Outcomes of Treatment Using the ERMI Shoulder Flexionater ®

Last updated: June 20, 2024
Sponsor: Foundation for Orthopaedic Research and Education
Overall Status: Active - Recruiting

Phase

N/A

Condition

Bursitis

Treatment

High Intensity Stretch Device

Clinical Study ID

NCT05384093
FORE AC 2019
  • Ages > 18
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

Study 1 - Adhesive Capsulitis Study - 110 patients The purpose of this study is to compare treatment of patients with symptoms of adhesive capsulitis, primary and secondary, between three groups: I) Physical Therapy alone; II) ERMI Shoulder Flexionater® alone; III) PT + Device.

Study 2 - Postoperative Shoulder Stiffness Study - 90 patients The purpose of this study is to compare treatment of patients with post-operative stiffness indicative of secondary adhesive capsulitis between three groups: I) Physical Therapy alone; II) ERMI Shoulder Flexionater® alone; III) PT + Device.

Study 3 - Stiffness after MUA Study - enroll all eligible patients (goal of at least 15) The purpose of this study is to compare treatment of patients who have undergone manipulation under anesthesia or lysis of adhesions between three groups: I) Physical Therapy alone; II) ERMI Shoulder Flexionater® alone; III) PT + Device.

Eligibility Criteria

Inclusion

For Study Group 1- Adhesive Capsulitis (AC)

Inclusion Criteria:

  • Exhibits symptoms of adhesive capsulitis i. Shoulder pain with limited motion formore than one month ii. AND ≤ 30 degrees external rotation with arm at side iii. AND ≤ 130 degrees forward flexion d. Cortisone shot for all patients

Exclusion

Exclusion Criteria:

  • a. No prior shoulder surgery b. Infection c. Rheumatoid arthritis d. Any structuralor systemic disorder that could result in pain or ROM limitation i. Such asinflammatory joint disease, osteoarthritis evidenced on radiographs ii. fullthickness rotator cuff tear as shown by ultrasound imaging iii. history of majortrauma or surgery involving the shoulder

For Study Group 2 - Postoperative Shoulder Stiffness Study (POS)

Inclusion Criteria:

c. Is not recovering normally based on objective criteria set for screening process i. Step 1 - Follow patients -all post-op patients with indicated procedures (see # 7 for list.) ii. Step 2 - Screen Patients -does patient meets inclusion criteria at 6 weeks or 3 months of follow-up?

  1. < 15 degrees external rotation with arm at side at 6 weeks post-op

  2. OR < 90 degrees forward flexion at 3 months post-op iii. Step 3 - Enroll patientsthat meet inclusion criteria and assign group

Exclusion Criteria:

a. Revision surgery b. Infection c. Rheumatoid arthritis

  1. Procedures included

  2. Shoulder arthroscopic procedures (29827, 29828, 29823,29824, 29826)

  3. ORIF Humerus fracture (23615) For Study Group 3, Secondary Surgery Study (SAM) Inclusion Criteria:

  4. Underwent a manipulation under anesthesia or a lysis of adhesions procedure

Exclusion Criteria:

a. Infection b. Rheumatoid arthritis c. Any structural or systemic disorder that could result in pain or ROM limitation i. Such as inflammatory joint disease, osteoarthritis evidenced on radiographs ii. full thickness rotator cuff tear as shown by ultrasound imaging iii. history of major trauma or surgery involving the shoulder

  1. Procedures included

  2. Manipulation under anesthesia (23700)

  3. Lysis of adhesions (29825)

Study Design

Total Participants: 210
Treatment Group(s): 1
Primary Treatment: High Intensity Stretch Device
Phase:
Study Start date:
June 25, 2019
Estimated Completion Date:
June 25, 2026

Study Description

Study 1 - Adhesive Capsulitis Study (AC)

Objective: The purpose of this study is to compare treatment efficacy of patients with symptoms of primary and secondary adhesive capsulitis between three groups: 1) Patients treated with Physical Therapy alone; 2) Patients treated with the ERMI Shoulder Flexionater® alone; 3) Patients treated with PT + Device in the treatment.

  1. Prospective randomized control trial

  2. Sample size - 110 patients

  3. Study Groups:

    1. Group I - Physical Therapy Only

    2. Group II - Flexionater® only

    3. Group III - Flexionater® and Physical Therapy

  4. Length of study - 2-year follow-up from last enrolled patient

Study 2 - Postoperative Shoulder Stiffness Study (POS)

Objective: The purpose of this study is to compare treatment efficacy of patients with post-operative stiffness indicative of secondary adhesive capsulitis between three groups: I) Patients treated with Physical Therapy alone; II) Patients treated with the ERMI Shoulder Flexionater® alone; III) Patients treated with PT + Device in the treatment.

  1. Prospective randomized control trial

  2. Sample size - 90 enrolled patients

  3. Study Groups:

    1. Group I - Physical Therapy only

    2. Group II - Flexionater® only

    3. Group III - Flexionater® and Physical Therapy

  4. Length of study - 2-year follow-up from last enrolled patient

Study 3 - Secondary Surgery Study (SAM)

Objective: The purpose of this study is to compare recovery of patients who have undergone a manipulation under anesthesia or a lysis of adhesions between three groups:

  1. Patients treated with Physical Therapy alone; 2) Patients treated with the ERMI Shoulder Flexionater® alone; 3) Patients treated with PT + Device in the treatment.

  1. Prospective randomized control trial

  2. Sample size - 10 enrolled patients

  3. Study Groups:

    1. Group I Physical Therapy Only

    2. Group II - - Flexionater® only

    3. Group III - Flexionater® and Physical Therapy

  4. Length of study - 2-year follow-up from last enrolled patient

Connect with a study center

  • Foundation for Orthopaedic Research and Education

    Tampa, Florida 33607
    United States

    Active - Recruiting

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