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Predicting ROtator Cuff Tears Outcomes After Physical Therapy Treatment

NCT05913050 · Status: SUSPENDED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 386

Last updated 2025-05-25

No results posted yet for this study

Summary

The aim of this multicenter non-controlled study is to develop a multivariable prediction model of pain/disability improvements in patients with full-thickness rotator cuff tears, after a physical therapy treatment based on therapeutic exercise and education.

Conditions

  • Rotator Cuff Injuries

Interventions

OTHER

Therapeutic resistance exercise

Therapeutic exercise program based on individualized progressive resistance exercises performed during 3 months at home, with a frequency of 1-3 sessions per week at the hospital.

OTHER

Education

Education applied during all the therapeutic process, focusing on diverting the patient's attention away from the structural lesion, explaining the relationship between pain/disability and tissue injury, explaining the meaning of pain during exercises, and explaining the objectives of the implemented treatments.

Sponsors & Collaborators

  • Hospital Universitario de Fuenlabrada

    collaborator OTHER

  • Hospital Universitario Infanta Leonor - Vallecas / Hospital Virgen de la Torre

    collaborator UNKNOWN

  • Hospital Universitario La Paz

    collaborator OTHER

  • Hospital Universitario Ramon y Cajal

    collaborator OTHER

  • Hospital Universitario La Princesa

    collaborator UNKNOWN

  • Hospital General Universitario Gregorio Marañon

    collaborator OTHER

  • Hospital Universitario Principe de Asturias

    collaborator OTHER

  • Hospital Universitario Fundación Alcorcón

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
30 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-05-01
Primary Completion
2026-09-18
Completion
2026-09-18

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05913050 on ClinicalTrials.gov