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Effectiveness of Telerehabilitation With Trak in Knee and Shoulder Pathology: A Randomized Clinical Trial

NCT06498453 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2024-12-03

No results posted yet for this study

Summary

The main objective of this clinical trial is to compare the effectiveness of digital physiotherapy treatment using the Trak telerehabilitation platform and the application of conventional means on two different health conditions (mild or moderate knee osteoarthritis and shoulder tendinopathy)

Participants will undergo telerehabilitation treatment through the TRAK platform for six weeks (treatment group) or follow the instructions and guidelines collected by health personnel for the same time in face-to-face rehabilitation sessions (control group).

Conditions

  • Shoulder Injury
  • Knee Injury

Interventions

DEVICE

Trak-Physio knee condition

The exercise protocol designed for knee conditions is carried out through Trak, the digital rehabilitation tool.

DEVICE

Trak-Physio in shoulder condition

The exercise protocol designed for knee conditions is carried out through Trak, the digital rehabilitation tool.

OTHER

Knee conventional rehabilitation program

Exercise protocol with the methodology of conventional clinical practice.

OTHER

Shoulder conventional rehabilitation program

Exercise protocol with the methodology of conventional clinical practice.

Sponsors & Collaborators

  • Trak Health Solutions S.L.

    lead INDUSTRY

Principal Investigators

  • María A García Velázquez · Asunción Klinika

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-03-01
Primary Completion
2023-06-06
Completion
2023-06-06

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06498453 on ClinicalTrials.gov