Telerehabilitation in Patients With Osteoarthritis (TABLET)

Istituto Ortopedico Rizzoli

Status: Completed

Conditions: Osteoarthritis

Treatments: Other: Exercises for Knee

Study type: Interventional

Funder types: Other

Identifiers

NCT05719350

0001333

Details and patient eligibility

About

Randomized controlled study on the effectiveness of Telerehabilitation intervention on subjects with knee osteoarthritis. Subjects will be randomized into two groups. The experimental group perform 3 sessions a week for 4 weeks of TR, the control group 3 sessions a week for 4 weeks of conventional rehabilitation c/o IOR rehabilitation gym. Follow-up at 3 months.

Inclusion criteria

1. Subjects must have a diagnosis of rheumatologic disease, osteoarthritis of one or more indications, OARSI criteria.

2. Male or Female, aged > 18 years

3. Participant is willing and able to provide informed consent for participation in the study.

4. Subjects must be able to use an electronic device (pc, tablet, smartphone). Exclusion criteria

5. Participation in another clinical study with any investigational agent within 30 days prior of the study screening.

6. Inability to use an electronic device (pc, tablet, smartphone) 4. Diagnosed with dementia or neurological disease that impairs speech comprehension e Not verbal.

7. Uncontrolled intercurrent illnesses including, without limitation, current infection or active, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia or psychiatric illnesses/social situations that would limit compliance with study requirements, illnesses neurological.

8. Children under the age of 18 8. NPRS value <3 7. BMI >25

Enrollment: 50 patients

Sex: All

Ages: 18 to 90 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Subjects must have a diagnosis of rheumatologic disease, osteoarthritis of one or more articulations, OARSI criteria.
• Male or Female, aged &gt; 18 years
• Participant is willing and able to provide informed consent for participation in the
• study.
• Subjects must be able to use

Exclusion criteria

• Participation in another clinical study with any investigational agent within 30 days prior
• of the study screening.
• Inability to use an electronic device (pc, tablet, smartphone)
• Diagnosed with dementia or neurological disease that impairs speech comprehension e Not verbal.
• Uncontrolled intercurrent illnesses including, without limitation, current infection or active, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia or psychiatric illnesses/social situations that would limit compliance with study requirements, illnesses neurological.
• hildren under the age of 18
• Numeric Pain Rating Scale(NPRS) value <3
• BMI >25

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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50 participants in 2 patient groups

Experimental Group

Experimental group

Description:

Tele-rehabilitation exercises for the knee joint to reduce pain

Treatment:

Other: Exercises for Knee

Control Group

Active Comparator group

Description:

Exercises in presence for the knee joint to decrease pain

Treatment:

Other: Exercises for Knee