the project, co-operate with the interview process and are willing to be interviewed in person.
  • Healthcare Professionals who are able to give voluntary, written informed consent to participate in this project and from whom consent has been obtained.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Interview

Time Frame: 30 minutes

The interview carried out with the HCPs will ascertain their opinions of the issues that patients report after undergoing TKR. The replies (data) collected could be different for each HCP so there is no outcome measure as such for this data. This information collected will be structured around a set number of questions asked in the interview and will be used to form the potential structure and layout of a Patient Reported Outcome Measure (PROM) and to provide background information for the subsequent Phase One of the project which will take place in the UK.

Study Sites (1)

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