Skip to main content
OpenTrials
Completed

NCT Number: NCT07301671

Prospective Cohort of Digital Shoulder Rehabilitation Using the REHABI System in Routine Clinical Practice

This is a prospective longitudinal observational cohort study of patients with shoulder disorders undergoing a standardized rehabilitation program supported by the REHABI digital automated model in a private physiotherapy clinic. The study aims to describe clinical outcomes in routine practice and to optimize a 24-test functional assessment battery based on deficit prevalence, magnitude, and responsiveness.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–71 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Lorena Castaño de Egues

Noáin, Navarre, 31110, Spain

About this study

This is a prospective longitudinal observational cohort study of 129 adult patients (≥18 and ≤71 years) with acute non-traumatic shoulder pain and/or dysfunction treated in a private sports physiotherapy clinic in Pamplona, Spain. All patients undergo a standardized rehabilitation program supported by the REHABI automated digital model, which links quantified deficits obtained from a 24-test functional assessment battery to specific exercise prescriptions and progression rules. The study aims to describe clinical outcomes in routine practice (global clinical deficit score, shoulder pain intensity, number of treatment sessions, and days to discharge) and to optimize the initial 24-test battery based on deficit prevalence, magnitude, and responsiveness to change between baseline and discharge.

The main objectives are: (1) to evaluate the clinical effectiveness and feasibility of the REHABI model in routine clinical practice; and (2) to reduce the initial 24-test assessment battery to a smaller core set of tests using mixed criteria based on prevalence, magnitude of deficit, and responsiveness to change.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18-71 years of age, acute non-traumatic shoulder pain/dysfunction, and access to a smartphone to view the exercises.

Exclusion criteria

  • Acute fractures or dislocations, arthritis/arthrosis, osteosarcoma, osteomyelitis, and recent shoulder surgeries.

Treatment and study plan

Primary outcomes

  1. Change in global clinical deficit score from baseline to discharge

    Time frame: Baseline and discharge (approximately 1-6 months after baseline, depending on clinical evolution)

    Global clinical score summarizing the number and magnitude of positive findings in the functional test battery. Higher scores indicate greater functional deficit. Change is calculated as discharge score minus baseline score.

Secondary outcomes

  1. Change in selected functional tests from the optimized core battery

    Time frame: Baseline and discharge (ranging from 1 month to 6 month after baseline)

    Change in performance on selected shoulder functional tests (e.g., Yocum, Speed, Jobe, external rotation at 90° abduction, etc.) identified as part of the optimized core test battery.

  2. Number of rehabilitation sessions until discharge

    Time frame: From baseline to discharge (approximately 1-6 months)

    Total number of physiotherapy sessions attended from baseline to discharge within the REHABI program.

  3. Days from baseline to clinical discharge

    Time frame: Baseline to discharge (ranging from 1 to 6 months)

    Number of days between the first assessment and the discharge visit recorded in the REHABI system.

  4. Change in shoulder pain intensity (Numeric Rating Scale, 0-10)

    Time frame: Baseline and discharge (approximately 1-6 months)

    Shoulder pain intensity during movement, measured using an 11-point Numeric Rating Scale (EVA 0-10). Change is calculated as discharge score minus baseline score.

Sponsors and collaborators

Lead sponsor

Universidad Pública de Navarra

Other

Collaborators

  • Government of Navarra

Registry information

Official study title

Prospective Longitudinal Observational Cohort Study of a Digital Automated Rehabilitation Model for Shoulder Disorders (REHABI) in a Private Physiotherapy Clinic

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Dec 24, 2025
Registry last updated
Dec 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.