Full Thickness Rotator Cuff Tear Clinical Trial
Official title:
Rehabilitation of Patients With Full-thickness Rotator Cuff Tears: Planning and Pilot Study for Feasibility and Efficacy
A single arm design will be used to assess the feasibility and preliminary efficacy of a closed-chain rehabilitation protocol for patients with full thickness rotator cuff tears of the shoulder. Full thickness rotator cuff tears will be documented using MRI or ultrasound images. 30 participants will be recruited for this study. The rehabilitation protocol will include two stages: stage 1, physical therapy, and stage 2, gym program. Stage I will include a total number of session between 12 and 24. The number of session included in stage 2, will depend on the total number of session completed during stage 1. The total duration of both stages will 5 months.
Closed-chain exercises have been used extensively in rehabilitation approaches to treat a
diverse range of musculoskeletal diagnoses. The closed-chain approach theoretically
facilitates co-contraction to improve joint mobility, stability and motor control, as well as
decreasing potential compression of the RC tendons in the subacromial space. The closed-chain
exercises are performed with the hands in contact with the floor/table, while the shoulder
joint moves and gravity provides resistance. This approach may prevent tear progression and
improve joint mechanics, shoulder pain, and function.
STAGE 1 - Physical therapy
Participants will be provided closed-chain exercises in the physical therapy treatment by a
licensed physical therapist. The length of each session will be 1 hour. Participants will
attend 2 sessions per week, for a minimum of 12 sessions. The maximum number of sessions to
complete Stage I of the protocol is 24. Each physical therapy session will consist of
closed-chain strengthening, along with stretching and aerobic exercises.
During the closed-chain strengthening portion, participants will be asked to perform 6
exercises focusing on the shoulder girdle. Closed-chain strengthening will be performed with
the shoulder moving over a fixed hand. Resistance will be provided by body weight against
gravity. To off-load and progress the amount of body-weight resistance, elastic bands will be
used to support body weight. The elastic bands will be attached to support frame used for the
exercises. As the patient improves, less elastic band support will be provided to allow
increased resistance via the patient's body weight. The criteria for determining if the
resistance is too high or the exercise is too difficult will be based on 2 criteria: 1.)
after the exercise is completed, the participant rates their shoulder pain > 2/10 increase as
compared to baseline pain taken at the start of that day's treatment session, on the numeric
pain rating scale, and 2.) BORG scale > 3 (moderate difficulty) and an inability of the
participant to maintain proper exercise form and full range of motion. If these criteria are
met then the physical therapist will modify the exercise so the subject can perform similar
movement pattern without pain. The goal will be for the participant to perform 2 sets of 20
repetitions, of each exercise. When the participant is able to perform 24 repetitions with
the given load, over 2 successive treatment sessions, then the resistance will be increased.
The investigators recognize that there is limited evidence regarding the effectiveness and
safety of closed-chain exercises in patients with full-thickness rotator cuff tears.
Therefore, the investigators are employing several steps to assure safety. At the beginning
of each session, each patient will fill out a questionnaire to assess for adverse effects of
exercises (such as severe joint pain). After each exercise, participants will rate their
shoulder pain level and their perceived difficulty with the exercise. This information will
be used to tailor the intervention according to the response to the intervention.
Furthermore, it will allow for monitoring for adverse outcomes of the intervention.
Participants will perform aerobic exercises of a stationary bike, elliptical, and treadmill.
Aerobic exercise will last about 10 to 15 minutes each session. Intensity of aerobic
exercises will be adjusted throughout stage I. The target is to exercise at least at a 4
level (somewhat hard) on the BORG scale.
STAGE 2 - Gym program
Participants will be enrolled in a gym program following discharge from Stage 1. The Gym
Program will be provided by a health care professionals trained in the delivery of exercise.
Each session will be 1 hour. Participants will attend 2 sessions per week, for 8- 12 weeks
depending on when they are discharged from Stage I. Each session will consist of closed-chain
strengthening, stretching, and aerobic exercises.
During the closed-chain strengthening portion, participants will execute the same
six-strengthening exercises as stage I. The next phase involves progressing to a moderate
resistance load that will allow the participant to complete 2 sets of 8 to 12 repetitions of
a given exercise. When the participant is able to perform more than 12 repetitions with a
given load, over the course of 2 successive training sessions, then the resistance will be
incrementally increased. The maximum resistance will be against body weight (no support from
bands).
Participants will perform aerobic exercises alternating each session between a stationary
bike, elliptical, and treadmill. Aerobic exercise will last about 15 to 20 minutes each
session. Intensity of aerobic exercises will be adjusted throughout stage II. The target will
be to exercise at least at a 4 level (somewhat hard) on the BORG scale.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01256242 -
Pilot Study of Augment Rotator Cuff for Surgical Treatment of Full Thickness Rotator Cuff Tears
|
N/A | |
Active, not recruiting |
NCT02484950 -
Mesenchymal Stem Cell Augmentation in Patients Undergoing Arthroscopic Rotator Cuff Repair
|
N/A | |
Completed |
NCT01557309 -
Clinical and Structural Outcome After Early Repair of the Traumatic Rotator Cuff Tear
|
N/A | |
Completed |
NCT01819909 -
Effectiveness Study of Postoperative Rotator Cuff Repair Rehabilitation
|
N/A | |
Terminated |
NCT04115644 -
Effectiveness of Corticosteroid vs. Ketorolac Shoulder Injections: A Prospective Double-Blinded Randomized Trial
|
Phase 4 | |
Completed |
NCT01849458 -
BioFiber Scaffold Post-Market Observational Study
|
N/A | |
Completed |
NCT02915588 -
Early Active Rehabilitation After Arthroscopic Rotator Cuff Repair
|
N/A | |
Completed |
NCT01499992 -
Rehabilitation of Reconstructed Shoulder Rotator Cuff
|
N/A | |
Completed |
NCT01987973 -
Allograft Reconstruction of Massive Rotator Cuff Tears vs Partial Repair Alone
|
N/A | |
Completed |
NCT03021733 -
A Pilot Cohort Study of Surgical and Non-surgical Management of Rotator Cuff Tears
|
N/A | |
Active, not recruiting |
NCT01481480 -
Latissimus Dorsi Tendon Transfer or Partial Arthroscopic Repair of Massive Rotator Cuff Tears
|
N/A | |
Completed |
NCT02740946 -
Enhanced Function and Quality of Life Following 5 Months of Exercise Therapy for Patients With Rotator Cuff Tears
|
N/A |