The Effect of Cognitive-Motor Dual Task Training on Knee Osteoarthritis

The Effect of Water-Based Cognitive-Motor Dual Task Training on Pain Intensity, Gait Pattern, Postural Control and Cognitive Function in Women with Knee Osteoarthritis

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20250228064877N1

Enrollment

Registered

2025-03-12

Start date

2025-05-05

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

Knee osteoarthritis. Osteoarthritis of knee

Interventions

Intervention 1: Intervention group: Water training interventions will be implemented for 8 weeks, 3 sessions per week and each session will be 45 minutes in the swimming pool of Razi University. Each

Eligibility

Sex/Gender

Female

Age

45 Years to 65 Years

Inclusion criteria

Inclusion criteria: Female gender Age range 45-65 years Having clinical criteria for osteoarthritis of the knee of the American College of Rheumatology Having a score of 112 in the radiography criteria of Kellgren and Lawrence Having a minimum score of 4 (from zero to 10) on the visual analog scale (VAS) for pain intensity

Exclusion criteria

Exclusion criteria: History of knee surgery Fracture in the lower limb Receiving an intervention that can affect the relationship between pain and inflammation (such as drug therapy) Receiving other exercise or nutritional treatments Having inflammatory joint diseases (such as rheumatoid arthritis) Having neuromuscular diseases (Parkinson's, MS, etc.) Having cardiovascular disease Vestibular disorder, uncorrected visual impairment Using any other type of therapeutic intervention during the period when the subjects are in the course of the study

Design outcomes

Primary

Measure	Time frame
Pain intensity. Timepoint: Measurement of pain intensity at the beginning of the study and 8 weeks after the start and end of interventions. Method of measurement: Visual Analog Scale (VAS).;Gait pattern. Timepoint: Measuring the pattern of walking at the baseline and 8 weeks after the interventions. Method of measurement: PT-Scan device.;Postural control. Timepoint: Measurement of postural control at the baseline and 8 weeks after the interventions. Method of measurement: Tecnobody device.;Cognitive function. Timepoint: Measurement of postural control at the baseline and 8 weeks after the interventions. Method of measurement: Montreal Cognitive Assessment or The MoCA Test.	—

Measure

Time frame

Pain intensity. Timepoint: Measurement of pain intensity at the beginning of the study and 8 weeks after the start and end of interventions. Method of measurement: Visual Analog Scale (VAS).;Gait pattern. Timepoint: Measuring the pattern of walking at the baseline and 8 weeks after the interventions. Method of measurement: PT-Scan device.;Postural control. Timepoint: Measurement of postural control at the baseline and 8 weeks after the interventions. Method of measurement: Tecnobody device.;Cognitive function. Timepoint: Measurement of postural control at the baseline and 8 weeks after the interventions. Method of measurement: Montreal Cognitive Assessment or The MoCA Test.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahdiyeh Babajani

Razi University

mahdyeh.babajani@stu.razi.ac.ir+98 83 3836 8024

Outcome results

None listed

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