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A study to see how physiotherapy exercises can help to improve the overall well being in neck pain patients

Effectiveness of Sensorimotor Training on Physical, Physiological and Psychosocial Parameters in Non-Specific Chronic Neck Pain - NIL

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/089488
Enrollment
66
Registered
2025-06-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: M629- Disorder of muscle, unspecified

Interventions

Intervention1: Sensorimotor training: A combination of cervical proprioception (LASER-guided head relocation, LASER-guided pattern tracing) occulomotor (Eye follow, saccades, gaze stability and Eye-he

Sponsors

none
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Individuals with chronic neck pain lasting for at least three months on and off with a score of more than or equal to 10 on NDI. (10) NPRS less than 6 Participants aged 25 to 40 years old. (3) Subjects with impaired joint position sense and balance will be included. Patients with an average of more than 4.5 degrees joint position error in rotation or extension and an inability to maintain tandem stance on a firm surface with eyes closed (age less than or equal to 45 years) for 30 seconds.(10) Patients who have not taken treatment for neck pain for the past three months will be included. Patients with BMI between 18 to 25 will be included.

Exclusion criteria

Exclusion criteria: Individuals with chronic neck pain attributed to specific pathologies such as spinal stenosis, inflammatory conditions (e.g. rheumatoid arthritis), or neurological disorders (e.g.Cervical radiculopathy, stroke) will be excluded.(10) Participants who have experienced recent trauma (e.g., whiplash injury) or undergone neck surgery or any implant will be excluded.(10) Participants with uncontrolled medical conditions such as cardiovascular disease, respiratory disorders, or uncontrolled hypertension that could interfere with participation or outcomes will be excluded. Malignancies. Diabetes Impaired vision that cannot be corrected with glasses. Pregnant individuals will be excluded due to potential risks associated with participation in physical training programs and assessments. Lactating mothers Patients with pain in other joints such as hip, knee, ankle, sacroiliac joint and lumbosacral spine. Patient with history of ENT disorder or vestibular disorder(10)

Design outcomes

Primary

MeasureTime frame
Physical Outcomes 1. Forward head angle 2. Cervical muscle endurance 3. Pain Pressure Threshold Physiological Outcomes 1. Cervical Joint Position Sense 2. Sleep Quality 3. Electromyography 4. Balance Psychosocial Outcomes Anxiety, depression, stress and fear of movementTimepoint: Day 1 after 3 weeks after 6 weeks

Secondary

MeasureTime frame
C Reactive protein 2 point discrimination Timepoint: At day 1. At the end of 6 weeks

Countries

India

Contacts

Public ContactProf Sohrab Ahmad Khan

Jamia Hamdard

sakhan_ahs@jamiahmdard.ac.in8802648164

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026