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Telerehabilitation in Shoulder Pathology

Effectiveness of Telerehabilitation in Shoulder Pathology

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07321444
Enrollment
68
Registered
2026-01-07
Start date
2025-10-01
Completion date
2026-02-15
Last updated
2026-08-18

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

Conditions

Rotator Cuff Pathology

Keywords

Telerehabilitation, Physiotherapy, Physical Therapy, Shoulder

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.

Detailed description

Digital health is undergoing significant development in various healthcare settings, especially in primary care. Digital physiotherapy, or telerehabilitation, is a resource that promotes self-care and allows for remote monitoring and follow-up. This study focuses on its application to degenerative rotator cuff disease of the shoulder. This is justified by its high prevalence and the geographical dispersion of the population served by the Primary Care Physiotherapy Unit of Teruel Ensanche. Objectives: The main objective is to evaluate the effectiveness of a primary care telerehabilitation program for patients with degenerative rotator cuff disease of the shoulder, compared to traditional physiotherapy. Secondary objectives are to assess patients' perception and satisfaction with this intervention and to analyze the usability and acceptance of the telerehabilitation program. Methodology: A 12-week randomized clinical trial will be conducted at the Teruel Ensanche Health Center. A sample of 68 adults aged 34 to 87 years with degenerative rotator cuff disease of the shoulder was estimated. Participants require internet access and an electronic device. The variables measured: shoulder function (Constant-Murley test), degree of disability (DASH questionnaire), quality of life (COOP/WONCA questionnaire), and pain perception (numerical rating scale). The intervention group (IG) receive an individualized program with remotely guided and supervised exercises, supplemented by a weekly in-person session. The control group (CG) receive standard treatment: 10 in-person physiotherapy sessions, followed by unsupervised home exercises. Assessments will be conducte at baseline and at 2, 5, 8, and 12 weeks.

Interventions

PROCEDUREtelerehabilitation in physiotherapy

Exercises supervised by videoconference.

PROCEDUREface to face physiotherapy

Exercises performed in a physical therapy room.

Sponsors

Instituto de Investigación Sanitaria Aragón
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Minimum age 18. * Diagnosis of degenerative shoulder rotator cuff disease. * Internet access. * Access to a video calling device.

Exclusion criteria

* Previous shoulder surgery. * Cognitive impairment that prevents them from performing the task.

Design outcomes

Primary

MeasureTime frameDescription
Shoulder functionalityAt baseline, at 2, 5, 8, and 12 weeks.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.

Secondary

MeasureTime frameDescription
Health-related quality of lifeAt baseline, and at 2, 5, 8, and 12 weeks.The COOP-WONCA questionnaire The COOP-WONCA questionnaire is a brief instrument for assessing health status and health-related quality of life (HRQoL), widely used in primary care and clinical studies to obtain a global and functional view of the patient's perceived health status. It consists of 7 items, and scores were processed using a 5-point Likert scale, with higher scores corresponding to a poorer quality of life.
Level of shoulder disabilityAt baseline, 5 and 12 weeksShoulder disability will be analyzed using the DASH questionnaire (Disabilities of the Arm, Shoulder and Hand). The DASH consists of 30 items. Each question must be answered using a 5-point scale, where 1 indicates "No difficulty" and 5 indicates "Unable to perform." A higher score indicates greater disability.
Pain perceptionAt baseline, 2,5,8 and 12 weeksPain perception will be analyzed using the Numerical Pain Rating Scale. It is scored from 1 to 10. The higher the score, the greater the perception of pain.
Level of satisfaction with telerehabilitationAt 12 weeks.Satisfaction with the use of telerehabilitation will be measured using the TUQ questionnaire (Telehealth Usability Questionnaire). It has 12 items, rated on a Likert scale from 1 to 7, the higher the score, the greater the satisfaction.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 19, 2026