Ignite Creation Date:
2024-05-06 @ 4:11 PM
Last Modification Date:
2024-10-26 @ 2:05 PM
Study NCT ID:
NCT04900857
Status:
COMPLETED
Last Update Posted:
2021-05-26
First Post:
2021-05-20
Brief Title:
Comparison of Vibration and Dry Needle in Trigger Point Therapy
Sponsor:
Istanbul Physical Medicine Rehabilitation Training and Research Hospital
Organization:
Istanbul Physical Medicine Rehabilitation Training and Research Hospital
Study Overview
Official Title:
Comparison of Vibration Applied to the Trigger Point and Dry Needle in Acute Myofascial Pain Syndrome a Prospective Randomized Controlled Research
Status:
COMPLETED
Status Verified Date:
2021-05
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 this study is to compare the effects of localized vibration and dry needling applied to the trigger point in the individuals with acute myofascial pain syndromePressure pain threshold PPT was used for the primary outcome measure of the study and pain intensity pain tolerance and short form SF-36 were used for secondary outcome measures
Detailed Description:
The patients were divided into two groups as dry needling and localized vibration using the permuted block randomization method The study was completed with 20 17 women 3 men in the dry needling group and 20 in localized vibration 15 women 5 men In both applications a total of 3 sessions were made to the patients at 1-day intervalsPatients age gender duration of pain localization presence of additional disease drug use were questioned and recorded Pressure pain threshold PPT was used for the primary outcome measure of the study and pain intensity pain tolerance and short form SF-36 were used for secondary outcome measures All evaluation criteria except SF-36 were made before immediately after and 1 day after each session 1 week after the last session SF-36 was evaluated before the 1st session treatment after the 3rd session treatment and 1 week after the 3rd session treatment
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