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Breathing reeducation in neck pain

Effects of breathing Reeducation on clinical outcomes in non specific chronic neck pain.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200226046623N1
Enrollment
80
Registered
2020-04-17
Start date
2020-02-27
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Non specific Neck pain.

Interventions

Intervention 1: Intervention group: Group will receive supervised breathing exercises focusing on proper inhalation, exhalation and chest expansion for 15 minutes with routine physical therapy treatme

Sponsors

University of Lahore
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 50 Years

Inclusion criteria

Inclusion criteria: Patients having non specific neck pain for more than 3 months• Patients having no history of respiratory disease• Patients having FEV1/FVC ratio=0.7 or 70% of the predicted value• Patients having no history of antidepressant drug treatment• Both genders Age between 25-50 years

Exclusion criteria

Exclusion criteria: Smokers• Known history of depression• Patients having any sort of Asthma• Patients with upper cervical signs and symptoms• Prolong sitting.

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before intervention and at 4th ,8th week. Method of measurement: Visual Analogue scale (VAS).;Range of motion neck. Timepoint: Before intervention,at 4th and 8th week. Method of measurement: CROM device.;Cervical muscle strength. Timepoint: Before intervention,and at 4th week and 8th week. Method of measurement: Dynamometer.;Neck muscles endurance. Timepoint: Before intervention,4th week and 8th week. Method of measurement: Craniocervical Flexion test, Biopressure feedback.;Neck disability. Timepoint: Before intervention,at 4th and 8th week. Method of measurement: Neck disability index questionire.;Quality of life. Timepoint: Before intervention and at 4th and 6th week. Method of measurement: NOOS Questioire.;Pulmonary Function Test. Timepoint: Before intervention, at 4th and 6th week. Method of measurement: Spirometry.

Countries

Pakistan

Contacts

Public ContactSahreen Anwar

The University of Lahore

sahreenanwar@yahoo.com+92 41 8750106

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 12, 2026