Postoperative Rotator Cuff Rehabilitation: Functional, Pain and Sleep Quality

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50+
SponsorLAURA CASTILLO VEJAR

About this trial

Rotator cuff injuries are the third leasing cause of pain and disability, accounting for 16% of all musculoskeletal injuries. Following surgical intervention, patients typically undergo a 4 to 6 week immobilization period before starting physical therapy. This rehabilitation phase can last between 4 to 6 months. Despite this, there is currently a lack of clear guidelines regarding specific physical therapy protocols or the expected post surgical recovery for patients who have undergone rotator cuff repair.

Eligibility criteria

Qualifiers

People over 50 years of age

People have undergone arthroscopic rotator cuff of one or more tendons.

Patients must sign informed consent and undergo physical therapy center (up to week 12 postoperatively).

Disqualifiers

Patients who develop postoperative stiffness or adhesive capsulitis during the rehabilitation process.

Patients with symptoms of cervical radiculopathy or previously diagnosed sleep disorders.

Patients with neurological or cognitive disorders who have difficulty following instructions

Trial design

Treatments tested in this trial

  • Rehabilitation protocol

Treatment groups

50 Participants
are divided into 2 treatment groups

Sponsors and collaborators

LAURA CASTILLO VEJAR

Lead sponsor

TRIMEDKINE

Sponsor institution