Skip to content

Trial of 2 conservative therapies for knee arthritis patients

Comparative impact of two packages of non pharmacological interventions on quality of life of knee osteoarthritis patients reporting at a tertiary care institution - A randomized control trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2014/01/004270
Enrollment
120
Registered
2014-01-02
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- mild and moderate grade of Knee osteoarthritis

Interventions

Intervention1: The diagnosed KOA (Knee osteoarthritis) patients who consult PGI Chandigarh during study period will be assigned to group A: An introductory session will be held by the researcher on th

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.Self-reported knee pain 2.Radiological /clinical grade 1, 2, 3 as per Kellgren Lawrence scale (table - ) certified by clinician. 3.Demonstrated minimal knee OA related dysfunction as per WOMAC score 4.Motivated and willing to alter their lifestyle and able to comply with the planned schedule for follow up

Exclusion criteria

Exclusion criteria: 1.Candidates for surgery due to deformity or intra â??articular pathology 2.Excessive obesity (BMI >40)or any co-morbidity not allowing proper exercise protocol 3.Unresolved balance disorder 4.Unresolved neurological disorder 5.History of knee surgery or knee trauma 6.Hip or ankle instability, excessive weakness 7.Hip or knee replacement 8.Intra-articular joint injection within 4 weeks of the study 9.Inadequate communication skills in Hindi /Punjabi 10.Illiterate (nor have any literate caregivers) 11.Unable to comply with exercise protocol. Participants will also be excluded if they have a significant medical condition that will increase their risk of a significant adverse health event during physical activity (eg, myocardial infarction in the previous 6 months, abnormal blood pressure response to exercise, etc.); have any other known organic disease that would contraindicate safe participation in the study (eg, cancer); have a non-OA inflammatory arthropathy or another arthritic disorder (eg, rheumatoid arthritis); use oral corticosteroids regularly.

Design outcomes

Secondary

MeasureTime frame
1.Difficulties faced by participants in complying with the intervention package. 2.Impact of KOA on daily routine, treatment taken by different agenciesTimepoint: visit 0- visit 26

Primary

MeasureTime frame
â?¢ Quality of life â?¢ Measure of function â?¢ Visual analogue scale â?¢ 50-Foot Timed Walk, â?¢ 30-second Chair Stand Test â?¢ Timed up and go test â?¢ BMITimepoint: visit 0- visit 26

Countries

India

Contacts

Public ContactMeenakshi

PGIMER

amarminhas56@rediffmail.com

Outcome results

None listed

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