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Multimedia Animations to Support Therapeutic Exercise for Rotator Cuff Shoulder Pain

NCT05770908 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 154

Last updated 2025-05-30

No results posted yet for this study

Summary

The goal of this randomized controlled trial is to evaluate the benefits from adding multimedia animations to a paper-based therapeutic exercise program in subjects with rotator cuff related shoulder pain. The main question\[s\] it aims to answer are:

* Does subjects improve more regarding shoulder disability and pain?
* Are the subjects more satisfied with the treatment received?
* Do the subjects adhere more to the exercise program?
* Do the subjects have greater expectations with the treatment received? Participants will perform a therapeutic exercise program within 6 months. Researchers will compare the addition of web-app animations to the classical paper-based information.

Conditions

  • Rotator Cuff Impingement Syndrome
  • Rotator Cuff Tendinitis
  • Rotator Cuff Related Shoulder Pain

Interventions

OTHER

Therapeutic exercise program

Therapeutic exercise program based on increasing resistance with elastic bands or weights. The programmes are composed of combinations of the following exercises: * Scaption with elastic band. * External rotation at 0º of abduction with elastic band. * Internal rotation at 0º of abduction with elastic band. * Shoulder protraction in supine position with weights. * Low row with elastic band. * Horizontal adduction stretching.

OTHER

Multimedia animation information

Multimedia animation videos (including audio) showing the performance of the prescribed exercises.

OTHER

Paper-based information

Paper-based information showing the performance of the prescribed exercises, based on figures and a brief description of the exercise performance.

Sponsors & Collaborators

  • Instituto de Salud Carlos III

    collaborator OTHER_GOV

  • European Union

    collaborator OTHER

  • Hospital Universitario Fundación Alcorcón

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-04-07
Primary Completion
2024-12-01
Completion
2024-12-01

Countries

  • Spain

Study Locations

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Entities

Companies

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 NCT05770908 on ClinicalTrials.gov