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The effect of ergonomic latex pillow on neck arthrosis treatment

Control trial of the effect of ergonomic latex pillow on pain and disability, range of motion, cervical flexor muscles endurance and head and neck posture in patients with cervical spondylosis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014021916643N1
Enrollment
42
Registered
2016-12-28
Start date
2017-01-17
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

cervical spondylosis. arthrosis or osteoarthritis of spine degeneration of facet joints

Interventions

Intervention 1: Intervention group: physiotherapy + ergonomic latex pillow. Patients in this group sleep on ergonomic latex pillow for 4 weeks and will receive physiotherapy 3 sessions a week (12 sess
Lifestyle
Rehabilitation
Intervention group: physiotherapy + ergonomic latex pillow. Patients in this group sleep on ergonomic latex pillow for 4 weeks and will receive physiotherapy 3 sessions a week (12 sessions) for 30-45
Control group: physiotherapy + his/her usual pillow. Patients in this group sleep on their usual pillow for 4 weeks and will receive physiotherapy 3 sessions a week (12 sessions) for 30-45 minutes.

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: people at the age of 30 to 60 year; Reporting a chronic and/or dull pain in the neck, with or without a radicular pain through the upper limbs; Grade 2 and 3 cervical spondylosis with at least two out of four of the following radiographic changes in the cervical region: Intervertebral disc space narrowing; Sclerosis of subchondral bone; Osteophyt formation between adjacent vertebral bodies or articular facets; The narrowing of the space between articular processes (facet joints); Positive compression and distraction test; Score = 2 of 10 in Numerical Pasin Rating Scale (NPRS); Score = 20% in Neck Disability Index (NDI) questionnaire. Exclusion criteria: Other non-specific neck pain lesions, acute neck strain, postural neck ache, or whiplash; Metabolic diseases, Paget’s disease, osteoporosis, gout, or pseudo-gout; Inflammatory disease—rheumatoid arthritis, ankylosing spondylitis, or polymyalgia rheumatic; Infections—osteomyelitis or tuberculosis; tumors; Fibromyalgia and psychogenic neck pain; Temporomandibular joint surgery or disorder; Trauma or disease affecting the cervical and cervicothoracic spine in the preceding year or a history of cervical surgery; Spinal cord canal stenosis; Congenital anomalies involving the spine (cervical, thoracic, lumbar and scoliosis); Pregnancy or breast-feeding; Persistent respiratory difficulties over the last 5 years that have necessitated absence from work, have required long-term medication, or have interfered with daily activities; Recurrent middle ear infections over the last 5 years or any hearing impairment requiring the use of a hearing aid; Any change (increase or decrease) in head and neck support or people who use more than one pillow; Patients who don’t complete a 12-sessions therapeutic period, or follow up evaluation; Subjects normally using no pillow or anything other than a conventional pillow (which is common in Iranian culture like feather or cotton pillow) or if they have a history of using a cervical ruff or pillow (medical pillow); Subjects who received physiotherapy or manipulation because of the neck pain during last three months; Wearing collar.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Range of motion. Timepoint: preintervention and post intervention. Method of measurement: inclinometer.;The amount of craniovertebral angle. Timepoint: Preintervention and post intervention. Method of measurement: Photo will be taken from patient and then the photo will be entered into the Adobe Acrobat Professional and craniovertebral angle will be calculated.;The amount of cervical short flexor muscles endurance. Timepoint: preintervention and post intervention. Method of measurement: the subject lying supine on bed then he/she gets his/her head up meanwhile retracting chin. The time of maintaining of this position is calculated by stop watch.;Pain. Timepoint: Before intervention, 1, 2 and 3 weeks later when intervention was applied and finally post intervention when treatment was done. Method of measurement: Numerical Pain Rating Scale (The patient scores).;The amount of disability caused by neck pain. Timepoint: Before intervention, 1, 2 and 3 weeks later when intervention was applied and finally post intervention when treatment was done. Method of measurement: Persian translation of Neck Disability Index questionnaire.

Secondary

MeasureTime frame
The amount of cervical extensor muscles endurance. Timepoint: preintervention and post intervention. Method of measurement: The subject lying prone on bed with their head and neck initially supported over the end while a 105 gr wheight suspended from his/her head then he/she extends his/her neck. The time of maintaining of this position is calculated by stop watch.;The amount of satisfaction from ergonomic latex pillow. Timepoint: post intervention. Method of measurement: self-made questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBehshid Farahmand

Iran University of Medical Sciences

farahmandb1@yahoo.com+98 21 2222 8051

Outcome results

None listed

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