This study targets adult patients with periodontal disease, mainly including those with gingivitis and periodontitis. Clinical manifestations may include gingival bleeding, gingival redness and swelling, oral malodor, plaque and calculus accumulation, periodontal pocket formation, gingival recession, attachment loss, tooth mobility, and discomfort during chewing.
Conditions
Interventions
Control group:Control group: routine care
Intervention group:Intervention group: periodontal nursing intervention
Sponsors
Zhenjiang First People's Hospital (Affiliated People’s Hospital of Jiangsu University)
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1.Aged 18 to 60 years, with no restriction on sex. 2.Patients attending the Department of Stomatology of this hospital and clinically diagnosed with periodontal disease. 3.Periodontal examination indicates one or more of the following manifestations: a) gingival redness, swelling, and bleeding; b) positive bleeding on probing; c) periodontal pocket formation; d) clinical attachment loss; e) alveolar bone resorption shown on X-ray examination. 4.Participants are currently planned to receive or have already entered the stage of standardized basic periodontal treatment, and are suitable for inclusion in the nursing intervention study. 5.Participants have no obvious cognitive or communication impairment, are able to understand the study content, and can cooperate with health education, behavioral guidance, and follow-up observation. 6.Voluntarily agree to participate in this study and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1.Patients with severe diseases of major organs, such as the heart, brain, liver, or kidneys, who cannot tolerate the examinations or interventions related to this study. 2.Patients with severe mental disorders, cognitive impairment, or communication disorders who are unable to cooperate with the study procedures. 3.Patients with other serious oral diseases or those requiring priority specialist treatment, which may affect the observation results of this study. 4.Patients who have received systematic periodontal treatment or participated in similar interventional studies within the past 3 months. 5.Pregnant or lactating women (may be listed as an exclusion criterion if not specifically included in the study protocol). 6.Patients deemed unsuitable for participation in this study by the investigators. 7.Patients who are unwilling to sign the informed consent form or have poor compliance and are expected to be unable to complete follow-up.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| oral health behaviors;Oral health literacy; | — |
Secondary
| Measure | Time frame |
|---|---|
| Bleeding on Probing (BOP);Plaque Index (PI);COM-B questionnaire score;Follow-up adherence;Score on the Oral Health Impact Profile-14 (OHIP-14); | — |
Countries
China
Contacts
Public ContactJishasha
Zhenjiang First People's Hospital (Affiliated People’s Hospital of Jiangsu University)
Outcome results
None listed