Efficacy Evaluation of Intelligent Rehabilitation Programs Based on AI-Powered Digital Rehabilitation System for Subacromial Impingement Syndrome

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorPeking University Third Hospital

About this trial

This non-randomized controlled trial will compare the efficacy of a conventional rehabilitation program versus an AI-based digital rehabilitation system in patients with subacromial impingement syndrome (SIS).

Eligibility criteria

Qualifiers

MRI shows hyperintensity indicating subacromial bursitis;

Aged 18-60 years;

Conscious, able to understand and cooperate with rehabilitation training, and willing to accept regular follow-up; ⑤ No shoulder surgery within the past 1 year, no other shoulder joint-related diseases, and no need for surgical intervention; ⑥ Voluntarily sign the informed consent form and commit to participating in the entire study.

Disqualifiers

History of shoulder surgery or current injury is an old tear (course >6 months without standardized treatment);

Suffering from severe cardiovascular or cerebrovascular diseases, diabetes, rheumatoid arthritis, osteoporosis, or other systemic diseases that may affect rehabilitation outcomes;

Cognitive impairment that prevents normal participation in rehabilitation training, or other conditions judged by the physician as making the patient unsuitable for the trial;

Trial design

Treatments tested in this trial

  • Home-based Rehabilitation Training Combined with Intelligent Rehabilitation Training
  • Traditional Rehabilitation Training
  • Prescribe home-based rehabilitation prescriptions for home rehabilitation training

Treatment groups

93 Participants
are divided into 3 treatment groups