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TeleRehabilitation Following Arthroscopic Rotator Cuff Repair

TeleRehabilitation Following Arthroscopic Rotator Cuff Repair

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04541953
Enrollment
32
Registered
2020-09-09
Start date
2020-09-16
Completion date
2022-06-01
Last updated
2022-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rotator Cuff Injuries

Brief summary

Telerehabilitation is a form of tele-treatment in which rehabilitation services are dispensed at patients' home utilizing video telecommunication services with real-time synchronous exchange of information. The advantages of telerehabilitation include reducing unnecessary travel to the hospital and person to person contact while maintaining social distancing. While some of the patients are truly staying at remote areas, others are unable to manage travel in the lockdown period. Telemedicine offers the opportunity to deliver rehabilitative services in the patients' home, closing geographic, physical, and motivational gaps. Punctuality on either side is also assured since the travel times are saved on both the ends. The purpose of the research study is to compare two standard of care rehabilitation methods (telerehabilitation vs in-person rehabilitation) following routine rotator cuff repair. Objectives include assessing range of motion and patient reported functional outcomes.

Interventions

Rehabilitation services will be dispensed at patients' home utilizing video telecommunication services with real-time synchronous exchange of information - range of motion exercises and stretching.

Range of motion exercises and stretching

Sponsors

NYU Langone Health
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Scheduled to undergo Rotator Cuff repair * Age 40-80 * Ability to comply with a standardized postoperative protocol * Willing and able to provide consent

Exclusion criteria

* Pregnant patient * Age \<40 years * Previous shoulder surgery * Unable to speak English or perform informed consent

Design outcomes

Primary

MeasureTime frameDescription
Level of Range of Motionup to 1 year post-opActive and passive range of motions will be tested in participants: forward flexion, abduction and internal/external rotation at 0° and 90°.

Secondary

MeasureTime frameDescription
Visual Analogue Scale (VAS) Scoreup to 1 year post-opVAS is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between no pain and worst pain. The total score ranges from 0-10. The higher the score, the worse the pain.
American Shoulder and Elbow Surgeons (ASES) Questionnaire Scoreup to 1 year post-opThe ASES score contains a physician-rated and patient-rated section; however, only the pain visual analog scale (VAS) and 10 functional questions will be used to tabulate the reported ASES score. The total score - 100 maximum points - is weighted 50% for pain and 50% for function. The final pain score (maximum 50 points) is calculated by subtracting the VAS from 10 and multiplying by five. For the functional portion, each of 10 separate questions is scored on an ordinal scale from 0-3 for a maximal raw functional score of 30 points. The raw score is multiplied by 5/3 to make the maximal functional score out of 50 possible points. The pain and functional portions are then summed to obtain the final ASES score. The higher the score, the worse the pain and level of function.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026