RECRUITING

Using VirtuaCareTM Platform for Home Programs in Acute and Chronic Shoulder Conditions: A Pilot Study

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Using VirtuaCareTM Platform for Home Programs in Acute and Chronic Shoulder Conditions: A Pilot Study

Quick Facts

Study Start:2024-02-01
Study Completion:2025-07-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06016257

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Subject 18 years or older
  2. * Outpatient physical therapy prescribed by doctor for shoulder rehabilitation.
  3. * No previous neurological condition
  4. * Understand English (exercises are only in English) Physical therapists
  5. * The therapists will be the ones who provide physical therapy treatment to the acute and chronic shoulder population.
  1. * Prior surgery within the last 5 years or less than 6 months between surgery
  2. * Neurologic comorbidities that have functional deficits
  3. * Uncontrolled diabetes
  4. * Diagnosis with active cancer in the last two years
  5. * Unable to understand English

Contacts and Locations

Study Contact

Pamela S Roberts
CONTACT
18185900004
pamela.roberts@cshs.org

Principal Investigator

Pamela S Roberts, PhD
PRINCIPAL_INVESTIGATOR
Cedars-Sinai Medical Center

Study Locations (Sites)

Cedars-Sinai Medical Center Outpatient Rehabilitation
Los Angeles, California, 90048
United States
Cedars-Sinai Medical Center
Los Angeles, California, 90048
United States

Collaborators and Investigators

Sponsor: Cedars-Sinai Medical Center

  • Pamela S Roberts, PhD, PRINCIPAL_INVESTIGATOR, Cedars-Sinai Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-01
Study Completion Date2025-07-31

Study Record Updates

Study Start Date2024-02-01
Study Completion Date2025-07-31

Terms related to this study

Keywords Provided by Researchers

  • Home program
  • Shoulder conditions
  • Adherence

Additional Relevant MeSH Terms

  • Shoulder Disease
  • Shoulder Injuries