Ignite Creation Date:
2024-07-17 @ 10:57 AM
Last Modification Date:
2024-10-26 @ 3:32 PM
Study NCT ID:
NCT06464809
Status:
COMPLETED
Last Update Posted:
2024-06-18
First Post:
2024-06-04
Brief Title:
Treatment Intervention of Patients With Carpal Tunnel Syndrome CTS
Sponsor:
China Medical University Hospital
Organization:
China Medical University Hospital
Study Overview
Official Title:
Treatment Effects of Transcutaneous Electrical Nerve Stimulation and Kinesio Taping on Hand Functions for Patients With Carpal Tunnel Syndrome
Status:
COMPLETED
Status Verified Date:
2024-06
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 purpose of this study was to investigate the effectiveness of KT versus TENS combining self-myofascial stretching in treatment of CTS through clinical functional assessment and sensory measurements
Primary hypothesis The KT group has a more substantial improvement in hand grip pain relief enhancing proprioceptive sensitivity and dexterity compare to the TENS group treatment program
Primary hypothesis The KT group has a more substantial improvement in hand grip pain relief enhancing proprioceptive sensitivity and dexterity compare to the TENS group treatment program
Detailed Description:
Objective To compare the effectiveness of a home-based treatment program involving Kinesio taping KT or transcutaneous electrical nerve stimulation TENS among carpal tunnel syndrome CTS patients
Methods
30 participants with CTS were enrolled age range 30 to 60 years The participants who met the inclusion criteria were randomized into one of two treatment groups KT group and TENS group Participants were blinded to the treatments used in the other group
Patients with CTS received aforementioned treatments compared with reliable qualitative and quantitative evaluation tools before and after 4-week treatment as well as at a additional 4-week follow-up The main parameters include the Symptom Severity Scale SSS and Functional Status Scale FSS hand grip and key pinch strengths two-point discrimination 2PD Modified Moberg pick-up test MMPUT and Pain assessment visual analog scale VAS
Methods
30 participants with CTS were enrolled age range 30 to 60 years The participants who met the inclusion criteria were randomized into one of two treatment groups KT group and TENS group Participants were blinded to the treatments used in the other group
Patients with CTS received aforementioned treatments compared with reliable qualitative and quantitative evaluation tools before and after 4-week treatment as well as at a additional 4-week follow-up The main parameters include the Symptom Severity Scale SSS and Functional Status Scale FSS hand grip and key pinch strengths two-point discrimination 2PD Modified Moberg pick-up test MMPUT and Pain assessment visual analog scale VAS
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