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A study to see how Tai Chi helps reduce knee pain and improve daily movement in people with knee osteoarthritis

EFFICACY OF TAI CHI ON PAIN AND PHYSICAL FUNCTION IN INDIVIDUALS WITH KNEE OSTEOARTHRITIS - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/12/098322
Enrollment
183
Registered
2025-12-02
Start date
Unknown
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Health Condition 1: M179- Osteoarthritis of knee, unspecified

Interventions

Intervention1: 8 - form Tai Chi Program: Participants in the 8-Form Tai Chi group will receive supervised Tai Chi sessions lasting 60 minutes, consisting of 10 minutes of warm up, 45 minutes of Tai Ch

Sponsors

Amity University Noida Amity Institute of Physiotherapy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age range: 45 60 years Clinical diagnosis of primary osteoarthritis of the knee Radiographic evidence Mild to moderate osteoarthritis (Kellgren Lawrence Grade I III) confirmed by X-ray Able to understand and follow exercise instructions Provides written informed consent to participate At least Grade 3/5 muscle strength in key lower limb muscles (quadriceps and hamstrings) based on the Oxford Scale for Manual Muscle Testing

Exclusion criteria

Exclusion criteria: Knee pain caused by other conditions (example rheumatoid arthritis, inflammatory arthritis, post-traumatic arthritis) History of total knee replacement on the affected knee, or planned knee surgery during the study period Intra-articular steroid injection in the knee within the past 3 months Significant knee instability or severe deformity Neurological or musculoskeletal disorder affecting lower limb function Participation in any formal exercise program for the knee in the last 6 months Any unstable medical condition where exercise is not advised Inability to follow instructions due to cognitive impairment

Design outcomes

Primary

MeasureTime frame
KOOS Score ( Pain, Function, Quality of Life ) NPRS (Numeric Pain Rating Scale)Timepoint: Baseline, 4 weeks, 8 weeks, 12 weeks

Secondary

MeasureTime frame
Timed Up & Go TUG TESTTimepoint: Baseline, 4 weeks, 8 weeks, 12 weeks

Countries

India

Contacts

Public ContactDr Sanjib Kumar Das

Amity University, Noida

skdas@amity.edu8879485847

Outcome results

None listed

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