Clinical Applicability of the Device Belk in the Rehabilitation Process

Basque Health Service

Status: Completed

Conditions: Application Site Atrophy

Treatments: Other: Standard Rehabilitative treatment; Device: Belk Device

Study type: Interventional

Funder types: Other

Identifiers

NCT04159623

Belk

Details and patient eligibility

About

Pilot, interventional, randomized of parallel groups and multicenter clinical trial.

Enrollment: 20 patients

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients of both sexes.
• Patients aged between 18 and 85 years.
• Patients with knee arthroplasty in the immediate postoperative period.
• Sign in informed consent.

Exclusion criteria

• Physical or psychological pathologies that prevent patient participation.
• Tumor arthroplasty.
• Knee replacement prosthesis.
• Impossibility of holding the device.
• Patients with a pacemaker.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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20 participants in 2 patient groups

Belk Device

Experimental group

Description:

With Belk Device

Treatment:

Device: Belk Device

Standard Rehabilitative treatment

Other group

Description:

With the standard rehabilitative treatment

Treatment:

Other: Standard Rehabilitative treatment