Using Band Connect to improve physical therapy for shoulder surgeries
Official title: Innovating Physical Therapy: A Pilot Study on Band Connect's Impact on Compliance, Satisfaction, and Revenue
Run by University Hospitals Cleveland Medical Center · NCT06733480 · Data updated 2026-11-12
This study is testing if using the Band Connect platform can help people recovering from shoulder surgery stick to their exercise programs and feel more satisfied with their recovery.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 89 Years |
| Sex | All |
| Enrollment | 499 (estimated) |
| Sponsor | University Hospitals Cleveland Medical Center Academic / other |
| Locations | 1 site (Cleveland, Ohio) |
| Status | Recruiting |
| Started | February 4, 2025 |
| Main results expected | June 1, 2027 |
| Study ends | June 1, 2027 |
| Registry record updated | July 6, 2026 |
| Trial ID | NCT06733480 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18 to 89 who are undergoing primary anatomic or reverse total shoulder arthroplasty or rotator cuff repair and are prescribed outpatient physical therapy.
✕Probably not a fit
Patients undergoing hemiarthroplasty or revision total shoulder arthroplasty may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This research investigates how Band Connect, a connected health platform, can enhance compliance with home exercise programs for patients recovering from total shoulder replacement or rotator cuff repair. Participants will be monitored during their post-operative physical therapy rehabilitation to assess the platform's impact on patient engagement and satisfaction. Additionally, the study will evaluate the economic benefits of implementing this hybrid care model on revenue generation for healthcare providers. The goal is to determine if increased compliance leads to better outcomes for both patients and clinicians.
Why it matters
Potential benefit: If successful, this approach could significantly improve patient adherence to rehabilitation exercises, leading to better recovery outcomes.
How similar studies have gone: Other studies have shown promising results with connected health platforms in enhancing patient compliance and satisfaction, suggesting this approach may be effective.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age range: from 18 to 89 years old * Surgery performed by Dr. Robert Gillespie and will be undergoing post-op physical therapy rehabilitation at University Hospitals * Patients undergoing primary anatomic total shoulder shoulder arthroplasty (aTSA) or primary reverse total shoulder arthroplasty (rTSA) * Patients undergoing primary rotator cuff repair * Prescribed outpatient physical therapy for post-operative rehabilitation Chart Review Inclusion Criteria: * Age range: from 18 to 89 years old * Surgery performed by Dr. Robert Gillespie who underwent post-op physical therapy rehabilitation at University Hospitals * Patients who underwent primary anatomic total shoulder shoulder arthroplasty (aTSA) or primary reverse total shoulder arthroplasty (rTSA) * Patients who underwent primary rotator cuff repair * Prescribed outpatient physical therapy for post-operative rehabilitation Exclusion Criteria: * Patients undergoing hemiarthroplasty or revision TSA * Patients undergoing revision rotator cuff repair * TSA performed for proximal humerus fractures * Length of stay in hospital following shoulder surgery greater than 3 days * Shoulder injuries related to workers compensation or involved in any pending litigation * Pregnant individuals Chart Review Exclusion Criteria: * Patients undergoing hemiarthroplasty or revision TSA * Patients undergoing revision rotator cuff repair * TSA performed for proximal humerus fractures * Length of stay in hospital following shoulder surgery greater than 3 days * Shoulder injuries related to workers compensation or involved in any pending litigation * Pregnant individuals
Where it's running
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University Hospitals Cleveland Medical Center
Cleveland, Ohio, United States Recruiting
Study contacts
- Principal investigator: Robert Gillespie — University Hospitals Cleveland Medical Center
- Study coordinator: Kira Smith, MD
- Email: kira.smith@uhhospitals.org
- Phone: 216-844-3233
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Rotator cuff repair with biceps rerouting and dermal graft augmentation for large, difficult tears
This study tests a combined surgical approach to see if it helps tendon retear rates in adults with large rotator cuff tears that are hard to repair.
-
Biomarkers to see if rotator cuff repairs will heal after surgery
This study tests whether biomarkers in shoulder tissue and synovial fluid can predict whether a rotator cuff repair will heal, using MRI after surgery to compare those who heal with those who don’t.
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Partial coracoidectomy with reverse total shoulder arthroplasty may improve functional internal rotation
A randomized trial tests whether adding partial coracoidectomy to reverse total shoulder arthroplasty helps people move their shoulder better in daily life.
-
Mobilization with Movement for people with rotator cuff lesions
This trial will test whether Mobilization with Movement helps reduce pain, improve shoulder function, and restore joint position sense in adults with rotator cuff lesions.
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Does age-related muscle loss change rotator cuff tear patterns?
We will see if age-related muscle loss (sarcopenia) is linked to the location and type of rotator cuff tears in adults aged 40–75 with rotator cuff syndrome.
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Impact of neck nerve compression (cervical radiculopathy) on recovery after rotator cuff repair
This study sees if people under 65 who had cervical radiculopathy before rotator cuff repair have different shoulder function and quality of life after surgery compared with those who did not.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.