Dry Needling and Maitland Joint Mobilization Techniques in Patients With Myofacial Chronic Neck Pain
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| ClinicalTrials.gov Identifier: NCT04568915 |
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Recruitment Status :
Completed
First Posted : September 29, 2020
Last Update Posted : September 29, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Myofacial Pain Neck Pain | Other: Dry Needling Other: Maitland Mobilization | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 30 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Double (Participant, Outcomes Assessor) |
| Primary Purpose: | Treatment |
| Official Title: | Comparison Between Dry Needling and Maitland Joint Mobilization Techniques in Patients With Myofacial Chronic Neck Pain |
| Actual Study Start Date : | September 15, 2019 |
| Actual Primary Completion Date : | June 20, 2020 |
| Actual Study Completion Date : | June 28, 2020 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: Dry Needling-Group
Tens, Stretching, Strengthening(girdle), Neck Isometrics, DN
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Other: Dry Needling
TENS 10 minutes, Stretching, Strengthening(girdle),Neck Isometrics, DN |
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Active Comparator: Maitland-Group
Tens Stretching, Strengthening(girdle), Neck Isometrics, Maitland joint mobilization
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Other: Maitland Mobilization
TENS 10 minutes, Stretching, Strengthening(girdle),Neck Isometrics, Maitland joint mobilization |
- Numeric Pain Rating Scale NPRS [ Time Frame: 4 months ]The Numerical Pain Rating Scale (NPRS) is a subjective measure in which individuals rate their pain on an eleven-point numerical scale. The scale is composed of 0 (no pain at all) to 10 (worst imaginable pain).
- Range of Motion [ Time Frame: 4 months ]Standard Goniometer will be used.Higher score shows improvement.
- Disability [ Time Frame: 4 months ]Scoring: For each section the total possible score is 5: if the first statement is marked the section score = 0, if the last statement is marked it = 5. If all ten sections are completed the score is calculated as follows: Example:16 (total scored) 50 (total possible score) x 100 = 32% If one section is missed or not applicable the score is calculated: 16 (total scored) 45 (total possible score) x 100 = 35.5% Minimum Detectable Change (90% confidence): 5 points or 10 %points
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| Ages Eligible for Study: | 25 Years to 45 Years (Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Bilateral pain involving the upper trapezius and elevator muscle of the scapula;
- Duration of pain of at least 3 months;
- A pain intensity corresponding to at least 20 mm on a 100 mm visual analogue scale (VAS)
- Neck pain with symptoms provoked by either neck postures or neck movement;
- Pain localized at least in the cervical and occipital regions but not in the orofacial region;
- Neck disability index (NDI) greater than or equal to 15 points;
- Restricted cervical range of movements (flexion, extension, rotation, and sidebending); (i) Presence of bilateral MTrPs in upper trapezius and levator scapulae muscles
Exclusion Criteria:
- Any signs, symptoms, or history of the following diseases:
- Orofacial pain and temporo-mandibular disorders
- A history of traumatic injuries (e.g., contusion, fracture, and whiplash injury);
- Systemic diseases such as fibromyalgia, systemic erythematous lupus, and arthritis; (d) Neurologic disorders (e.g., trigeminal neuralgia or occipital neuralgia);
- Concomitant medical diagnosis of any primary headache (tension type or migraine);
- Unilateral neck pain;
- Cervical spine surgery;
- Clinical diagnosis of cervical radiculopathy or myelopathy;
- Needle phobia;
- History of previous physical therapy intervention for the cervical region in last 6 months.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04568915
| Pakistan | |
| Riphah IU | |
| Lahore, Pakistan, 54000 | |
| Principal Investigator: | Maryam Shabbir, PHD | Riphah International University |
| Responsible Party: | Riphah International University |
| ClinicalTrials.gov Identifier: | NCT04568915 |
| Other Study ID Numbers: |
MS-OMPT/Spring19/030 Momna Momna Ghaffar ( Other Identifier: Riphah ) |
| First Posted: | September 29, 2020 Key Record Dates |
| Last Update Posted: | September 29, 2020 |
| Last Verified: | September 2020 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Neck Pain Myofacial Pain |
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Neck Pain Facial Pain Pain Neurologic Manifestations |

