Ignite Creation Date:
2024-06-16 @ 11:49 AM
Last Modification Date:
2024-10-26 @ 3:31 PM
Study NCT ID:
NCT06437483
Status:
RECRUITING
Last Update Posted:
2024-05-31
First Post:
2024-05-27
Brief Title:
Effects of Sustained Natural Apophyseal Glides Combined With Kinesiotaping in Patients With Chronic Mechanical Neck Pain A Randomised Controlled Trial
Sponsor:
Foundation University Islamabad
Organization:
Foundation University Islamabad
Study Overview
Official Title:
Effects of Sustained Natural Apophyseal Glides Combined With Kinesiotaping in Patients With Chronic Mechanical Neck Pain A Randomised Controlled Trial
Status:
RECRUITING
Status Verified Date:
2024-05
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:
This study is a randomized controlled trial and its purpose is to determine the combined effects of sustained natural apophyseal glides and kinesiotaping on pain range of motion and neck disability in patients with chronic mechanical neck pain
Detailed Description:
This study aims to determine the combined effects of sustained natural apophyseal glides and kinesiotaping in chronic mechanical neck pain patients of age range 18-40 Outcome variables are pain range of motion and functional disability of neck which will be determined by using the following respective data collection tools
1 Numeric pain rating scale
2 Inclinometer
3 Neck Disability Index
Participants of interest will be approached and explained about the research They will be randomly allocated in to two groups Informed written consent will be taken The intervention protocol will be comprised of six sessions over a 2-week period 3 sessions per week on alternate days Outcome measures will be assessed at baseline and after 2 weeks Data will be analyzed and interpreted using SPSS
1 Numeric pain rating scale
2 Inclinometer
3 Neck Disability Index
Participants of interest will be approached and explained about the research They will be randomly allocated in to two groups Informed written consent will be taken The intervention protocol will be comprised of six sessions over a 2-week period 3 sessions per week on alternate days Outcome measures will be assessed at baseline and after 2 weeks Data will be analyzed and interpreted using SPSS
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