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Studying the effects of Nordic Walking and Simple Walking on the quality of life of Women With Knee Osteoarthritis

Studying the Effects of Nordic Walking on Balance, Cognitive Function and Disabilities Related to Knee Osteoarthritis in Elderly Women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241027063512N1
Enrollment
45
Registered
2024-11-24
Start date
2025-04-09
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Knee osteoarthritis. Other internal derangements of knee

Interventions

Intervention 1: Intervention Group 1: This group, which consists of 15 participants, walks with the help of adjustable Nordic walking poles. The duration of our intervention is six weeks, three sessio

Sponsors

Razi University of Kermanshah
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age over 45 to 65 years Chronic Knee pain on most days, for at least 3 months, pain score of at least4 on a Visual analog pain scale No intra-articular injections in the past 3 months Having the American College of Rheumatology clinical criteria for Knee Osteoarthritis

Exclusion criteria

Exclusion criteria: Uncontrolled diabetes Body mass index greater than or equal(BMI>40kg>m2), patients With severe obesity Lower limb arthroplasty Intra-articular steroid injections (within the past 6 months) Systemic arthritis Neuromuscular disorders that interfere with daily functioning, such as (stroke, uncontrolled muscle stiffness, tumor, etc.) Patients who are unable to walk without assistive devices Patients who have undergone other exercise or nutritional treatments in the past three months Neuromuscular diseases (such as MS and Parkinson's) that interfere with exercise programs Fractures and surgery in the lower extremities Use of any other type of therapeutic intervention during the period in which the subjects are in the study

Design outcomes

Primary

MeasureTime frame
Assessing pain intensity. Timepoint: Measuring pain intensity before and after the test. Method of measurement: Measuring pain intensity with the McGill Index.

Secondary

MeasureTime frame
Balance assessment. Timepoint: Measurement before the intervention and after the intervention. Method of measurement: Technobody device,Pro-kin252N.;Muscle strength assessment. Timepoint: Measurement before the intervention and after the intervention. Method of measurement: pull-push dynomometer.;Proprioception of the knee joint assessment. Timepoint: Measurement before the intervention and after the intervention. Method of measurement: Inclinometer device.;Motor function assessment. Timepoint: Measurement before the intervention and after the intervention. Method of measurement: Osteoarthritis Index Questionnaire, Up&Go Test, 40 Merer Walking Time.;Cognitive function assessment. Timepoint: Measurement before the intervention and after the intervention. Method of measurement: Montreal Cognitive Assessment questionnaire.;Checking the level of quality of life. Timepoint: Measurement before the intervention and after the intervention. Method of measurement: Medical Outcomes Study Short Form Scale (SF-36).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSosan Panjalizad

Razi University of Kermanshah

sosanpanjali@gmail.com+98 83 3822 2539

Outcome results

None listed

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