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Postoperative Rotator Cuff Rehabilitation: Functional, Pain and Sleep Quality

Postoperative Rotator Cuff: Functional, Pain and Sleep Quality

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07135375
Acronym
REHAB-PSF
Enrollment
50
Registered
2025-08-22
Start date
2025-08-26
Completion date
2026-03-30
Last updated
2025-09-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rotator Cuff Injuries, Functionality, Pain, Sleep, Rehabilitation, Rotator Cuff

Keywords

Rehabilitation, Rotator cuff

Brief summary

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.

Detailed 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.

Interventions

The modified protocol will be implementen based on available scientific evidence and guided by the consensus remaches with the traumatologist at the physiotherapy center

Sponsors

LAURA CASTILLO VEJAR
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

Quasi-experimental study using non probability convenience sampling

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Functionality3,6,9 and 12 weeks postoperativelyQuickDash questionnaire will be administered, which provides information on the level of shoulder disability. The results of this questionnaire are reported as a percentage ranging from 0 to 100%. The higher the score, the greater the level of disability.
Pain nocturnal, dynamic and static3,6,9 and 12 weeks postoperativelyNumeric visual scale, considering 0 as no pian and 10 as the maximum perceived pain. The patient will be asked about his pain at rest, movement, and at night.
Sleep quality3,6,9 and 12 weeks postoperativelySubjective perception of sleep quality was assessed through questions regarding hours of sleep, number of times awakened due to pain, and use of medication to control nigth time sleep.

Secondary

MeasureTime frameDescription
Range of movility3,6,9 and 12 weeks postoperativelyThe movement of flexion, abduction, internal and external rotation of the shoulder are evaluated by means of goniometry.

Countries

Chile

Contacts

Primary ContactLaura A Castillo Vejar
lauracastillovejar@gmail.com9-82692727

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026