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Postoperative Rotator Cuff Rehabilitation: Functional, Pain and Sleep Quality (REHAB-PSF)

L

LAURA CASTILLO VEJAR

Status

Enrolling

Conditions

Rehabilitation
Functionality
Pain
Sleep
Rotator Cuff
Rotator Cuff Injuries

Treatments

Other: Rehabilitation protocol

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Full description

Objective: To compare the effectiveness of a differentiated rehabilitation protocol based on the number of tendons repaired versus a standard rehabilitation protocol, regarding functionality, pain, subjective perception of sleep quality, and mobility, in patients who have undergone surgical rotator cuff repair.

Enrollment

50 estimated patients

Sex

All

Ages

50+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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).

Exclusion criteria

  • 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

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

Standard protocol
Active Comparator group
Description:
According American Society of Shoulder and elbow therapist
Treatment:
Other: Rehabilitation protocol
Modified protocol
Experimental group
Description:
According to the number of tendons treated
Treatment:
Other: Rehabilitation protocol

Trial contacts and locations

2

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Central trial contact

Laura A Castillo Vejar

Data sourced from clinicaltrials.gov

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