This is a single-center, randomized, parallel-controlled trial evaluating the efficacy and safety of an artificial intelligence-based exercise prescription system for rehabilitation in rheumatoid arthritis (RA) patients. A total of 147 patients with low-to-moderate disease activity will be randomly assigned to three groups: AI exercise prescription group (personalized AI system guidance), paper exercise prescription group (traditional paper guidance), and routine care group. The intervention will last for 6 weeks with 6-month follow-up assessments evaluating joint function, pain, and quality of life indicators.
This three-arm randomized controlled trial (RCT) uses Redcap system for 1:1:1 randomization. The AI exercise prescription group receives intervention through the "Yidong Health AI Exercise Prescription System" delivered via WeChat mini-program; the paper exercise prescription group receives traditional paper-based guidance; and the routine care group receives standardized health education and basic exercise instructions. The primary outcome measure is knee flexion range of motion (ROM) at 6 months, with secondary outcomes including HSS score, WOMAC index, TUG test, BBS balance scale, and other functional assessment measures.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
147
Uses "Yidong Health AI Exercise Prescription System" delivered via WeChat mini-program, providing personalized exercise prescriptions (three sets: A/B/C) with AI Q\&A module. Physicians adjust prescriptions weekly based on patient feedback.
Receives standardized RA disease management education and basic joint mobility exercises provided by rheumatology nurses.
Receives paper-based exercise prescription developed by rehabilitation therapists, including warm-up, formal training (bridging, modified bird-dog exercise, etc.) and cool-down stretching.
Department of Rehabilitation Medicine, Peking University People's Hospital
Beijing, Beijing Municipality, China
Knee flexion range of motion
Knee Flexion Range of Motion Unit of Measure: Degrees (°) Knee flexion range of motion refers to the maximum angle through which the knee joint can bend, measured from the straight (extended) position to the farthest point the lower leg can move toward the thigh. This assessment evaluates the flexibility and functional mobility of the knee, which is critical for daily activities such as walking, climbing stairs, and sitting. Relevant definitions and criteria: A "normal" range of motion for knee flexion in adults is generally considered to be 135° to 150°, though this can vary slightly based on age, physical conditioning, and individual anatomy. Limited knee flexion (e.g., less than 90°) may indicate joint stiffness, muscle tightness, or underlying issues such as injury, arthritis, or post-surgical scarring.
Time frame: Baseline, post-intervention (6 weeks), 3-month follow-up, 6-month follow-up
Hospital for Special Surgery (HSS) Score
Hospital for Special Surgery (HSS) Score Unit of Measure: Points (out of 100) The Hospital for Special Surgery (HSS) Score is a comprehensive assessment tool used primarily in orthopedics, especially in evaluating the condition of the knee joint. It helps medical professionals determine the overall function and well - being of the knee, which is crucial for guiding treatment decisions, such as whether conservative management or surgical intervention is more appropriate.Total Score Range: The HSS Score ranges from 0 to 100 points. Interpretation of Scores: \> 85 points: Considered "excellent". At this level, the knee is functioning very well, with minimal pain and good functional ability. In many cases, patients with such scores may not require significant medical intervention or may only need conservative measures like rest and exercise adjustments. 70 - 85 points: Rated as "good". The knee has some minor issues, but overall function is still acceptable. Appropriate conservative
Time frame: Baseline, post-intervention (6 weeks), 3-month follow-up, 6-month follow-up
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)
Time frame: Baseline, post-intervention (6 weeks), 3-month follow-up, 6-month follow-up
Timed Up and Go (TUG) Test
Time frame: Baseline, post-intervention (6 weeks), 3-month follow-up, 6-month follow-up
Berg Balance Scale (BBS)
Time frame: Baseline, post-intervention (6 weeks), 3-month follow-up, 6-month follow-up
Isokinetic Muscle Strength Test
Time frame: Baseline, post-intervention (6 weeks), 3-month follow-up, 6-month follow-up
Gait and Plantar Pressure Analysis
Time frame: Baseline, post-intervention (6 weeks), 3-month follow-up, 6-month follow-up
Arthritis Self-Efficacy Scale (ASES-8)
Time frame: Baseline, post-intervention (6 weeks), 3-month follow-up, 6-month follow-up
Patient Health Questionnaire-9 (PHQ-9)
Time frame: Baseline, post-intervention (6 weeks), 3-month follow-up, 6-month follow-up
Generalized Anxiety Disorder-7 (GAD-7)
Time frame: Baseline, post-intervention (6 weeks), 3-month follow-up, 6-month follow-up
Pittsburgh Sleep Quality Index (PSQI)
Time frame: Baseline, post-intervention (6 weeks), 3-month follow-up, 6-month follow-up
Health Assessment Questionnaire (HAQ)
Time frame: Baseline, post-intervention (6 weeks), 3-month follow-up, 6-month follow-up
Laboratory indicators (RF, CRP, complete blood count)
Time frame: Baseline, post-intervention (6 weeks), 3-month follow-up, 6-month follow-up
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