Integrated Approach of Yoga Therapy (IAYT) for Chronic low back pain

Evaluating the long term effect of Integrated Approach of Yoga Therapy (IAYT) on physical and mental health, quality of life and biomarkers in patients with chronic low back pain and comparing it with physical exercise or usual care: A community based randomized Controlled Trial. - NIL

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/01/062077

Enrollment

264

Registered

2024-01-30

Start date

Unknown

Completion date

Unknown

Last updated

2025-09-15

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

Conditions

Health Condition 1: M998- Other biomechanical lesions

Interventions

Intervention1: YOGA GROUP: Yoga Therapy (IAYT) protocol has been designed for Chronic Low back pain patients by the expert fraternity will be provided by trained personal as follows Initial supervise

Eligibility

Inclusion criteria

Inclusion criteria: Patients, with a history of non-specific low back pain with or without leg pain for more than 3 months, with average pain intensity of = 4 on a Numeric Rating scale (NRS), who are willing to participate, who are ready to attend Yoga classes or physical exercise, and are willing to continue home practise will be recruited.

Exclusion criteria

Exclusion criteria: Patients with chronic pain occurring due to cancer or involvement of fibromyalgia, diabetic neuropathy and other systematic complications such as cardiac, kidney disorders, patients who have undergone lower back region surgery, pregnant females and patients with pre-existing major psychiatric illness will also be excluded. Patients with chronic pain occurring due to cancer or involvement of fibromyalgia, diabetic neuropathy and other systematic complications such as cardiac, kidney disorders, patients who have undergone lower back region surgery, pregnant females and patients with pre-existing major psychiatric illness will also be excluded

Design outcomes

Primary

Measure	Time frame
Change in dysfunction as measured by MODQ and Pain as measured by VNRSTimepoint: 6 months	—

Secondary

Measure	Time frame
improvement in MODQ as = 50% and effective pain relief as = 50% reduction from baseline on VNRS. Proportion of patients achieving clinically meaningful improvement on MODQ and effective pain relief (EPR) in each group will considered as primary endpoint.Timepoint: 1, 3, AND 6 months	—

Countries

India

Contacts

Public ContactBabita Ghai

Post Graduate Institute of Medical Education and Research, Chandigarh

ghaibabita1@gmail.com7087009533

Outcome results

None listed

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