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Comparison of Outpatient and Inpatient Spa Therapy

Comparison of Outpatient and Inpatient Spa Therapy in Knee Osteoarthritis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04531969
Enrollment
74
Registered
2020-08-31
Start date
2020-09-08
Completion date
2022-12-15
Last updated
2023-09-25

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

Conditions

Osteoarthritis, Knee

Keywords

Spa therapy, Electrotherapy, Ultrasound, Hotpack

Brief 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.

Detailed 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.

Interventions

OTHERSpa 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.

Sponsors

Abant Izzet Baysal University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Patients will be aware of group distribution due to the nature of the study. Therefore, the only outcome assessor will be blinded

Intervention model description

Parallel Assignment

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Western Ontario and McMaster University (WOMAC) osteoarthritis indextwo weeksThe 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.

Secondary

MeasureTime frameDescription
Visual Analog Scale (VAS)two weeksThe 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).
Timed Up and Go (TUG)two weeksThe 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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026