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Clinical Trials in China / NCT07422714
Recruiting Not applicable

Application of a Wearable Device-Based Intelligent Rehabilitation System in the Rehabilitation of Patients With Frozen Shoulder

NCT07422714 · tracked via the Priya Life Science China tracker
Sponsor
Peking University Third Hospital
Phase
Not applicable
Started
2026-09-17
Last updated
2026-09-22

Condition(s) studied

Range of Motion, Articular

Investigational drug(s) / intervention(s)

Artificial and intelligent combination of shoulder joint function exerciseTraditional rehabilitation trainingIntelligent rehabilitation training

Artificial and intelligent combination of shoulder joint function exercise: Rehabilitation therapist rehabilitation and intelligent rehabilitation are combined

Traditional rehabilitation training: Shoulder joint function training is performed by a rehabilitation therapist

Intelligent rehabilitation training: Shoulder joint rehabilitation training is carried out according to the intelligent rehabilitation system

Study summary

A Comparative Study of Traditional Rehabilitation and Remote Intelligent Rehabilitation: Exploring the Application Effectiveness of Intelligent Rehabilitation in Frozen Shoulder Rehabilitation

Eligibility

Sex
ALL
Min age
40 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria:① Subjects are aged between 40 and 60 years (inclusive), regardless of gender; * Diagnosed with the adhesive phase of frozen shoulder by the Department of Sports Medicine, with patients potentially coming from different physicians; * Have not participated in any other clinical trials within the past 3 months; ④ Patients voluntarily agree to participate in the clinical trial, sign the informed consent form, and are able to cooperate with clinical follow-up. Exclusion Criteria:① Patients with combined cardiovascular or cerebrovascular diseases, severe liver or kidney dysfunction, coagulation disorders, severe electrocardiogram abnormalities, etc.; * Patients with local lesions in the affected shoulder or arm, such as skin damage, infection, tuberculosis, tumors, or skin diseases; * Patients with poor physical condition who are unable to tolerate the intensity of rehabilitation training; ④ Patients with cognitive impairments who cannot undergo normal rehabilitation training, or other conditions deemed by the physician as unsuitable for trial participation; ⑤ Pregnant or breastfeeding women; ⑥ Patients with other shoulder conditions, such as rotator cuff tears or shoulder dislocation.

Primary outcome measure(s)

  • Constant-Murley Shoulder Assessment Score Scale — Week 0、Week 4 and Week 8
    The Constant-Murley Shoulder Assessment Score Scale consists of four components: activities of daily living (20 points), pain (15 points), muscle strength (25 points), and range of motion (40 points), with a total score of 100 points. A lower score indicates a higher percentage of dysfunction, while a higher score indicates the opposite. The questionnaire demonstrates high accuracy and reliability and is commonly used to assess patients' shoulder joint conditions.

Trial sites (1)

FacilityCityRegionStatus
Peking University Third Hospital Beijing China Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07422714 on ClinicalTrials.gov ↗ ← All trials in China