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Development of a Clinical Assessment Tool for Oral Frailty and Exploration of Intervention Strategies in Patients with Sjögren's Syndrome

Development of a Clinical Assessment Tool for Oral Frailty and Exploration of Intervention Strategies in Patients with Sjögren's Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122733
Enrollment
Unknown
Registered
2026-04-16
Start date
2026-04-16
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

Patients with Sjögren's syndrome meet the 2016 American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) classification criteria, which include: clinically manifest xerostomia (patients report significant dry mouth lasting =3 months) along with reduced salivary gland function, or diagnosis confirmed by salivary gland biopsy/anti-SSA antibody testing.

Interventions

Pre-experiment group:Comprehensive Management Strategy for Oral Frailty in Patients with Sj?gren's Syndrome

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients aged >= 18 years who meet the 2016 American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) classification criteria for Sjögren's syndrome. 2.Patients are able to cooperate with relevant examinations and follow-up. 3.Both genders are included; considering the higher prevalence of Sjögren's syndrome in women, efforts will be made to ensure a representative gender ratio.

Exclusion criteria

Exclusion criteria: 1.Comorbid other autoimmune diseases, such as systemic lupus erythematosus, systemic scleroderma, etc.; 2.Use of medications that affect salivary secretion, such as anticholinergics, antidepressants, antihistamines, etc., in the recent period (within the last 3 months); 3.Presence of active oral infection, severe periodontal disease, oral malignancy, or oral mucosal lesions; 4.Pregnant or breastfeeding women; 5.Patients with cognitive impairment or mental disorders, making it difficult to cooperate with the study procedures; 6.Presence of severe systemic diseases, such as severe cardiopulmonary, hepatic, or renal insufficiency, etc.

Design outcomes

Primary

MeasureTime frame
Unstimulated salivary flow rate;Oral Frailty Index-8, OFI-8;Fatigue,Resistance,Ambulation,Illness,and Loss, FRAIL;Decay Missing Fill, DMFT;

Countries

China

Contacts

Public ContactAdalia

Beijing Hospital

jiashuyuancindy@163.com+86 10 8513 5062

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026