Symmetrical Scapula-pelvis Proprioceptive Neuromuscular Facilitation and Superficial Back Line in Chronic Neck Pain With Hamstring Tightness

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-40
SponsorUniversity of Karachi

About this trial

A research study will be conducted at Physiotherapy department of the Sindh Institute of Physical Medicine and Rehabilitation, Karachi, Pakistan. Overall 156 patients with 18-40 years old individuals with neck pain will be eligible and they will be included through non-probability, purposive sampling technique. The written informed consent will be taken from all the patients. They will be divided through Simple random sampling (computer generated software) method into two groups, 78 in each group. Group A (experimental group) will receive PNF Symmetrical Scapula-Pelvis Patterns (PNF-SSPP), group B (control group) will receive sub occipital muscle inhibition technique (SMI) and static stretching (SS) of hamstring muscle. All participants will be assessed using assessment form. Outcome measures will be Pain, disability, disability, neck range of motions, hamstring tightness, head posture, and levator scapulae index. An independent assessor blinded to the treatment will assess all the patients for treatment outcome assessment at baseline, after first session and post treatment. Treatment sessions will be given thrice a week for 6 weeks.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Individual with both male and female gender

Individuals with chronic neck pain (pain for > 3 month) with hamstring tightness

Disqualifiers

Any history related to spinal surgery

Previous administration of epidural injections

Neck pain due to specific pathology

Patients with radiculopathy or myelopathy

Trial design

Design model

Parallel

Treatments tested in this trial

  • Suboccipital muscle inhibition technique

    Other intervention

    The Suboccipital Muscle Inhibition technique is a manual therapy method used by practitioners to relieve tension in the suboccipital muscles, which are located at the base of the skull.

  • Symmetrical Scapula-Pelvis Patterns Exercises

    Other intervention

    Symmetrical scapula-pelvis patterns refer to a balanced, aligned posture and movement of the shoulder blades and pelvis which is often a therapeutic goal in physical rehabilitation with proprioceptive neuromuscular facilitation.

  • Static stretching of hamstring muscle

    Other intervention

    Static stretching for hamstrings involves holding a position that creates tension in the back of the thigh for 30 seconds.

Treatment groups

156 Participants
are divided into 2 treatment groups
Group A: Symmetrical Scapula-Pelvis Pattern ExercisesExperimental treatment 1 intervention
Group B: Control TreatmentActive comparator 2 interventions

Trial outcomes

Primary outcomes

1

Change in pain intensity with visual analogue scale for pain at Day 1

The Visual Analogue Scale is a 10 cm line used to measure pain intensity, where the patient marks a point on the line to indicate their pain level, with 0 representing "no pain" and 10 representing "pain as bad as it could possibly be". A score is obtained by measuring the distance from the "no pain" end to the patient's mark, which can be done in centimeters (0-10) or millimeters (0-100). Higher scores indicate greater pain intensity, and this score helps healthcare providers assess severity, which can be categorized as mild (1-3), moderate (4-6), or severe (7-10)

Time frame
From enrolment to the end of the first treatment session at Day 1.
2

Change in pain intensity with visual analogue scale for pain at 6 weeks

The Visual Analogue Scale (VAS) is a 10 cm line used to measure pain intensity, where the patient marks a point on the line to indicate their pain level, with 0 representing "no pain" and 10 representing "pain as bad as it could possibly be". A score is obtained by measuring the distance from the "no pain" end to the patient's mark, which can be done in centimeters (0-10) or millimeters (0-100). Higher scores indicate greater pain intensity, and this score helps healthcare providers assess severity, which can be categorized as mild (1-3), moderate (4-6), or severe (7-10).

Time frame
From enrolment to the end of 18 treatment session at 6 weeks
3

Change in range of motion with goniometry at Day 1

Goniometry measures the change in range of motion of a joint in degrees by using a goniometer to calculate the joint's angle. The increase in degrees suggests increase in range of motion and decrease suggests decrease in range of motion.

Time frame
From enrolment to the end of first treatment at Day 1
4

Change in range of motion with goniometry at 6 weeks

Goniometry measures the change in range of motion of a joint in degrees by using a goniometer to calculate the joint's angle. The increase in degrees suggests increase in range of motion and decrease suggests decrease in range of motion.

Time frame
From enrolment to the end of 18 treatment sessions at 6 weeks.

Secondary outcomes

1

Change in head posture with goniometry at Day 1

Goniometry can measure changes in forward head posture by using a goniometer to calculate the craniovertebral angle. This involves placing the goniometer's base on the C7 spinous process and the moving arm on the tragus of the ear, with a smaller CVA angle indicating a greater degree of forward head posture and vice versa. Changes are tracked by taking repeated measurements over time to see if the CVA increases (improving posture) or decreases (worsening posture).

Time frame
From enrolment to the end of first treatment session at Day 1
2

Change in head posture with goniometry at 6 weeks

Goniometry can measure changes in forward head posture by using a goniometer to calculate the craniovertebral angle. This involves placing the goniometer's base on the C7 spinous process and the moving arm on the tragus of the ear, with a smaller CVA angle indicating a greater degree of forward head posture and vice versa. Changes are tracked by taking repeated measurements over time to see if the CVA increases (improving posture) or decreases (worsening posture).

Time frame
From enrolment to the end of 18 treatment sessions at 6 weeks
3

Change in levator scapulae index with vernier caliper at Day 1

The levator scapulae index is a measurement technique used to assess the relative length of the levator scapulae muscle. It provides a normalized value by comparing the muscle's length to an individual's total body height, which accounts for variations in size between patients. A vernier caliper is the tool used for this measurement due to its accuracy. A normal levator scapulae index range is greater than or equal to 7.44. Decrease in score suggests decrease in muscle length and increase suggests increase in length.

Time frame
From enrolment to the end of first treatment session at Day 1
4

Change in levator scapulae index with vernier caliper at 6 weeks

The levator scapulae index is a measurement technique used to assess the relative length of the levator scapulae muscle. It provides a normalized value by comparing the muscle's length to an individual's total body height, which accounts for variations in size between patients. A vernier caliper is the tool used for this measurement due to its accuracy. A normal levator scapulae index range is greater than or equal to 7.44. Decrease in score suggests decrease in muscle length and increase suggests increase in length.

Time frame
Time Frame: From enrolment to the end of 18 treatment sessions at 6 weeks

Other outcomes

Sponsors and contacts

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University of Karachi

Lead sponsor

Sindh Institute of Physical Medicine and Rehabilitation

Collaborator