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Rehabilitation of Reconstructed Shoulder Rotator Cuff

Rehabilitation of Reconstructed Shoulder Rotator Cuff : Optimizing Physical Therapy Dosage and Effect of Aquatic Physical Therapy - A Randomized, Factorial Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01499992
Enrollment
14
Registered
2011-12-26
Start date
2012-01-31
Completion date
2013-01-31
Last updated
2014-03-19

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

Conditions

Full Thickness Rotator Cuff Tear

Keywords

Shoulder rehabilitation, Rotator cuff tear, Physiotherapy, aqua therapy, Therapy dosage, adjunctive aquatic physical therapy

Brief summary

The aim of this study to define the optimal rehabilitation for clients with full thickness rotator cuff reconstruction, with two goals: 1. Finding the optimal physical therapy dosage in enhancing post-operative outcomes of shoulder pain, shoulder joint range of motion, shoulder muscle strength, upper extremity function; and 2. Finding the effect of aquatic physical therapy in enhancing the post-operative outcomes.

Detailed description

Measurement devices: Biodex: Biodex system is a muscle strength testing and rehabilitation instrument used in the testing and rehabilitation services for shoulder, elbow, wrist, hip, knee and ankle. Modes of operation for exercise and testing include isokinetic, passive, isometric, isotonic, and reactive eccentric. Patients are tested for their muscle performance for the required number of repetitions in the required mode. The muscle performance is measured by calculating the average peak torque (in Nm) and analyzed across the group of patients. Goniometer: A manual devise used to measure joint range of motion. Visual Analogue Scale: A scale with 0 to 10, with 0 being no pain, and 10 being severe pain. Measurement procedure: All the subjects posted for surgery will be tested prior to and again 6 weeks following surgery for: Shoulder Pain is measured using a visual analog scale. Shoulder Range of motion is measured using a standard goniometer. Shoulder Muscle performances are measured using Biodex.

Interventions

PROCEDUREStandard physical therapy program PLUS aquatic physical therapy

2\. Standard physical therapy program PLUS aquatic physical therapy: The above PLUS a aquatic physical therapy program which will be conducted twice weekly for 10 weeks and will include a 40-50 minute hydrotherapy session emphasizing range of motion and light resistive exercises of the arm, primarily focusing on the shoulder. The program will start with general mobility of the other upper limb joints to allow time for preconditioning of the painful shoulder. Shoulder exercises will emphasize flexion, rotation and abduction and a slow transition from pain-free range to the restricted range of motion to maximize the effectiveness of the heat and buoyancy.

OTHERstandard care

Total of 12 weeks; each exercise session will be 20 -30 minutes of direct contact and additional supervised exercise as defined by assignment and stage.

Sponsors

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* full thickness rotator cuff tear treated by arthroscopic or mini-open repair by a specialized upper extremity surgeons * mentally competent * able to read and write * able to return for follow-up * 18-65 years old

Exclusion criteria

* associated surgical procedures (Concomitant fractures, capsular releases surgical decompression) * nerve injury * neurological conditions * irreparable massive rotator cuff tear, and * comorbid health problems that limit rehabilitation potential (Rheumatoid arthritis, Diabetes).

Design outcomes

Primary

MeasureTime frame
strength3 month after the surgery

Secondary

MeasureTime frame
patient satisfaction3 and 6 months after the surgery

Countries

Canada

Outcome results

None listed

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