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Effect of combination of two physiotherapeutic interventions for the treatment of neck pain.

Combined effect of dry needling and muscle energy technique on neck pain of myofascial origin.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/03/040750
Enrollment
36
Registered
2022-03-02
Start date
Unknown
Completion date
Unknown
Last updated
2022-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Dry Needling (DN), and Muscle Energy Technique (MET): Dry needling is and invasive technique used for the management of myofascial trigger points, and Muscle energy technique is an oste

Sponsors

There is no primary sponser
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Neck pain for atleast 3 months (or more). 2. Subjects having unilateral and bilateral pain involving the upper trapezius and levator scapulae muscles. 3. Presence of myofascial trigger points in upper trapezius and levator scapulae muscles

Exclusion criteria

Exclusion criteria: 1. Orofascial pain and temporomandibular disorders according to the Reseach Diagnostic Criteria of Temporomandibular disorders (RDC/TMD) 2. A history of traumatic injuries (e.g., contusion, fractures, and whiplash injuries) 3. Systemic diseases such as fibromyalgia, systemic lupus erythematosis, and psoriatic arthritis. 4. Neurologic disorders (e.g., trigeminal neuralgia or occipital neuralgia). 5. Concomitant medical diagnosis of any primary headache (tension type or migraine). 6. Cervical spine surgery 7. Clinical diagnosis of cervical radiculopathy or myelopathy. 8. Needle phobia 9. History of previous physical therapy intervention fpr the cervical region. 10. Furthermore, subjects with shoulder diseases like tendonitis, bursitis, and capsulitis will be excluded.

Design outcomes

Primary

MeasureTime frame
Pain, Range of motion, and disability level of the subjects.Timepoint: 4 weeks (Baseline measurements Post- intervention immediate Post intervention Day 4 Post intervention Day 7)

Secondary

MeasureTime frame
Changes in the Quality of lifeTimepoint: 1 month

Countries

India

Contacts

Public ContactDr Pankajpreet Singh

Sri Guru Granth Sahib World University, Fatehgarh Sahib

physio.supreet@gmail.com9781526644

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026