Skip to content

Calisthenic Exercise v/s Conventional Treatment on Non Specific Neck Pain

Effect of calisthenic exercise versus conventional treatment on non specific neck pain : A Randomised control trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/073538
Enrollment
32
Registered
2024-09-06
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: M258- Other specified joint disorders

Interventions

Intervention1: Calisthenic Exercise + Conventional treatment: Calisthenic exercise with Conventional treatment will be given for 4 weeks alternate days 12 session in total Control Intervention1: Conve

Sponsors

KLE Academy of Higher Education and Research Belagavi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Individuals within the age group 18-50 years, with with non-specific neck pain. 2.Pain intensity more than 3 out of 10 on NPRS(Numerical Pain Rating Scale) 3.Individuals willing to participate in the study.

Exclusion criteria

Exclusion criteria: 1.History of fracture, trauma, injury or recent surgeries of cervical, spine and upper limb that would prevent the participants to perform the exercise. 2.Past six month history of fracture, trauma, injury or recent surgeries of cervical, spine and upper limb & lower limb that would prevent the participants to perform the exercise. 3.Pregnant women. 4.Diagnosed cases of serious pathology such as specific neck pain due to disc prolapsed, tumor of cervical spine, whiplash injury, cervical fractures, Cervicogenic head ache, and any neurological signs consistent with nerve root compression.

Design outcomes

Primary

MeasureTime frame
Pain will be recorded using Numeric Pain Rating Scale,Assessment of disability using Neck Disability Index, Assessment using Pressure Biofeedback, Craniovertebral angle measured using MB ruler5.3Timepoint: will be done at baseline and after 4 weeks

Secondary

MeasureTime frame
NILTimepoint: NIL

Countries

India

Contacts

Public ContactAarti Welling

KAHER INSTITUTE OF PHYSIOTHERAPY BELGAUM

aaartiwell88@gmail.com9448814569

Outcome results

None listed

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