Effectiveness Study of Postoperative Rotator Cuff Repair Rehabilitation

Sponsor
Orthopedic Institute, Sioux Falls, SD (Other)
Overall Status
Completed
CT.gov ID
NCT01819909
Collaborator
(none)
53
1
2
92
0.6

Study Details

Study Description

Brief Summary

There are very few level 1 or level 2 evidence studies that examine postoperative rehabilitation of rotator cuff repair and shoulder arthroplasty. A systematic review of level 1 or level 2 evidence studies was performed (Baumgarten et al., Sports Health, 2009) that found only four studies that examined rotator cuff repair rehabilitation.

The current study was performed to determine if there is a significant difference in passive glenohumeral joint range of motion, active glenohumeral joint range of motion, scapular substitution, and subjects measured outcome scores (clinimetrics) in patients who undergo rotator cuff repair when treated postoperatively with pulley exercises compared to Jackins' exercises.

Null Hypothesis: There will be no significant difference in passive range of motion, active range of motion, scapular substitution, and subject measured outcomes scores in subjects who undergo rotator cuff repair when treated with pulley exercises compared to Jackins' exercises.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Postoperative Jackins Exercise Protocol
  • Procedure: Postoperative Pulleys Exercise Protocol
N/A

Detailed Description

Scapulothoracic substitution for forward elevation is seen clinically when patients have shoulder pain. The patient uses the trapezius musculature to superiorly elevate the upper extremity instead of using the deltoid and the rotator cuff for upper extremity elevation. Scapulothoracic substitution does not occur in healthy shoulders. Excessive scapular movement can be due to an attempt to substitute for poorly functioning shoulder musculature or tightness of the capsular structures of the glenohumeral joint.

Pulleys have been used in postoperative shoulder rehabilitation to improve passive as well as active range of motion and develop strength. Jackins described a series of exercises that are used to improve active range of motion and develop strength without the use of pulleys. The use of pulleys in the post-operative care for patients who have had shoulder surgery is thought to contribute to excessive scapular motion. To date, there has not been any study that compares the use of pulleys and Jackins' exercises with respect to active range of motion, scapulothoracic substitution, and objective patient outcomes measures. Due to the lack of level 1 or 2 evidence postoperative rehabilitation studies, a prospective randomized study should be performed on patients that have underwent rotator cuff repair.

Study Design

Study Type:
Interventional
Actual Enrollment :
53 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Treatment
Official Title:
Prospective Randomized Trial of Rotator Cuff Repair Postoperative Rehabilitation: Jackins' Exercises Versus Pulleys
Actual Study Start Date :
Nov 1, 2008
Actual Primary Completion Date :
Oct 1, 2015
Actual Study Completion Date :
Jul 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Postoperative Jackins Exercise Protocol

Jackin's exercises were initially designed for patients with difficulty performing forward elevation. The patient initially is positioned supine to perform shoulder flexion. When the patient can actively elevate in the supine position, one to two pounds of weight is placed in the patients hand and the patient is asked to repeat the maneuver of supine active elevation. When the patient can do this with little difficulty, the head of the bed is elevated approximately 20 degrees from the supine position and the sequence is repeated. Once the patient is able to perform flexion in this elevated head position, the inclination of the patient is increased in 20 degree increments until the patient is able to perform upright sitting shoulder flexion.

Procedure: Postoperative Jackins Exercise Protocol
Jackin's exercises were initially designed for patients with difficulty performing forward elevation. The patient initially is positioned supine to perform shoulder flexion. When the patient can actively elevate in the supine position, one to two pounds of weight is placed in the patients hand and the patient is asked to repeat the maneuver of supine active elevation. When the patient can do this with little difficulty, the head of the bed is elevated approximately 20 degrees from the supine position and the sequence is repeated. Once the patient is able to perform flexion in this elevated head position, the inclination of the patient is increased in 20 degree increments until the patient is able to perform upright sitting shoulder flexion.

Experimental: Postoperative Pulleys Exercise Protocol

Pulleys have been used in postoperative shoulder rehabilitation to improve passive as well as active range of motion and develop strength.

Procedure: Postoperative Pulleys Exercise Protocol
Pulleys have been used in postoperative shoulder rehabilitation to improve passive as well as active range of motion and develop strength.

Outcome Measures

Primary Outcome Measures

  1. Change in Western Ontario Rotator Cuff Index (WORC) [Baseline, 6 weeks, 12 weeks, 6 months, 1 year]

    The WORC(ref 6) is a valid,reliable, and responsive patient-reported outcomes measures that assesses response to treatment for rotator cuff disease. A minimally important clinical difference (MCID) has been determined. Its use has been recommended in clinical trials.

Secondary Outcome Measures

  1. Change in scapular substitution (centimeters) [Baseline, 6 weeks, 12 weeks, 6 months, 1 year]

    A novel technique for measuring scapular substitution has been developed by the investigators of this study (Baumgarten et al. Int J Sports Phys Ther. 2012; 7: 39-48).

  2. Change in range of motion (degrees) [Baseline, 6 weeks, 12 weeks, 6 months, 1 year]

  3. Change in strength (N) [Baseline, 6 weeks, 12 weeks, 6 months, 1 year]

  4. Change in Simple Shoulder Test9 [Baseline, 6 weeks, 12 weeks, 6 months, 1 year]

    The Simple Shoulder Test9 is a self-reported patient outcome score that has been specifically validated to examine post-operative rotator cuff repair outcomes.

  5. Change in American Shoulder and Elbow Surgeon (ASES) Shoulder Score [Baseline, 6 weeks, 12 weeks, 6 months, 1 year]

    The ASES Shoulder Score (ref 12) is a self-reported patient outcome score that has been specifically validated to examine rotator cuff disease outcomes. Minimal clinically important differences and the minimal detectable change have been determined.

  6. Change in Marx Shoulder Activity Score2 [Baseline, 6 weeks, 12 weeks, 6 months, 1 year]

    The Marx Shoulder Activity Score2 is a validated, patient self-reported outcome score that determines activity level. This is a supplement to outcome scores that measure pain and function.

  7. Change in Single Assessment Numeric Evaluation (SANE) rating [Baseline, 6 weeks, 12 weeks, 6 months, 1 year]

    The SANE rating (ref 15) is a simple patient self-reported outcome score that asks the patient to rate their shoulder as a percentage of normal (range 0 to 100%).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients undergoing post-operative rehabilitation for a rotator cuff repair
Exclusion Criteria:
  • Patients who do not have permission from their treating surgeon to enroll in this study.

Patients who have undergone a previous rotator cuff repair on the non-operated side.

Patients who have undergone a previous rotator cuff repair on the ipsilateral shoulder.

Patients who have a history of adhesive capsulitis. Patients who are unwilling to participate in all aspects of the study. Patients who are cognitively impaired. Patients with known axillary or suprascapular neuropathy. Patients with a painful or dysfunctional contralateral shoulder.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Orthopedic Institute Sioux Falls South Dakota United States 57117

Sponsors and Collaborators

  • Orthopedic Institute, Sioux Falls, SD

Investigators

  • Principal Investigator: Keith M Baumgarten, MD, Orthopedic Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Keith Baumgarten, MD, Orthopedic Institute, Sioux Falls, SD
ClinicalTrials.gov Identifier:
NCT01819909
Other Study ID Numbers:
  • Jackins
First Posted:
Mar 28, 2013
Last Update Posted:
Mar 2, 2022
Last Verified:
Feb 1, 2022
Keywords provided by Keith Baumgarten, MD, Orthopedic Institute, Sioux Falls, SD
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 2, 2022