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RecruitingNCT07611981SLD-OHUpdated Jun 16, 2026

Dental Caries and Oral Hygiene Status in Children With Specific Learning Disabilities

An observational study in Specific Learning Disabilities, Dental Caries and Oral Hygiene, sponsored by Alanya Alaaddin Keykubat University. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 7 Years to 12 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-16.

Sponsored by Alanya Alaaddin Keykubat University · Observational

From the registry’s dates

  • Started Jun 2026; still recruiting 4 months later.
Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
70
Ages
7 Years to 12 Years
Sex
All
01

Study summary

This study aims to evaluate dental caries and oral hygiene status in children aged 7-12 years with specific learning disabilities (SLD) and to compare the findings with healthy children. Clinical oral examinations, including dmft/DMFT, ICDAS II, Plaque Index, and Gingival Index assessments, will be performed. In addition, questionnaire-based evaluations of oral hygiene habits, dietary habits, and parental supervision during toothbrushing will be conducted.

02

Conditions studied

  • Specific Learning Disabilities
  • Dental Caries
  • Oral Hygiene

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Keywords

  • Specific Learning Disabilities
  • Dental Caries
  • Oral Health
  • dmft/DMFT
  • Pediatric Dentistry
  • Plaque Index
  • Gingival Index
03

In context

Dental Caries

1,171 studies on the registry are indexed under Dental Caries; 209 are open to participants now.

This study's planned enrollment of 70 is below the median of 174 across 187 observational studies indexed under Dental Caries.

Browse Dental Caries studies →

Lead sponsor

Alanya Alaaddin Keykubat University is the lead sponsor of 51 studies on the registry; 17 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
7 Years to 12 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Children aged 7-12 years presenting to Alanya Alaaddin Keykubat University Faculty of Dentistry Paediatric Dentistry Clinic. The study group consists of children diagnosed with specific learning disorder (SLD) by a psychiatrist. The control group consists of healthy children with no psychiatric diagnosis, confirmed by a psychiatrist.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Children aged 7-12 years
  • For the study group: diagnosis of specific learning disorder (SLD) confirmed by a psychiatrist
  • For the control group: confirmed healthy with no psychiatric diagnosis by a psychiatrist
  • Written obtained from the parent or guardian

Exclusion criteria

Exclusion Criteria:

  • Children with additional psychiatric diagnoses (e.g., autism spectrum disorder, attention-deficit/hyperactivity disorder, intellectual disability)
  • Children with systemic disease or physical disability that may prevent participation in the study
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
70 participants (estimated)
Patient registry
No

Groups and cohorts

  • Children with Specific Learning Disorder (SLD)

    Children aged 7-12 years diagnosed with specific learning disorder by a psychiatrist, presenting to Alanya Alaaddin Keykubat University Faculty of Dentistry. Dental caries experience (dmft/DMFT), caries severity (ICDAS II), plaque index and gingival index will be assessed.

  • Healthy Control Children

    Children aged 7-12 years with no psychiatric diagnosis, confirmed healthy by a psychiatrist, presenting to Alanya Alaaddin Keykubat University Faculty of Dentistry Paediatric Dentistry Clinic. Dental caries experience (dmft/DMFT), caries severity (ICDAS II), plaque index and gingival index will be assessed.

06

What researchers measure

Primary outcomes

  1. Dental Caries Experience (dmft/DMFT)

    Decayed, missing, and filled teeth index for primary (dmft) and permanent (DMFT) dentition, assessed according to WHO criteria using mirror and periodontal probe under dental unit light.

    Time frame: Single assessment at the time of clinical examination

  2. Caries Severity (ICDAS II)

    International Caries Detection and Assessment System II score recorded for each tooth using visual and tactile examination. The highest ICDAS II code recorded for each patient is used as the individual score.

    Time frame: Single assessment at the time of clinical examination

Secondary outcomes

  1. Plaque Index (PI)

    Loe \& Silness Plaque Index assessing dental plaque thickness at the gingival margin, scored 0-3.

    Time frame: Single assessment at the time of clinical examination

  2. Gingival Index (GI)

    Loe \& Silness Gingival Index assessing quality, severity and localisation of gingival disease, scored 0-3.

    Time frame: Single assessment at the time of clinical examination

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No — Individual participant data (IPD) will not be shared due to participant confidentiality and privacy considerations.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07611981
Lead sponsor
Alanya Alaaddin Keykubat University
Responsible party
Gül Keskin (Associate Professor, DDS, PhD, Alanya Alaaddin Keykubat University) — Principal investigator
First posted
May 28, 2026
Start date
Jun 15, 2026
Primary completion
Oct 2026 (estimated)
Completion
Oct 2026 (estimated)
Last update
Jun 16, 2026

Study contacts

Gül Keskin, Associate Professor, DDS, PhD
Contact
gul.keskin@alanya.edu.tr
+90 242 510 61 40
Fatma Yaman Toktasır, Research Assistant, DDS
Contact
yamanfatma07@gmail.com
+905055881265

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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