NCT07321444

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
68

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
22 days until next milestone

First Submitted

Initial submission to the registry

September 23, 2025

Completed
4 months until next milestone

First Posted

Study publicly available on registry

January 7, 2026

Completed
26 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 2, 2026

Completed
13 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 15, 2026

Completed
Last Updated

April 8, 2026

Status Verified

April 1, 2026

Enrollment Period

5 months

First QC Date

September 23, 2025

Last Update Submit

April 7, 2026

Conditions

Keywords

TelerehabilitationPhysiotherapyPhysical TherapyShoulder

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

EXPERIMENTAL

exercises supervised by videoconference

Procedure: telerehabilitation in physiotherapy

Face to face physiotherapy

ACTIVE COMPARATOR

Face to face exercise sessions in the physiotherapy room

Procedure: face to face physiotherapy

Interventions

Exercises supervised by videoconference.

Telerehabilitation

Exercises performed in a physical therapy room.

Face to face physiotherapy

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Interventions

TelerehabilitationPhysical Therapy Modalities

Intervention Hierarchy (Ancestors)

RehabilitationAftercareContinuity of Patient CarePatient CareTherapeuticsHealth ServicesHealth Care Facilities Workforce and ServicesTelemedicineDelivery of Health CarePatient Care ManagementHealth Services Administration

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.

Locations