Neck Pain Clinical Trial
Official title:
A Randomized Clinical Trial To Review The Effectiveness Of Dry Needling Versus Trigger Point Compression Release Among Patients With Neck Pain
Verified date | May 2023 |
Source | Health Education Research Foundation (HERF) |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This randomized control trial was conducted to investigate the efficacy of trigger point dry needling which is a modern treatment intervention compared with ischemic compression release in the patients having neck pain due to myofascial trigger points.
Status | Completed |
Enrollment | 30 |
Est. completion date | October 31, 2021 |
Est. primary completion date | September 30, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 40 Years |
Eligibility | Inclusion Criteria: - Patients between the age group of 20 to 40 years. - Both Male and female patients. - Patients presenting with neck pain due to MTrP's. - The presence of a palpable taut band in the neck region. - Patients reporting typically referred pain pattern of the MTrP in response to compression. Exclusion Criteria: - Patients with any associated comorbidities such as hypertension and diabetes. - Patients with known history of fibromyalgia syndrome, whiplash injury, cervical spine surgery fracture and cervical radiculopathy. - Patients with any systemic disease such as rheumatism and tuberculosis or cervical myelopathy and multiple sclerosis. - Patients with history of myofascial trigger point therapy one month prior to enrollment. - Patients with non-cooperative attitude, fear or any contraindications to needling. |
Country | Name | City | State |
---|---|---|---|
Pakistan | Bashir Institute of Health Sciences,Bashir General & Dental Hospital | Islamabad |
Lead Sponsor | Collaborator |
---|---|
Health Education Research Foundation (HERF) |
Pakistan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Pain assessed through Visual Analogue Pain Scale | To measure the change in terms of betterment or aggravation in the intensity of pain baseline then after week 1,week 2 and after week 3. | Data was Collected at Baseline and after week 1,2 & 3. | |
Primary | Change in degree of disability assessed through Northwick Park Neck Pain Questionnaire. | To measure change in the intensity of neck pain and the consequent patient disabilities at baseline then after week 1,week 2 and after week 3. | Data was Collected at Baseline and after week 1,2 & 3. |
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