Recruiting

VirtuaCareTM

Sponsor:

Cedars-Sinai Medical Center

Code:

NCT06016257

Conditions

Shoulder Disease

Shoulder Injuries

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Use of VirtuaCare™ for home program

Study Details

Brief summary:

This study will be performed to determine if Band Connect's VirtuaCare™ platform increases patient compliance and provides an effective alternative to current physical therapy treatment while reducing the frequency of visits compared with standard orthopedic physical therapy treatment performed in the outpatient clinic.

Participants are being asked to take part in this research study if 18 years and older and have been prescribed physical therapy rehabilitation for an acute or chronic shoulder condition and as part of the participant's physical therapy will receive a shoulder exercise home program.

Conditions

Shoulder Disease

Shoulder Injuries

Study ID

NCT06016257

Start date

Feb 1, 2024

Status verified date

Mar, 2026

Completion date

Dec 31, 2026

Anticipated

Primary completion date

Dec 31, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

Physical therapy home program subjects

  • Subject 18 years or older
  • Outpatient physical therapy prescribed by doctor for shoulder rehabilitation.
  • No previous neurological condition
  • Understand English (exercises are only in English) Physical therapists
  • The therapists will be the ones who provide physical therapy treatment to the acute and chronic shoulder population.

Patients who had usual and customary treatment for acute and chronic shoulder conditions

• Any patient referred based on inclusion criteria noted above that are referred for outpatient physical therapy and had a previous acute or chronic shoulder condition, were 18 years and older and had no previously documented neurological condition.

Exclusion Criteria:

Physical therapy home program subjects

  • Prior surgery within the last 5 years or less than 6 months between surgery
  • Neurologic comorbidities that have functional deficits
  • Uncontrolled diabetes
  • Diagnosis with active cancer in the last two years
  • Unable to understand English

Physical therapists • Any therapist who does not provide physical therapy treatment for acute and chronic shoulder conditions.

Patients who had usual and customary treatment for acute and chronic shoulder conditions

• Any patient who had prior surgery within the last 5 years or less than 6 months between surgery, had neurological comorbidities that had documented functional deficits, documented uncontrollable diabetes, documented diagnosis of active cancer within the last two years.

Study Design

Enrollment

20 participants

Anticipated

Allocation

Non randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: VirtuaCare Group

For the subjects in Group 1, the physical therapist will set up the patients within the VirtuaCare™ system and build their treatment plan.

Each time a patient in the VirtuaCare returns for a clinic visit, the physical therapist will review their VirtuaCare™ patient report displaying information such as exercises completed along with their measured form, pace, range of motion, and exertion. From the review, they will help the patient understand any corrections they need to make in the following week when at home. The therapist can add or adjust any exercises they deem necessary for the next phase of the patient's rehabilitation.

no intervention: Usual and Customary Group

This study involves a medical record review for the control group. Data will be abstracted from closed medical records after completion of shoulder physical therapy.

Interventions

Use of VirtuaCare™ for home program

Use of VirtuaCare™ system for the Home Program.

Primary outcome measure

  • Reduced Number of Visits [ Time Frame: 4-8 weeks ]

Central Contacts and Locations

Central contacts

Locations

Cedars-Sinai Medical Center Outpatient Rehabilitation

Recruiting

Los Angeles, California, United States, 90048

Principal Investigator:

Pamela Roberts, PhD

Cedars-Sinai Medical Center

Recruiting

Los Angeles, California, United States, 90048

Contacts

Jeffrey Wertheimer, PhD

Jeffrey.wertheimer@cshs.org

More Information

Sponsor

Cedars-Sinai Medical Center

Last update posted

Mar 27, 2026

Last verified

Mar, 2026

Keywords

  • Home program
  • Shoulder conditions
  • Adherence

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Cedars-Sinai Medical Center on 2026-03-27.