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Construction and Validation of Long-term Rehabilitation Exercise Patterns for Ankylosing Spondylitis Participants Based on the ASE Model: A Decentralized Randomized Controlled Trial

Construction and Validation of Long-term Rehabilitation Exercise Patterns for Ankylosing Spondylitis Participants Based on the ASE Model: A Decentralized Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102260
Enrollment
Unknown
Registered
2025-05-12
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ankylosing spondylitis

Interventions

Experimental group:''Exercise Management Method based on ASE Model (EMM-ASE)'' for rehabilitation exercise management
Control group:Regular rehabilitation exercise management

Sponsors

The Third Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Meets the 2009 classification criteria for ankylosing spondylitis; 2. Inpatients over 18 years of age, whose condition has improved, with a BASDAI score below 4, and who meet the discharge criteria; 3. Participants who understand the purpose, procedures, and content of the study and voluntarily participate in the trial, signing an informed consent form; 4. Participants who are able to communicate orally with researchers in Mandarin or Cantonese

Exclusion criteria

Exclusion criteria: 1. Participants suffering from fibromyalgia syndrome, pelvic inflammatory sclerosis, localized pain caused by lumbar or cervical spinal cord compression, or moderate to severe pain that may be confused with radicular pain or other pains possibly related to ankylosing spondylitis (AS); 2. Participants with severe osteoporosis or pathological fractures; 3. Participants with severe systemic diseases and significant impairment of major organ function; 4. Participants without experience using WeChat software on computers or smartphones.

Design outcomes

Primary

MeasureTime frame
Physical activity level;Bath Ankylosing Spondylitis Functional Index, BASFI;

Secondary

MeasureTime frame
Bath ankylosing spondylitis disease activity index, BASDAI;Fatigue Severity Scale, FSS;Quality of life;Exercise compliance;

Countries

China

Contacts

Public ContactHuang Lei

The Third Affiliated Hospital of Sun Yat-sen University

zaokou123@126.com+86 135 7048 7964

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026