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OpenTrials
Completed

NCT Number: NCT05719350

Telerehabilitation in Patients With Osteoarthritis

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

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

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Key information

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Roberto Tedeschi

Bologna, 40141, Italy

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Exercises for Knee

Other

Four exercises for strengthening and mobility of the knee joint two in a sitting position and two in a standing position for a total of 20-25 minutes

Primary outcomes

  1. Rating of Pain

    Time frame: one Month

    rating of pain in the knee joint with osteoarthritis measured with the nprs pain scale

Secondary outcomes

  1. Quality of life improvement

    Time frame: one month, three month

    Improved quality of life as measured by the Short Form Health Survey scale

  2. Assessment of knee joint function

    Time frame: one month, three month

    Assessment of knee joint function as measured by the Womac scale

Sponsors and collaborators

Lead sponsor

Istituto Ortopedico Rizzoli

Other

Registry information

Official study title

Effectiveness of Telerehabilitation in Patients With Osteoarthritis. A Randomized Controlled

Acronym: TABLET

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Feb 8, 2023
Registry last updated
Apr 3, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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