Skip to main content
OpenTrials
Completed

NCT Number: NCT07321444

Telerehabilitation in Shoulder Pathology

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Teruel Ensanche Primary Care

Teruel, Aragon, 44002, Spain

About this study

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.

Who can participate

Healthy volunteers accepted: No

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

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.

Treatment and study plan

telerehabilitation in physiotherapy

Procedure

Exercises supervised by videoconference.

face to face physiotherapy

Procedure

Exercises performed in a physical therapy room.

Primary outcomes

  1. Shoulder functionality

    Time frame: At 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 outcomes

  1. Health-related quality of life

    Time frame: At 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.

  2. Level of shoulder disability

    Time frame: At baseline, 5 and 12 weeks

    Shoulder 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.

  3. Pain perception

    Time frame: At baseline, 2,5,8 and 12 weeks

    Pain 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.

  4. Level of satisfaction with telerehabilitation

    Time frame: At 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.

Sponsors and collaborators

Lead sponsor

Instituto de Investigación Sanitaria Aragón

Other

Registry information

Official study title

Effectiveness of Telerehabilitation in Shoulder Pathology

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jan 7, 2026
Registry last updated
Apr 8, 2026

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.