Effects of Dry Needling in Patients With Upper Cross Syndrome
Effects of Dry Needling on Pain, Range of Motion and Function in Patient With Upper Cross Syndrome
1 other identifier
interventional
34
1 country
1
Brief Summary
The study will be done to evaluate the effectiveness of dry needling of muscles involved in Upper Cross Syndrome. Muscles involved in upper cross syndrome are tight upper trap, Levator Scapulae, Sternocledomastoid , Pectorals major and minor and rhomboids. Physical assessment of trigger points will locate the target area for dry needling. After pre treatment measurements, dry needling will be performed to treatment group and stretching, hot pack and tens will be apply in control group. Study design will be randomized controlled trial and sample size will be 34 participants. Data will be collected from Riphah Rehabilitation Center. Patients of 20-50 years old with UCS diagnosed through observation and physical examination will be included. Patients with systemic soft tissue and bony diseases will be excluded. Intervention duration will be two session of DNT with two weeks routine management. Basic tools will be Visual analog scale (VAS), Neck Disability Index (NDI) and Goniometry
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2020
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 30, 2020
CompletedFirst Submitted
Initial submission to the registry
December 16, 2020
CompletedFirst Posted
Study publicly available on registry
December 19, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
January 30, 2021
CompletedMarch 8, 2021
March 1, 2021
9 months
December 16, 2020
March 4, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Visual Analogue Scale
A Visual Analogue Scale (VAS) 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
2nd Week
Secondary Outcomes (1)
Neck Disability Index Questionnaire
2nd Week
Other Outcomes (1)
Goniometer
2nd Week
Study Arms (2)
Group A
EXPERIMENTALDry Needling
Group B
ACTIVE COMPARATORHot pack , TENS , Stretching
Interventions
Dry needling on Upper trapezius, Levator Scapulae, Sternocledomastoid , Pectorals major and minor and rhomboids for 10 min
Treatments are 1. Hot Pack for 15 minutes 2. TENS for 10 minutes 3. Stretching The third treatment which is Stretching will be given one time on each muscle (tight upper trap, Levator Scapulae, Sternocledomastoid , Pectorals major and minor and rhomboids) of upper spine
Eligibility Criteria
You may qualify if:
- Stiffness and gradual pain in neck and shoulder
- Pain due to Postural Dysfunction
- Trauma or insidious onset
You may not qualify if:
- Any systemic soft tissue and bony disease.
- Patient with spinal tuberculosis, spinal fractures, pregnancy, cancer.
- Any recent surgery.
- Patient with any cervical or thoracic problem.
- Patients with any other serious pathology/red flags
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sheikh Zaid Hospital
Rahim Yar Khan, Punjab Province, Pakistan
Related Publications (9)
Dunning J, Butts R, Mourad F, Young I, Flannagan S, Perreault T. Dry needling: a literature review with implications for clinical practice guidelines. Phys Ther Rev. 2014 Aug;19(4):252-265. doi: 10.1179/108331913X13844245102034.
PMID: 25143704BACKGROUNDTough EA, White AR, Cummings TM, Richards SH, Campbell JL. Acupuncture and dry needling in the management of myofascial trigger point pain: a systematic review and meta-analysis of randomised controlled trials. Eur J Pain. 2009 Jan;13(1):3-10. doi: 10.1016/j.ejpain.2008.02.006. Epub 2008 Apr 18.
PMID: 18395479BACKGROUNDGerber LH, Shah J, Rosenberger W, Armstrong K, Turo D, Otto P, Heimur J, Thaker N, Sikdar S. Dry Needling Alters Trigger Points in the Upper Trapezius Muscle and Reduces Pain in Subjects With Chronic Myofascial Pain. PM R. 2015 Jul;7(7):711-718. doi: 10.1016/j.pmrj.2015.01.020. Epub 2015 Feb 4.
PMID: 25661462BACKGROUNDKalichman L, Vulfsons S. Dry needling in the management of musculoskeletal pain. J Am Board Fam Med. 2010 Sep-Oct;23(5):640-6. doi: 10.3122/jabfm.2010.05.090296.
PMID: 20823359BACKGROUNDLiu L, Huang QM, Liu QG, Ye G, Bo CZ, Chen MJ, Li P. Effectiveness of dry needling for myofascial trigger points associated with neck and shoulder pain: a systematic review and meta-analysis. Arch Phys Med Rehabil. 2015 May;96(5):944-55. doi: 10.1016/j.apmr.2014.12.015. Epub 2015 Jan 7.
PMID: 25576642BACKGROUNDGonzalez-Perez LM, Infante-Cossio P, Granados-Nunez M, Urresti-Lopez FJ. Treatment of temporomandibular myofascial pain with deep dry needling. Med Oral Patol Oral Cir Bucal. 2012 Sep 1;17(5):e781-5. doi: 10.4317/medoral.17822.
PMID: 22549679BACKGROUNDAhmad Z, ur Rehman S, Ahmad S, Afzal MF. Effects of combined manual postural correction technique in patient with upper cross syndrome. Rawal Medical Journal. 2019;44(3):486-9.
BACKGROUNDThacker D, Jameson J, Baker J, Divine J, Unfried A. Management of upper cross syndrome through the use of active release technique and prescribed exercises. Logan College of Chiropractic. 2011 Apr
BACKGROUNDYeganeh Lari A, Okhovatian F, Naimi Ss, Baghban AA. The effect of the combination of dry needling and MET on latent trigger point upper trapezius in females. Man Ther. 2016 Feb;21:204-9. doi: 10.1016/j.math.2015.08.004. Epub 2015 Aug 14.
PMID: 26304789BACKGROUND
MeSH Terms
Conditions
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Syed Shakil Ur Rehman
Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 16, 2020
First Posted
December 19, 2020
Study Start
March 30, 2020
Primary Completion
December 30, 2020
Study Completion
January 30, 2021
Last Updated
March 8, 2021
Record last verified: 2021-03
Data Sharing
- IPD Sharing
- Will not share