Sub-Occipital MIT With and Without HR Agonist Contraction of Hamstrings in Neck Pain Patients With Hamstring Tightness

Riphah International University

Status: Enrolling

Conditions: Neck Pain Patients With Hamstring Tightness

Treatments: Other: Sub Occipital Muscle Inhibition; Other: Sub Occipital Inhibition with Hold Relax Agonist Contraction

Study type: Interventional

Funder types: Other

Identifiers

NCT05353075

REC/Lhr/22/0133 Sumaiya

Details and patient eligibility

About

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.

Enrollment: 30 estimated patients

Sex: All

Ages: 25 to 40 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Age 25-40 years Both Genders ( Male and Female) Neck Pain on NPRS ≥5 NDI score ≥14 ( Moderate disability) Active knee extension lag ≥30 and considered as tight hamstrings

Exclusion criteria

Acute Low back or Neck pain History of lumbar and cervical herniated disc and spinal stenosis History of cervical spine surgery and Trauma History of vascular disease in head and neck Progressive neurological deficit or Inflammatory condition ( such as peripheral neuropath, rheumatoid arthritis) History of abdominal or pelvic surgery in last 6 months

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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30 participants in 2 patient groups

Sub Occipital Muscle Inhibition

Other group

Description:

Subjects in this group will receive only Sub Occipital Muscle Inhibition Technique and heating pad for 10 minutes.

Treatment:

Other: Sub Occipital Muscle Inhibition

Sub Occipital Inhibition with Hold Relax Agonist Contraction

Experimental group

Description:

Subjects in this group will receive Sub Occipital Inhibition and Hold Relax Agonist Contraction of hamstrings.

Treatment:

Other: Sub Occipital Muscle Inhibition

Other: Sub Occipital Inhibition with Hold Relax Agonist Contraction