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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04540341
Other study ID # 60116787-020/48052
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 14, 2020
Est. completion date April 20, 2022

Study information

Verified date April 2022
Source Pamukkale University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Osteoarthritis (OA) is a chronic disease process characterized by degeneration and inflammation in the joint cartilage and subchondral bone, synovial fluid and joint capsule. One of the most affected joints in OA is the knee joint, and the incidence of OA increases with age. Different treatment approaches are used in the treatment of osteoarthritis. The aim of the study is to examine the effectiveness of Mulligan technique and core exercises applied to female patients with knee osteoarthritis. In addition, the investigators did not find any study examining the effect of Mulligan technique on static balance in the treatment of OA. This is the secondary aim of the study.


Recruitment information / eligibility

Status Completed
Enrollment 42
Est. completion date April 20, 2022
Est. primary completion date February 1, 2022
Accepts healthy volunteers No
Gender Female
Age group 40 Years to 70 Years
Eligibility Inclusion Criteria: - Being diagnosed with knee osteoarthritis - To be in the age range of 40-70 - No lower extremity surgery in the last 6 months. - Agree to participate in the study Exclusion Criteria: - Having had hip-knee replacement surgery - Surgery planned in the last 6 months - Having received physical therapy in the last 6 months - Having uncontrollable hypertension and cardiac problems - Having been diagnosed with rheumatoid arthritis

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Mulligan mobilization
Mulligan mobilization technique will be apply.
Core stabilization
Core stabilization technique will be apply.
Conventional therapy
Conventional therapy exercise will be apply.

Locations

Country Name City State
Turkey Pamukkale University Denizli

Sponsors (1)

Lead Sponsor Collaborator
Pamukkale University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain assessment Visual Analog Scale: This scale consists of a straight line with the end points defining extreme limits such as 'no pain at all', which is 0 cm, and 'pain as bad as it could be', which is 10cm. 10 minutes
Primary Range of motion assessment Goniometric measurement 10 minutes
Primary muscle strength assessment by handheld device (Commander Powertrack II brand) 10 minutes
Primary functional level assessment Western Ontario and McMaster Universities Arthritis Index (WOMAC) 5 minutes
Primary aerobic endurance assessment 6 minute walk test 6 minutes
Primary balance assessment Stand on one leg test 5 minutes
Primary Timed Up& Go Test Timed Up& Go Test 5 minutes
Primary assessment of quality of life survey Nottingham Health Profile 5 minutes
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