The Effect of Adding Instrumented Hip Concentric Abductor Strengthening Exercise in Knee Osteoarthritis
NCT ID: NCT06331858
Last Updated: 2025-03-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
70 participants
INTERVENTIONAL
2023-09-20
2024-03-29
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
2. CONTROL GROUP
TREATMENT
DOUBLE
Study Groups
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Study group
The study group received hip device-assisted concentric abductor strengthening (HDACAS) program in addition to knee device-assisted concentric flexor-extensor strengthening (KDACFES) program.
hip device-assisted concentric abductor strengthening (HDACAS)
All participants received device-assisted strengthening exercises with increasing doses according to a pre-determined strengthening program for a total of 6 weeks, 4 days a week, and a total of 24 sessions
knee device-assisted concentric flexor-extensor strengthening (KDACFES)
All participants received device-assisted strengthening exercises with increasing doses according to a pre-determined strengthening program for a total of 6 weeks, 4 days a week, and a total of 24 sessions
Control group
The control group received only KDACFES program
knee device-assisted concentric flexor-extensor strengthening (KDACFES)
All participants received device-assisted strengthening exercises with increasing doses according to a pre-determined strengthening program for a total of 6 weeks, 4 days a week, and a total of 24 sessions
Interventions
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hip device-assisted concentric abductor strengthening (HDACAS)
All participants received device-assisted strengthening exercises with increasing doses according to a pre-determined strengthening program for a total of 6 weeks, 4 days a week, and a total of 24 sessions
knee device-assisted concentric flexor-extensor strengthening (KDACFES)
All participants received device-assisted strengthening exercises with increasing doses according to a pre-determined strengthening program for a total of 6 weeks, 4 days a week, and a total of 24 sessions
Eligibility Criteria
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Inclusion Criteria
* Having symptomatic unilateral or bilateral knee pain with a VAS (0-10) pain score \> 4
* Being able to ambulate independently without orthosis/prosthesis
* Having a body mass index less than 35
Exclusion Criteria
* Presence of lesions, atrophy, or scars in the skin area
* Intra-articular injection to the knee within the last 6 months
* Receiving active physiotherapy, physical therapy, or spa treatment in the last 6 months
* Patients with chronic diseases such as COPD, coronary artery disease
* Those with oxygen saturation levels \<95%
* Individuals with any pathological condition that may impair normal walking
* Patients with diseases such as vertigo, epilepsy that may pose a risk during physical performance tests
* Patients with contraindications to strength training exercises
45 Years
70 Years
ALL
No
Sponsors
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Kutahya Health Sciences University
OTHER
Responsible Party
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Hasan Hüseyin Gökpınar
Assistant professor
Principal Investigators
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Hasan H Gökpınar
Role: STUDY_DIRECTOR
Kutahya Health Sciences University
Locations
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Kutahya Health Sciences University
Kütahya, Kütahya, Turkey (Türkiye)
Countries
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Other Identifiers
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KutahyaHSU-DRGOKPINARDROMER-43
Identifier Type: -
Identifier Source: org_study_id
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