CClinicalTrials.gg
CompletedNCT05597046Updated Nov 9, 2022

Qualitative Interviews With Healthcare Professionals

An observational study in Total Knee Replacement, sponsored by Invibio Ltd. Completed at 1 site in United States. Per ClinicalTrials.gov, last updated 2022-11-09.

Sponsored by Invibio Ltd · Observational

Study type
Observational
Model
Other
Time perspective
Other
Enrollment
6
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Total Knee Replacement

Keywords

  • TKR
03

In context

Lead sponsor

Invibio Ltd is the lead sponsor of 6 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Healthcare Professionals attending the AAKHS conference, Dallas during Thursday 3rd to Saturday 5th November 2022.

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.
05

Study design

Observational model
Other
Time perspective
Other
Enrollment
6 participants (actual)
Patient registry
No

Groups and cohorts

  • Healthcare Professionals

    Planning Phase Interviews

    Other: Interview

Interventions

  • OtherInterview

    Interviews

06

What researchers measure

Primary outcomes

  1. Interview

    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.

    Time frame: 30 minutes

07

Study locations

1 site
  • AAKHS conference, Dallas
    Dallas, Texas 76051, United States
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 9, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05597046
Lead sponsor
Invibio Ltd
Responsible party
Sponsor
First posted
Oct 27, 2022
Start date
Nov 3, 2022
Primary completion
Nov 5, 2022
Completion
Nov 5, 2022
Last update
Nov 9, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2022. You cannot join it, but the record below documents what was studied.

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