Ignite Creation Date:
2024-10-26 @ 3:43 PM
Last Modification Date:
2024-10-26 @ 3:43 PM
Study NCT ID:
NCT06648070
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-10-01
Brief Title:
Effects of Neuromuscular Reeducation Versus Post Facilitation Stretch Technique for Upper Cross Syndrome Among IT Professionals
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Effects of Neuromuscular Reeducation Versus Post Facilitation Stretch Technique for Upper Cross Syndrome Among IT Professionals
Status:
RECRUITING
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study is a randomised control trial and the purpose of this study is to determine the Effects of Neuromuscular Reeducation Versus Post Facilitation Stretch Technique for Upper Cross Syndrome among IT professionals
Detailed Description:
The purpose of this study is to determine the Effects of Neuromuscular Reeducation Versus Post Facilitation Stretch Technique for Upper Cross Syndrome among IT professionals
we make 2 groups control and treatment group we give NMR technique to treatment group and PFS technique to control group in patients with upper cross syndrome
first we take base line readings of cervical ROM NPRS AND neck diasbilty index
after 2 weeks of treatment again we take same readings and compare both readings
with techniques we also perform strengthning excercise of weal muscles for both groups
we make 2 groups control and treatment group we give NMR technique to treatment group and PFS technique to control group in patients with upper cross syndrome
first we take base line readings of cervical ROM NPRS AND neck diasbilty index
after 2 weeks of treatment again we take same readings and compare both readings
with techniques we also perform strengthning excercise of weal muscles for both groups
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None