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Not yet recruitingNCT07433595Updated Feb 25, 2026

Association Between Child and Parental Stress and Bruxism in Children Aged 8-11 Years

An observational study in Bruxism, Stress and Parent Stress, sponsored by Bezmialem Vakif University. Not yet recruiting at 1 site in Turkey (Türkiye). Open to participants aged 8 Years to 11 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-25.

Sponsored by Bezmialem Vakif University · Observational

From the registry’s dates

  • Primary completion was expected by Apr 2026, 7 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
100
Ages
8 Years to 11 Years
Sex
All
01

Study summary

This prospective observational case-control study aims to evaluate the association between perceived stress levels in children and their parents and the presence of clinically diagnosed bruxism in children aged 8-11 years. Children with bruxism and age-matched controls will be recruited from the Department of Pediatric Dentistry. Child perceived stress, parental perceived stress, parenting-related stress, and parental awareness of child stress/anxiety will be assessed using validated questionnaires. Associations between stress-related measures and bruxism status will be analyzed.

Read the detailed description

This study is a prospective observational case-control study designed to investigate the association between perceived stress levels in children and their parents and the presence of clinically diagnosed bruxism in children aged 8-11 years. Participants will be recruited from children presenting to the Department of Pediatric Dentistry at Bezmialem Vakıf University Faculty of Dentistry for dental treatment.

Children will be allocated into two groups based on clinical evaluation: a bruxism group consisting of children diagnosed with bruxism, and a control group consisting of children without clinical signs of bruxism. Bruxism diagnosis will be established using parental reports and standardized clinical examination findings, including tooth wear assessed according to the Smith and Knight Tooth Wear Index, temporomandibular joint findings, masticatory muscle symptoms, and intraoral soft tissue signs.

Perceived stress levels in children will be assessed using the Perceived Stress Scale for Children (8-11 years). Parenting-related stress will be evaluated using the Parenting Stress Scale. Parents' own perceived stress levels will be measured using the Perceived Stress Scale (PSS). Parental awareness of the child's stress and anxiety will be assessed using the parent form of the Screen for Child Anxiety Related Emotional Disorders (SCARED) developed by Birmaher et al.

All assessments will be conducted at baseline during the clinical visit. The primary outcome is the association between child perceived stress levels and bruxism status. Secondary outcomes include associations between parental stress-related measures and child bruxism status. Statistical analyses will be performed to evaluate group differences and associations between stress measures and the presence of bruxism.

02

Conditions studied

  • Bruxism
  • Stress
  • Parent Stress
  • Parent and Child Stress

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Keywords

  • Child stress
  • Parenting stress
  • Bruxism
  • Parental and child stress
03

In context

Bruxism

151 studies on the registry are indexed under Bruxism; 39 are open to participants now.

This study's planned enrollment of 100 is above the median of 89 across 55 observational studies indexed under Bruxism.

Browse Bruxism studies →

Lead sponsor

Bezmialem Vakif University is the lead sponsor of 354 studies on the registry; 59 are open to participants now.

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

04

Who can participate

Ages eligible
8 Years to 11 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The study population consists of children aged 8-11 years who present to the Department of Pediatric Dentistry at Bezmialem Vakıf University Faculty of Dentistry for dental treatment, along with their parents. Children will be classified into the bruxism and control groups based on clinical examination and parental reports.

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 8-11 years Mixed or permanent dentition Presentation to the Department of Pediatric Dentistry For bruxism group: clinically diagnosed bruxism For control group: absence of clinical signs of bruxism Written obtained from parent/legal guardian

Exclusion criteria

Exclusion Criteria:

Absence of signed Presence of chronic or systemic diseases

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
Prospective
Enrollment
100 participants (estimated)
Patient registry
No

Groups and cohorts

  • Bruxism Group

    Children aged 8-11 years with clinically diagnosed bruxism.

  • Control Group

    Children aged 8-11 years without clinical signs of bruxism.

06

What researchers measure

Primary outcomes

  1. Association between child perceived stress level and bruxism status

    Child perceived stress level assessed by the Perceived Stress Scale for Children (8-11 years); association with bruxism status (yes/no).

    Time frame: Baseline

Secondary outcomes

  1. Association between parenting-related stress and child bruxism status

    Parenting-related stress level assessed by the Parenting Stress Scale; association with child bruxism status.

    Time frame: Baseline

  2. Association between parental perceived stress level and child bruxism status

    Parental perceived stress level assessed by the Perceived Stress Scale (PSS); association with child bruxism status.

    Time frame: Baseline

  3. Association between parental awareness of child stress/anxiety and child bruxism status

    Parental awareness of child stress/anxiety assessed by the SCARED - Parent Form; association with child bruxism status.

    Time frame: Baseline

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No — Individual participant data (IPD) will not be shared.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Mar 2026; primary completion for Apr 2026, 1 month later.

Of 13 observational studies under Bruxism, half reached primary completion within 15 months of starting (the median), counting those still running; a quarter within 7 and three quarters within 28. This study's planned 1 month is below that.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 20, 2026
First posted
Feb 25, 2026
StartEst.
Mar 1, 2026
Primary completionEst.
Apr 1, 2026
CompletionEst.
Apr 15, 2026
Last update
Feb 25, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 25, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07433595
Responsible party
Basak Gunay (Principal Investigator, Bezmialem Vakif University) — Principal investigator
First posted
Feb 25, 2026
Start date
Mar 1, 2026 (estimated)
Primary completion
Apr 1, 2026 (estimated)
Completion
Apr 15, 2026 (estimated)
Last update
Feb 25, 2026

Study contacts

Başak Günay, DDS
Contact
dtbasakgunay@gmail.com
00905072929002
Narmin Soylu, DDS
Contact
dt.n.mammadli@gmail.com
00905522824827
Başak Günay, DDS
study director · Bezmialem Vakif University

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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