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| Name | Class |
|---|---|
| Band Connect | UNKNOWN |
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Participants are being invited to take part in this research study because you will be undergoing total shoulder replacement or rotator cuff repair and will be participating in physical therapy rehabilitation following the procedure. The purpose of this research is to investigate the effectiveness of Band Connect, a connected health platform, in enhancing compliance with home exercise programs among patients undergoing physical therapy. This study aims to evaluate the implications of increased compliance on improving patient engagement and increasing satisfaction for both patients and clinicians. Additionally, the study will analyze the economic implications of implementing Band Connect's hybrid care model on driving increased revenue per patient.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group 1 Band Connect | Experimental | Patients in group 1 will be set up with the Band Connect platform and build their treatment plan at the first in-clinic visit. |
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| Group 2 Standard Care | No Intervention | 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. |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Band Connect | Device | 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. |
| Measure | Description | Time Frame |
|---|---|---|
| Number of physical therapy visits as measured by medical record review. | Up to 6 months | |
| Number of home exercise programs completed as measured by medical record review. | Up to 6 months | |
| Number of in clinic visits as measured by medical record review. | Up to 6 months | |
| Number of patients who were able to return to work | This will be asked as a Yes/No question | Up to 6 months |
| Time to return to work measured in weeks | Up to 6 months | |
| Number of patients who returned to sports | This will be asked as a Yes/No question | Up to 6 months |
| Change in pain as measured by the Visual Analog Scale | The Visual Analogue Scale (VAS) measures pain intensity. The VAS consists of a 10cm line, with two end points representing 0 ('no pain') and 10 ('pain as bad as it could possibly be'). | Baseline, 1 month, 3 months, 6 months |
| Active range of motion measured in degrees | Up to 6 months | |
| Passive range of motion measured in degrees | Up to 6 months |
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Inclusion Criteria:
Chart Review Inclusion Criteria:
Exclusion Criteria:
Chart Review Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Kira Smith, MD | Contact | 216-844-3233 | kira.smith@uhhospitals.org |
| Name | Affiliation | Role |
|---|---|---|
| Robert Gillespie | University Hospitals Cleveland Medical Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University Hospitals Cleveland Medical Center | Recruiting | Cleveland | Ohio | 44106 | United States |
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| Strength will be measured on a scale of 0-5 | Strength scale:
| Up to 6 months |
| Patient satisfaction as measured by American Shoulder and Elbow Surgeons (ASES) Score | Scored out of 100, with higher scores indicating greater satisfaction | Up to 6 months |
| Number of adverse events as measured by medical record review. | Up to 6 months |
| ID | Term |
|---|---|
| D000070636 | Rotator Cuff Injuries |
| ID | Term |
|---|---|
| D012421 | Rupture |
| D014947 | Wounds and Injuries |
| D000070599 | Shoulder Injuries |
| D013708 | Tendon Injuries |
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