Innovating Physical Therapy: A Pilot Study on Band Connect's Impact on Compliance, Satisfaction, and Revenue
NCT ID: NCT06733480
Last Updated: 2025-02-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
499 participants
INTERVENTIONAL
2025-02-04
2026-06-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Group 1 Band Connect
Patients in group 1 will be set up with the Band Connect platform and build their treatment plan at the first in-clinic visit.
Band Connect
Band Connect provides a medical-grade and condition-specific platform that augments the clinician workflow by extending the in-clinic MSK rehabilitation experience into the patient's home - leading to higher quality personalized treatment and increased adherence with enhanced economics and reimbursement for the clinic.
Group 2 Standard Care
Group 2 will consist of retrospective chart review to as act a control group. Charts will be pulled from 1/1/2019-12/31/2023.
No interventions assigned to this group
Interventions
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Band Connect
Band Connect provides a medical-grade and condition-specific platform that augments the clinician workflow by extending the in-clinic MSK rehabilitation experience into the patient's home - leading to higher quality personalized treatment and increased adherence with enhanced economics and reimbursement for the clinic.
Eligibility Criteria
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Inclusion Criteria
* 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
* 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 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
* 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
18 Years
89 Years
ALL
No
Sponsors
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Band Connect
UNKNOWN
University Hospitals Cleveland Medical Center
OTHER
Responsible Party
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Robert J. Gillespie
Vice Chair of Education
Principal Investigators
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Robert Gillespie
Role: PRINCIPAL_INVESTIGATOR
University Hospitals Cleveland Medical Center
Locations
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University Hospitals Cleveland Medical Center
Cleveland, Ohio, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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STUDY20241277
Identifier Type: -
Identifier Source: org_study_id
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