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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04531969
Other study ID # Physical Med-2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 8, 2020
Est. completion date December 15, 2022

Study information

Verified date September 2023
Source Abant Izzet Baysal University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study, we aimed to compare the effectiveness of inpatient and outpatient physical therapy modalities and spa combination treatments on pain and functional status in patients with knee osteoarthritis.


Description:

Osteoarthritis (OA) has an important place in musculoskeletal diseases and is the most common rheumatic joint disorder characterized by progressive cartilage degeneration. Osteoarthritis of the knee is the most common symptomatic osteoarthritis characterized by chronic knee pain, joint stiffness, limited daily activities, and decreased quality of life. In this study, it was aimed to compare the effects of inpatient and outpatient applications of HP, US, TENS, spa combination treatments on pain and functional status in patients with knee osteoarthritis.


Recruitment information / eligibility

Status Completed
Enrollment 74
Est. completion date December 15, 2022
Est. primary completion date December 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Patients diagnosed with primary knee osteoarthritis Exclusion Criteria: - Patients who have secondary knee osteoarthritis due to various diseases - Patients with pronounced pathology in the waist, hip and ankle joint, patients with active tumors - Patients with febrile infectious disease - Having had serious surgical operations in the last 6 months - Patients who have undergone and/or have been injected with intraarticular steroid and hyaluronic acid into the knee joint - Patients who have received balneotherapy and peloidotherapy in the last one year - Patients with decompensated organ failure, those with inflammatory disease, those with pregnancy and breastfeeding - People with neurological diseases such as epilepsy, inner ear hearing aids, pacemakers and other individuals with a small metallic implant

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Spa therapy and conventional physical therapy
HP application +deep heater application + TENS. HP application: A hotpack wrapped in a towel for 20 minutes will be placed on the knee and surrounding soft tissues. Deep heater application: The application will be performed with a therapeutic ultrasound device at a dose of 1.5watt / cm2 for each string for 6 minutes. TENS application:TENS device with two electrodes surrounding tendon will be performed for 30 minutes at low-frequency current application. Spa therapy: A conventional water bath water at 38 ° C will be applied in the pool for 20 minutes a day.

Locations

Country Name City State
Turkey Abant Izzet Baysal University Bolu Merkez

Sponsors (1)

Lead Sponsor Collaborator
Abant Izzet Baysal University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Western Ontario and McMaster University (WOMAC) osteoarthritis index The form consists of three parts (pain, stiffness, and physical function) and 24 questions. High WOMAC values indicate an increase in pain and stiffness and impairment of physical function. two weeks
Secondary Visual Analog Scale (VAS) The patient was asked to mark the severity of his or her pain with active motion on a horizontal line 100 millimeters in length. The intensity of the pain was calculated by measuring the area in which the individual marked between 0 (no pain) and 10 (the most severe pain I felt in my life). two weeks
Secondary Timed Up and Go (TUG) The patient starts in a seated position and stands up upon therapist's command: walks 3 meters, turns around, walks back to the chair and sits down. The time stops when the patient is seated. The subject is allowed to use an assistive device. two weeks
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