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Mobile application-based support for treatment of patients with gum disease

Mobile application-based support for periodontal treatment improves clinical, cognitive, and psychomotor outcomes: a randomized controlled trial study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN12409366
Enrollment
40
Registered
2024-02-28
Start date
2022-01-21
Completion date
Unknown
Last updated
2024-03-18

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

Conditions

Improving clinical, cognitive, and psychomotor aspects of patients with gingivitis or periodontitis Oral Health

Interventions

Participants were listed and evenly distributed between the test (professional mechanical plaque removal including scaling and root planing and dental health education [PMPR-DHE] + mobile application)

Sponsors

Universitas Indonesia
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Gingivitis or periodontitis subjects 2. Aged between 35 and 55 years 3. Had never received periodontal therapy only during the previous 6 months 4. Android system-based smartphone users

Exclusion criteria

Exclusion criteria: 1. Systemic conditions related to periodontal disease such as cardiovascular disease, oral cancer, respiratory tract infection, and diabetes 2. Pregnancy or breastfeeding 3. On medication from a health provider 4. Current smokers

Design outcomes

Primary

MeasureTime frame
1. Clinical periodontal parameters: probing pocket depth (PPD) measured using periodontal probe UNC-15 and visual inspection on six tooth surfaces, namely the distobuccal, mid-buccal, mesiobuccal, distolingual, mid-lingual, and mesiolingual surfaces of all teeth, except for the third molars, and the average probing depth value was measured at baseline, 1 and 3 months 2. Clinical periodontal parameters: bleeding on probing (BoP) measured using periodontal probe UNC-15 and visual inspection by assessing the presence of bleeding lasting up to 30 seconds, the BoP was recorded during the PPD measurement at baseline, 1 and 3 months 3. Clinical periodontal parameters: oral hygiene index (OHIS) measured using a disclosing agent and visual inspection which stained plaque and calculus on all tooth surfaces to be evaluated at baseline, 1 and 3 months 4. Cognitive scores recorded by using pretest questions at baseline and post-test questions during the evaluation visits at baseline, 1 and 3 months 5. Psychomotor scores assessed using a checklist form of oral hygiene procedures at baseline, 1 and 3 months

Secondary

MeasureTime frame
Microbiology periodontal complexes measured using next-generation sequencing (NGS) at baseline, 1 and 3 months

Countries

Indonesia

Contacts

Public ContactBenso;Valdy Sulijaya;Hartono

;

bensosulijaya@gmail.com;valdy.hartono@gmail.com+62 (0)81212286089;+62 (0)81808050734

Outcome results

None listed

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