Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05876208

Increased Home-based Physical Therapy Adherence Using BAND Connect's VirtuaCare™ Platform

Led by University of Cincinnati · Updated on 2026-04-29

60

Participants Needed

1

Research Sites

264 weeks

Total Duration

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AI-Summary

What this Trial Is About

This study aims to enhance at-home therapy by introducing a new device called the BAND Connect's VirtuaCare™ platform. The study aims to determine whether patients can improve their adherence to at-home exercises using this device. Currently, research indicates that only 35% of patients undergoing physical therapy treatment fully comply with their prescribed plans of care, often neglecting their at-home exercises. To address this issue, a set of smart exercise tools called VirtuaCare™ has been developed. This platform provides patients with instructions on performing at-home exercises and offers real-time biofeedback to help them adjust their form if necessary. The study seeks to evaluate the effectiveness of BAND CVCP in assisting patients and improving their overall success with at-home therapy.

CONDITIONS

Official Title

Increased Home-based Physical Therapy Adherence Using BAND Connect's VirtuaCare™ Platform

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Surgery performed by Dr. Brian Grawe with post-operative physical therapy at UC Health
  • Undergoing primary total shoulder arthroplasty, primary reverse total shoulder arthroplasty, or primary rotator cuff repair
  • Outpatient physical therapy prescribed for post-operative rehabilitation
Not Eligible

You will not qualify if you...

  • Unplanned surgical procedures
  • Partial or revision shoulder replacements
  • Revision rotator cuff repair
  • Fracture surgeries
  • Prior shoulder surgery within last 5 years or surgery on opposite shoulder less than 6 months ago
  • Hospital stay longer than 3 days
  • Uncontrolled diabetes or cancer diagnosed in past 5 years or active disease
  • Any comorbidity affecting compliance with study protocol
  • Injuries related to workers' compensation
  • Injuries involved in pending litigation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Cincinnati

Cincinnati, Ohio, United States, 45267

Actively Recruiting

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Research Team

K

Kim Hasselfeld

CONTACT

M

Michael Kloby

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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