Ignite Creation Date:
2024-05-06 @ 7:39 PM
Last Modification Date:
2024-10-26 @ 3:11 PM
Study NCT ID:
NCT06088173
Status:
COMPLETED
Last Update Posted:
2024-07-03
First Post:
2023-10-08
Brief Title:
The Effects of Graded Motor Imagery Training Program in Patients With Flexor Tendon Repair
Sponsor:
Istanbul University - Cerrahpasa IUC
Organization:
Istanbul University - Cerrahpasa IUC
Study Overview
Official Title:
The Effects of Graded Motor Imagery Training Before and After the Rehabilitation Program in Patients With Flexor Tendon Repair
Status:
COMPLETED
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:
None
Brief Summary:
The aim of our study was to investigate the effects of graded motor imagery training applied during the immobilization period on hand functions range of motion proprioception and kinesiophobia before and after the rehabilitation program in patients with flexor tendon repair
Detailed Description:
After flexor tendon repair conditions such as limitation of joint movement in the injured finger contracture decreased proprioception decreased hand function and skills during activities of daily living may occur due to one or more reasons Various protocols have been applied in rehabilitation after flexor tendon repair but the search for new treatment methods to achieve the best results continues In this study our aim is to reorganize the cortex and incorporate graded motor imagery training which has been proven to be more effective in the treatment of chronic pain but promising in terms of increasing body awareness proprioception and function into flexor tendon rehabilitation to provide flexor tendon repair patients with more functional results and to contribute to the search for new treatment methods in the literature
The participants who volunteered to take part in the study will be randomly divided into two groups namely the Early passive mobilization group Group 1 and the graded motor imagery GMI training Group 2 using a computerassisted randomization program After the groups are assigned Group 1 will receive Modified Kleinert protocol and Group 2 will receive GMI training in addition to Modified Kleinert protocol with the help of hand recognize mobile application A total of 6 weeks of treatment will be applied GMI will be taught in sessions and practice will be continued at home Both groups will use a short modified Kleinert splint for postoperatif 6 weeks This splint does not allow the use of the hand but allows passive flexion and active extension with the help of a tire GMI training will be given and practiced as soon as rehabilitation starts The progression will be 2 weeks lateralization 2 weeks imagery 2 weeks mirror therapy and when the splint is removed at the end of postop 6 weeks In the remaining sessions standard rehabilitation will be continued in both groups
The participants who volunteered to take part in the study will be randomly divided into two groups namely the Early passive mobilization group Group 1 and the graded motor imagery GMI training Group 2 using a computerassisted randomization program After the groups are assigned Group 1 will receive Modified Kleinert protocol and Group 2 will receive GMI training in addition to Modified Kleinert protocol with the help of hand recognize mobile application A total of 6 weeks of treatment will be applied GMI will be taught in sessions and practice will be continued at home Both groups will use a short modified Kleinert splint for postoperatif 6 weeks This splint does not allow the use of the hand but allows passive flexion and active extension with the help of a tire GMI training will be given and practiced as soon as rehabilitation starts The progression will be 2 weeks lateralization 2 weeks imagery 2 weeks mirror therapy and when the splint is removed at the end of postop 6 weeks In the remaining sessions standard rehabilitation will be continued in both groups
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