Neck pain. Cervical disc disorder, unspecified
Conditions
Interventions
Intervention 1: Control group: conventional physiotherapy treatment, Individuals 12 sessions of therapy (4 weeks of frequency therapy 3 times a week) including 1-20 minutes of TENS and hot packs 2- Ex
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Age between 18-65 years Nonspecific neck pain with a history of at least 12 weeks (chronic) Ability to understanding, speaking and writing in Persian Has not used any other treatment 6 weeks before participating in this project and during it. (To get steady state) Minimum visual analog scale (VAS) 30 of100 mm Confirmation of central sensitization in people with CSI questionnaire (score above 40 CSI questionnaire is the reason for central sensitization)
Exclusion criteria
Exclusion criteria: Cancer, fracture, metabolic diseases, rheumatism, cardiovascular, neurological disorders and osteoporosis Neck radiculopathy, myelopathy and dizziness People with widespread pain disorders such as fibromyalgia syndrome or chronic fatigue syndrome Psychiatric disorders
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Score of 100 mm visual analog scale to assess pain intensity. Timepoint: Pre intervention, Post intervention, one month and 3 months after baseline. Method of measurement: Visual Analogue Scale.;Central Sensitization Inventory questionnaire to assess central sensitivity. Timepoint: Pre intervention, Post intervention, one month and 3 months after baseline. Method of measurement: Central Sensitization Inventory questionnaire score.;Lutron Model 5020 Digital Tensile and pressure Algometer for Measuring Pressure Pain Threshold (PPT). Timepoint: Pre intervention, Post intervention, one month and 3 months after baseline. Method of measurement: Digital Tensile and pressure Algometer.;Score of Neurophysiology of Pain Questionnaire to evaluate the concept of biological mechanism of pain. Timepoint: Pre intervention, Post intervention, one month and 3 months after baseline. Method of measurement: Neurophysiology of Pain Questionnaire.;Neck Disability Index questionnaire for disability evaluation. Timepoint: Pre intervention, Post intervention, one month and 3 months after baseline. Method of measurement: Neck Disability Index questionnaire score.;Pain Catastrophizing Scale to assess pain catastrophizing. Timepoint: Pre intervention, Post intervention, one month and 3 months after baseline. Method of measurement: Pain Catastrophizing Scale score.;Tampa Scale for Kinesiophobia Questionnaire to assess fear of movement. Timepoint: Pre intervention, Post intervention, one month and 3 months after baseline. Method of measurement: Tampa Scale for Kinesiophobia Questionnaire score.;Pain Awareness and Vigilance questionnaire to assess pain awareness and alertness. Timepoint: Pre intervention, Post intervention, one month and 3 months after baseline. Method of measurement: Pain Awareness and Vigilance questionnaire score. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life score. Timepoint: Pre Intervention, Post Intervention, one month and three months after baseline. Method of measurement: Score of SF3 6 questionnaires to assess the quality of life.;Score of a person's perception of their illness. Timepoint: Pre Intervention, Post Intervention, one month and three months after baseline. Method of measurement: Score of Brief illness perception questionnaire to assess a person's perception of their illness.;General measurement of the rate of change. Timepoint: Pre Intervention, Post Intervention, one month and three months after baseline. Method of measurement: General review of the amount of changes with the general form of the amount of changes. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactHosein Kouhzad Mohammadi
Ahvaz University of Medical Sciences
Outcome results
None listed