Ignite Creation Date:
2024-05-06 @ 3:47 PM
Last Modification Date:
2024-10-26 @ 1:56 PM
Study NCT ID:
NCT04752761
Status:
RECRUITING
Last Update Posted:
2023-07-21
First Post:
2020-12-23
Brief Title:
Compliance With PROMs Detection Through Digital Support and Correlation Compared Standard to Outpatient Detection in Knee Prosthetics
Sponsor:
Istituto Ortopedico Rizzoli
Organization:
Istituto Ortopedico Rizzoli
Study Overview
Official Title:
Compliance al Rilevamento PROMs Mediante Supporto Digitale e Correlazione Rispetto Alla Rilevazione Ambulatoriale Nella Protesica di Ginocchio
Status:
RECRUITING
Status Verified Date:
2024-07
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:
DIG-PROMs-k
Brief Summary:
Two methods for detecting outcomes after knee prosthetic surgery are compared the traditional one using paper questionnaires administered in the outpatient setting Oxford Knee Score VS detection using digital questionnaires created on Google Forms and sent to the patients smartphone on which the compilation takes place in the extra area outpatient
Detailed Description:
PROMs Patient Reported Outcomes Measures are used globally for the evaluation of the results of a prosthetic surgery One of the most used methods in the evaluation of PROMs in knee prosthetic surgery is the Oxford Knee Score usually measured in an outpatient setting using paper questionnaires
The aim of the study is to investigate the validity of an alternative method of evaluating PROMs in which the questionnaire will be administered to the patient digitally Google Forms in an out-of-patient setting
The questionnaire aimed at the subjective evaluation of the discomfort induced by arthrosis of the knee Oxford Knee Score will be administered during the pre-hospitalization visits and again during the follow-up visits carried out at 1 3 and 6 months after intervention The digital evaluation will be sent to the patient during the outpatient visits and will be considered valid only if completed within 48 hours of the same
On each patient the measurements will be carried out in both methods and differences in terms of compliance and satisfaction with the two methods under examination will be detected Any differences in the final result of the Oxford Knee Score compared to the two methods and the differences in terms of outpatient assessment times will also be evaluated
The aim of the study is to investigate the validity of an alternative method of evaluating PROMs in which the questionnaire will be administered to the patient digitally Google Forms in an out-of-patient setting
The questionnaire aimed at the subjective evaluation of the discomfort induced by arthrosis of the knee Oxford Knee Score will be administered during the pre-hospitalization visits and again during the follow-up visits carried out at 1 3 and 6 months after intervention The digital evaluation will be sent to the patient during the outpatient visits and will be considered valid only if completed within 48 hours of the same
On each patient the measurements will be carried out in both methods and differences in terms of compliance and satisfaction with the two methods under examination will be detected Any differences in the final result of the Oxford Knee Score compared to the two methods and the differences in terms of outpatient assessment times will also be evaluated
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None