Ignite Creation Date:
2024-05-06 @ 5:34 PM
Last Modification Date:
2024-10-26 @ 2:31 PM
Study NCT ID:
NCT05353075
Status:
UNKNOWN
Last Update Posted:
2022-06-16
First Post:
2022-04-21
Brief Title:
Sub-Occipital MIT With and Without HR Agonist Contraction of Hamstrings in Neck Pain Patients With Hamstring Tightness
Sponsor:
Riphah International University
Organization:
Riphah International University
Study Overview
Official Title:
Effects of Sub-Occipital Muscle Inhibition Technique With and Without Hold Relax Agonist Contraction of Hamstrings on Pain Disability and Craniovertebral Angle in Neck Pain Patients With Hamstring Tightness
Status:
UNKNOWN
Status Verified Date:
2022-06
Last Known Status:
RECRUITING
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:
Hamstrings and Sub occipital muscles are part of the superficial back line of the myofascial chain which connects the neck to the lower extremity and the soft tissue in the cervical spine links the dura and sub occipital muscle fascia Increased tension in one or other part of this myofascial chain disturbs the whole superficial back line and compromises the flexibility The objective of this study is to determine the Effects of Sub-Occipital Muscle Inhibition technique MIT with and without Hold Relax HR Agonist Contraction of Hamstrings on Pain Disability and Craniovertebral angle in Neck pain patients with Hamstring Tightness This study will be a randomized controlled trial and will be conducted in Physiotherapy center of AL-Mahmood Welfare Foundation Sahiwal This study will be completed in time duration of 10 months after the approval of synopsis and consecutive sampling technique will be used A sample size of 34 will be randomly assigned into two groups Group A will be given Sub Occipital Muscle Inhibition treatment while Group B will be given Sub occipital Muscle Inhibition and Hold Relax Agonist Contraction of hamstring Each group will be given three sessions per week Data will be collected from all participants before first session of treatment and after 6th session of treatment by using Numeric Pain Rating Scale NPRS Neck Disability Index NDI Cervical Range of motion CROM Craniovertebral Angle CVA and Active knee extension AKE test measurement
Detailed Description:
None
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