Ignite Creation Date:
2024-05-06 @ 8:21 PM
Last Modification Date:
2024-10-26 @ 3:26 PM
Study NCT ID:
NCT06357143
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-05-31
First Post:
2024-04-04
Brief Title:
Efficacy of Early Multimodal Physiotherapy in Patients with Reverse Shoulder Prosthesis
Sponsor:
University of Malaga
Organization:
University of Malaga
Study Overview
Official Title:
Efficacy of Early Multimodal Physiotherapy in Patients with Reverse Shoulder Prosthesis a Randomized Controlled Trial
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-10
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:
None
Brief Summary:
The present study try to evaluate the effectivenness of an early intervention program based on multimodal physiotherapy and focused on therapeutic exercise to improve the results of patients with a reverse shoulder phrostesis This trial will be a randomized controlled trial with parallel groups and outcomes variables will include psychometric properties through the use of specific questionnaries and laboratory variables such as strength with a dynamometer range of movement with a goniometer muscle mass with an ultrasound and kinematic parameters with inertial sensors This study aims to develop an original intervention program in order to try to establish new protocols in the management of these patients
Detailed Description:
Background Shoulder fractures shoulder osteoarthritis and rheumatoid arthritis have a high prevalence and many times they require a surgery in which a reverse shoulder phrostesis is colocated Nonetheless nowadays there is no a clear consensus protocol in order to manage the prehabilitation and rehabilitation of this patient so each physiotherapist use different techniques to treat this pathology
Objective This study aims to evaluate the effectiveness of an original intervention program REMOVE program focused on an early intervention based on therapeutic exercise manual therapy and education to improve the functionality of these patients after surgery
Methods This study is a randomized controlled trial with parallel groups The control group receive standard care and the experimental group is subjected to the REMOVE program Both groups are evaluated five times pre-surgery at baseline at 6 weeks at 12 weeks and at 24 weeks to assess psychometric and laboratory outcomes
Objective This study aims to evaluate the effectiveness of an original intervention program REMOVE program focused on an early intervention based on therapeutic exercise manual therapy and education to improve the functionality of these patients after surgery
Methods This study is a randomized controlled trial with parallel groups The control group receive standard care and the experimental group is subjected to the REMOVE program Both groups are evaluated five times pre-surgery at baseline at 6 weeks at 12 weeks and at 24 weeks to assess psychometric and laboratory outcomes
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