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Enhanced management of telemedicine for ankylosing spondylitis: a randomized controlled trial

Enhanced management of telemedicine for ankylosing spondylitis: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800014468
Enrollment
Unknown
Registered
2018-01-16
Start date
2018-02-01
Completion date
Unknown
Last updated
2018-01-29

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

Conditions

ankylosing spondylitis

Interventions

Intervention group :In addition to conventional therapy, participants in CT-GOHT group will receive a brief repeated GOH-based management every month via the GOHT platform.

Sponsors

Guangdong Second Provincial General hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Participants will be qualified for inclusion when they meet the following criteria: meeting the 1984 American College of Rheumatology (ACR) classification criteria for ankylosing spondylitis;patients in active stage(two of following: BASDAI=4cm; VAS=4cm in back;morning stiffness= 1 hour); aged over 18 years; availability of GOH telemedicine platforms in the community; ability to communicate and to understand the study.

Exclusion criteria

Exclusion criteria: Participants will be excluded if they have any of the following conditions: OA with severe joint deformity which needs surgery; other joint diseases, including rheumatoid arthritis and joint trauma; autoimmune diseases; hypertension; coronary heart disease; chronic digestive disorders including chronic gastritis and chronic hepatitis; stroke; diabetes mellitus; chronic kidney diseases; chronic respiratory diseases including chronic obstructive pulmonary disease; cancers; dementia or substantial cognitive impairment; psychotic illness; inability to give informed consent; unable to communicate or to understand the study; and no access to a GOH telemedicine platform.

Design outcomes

Primary

MeasureTime frame
Bath Ankylosing Spondylitis Disease Activity Index (BASDAI);Bath Ankylosing Spondylitis Functional Index (BASFI);

Secondary

MeasureTime frame
the Pittsburgh Sleep Quality Index (PSQI);the Multidimensional Fatigue Inventory (MFI);Hospital Anxiety and Depression Scale;

Countries

China

Contacts

Public ContactHuang Zhengping

Guangdong Second Provincial General Hospital

huangzhp2012@163.com+86 13802416733

Outcome results

None listed

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