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Recruiting NCT05719350

"Effectiveness of Telerehabilitation in Patients With Osteoarthritis. A Randomized Controlled Trial"

Conditions: Tele-rehabilitation in Patients With Knee Osteoarthritis

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: 1
Phase: NA
Enrollment: 50
Sponsor: Istituto Ortopedico Rizzoli

Location: Italy

Summary

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 criteriaSubjects must have a diagnosis of rheumatologic disease, osteoarthritis of one or more indications, OARSI criteria.Male or Female, aged > 18 yearsParticipant is willing and able to provide informed consent for participation in the study.Subjects must be able to use an electronic device (pc, tablet, smartphone). Exclusion criteria1. Participation in another clinical study with any investigational agent within 30 days prior of the study screening. 2. Inability to use an electronic device (pc, tablet, smartphone) 4. Diagnosed with dementia or neurological disease that impairs speech comprehension e Not verbal. 5. 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. 6. Children under the age of 18 8. NPRS value <3 7. BMI >25

Eligibility Criteria

Inclusion Criteria:1. Subjects must have a diagnosis of rheumatologic disease, osteoarthritis of one or more articulations, 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:1. Participation in another clinical study with any investigational agent within 30 days prior of the study screening. 2. Inability to use an electronic device (pc, tablet, smartphone) 4. Diagnosed with dementia or neurological disease that impairs speech comprehension e Not verbal. 5. 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. 6. Children under the age of 18 8. NPRS value <3 7. BMI >25

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05719350). StuddyBuddy aggregates publicly available trial information.