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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07332845
Enrollment
156
Registered
2026-01-12
Start date
2026-01-16
Completion date
2026-11-26
Last updated
2026-03-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Neck Pain, Hamstring Muscle Tightness, Neck Pain

Keywords

neck ache, Exercise, Muscle Stretching, Muscle Inhibition, PNF

Brief summary

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.

Detailed description

A maximum drop-out rate of 20% is expected. The Statistical package for the social sciences (SPSS) 23 version will be used for data analysing. The Mean ± SD will be calculated for quantitative variables like age. The qualitative variables will be shown through calculated frequencies and percentages. The outcome results of the study (decrease pain intensity, improve disability, improve ROM and improve muscle tightness) taken before, after 1st session and after 18th session will be compared and analyzed. The repeated measure of ANOVA will be used as the statistical test. The p-value of 0.05 will be considered as level of significant.

Interventions

OTHERSuboccipital muscle inhibition technique

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.

OTHERSymmetrical Scapula-Pelvis Patterns Exercises

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.

OTHERStatic stretching of hamstring muscle

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

Sponsors

University of Karachi
Lead SponsorOTHER
Sindh Institute of Physical Medicine and Rehabilitation
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Data analyst was also blinded.

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Individual with both male and female gender * Individuals with chronic neck pain (pain for \> 3 month) with hamstring tightness

Exclusion criteria

* Any history related to spinal surgery * Previous administration of epidural injections * Neck pain due to specific pathology * Patients with radiculopathy or myelopathy * Traumatic spinal cord injury * Neck pain associated with progressive neurological deficit or loss of strength

Design outcomes

Primary

MeasureTime frameDescription
Change in pain intensity with visual analogue scale for pain at Day 1From enrolment to the end of the first treatment session 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)
Change in pain intensity with visual analogue scale for pain at 6 weeksFrom enrolment to the end of 18 treatment session at 6 weeksThe 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).
Change in range of motion with goniometry at Day 1From enrolment to the end of first treatment at Day 1Goniometry 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.
Change in range of motion with goniometry at 6 weeksFrom enrolment to the end of 18 treatment sessions 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.
Change in neck disability with Neck Disability Index at day 1From enrolment to the end of first treatment session at Day 1.A change in the Neck Disability Index score indicates a change in a patient's self-reported neck disability. A higher score means greater disability.The NDI is scored from 0 to 50, or 0% to 100%. A score of 0 indicates no limitation, while a score of 50 represents complete limitation.
Change in neck disability with Neck Disability Index at 6 weeksFrom enrolment to the end of 18 treatment sessions at 6 weeks.A change in the Neck Disability Index score indicates a change in a patient's self-reported neck disability. A higher score means greater disability.The NDI is scored from 0 to 50, or 0% to 100%. A score of 0 indicates no limitation, while a score of 50 represents complete limitation.
Change in hamstring tightness with Sit and Reach (SR) test at Day 1From enrolment to the end of first treatment session at Day 1.A low Sit and Reach test score in centimetre indicates tight hamstrings, while a higher score shows better hamstring flexibility. When a person with tight hamstrings performs the Sit and Reach test, the muscles pull the pelvis into a posterior tilt, which limits the ability to reach as far and can cause the lower back to round instead of the spine flexing naturally. As hamstring tightness decreases through stretching, the SR score increases, signifying greater flexibility and improved superficial back line.
Change in hamstring tightness with Sit and Reach (SR) test at 6 weeksFrom enrolment to the end of 18 treatment sessions at 6 weeks.A low Sit and Reach test score in centimetre indicates tight hamstrings, while a higher score shows better hamstring flexibility. When a person with tight hamstrings performs the Sit and Reach test, the muscles pull the pelvis into a posterior tilt, which limits the ability to reach as far and can cause the lower back to round instead of the spine flexing naturally. As hamstring tightness decreases through stretching, the SR score increases, signifying greater flexibility and improved superficial back line.

Secondary

MeasureTime frameDescription
Change in head posture with goniometry at Day 1From enrolment to the end of first treatment session at Day 1Goniometry 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).
Change in head posture with goniometry at 6 weeksFrom enrolment to the end of 18 treatment sessions at 6 weeksGoniometry 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).
Change in levator scapulae index with vernier caliper at Day 1From enrolment to the end of first treatment session at Day 1The 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.
Change in levator scapulae index with vernier caliper at 6 weeksTime Frame: From enrolment to the end of 18 treatment sessions at 6 weeksThe 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.

Countries

Pakistan

Contacts

CONTACTAftab Ahmed Mirza Baig, PhD
ab.dptrm@gmail.com+923002739920
CONTACTBasit Ansari, PhD
basitansari@hotmail.com+923222279221
PRINCIPAL_INVESTIGATORAftab Ahmed Mirza Baig, PhD

University of Karach

STUDY_DIRECTORBasit Ansari, PhD

University of Karachi

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 11, 2026