NCT07888920|Not Yet Recruiting
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Sponsor study identifier
interventional
42
1 country
2
Study Start
October 28, 2026
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
Primary Completion
October 30, 2026
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
Study Completion
April 1, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
This study aims to investigate the effects of visual rehabilitation and vestibular rehabilitation added to conventional physiotherapy on postural stability, pain, and functional status in individuals with knee osteoarthritis. Participants will be randomly assigned to three groups: conventional physiotherapy, conventional physiotherapy combined with visual rehabilitation, or conventional physiotherapy combined with vestibular rehabilitation. The study will evaluate changes in balance, pain, and functional performance before and after the intervention.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
April 1, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
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Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
October 16, 2026
Actual (reported)October 22, 2026
Actual (reported)October 28, 2026
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
October 30, 2026
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
April 1, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
Postural Stability
Postural stability will be assessed using the Ottometriks Balance Platform. Center of pressure (COP) displacement and postural sway in the anteroposterior and mediolateral directions will be evaluated.
At baseline and immediately after the 6-week intervention
Pain Intensity
At baseline and immediately after the 6-week intervention
WOMAC
At baseline and immediately after the 6-week intervention
Participants in this arm will receive conventional physiotherapy, including transcutaneous electrical nerve stimulation (TENS), cold pack application, patellar mobilization, quadriceps isometric exercises, progressive resistance exercises, straight leg raises, and hamstring and gastrocnemius stretching.
Participants in this arm will receive conventional physiotherapy combined with peripheral vision-focused visual rehabilitation.
Participants will receive conventional physiotherapy consisting of transcutaneous electrical nerve stimulation (TENS), cold pack application, grade I-II patellar mobilization, quadriceps isometric exercises, progressive resistance exercises, straight leg raises, and static hamstring and gastrocnemius stretching. The intervention will be provided three times per week for six weeks, with a total of 18 sessions.
Istanbul Aydin University Medical Park Florya Hospital
Istanbul, Istanbul, 34295, Turkey (Türkiye)
Istanbul Aydin University
Istanbul, Istanbul, 34295, Turkey (Türkiye)
Kamer Ünal Eren
Istanbul Aydın University
First Submitted
October 16, 2026
First Posted
October 22, 2026
Study Start
October 28, 2026
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
Primary Completion
October 30, 2026
Estimated (date passed)Virtual Reality-Based Hypnotherapy for Pain, Sleep, and Mood in Spinal Cord Injury
Timed Up and Go Test (TUG)
At baseline and immediately after the 6-week intervention
Y Balance Test
At baseline and immediately after the 6-week intervention
Berg Balance Scale (BBS)
At baseline and immediately after the 6-week intervention
Participants in this arm will receive conventional physiotherapy combined with vestibular rehabilitation involving standardized rhythmic head movements.
Participants will receive conventional physiotherapy combined with peripheral vision-focused visual rehabilitation. Visual rehabilitation will involve peripheral visual stimuli presented using the Smart Optometry Pro application while participants maintain central fixation and respond to the stimuli with motor actions. The intervention will be provided for 20 minutes per session, three times per week for six weeks, for a total of 18 sessions.
Participants will receive conventional physiotherapy combined with vestibular rehabilitation involving standardized rhythmic head movements. Head movements will be performed in right-left and anterior-posterior directions at a standardized rhythm using a metronome application. The intervention will be provided for 20 minutes per session, three times per week for six weeks, for a total of 18 sessions.
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This estimate has passed. The registry has not confirmed an actual date for this milestone.
Study Completion
April 1, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
Last Updated
October 22, 2026
Record last verified: 2026-10
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