Telerehabilitation in Shoulder Pathology
Effectiveness of Telerehabilitation in Shoulder Pathology
1 other identifier
interventional
68
1 country
1
Brief Summary
A randomized clinical trial will be conducted to evaluate the effectiveness of telerehabilitation compared to in-person physiotherapy in the treatment of rotator cuff injuries of the shoulder. Follow-up assessments will be performed at 2, 5, and 8 weeks. Scales will be used to evaluate shoulder function, quality of life, pain perception, and satisfaction with the digital tool.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Sep 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2025
CompletedFirst Submitted
Initial submission to the registry
September 23, 2025
CompletedFirst Posted
Study publicly available on registry
January 7, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 2, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
February 15, 2026
CompletedApril 8, 2026
April 1, 2026
5 months
September 23, 2025
April 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Shoulder functionality
Shoulder function will be analyzed using the test Constant Murley.A maximum total score of 100 indicates optimal health and mobility in this joint. The results are divided into four main categories: pain (15 points), activities of daily living (20 points), mobility (40 points), and strength (25 points). It is essential to distinguish between scores below 60, which denote a severely dysfunctional state, and those above 80, which reflect optimal functionality.
At baseline, at 2, 5, 8, and 12 weeks.
Secondary Outcomes (4)
Health-related quality of life
At baseline, and at 2, 5, 8, and 12 weeks.
Level of shoulder disability
At baseline, 5 and 12 weeks
Pain perception
At baseline, 2,5,8 and 12 weeks
Level of satisfaction with telerehabilitation
At 12 weeks.
Study Arms (2)
Telerehabilitation
EXPERIMENTALexercises supervised by videoconference
Face to face physiotherapy
ACTIVE COMPARATORFace to face exercise sessions in the physiotherapy room
Interventions
Exercises supervised by videoconference.
Exercises performed in a physical therapy room.
Eligibility Criteria
You may qualify if:
- Minimum age 18.
- Diagnosis of degenerative shoulder rotator cuff disease.
- Internet access.
- Access to a video calling device.
You may not qualify if:
- Previous shoulder surgery.
- Cognitive impairment that prevents them from performing the task.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Teruel Ensanche Primary Care
Teruel, Aragon, 44002, Spain
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- PhD
Study Record Dates
First Submitted
September 23, 2025
First Posted
January 7, 2026
Study Start
September 1, 2025
Primary Completion
February 2, 2026
Study Completion
February 15, 2026
Last Updated
April 8, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share
This study is not complete.