- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04913441
Manual Therapy vs Stretching vs Routine Physical Therapy in Nonspecific Chronic Neck Pain
Effects of Manual Therapy Versus Stretching Versus Routine Physical Therapy on Pain, ROM, and Functional Disability in Restaurant Chef Workers With Nonspecific Chronic Neck Pain: A Randomised Controlled Trial
Study Overview
Status
Conditions
Detailed Description
Neck pain (NP) is one of the basic musculoskeletal issues. Neck pain can be due to stress about the musculoskeletal framework because of postural problems and may be related with different causes, such as: - Intervertebral disc herniation, -nerve compression -fracture.
Nonspecific neck pain is a pain located in the lateral and posterior neck that does not show pathognomonic signs and symptoms. When the duration of symptoms is greater than 12 weeks of evolution, it acquires the value of chronicity, being denominated non-specific chronic neck pain (NCNP). It is a common disorder, which generates a great impact and socio-economic cost .
In this study we evaluate the comparison of manual physical therapy vs routine physical therapy vs stretching physical therapy effects among restaurants chefs having non-specific chronic pain.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab Pakistan
-
Faisalabad, Punjab Pakistan, Pakistan, 3800
- Ripah International University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
Neck pain for atleast 3 months having no :
- Neurological Problem
- Rheumatological Problem
- Patient had taken any analgesic medication for neck pain for last 3 months.
- Non specific neck pain
- Age 18-60 years
Exclusion Criteria:
Neck pain due to,
- Tumors
- Ankylosings Spondylitis
- Fracture
- Dislocation
- Presence of cord compression
- Vertebrobasilar artery insufficiency
- Osteoprosis OR Osteopenia
- Long term use of anticoagulant or corticosteroid drugs
- Pain due to any congenital deformity, inflammation or any infection
- Carcinoma
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Routine physical therapy
Patients in this group will get every session of 30 min 3 times per week on alternative days for 12 weeks
|
Patients in this group will get every session routine physical therapy of 30 minutes 3 times per week on alternative days for 12 weeks
Other Names:
|
Experimental: Manual physical therapy with routine physical therapy
Patients in group B will get every session 30 minutes 3 times per week on alternative days
|
Patients in this group will get every session Manual physical therapy with routine physical therapy of 40 to 45 minutes 3 times per week on alternative days for 12 weeks
Other Names:
|
Experimental: Stretching physical therapy with routine physical therapy
Patients in this group will get every session 30 minutes 3 times per week on alternative days
|
Patients in this group will get every session of Stretching physical therapy with routine physical therapy of 40 to 45 minutes 3 times per week on alternative days for 12 weeks
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Visual Analog scale (VAS)
Time Frame: 3 months
|
Visual Analogue Scale is a measurement instrument that tries to measure a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured. It is often used in epidemiologic and clinical research to measure the intensity or frequency of various symptoms. The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain |
3 months
|
Bubble inclinometer
Time Frame: 3 months
|
Baseline's Bubble Inclinometer is a simple to use device for measuring range of motion in patients.
The inclinometer can be used to measure range of motion in the neck, the hip, the elbow, the knee, the shoulder, the spine, the ankle, the wrist, and the MCP joint
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Neck disability Index (NDI)
Time Frame: 3 months
|
This questionnaire has been designed to give us information as to how your neck pain has affected your ability to manage in everyday life.The NDI can be scored as a raw score or doubled and expressed as a percent.
Each section is scored on a 0 to 5 rating scale, in which zero means 'No pain' and 5 means 'Worst imaginable pain'.
Points summed to a total score.
|
3 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RCRAHS/FSD/REC/0260
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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