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Effect of yoga and physiotherapy in mechanical neck pain.

Effectiveness of Ardh Matsyendrasan Alongwith Mind Sound Resonance Technique and Proprioceptive Neuromuscular Facilitation in Mechanical Neck Pain.

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/01/016985
Enrollment
120
Registered
2019-01-08
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: M628- Other specified disorders of muscle

Interventions

Intervention1: Group 1: PNF group: Phase 1: 20 Sessions of PNF (5 times/week) (15 Minutes) Phase 2: Hot Pack (5 minutes) Phase 3: Ergonomic advice Intervention2: Group 2: Yoga group: Phase 1: Tadasa

Sponsors

Aditi Singh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Bilateral Mechanical neck pain of subacute duration (6week-3month), NDI 2. Age of 18- 30 years. 3. Both males and females. 4. Subjects with dull aching pain increased by sustained postures, neck movement, palpation of cervical musculature. 5. Subjects willing to participate and give consent to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Subjects excluded with spinal deformities. 2. Short neck. 3. Specific neck pain such as disc lesion, Cervical spondylitis with radiculopathy, inflammatory disease, neoplasm etc. 4. History of osteoporosis, fracture, whiplash injury. 5. Cervical surgery, cervicogenic headache. 6. Subjects with Low back pain.

Design outcomes

Primary

MeasureTime frame
1. Neck Pain and Disability: Neck Disability Index (NDI). 2. Pain Pressure Threshold (PPT): Algometer 3. Health related Quality of Life: SF-36 Timepoint: 4 week treatment protocol with 5 days/week for 20 min/day. Data will be collected first at baseline before start of treatment and then 4 weeks after treatment. Follow up is 15 days after 4 week of treatment.

Secondary

MeasureTime frame
Range of movement: Cervical GoniometerTimepoint: 4 week treatment protocol with 5 days/week for 20 min/day. Data will be collected first at baseline before start of treatment and then 4 weeks after treatment. Follow up is 15 days after 4 week of treatment.

Countries

India

Contacts

Public ContactProf Dr Jasobanta Sethi

Amity Institute of Physiotherapy, Amity University, Noida

jsethi@amity.edu

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 14, 2026